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Basso W, Moré G, Gliga D, Marti I, Müller N, Lundström-Stadelmann B, Frey CF. Detection of Trichinella spp. in free-ranging carnivores and wild boars in Switzerland. Vet Parasitol 2025; 336:110454. [PMID: 40147099 DOI: 10.1016/j.vetpar.2025.110454] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/08/2024] [Revised: 02/21/2025] [Accepted: 03/13/2025] [Indexed: 03/29/2025]
Abstract
Wolves (Canis lupus lupus) and lynx (Lynx lynx) are officially monitored species in Switzerland. Deceased individuals are subjected to post-mortem examination and collection of baseline health data. The procedure includes an assessment of different infectious agents, including Trichinella spp., the cause of a notifiable zoonotic infection. Between May 2009 and May 2023, a total of 100 wolves and 250 lynx were tested at the National Reference Laboratory for Trichinellosis by the artificial digestion method. Additionally, muscle samples from 8838 wild boars (Sus scrofa), 27 red foxes (Vulpes vulpes), and 23 European badgers (Meles meles), mainly submitted by Swiss hunters, were also analysed for Trichinella infection. Trichinella spp. larvae were detected in 16/100 (16 %) wolves, 41/250 (16.4 %) lynx, 2/27 (7.4 %) red foxes, 0/23 (0 %) badgers, and 1/8838 (0.01 %) wild boars. All positive samples were further tested by multiplex PCR to identify the parasite at the species/genotype level. Two species were detected: T. britovi (in 14 wolves, 33 lynx, 2 red foxes and 1 wild boar) and T. spiralis (in one lynx). In nine cases, the molecular identification was not possible. Although no cases of Trichinella spp. infection in domestic swine and horses were detected in the last decades in Switzerland, we revealed that these parasites, most frequently T. britovi, are still present in Swiss wildlife. Therefore, inspection of game meat remains very important, and the occurrence of sporadic infection in domestic animals cannot be excluded.
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Affiliation(s)
- Walter Basso
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122 3012, Bern, Switzerland.
| | - Gastón Moré
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122 3012, Bern, Switzerland
| | - Diana Gliga
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122 3012, Bern, Switzerland
| | - Iris Marti
- Institute for Fish and Wildlife Health, Vetsuisse Faculty, University of Bern, Länggassstrasse 122 3012, Bern, Switzerland
| | - Norbert Müller
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122 3012, Bern, Switzerland
| | - Britta Lundström-Stadelmann
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122 3012, Bern, Switzerland; Multidisciplinary Center for Infectious Diseases, University of Bern, Hallerstrasse 6, Bern 3012, Switzerland
| | - Caroline F Frey
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122 3012, Bern, Switzerland
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2
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Mahmoud YS, El-Wakil ES, Elsayad MH, Khodear GAM, Kazem A, Elhadad H. Metformin innovative repurposing as anti-parasitic drug in the treatment of murine trichinosis. J Helminthol 2025; 99:e55. [PMID: 40275564 DOI: 10.1017/s0022149x25000276] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 04/26/2025]
Abstract
Benzimidazoles are the most frequently prescribed therapeutic options for treating trichinellosis in clinical settings; however, they have a lot of disadvantages. Therefore, researchers are focusing on the hunt for substitute chemicals. The goal of the current study was to compare the effectiveness of albendazole and the anti-diabetic medication metformin loaded on chitosan nanoparticles in treating mice infected with various stages of T. spiralis infection. 160 mice were included in the present study and divided into 8 groups: 6 experimentally treated groups, and positive and negative control groups. For studying the intestinal and parenteral phase, each group was broken into two more subgroups (a and b) according to the time of drug administration. The effects of albendazole, albendazole-loaded NPs, metformin, metformin-loaded NPs, combined albendazole and metformin, and metformin and albendazole-loaded NPs were assessed using parasitological studies, histopathological examination, and ultrastructural examination using SEM.Statistically significant differences were detected in all studied subgroups compared to the control infected subgroup both in the intestinal and muscular phases. The greatest decrease in recovered adult worm and muscle larvae numbers was achieved by ABZ & MET/ Cs NPs. These findings were confirmed by histopathological examination. SEM examination of the tegument of T. spirals adult worms and muscle larvae showed destruction with multiple degenerative changes.Our results suggested that metformin and its combination with albendazole especially when loaded on chitosan nanoparticles could be potential therapeutic alternative drugs against trichinellosis.
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Affiliation(s)
- Y S Mahmoud
- Misr University for Science and Technology, 6th of October, Egypt
| | - E S El-Wakil
- Department of Parasitology, Theodor Bilharz Research Institute, Giza, Egypt
| | - M H Elsayad
- Department of Parasitology, Medical Research Institute, Alexandria University, Alexandria, Egypt
| | - G A M Khodear
- Medical Technology Centre, Medical Research Institute, Alexandria University, Egypt
| | - A Kazem
- Department of Pathology, Medical Research Institute, Alexandria University, Egypt
| | - H Elhadad
- Department of Parasitology, Medical Research Institute, Alexandria University, Alexandria, Egypt
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3
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Hammad SK, Almotayam MH, Mohamed ASN, Farag TI. The impact of ivermectin-loaded solid lipid nanoparticles on the enteric phase of experimental trichinellosis. J Helminthol 2025; 99:e53. [PMID: 40260506 DOI: 10.1017/s0022149x2500029x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 04/23/2025]
Abstract
Trichinellosis is a global zoonotic disease affecting humans and nearly all animal species. The intestinal (enteric) phase of trichinellosis is critical, as it determines the course and prognosis of the disease. The medications used in the management of trichinellosis demonstrate inadequate bioavailability, along with a significant level of resistance. Therefore, there is a need for the development of novel agents that enhance the bioavailability of administered medications. Nanobiotechnology has emerged as a significant strategy in treating parasitic diseases. This study examined the use of solid lipid nanoparticles (SLNs) to improve the efficacy of oral ivermectin (IVM) in treating the enteric phase of trichinellosis. Thirty-five Swiss albino mice were divided into seven equal groups as follows: negative control, positive control, albendazole, ivermectin, SLNs, ivermectin loaded on solid lipid nanoparticles (IVM-SLNs), and a combination of IVM-SLNs and albendazole. Mice were sacrificed on the seventh day post-infection. The drugs' effects were assessed using parasitological, biochemical, histological, histochemical and immunohistochemical analyses. The co-administration of albendazole and IVM-SLNs resulted in a significant decrease in adult burden, inflammatory cell infiltration, and apoptosis. Furthermore, a significant reduction in Cyclooxygenase-2 (COX-2) expression was observed compared to the infected untreated control group, along with improved liver and kidney function indices. In conclusion, the potent trichinocidal effect of a single oral dose of IVM-SLNs against Trichinella adults makes them a promising alternative or adjunct to existing nematicidal agents.
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Affiliation(s)
- S K Hammad
- Department of Medical Parasitology, Faculty of Medicine, Zagazig University, Zagazig, Egypt
| | - M H Almotayam
- Department of Medical Parasitology, Faculty of Medicine, Zagazig University, Zagazig, Egypt
| | - A S N Mohamed
- Department of Medical Parasitology, Fakous Faculty of Medicine, Fakous, Egypt
| | - T I Farag
- Department of Medical Parasitology, Faculty of Medicine, Zagazig University, Zagazig, Egypt
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Ahmed S, Raja J. Arthritis related to parasitic infections. Best Pract Res Clin Rheumatol 2025:102062. [PMID: 40240207 DOI: 10.1016/j.berh.2025.102062] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/28/2025] [Revised: 03/25/2025] [Accepted: 03/26/2025] [Indexed: 04/18/2025]
Abstract
Various parasitic infections can manifest with symptoms resembling inflammatory rheumatic diseases. Parasitic arthritis is uncommon, and the literature concerning rheumatic manifestations of specific parasitic infections tends to be limited to case reports. Despite its rarity, parasitic infections should always be included in the differential diagnosis of rheumatic presentations when there is a history of risk factors, particularly in patients from endemic regions and in atypical rheumatic presentations. Specific treatment of the parasitic infection often leads to significant improvement or resolution of symptoms. This account discusses various parasites that have been reported to be associated with arthritis and other related musculoskeletal manifestations.
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Affiliation(s)
- Shaheed Ahmed
- Division of Rheumatology, Department and Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia; Department of Medicine, Indira Gandhi Memorial Hospital, Male, Republic of Maldives.
| | - Jasmin Raja
- Division of Rheumatology, Department and Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia
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5
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Basso W, Moré G, Pischon H, Merz S, Beres A, Norkus P, Frey CF, Pantchev N. Cutaneous abdominal biopsy enabled the diagnosis of clinical Trichinella britovi infection in a hunting dog. Vet Parasitol 2025; 335:110433. [PMID: 40043332 DOI: 10.1016/j.vetpar.2025.110433] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/31/2024] [Revised: 02/20/2025] [Accepted: 02/21/2025] [Indexed: 03/16/2025]
Abstract
A six-year-old mixed-breed female hunting dog, which has been imported from Bulgaria to Germany, was admitted to a private veterinary clinic presenting a swelling (approx. 10 ×10 x 1 cm) with ulceration of the skin on the left abdominal flank. The dog evidenced difficulty to climb the stairs. The mass including skin and subcutaneous tissues was surgically removed and submitted for routine histological examination. Microscopically, a severe pyogranulomatous to mixed-cellular and lymphoplasmacytic inflammation, with demarcating fibrosis, involving cutis, subcutis and cutaneous muscle was observed. Multiple cyst-like structures (∼0.25 mm diameter) with an eosinophilic hyalinised wall, containing nematode larvae sections (∼26 µm wide) were detected intralesional, and a Trichinella infection was suspected. Consequently, DNA was extracted from formalin-fixed paraffin-embedded tissues and a multiplex PCR for Trichinella species/genotype identification was performed. After electrophoresis, two bands of 129 and 253 bp were observed, which corresponds to the banding pattern of T. britovi. Trichinella T8 and T9 show a similar banding pattern; however, these genotypes are assumed to exclusively circulate in sub-Saharan Africa and Japan, respectively. The localisation of Trichinella in the cutaneous muscle, and the high degree and extension of inflammatory reaction observed are unusual. Consumption of hunted prey was assumed as the most probable source of infection. Trichinella spp. should be considered in the differential diagnosis of nematodes, which may be observed in cutaneous and muscular biopsies in dogs.
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Affiliation(s)
- Walter Basso
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122, Bern 3012, Switzerland.
| | - Gastón Moré
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122, Bern 3012, Switzerland
| | - Hannah Pischon
- IDEXX Laboratories, Humboldtstr. 2, Kornwestheim 70806, Germany
| | - Sophie Merz
- IDEXX Laboratories, Humboldtstr. 2, Kornwestheim 70806, Germany
| | - Annemarie Beres
- Kleintierpraxis Norkus, Ostcharweg 101, Recklinghausen 45665, Germany
| | - Pierre Norkus
- Kleintierpraxis Norkus, Ostcharweg 101, Recklinghausen 45665, Germany
| | - Caroline F Frey
- Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggassstrasse 122, Bern 3012, Switzerland
| | - Nikola Pantchev
- IDEXX Laboratories, Humboldtstr. 2, Kornwestheim 70806, Germany
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6
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Golinar Oven I, Gorišek M, Posedi J. First detection of Trichinella nativa in red foxes (Vulpes vulpes) in Slovenia. Vet Parasitol 2025; 335:110424. [PMID: 39978293 DOI: 10.1016/j.vetpar.2025.110424] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/28/2024] [Revised: 02/13/2025] [Accepted: 02/15/2025] [Indexed: 02/22/2025]
Abstract
Trichinella spp. is the zoonotic agent that causes trichinellosis in humans. It is traditionally associated mainly with undercooked meat from susceptible species such as domestic and wild pigs and other wild animals containing Trichinella larvae. In the present study, we investigated the prevalence and species distribution of Trichinella spp. in red foxes (Vulpes vulpes) in Slovenia during the 2020-2021 hunting season. Six hundred and eighty red fox samples were examined and the presence of Trichinella spp. larvae was confirmed in six cases (0.8 %). Using multiplex PCR, T. britovi was detected in five cases and T. nativa in one case. The occurrence of T. nativa on the southern side of the Alps is of great epidemiological importance and raises very important public health issues.
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Affiliation(s)
- Irena Golinar Oven
- Clinic for Ruminants and Pigs, Clinic for Reproduction and Large Animals, Veterinary Faculty, University of Ljubljana, Ljubljana 1000, Slovenia.
| | - Maja Gorišek
- Unit for Parasitology, Institute of Microbiology and Parasitology, Veterinary Faculty, University of Ljubljana, Ljubljana 1000, Slovenia; National Reference Laboratory for Parasites, National Veterinary Institute, Veterinary Faculty, University of Ljubljana, Ljubljana 1000, Slovenia.
| | - Janez Posedi
- Unit for Parasitology, Institute of Microbiology and Parasitology, Veterinary Faculty, University of Ljubljana, Ljubljana 1000, Slovenia; National Reference Laboratory for Parasites, National Veterinary Institute, Veterinary Faculty, University of Ljubljana, Ljubljana 1000, Slovenia.
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7
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Dabrowska M, Kępczyńska A, Goździk K, Nowak N, Uram Ł, Skoneczny M, Doligalska M, Sikora E. Expression of angiogenic factors in the mammalian senescent cell sustaining Trichinella spp. muscle larvae. Histochem Cell Biol 2025; 163:33. [PMID: 40029443 DOI: 10.1007/s00418-025-02363-8] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 02/11/2025] [Indexed: 03/05/2025]
Abstract
Muscle larvae of the mammalian parasitic nematode Trichinella spp. live in a senescent nurse cell (NC). The NC is formed from a portion of the invaded myofiber and muscle satellite cells that fuse with it. In continuation of our previous research, which documented a senescent phenotype in a fully developed NC analyzed 7 months post-infection, we show in this current study that cellular senescence is a primary event during NC establishment, and occurs as early as 26 days post-infection. At both stages of the formation process, 26 days and 7 months post-infection, the NC was found to express angiogenic factors: angiopoietin 2, interleukin 1β, matrix metallopeptidase 2, platelet-derived growth factor D, and vascular endothelial growth factor C. We hypothesize that the nuclei of the degenerating myofiber transforms the senescent program to the fusing satellite cells. Hypersecretory activity of the senescent NC may facilitate the development of a circulatory rete, which has long been known to accompany the formation of the NC-larva complex.
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Affiliation(s)
- Magdalena Dabrowska
- Laboratory of Molecular Bases of Ageing, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-093, Warsaw, Poland.
- Laboratory of Electron Microscopy, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-093, Warsaw, Poland.
| | - Agnieszka Kępczyńska
- Laboratory of Electron Microscopy, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-093, Warsaw, Poland
| | - Katarzyna Goździk
- Department of Parasitology, Institute of Experimental Zoology, Faculty of Biology, University of Warsaw, 1 Miecznikowa St., 02-089, Warsaw, Poland
| | - Natalia Nowak
- Laboratory of Imaging Tissue Structure and Function, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-093, Warsaw, Poland
| | - Łukasz Uram
- Faculty of Chemistry, Rzeszow University of Technology, 6 Powstancow Warszawy Ave., 35-959, Rzeszow, Poland
| | - Marek Skoneczny
- Laboratory of Yeast Genetics and Molecular Biology, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 5a Pawinskiego St., 02-106, Warsaw, Poland
| | - Maria Doligalska
- Department of Parasitology, Institute of Experimental Zoology, Faculty of Biology, University of Warsaw, 1 Miecznikowa St., 02-089, Warsaw, Poland
| | - Ewa Sikora
- Laboratory of Molecular Bases of Ageing, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-093, Warsaw, Poland
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Burns JE, Mhapankar G, Kilabuk E, Penner J. Zoonoses dans l’Arctique canadien. CMAJ 2025; 197:E217-E228. [PMID: 40032290 PMCID: PMC11879373 DOI: 10.1503/cmaj.240541-f] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 03/05/2025] Open
Affiliation(s)
- James E Burns
- Département de médecine de laboratoire et de pathobiologie (Burns), University of Toronto; Département de microbiologie (Burns), Mount Sinai Hospital, Toronto, Ont.; Département des maladies infectieuses pédiatriques (Mhapankar, Penner), Centre hospitalier pour enfants de l'est de l'Ontario, Département de pédiatrie (Mhapankar, Penner), Université d'Ottawa; Département de médecine interne (Kilabuk), L'Hôpital d'Ottawa, Ottawa, Ont. Départements de médecine (Kilabuk), et de pédiatrie (Penner), Hôpital général Qikiqtani, Iqaluit, Nvt
| | - Gunjan Mhapankar
- Département de médecine de laboratoire et de pathobiologie (Burns), University of Toronto; Département de microbiologie (Burns), Mount Sinai Hospital, Toronto, Ont.; Département des maladies infectieuses pédiatriques (Mhapankar, Penner), Centre hospitalier pour enfants de l'est de l'Ontario, Département de pédiatrie (Mhapankar, Penner), Université d'Ottawa; Département de médecine interne (Kilabuk), L'Hôpital d'Ottawa, Ottawa, Ont. Départements de médecine (Kilabuk), et de pédiatrie (Penner), Hôpital général Qikiqtani, Iqaluit, Nvt
| | - Elaine Kilabuk
- Département de médecine de laboratoire et de pathobiologie (Burns), University of Toronto; Département de microbiologie (Burns), Mount Sinai Hospital, Toronto, Ont.; Département des maladies infectieuses pédiatriques (Mhapankar, Penner), Centre hospitalier pour enfants de l'est de l'Ontario, Département de pédiatrie (Mhapankar, Penner), Université d'Ottawa; Département de médecine interne (Kilabuk), L'Hôpital d'Ottawa, Ottawa, Ont. Départements de médecine (Kilabuk), et de pédiatrie (Penner), Hôpital général Qikiqtani, Iqaluit, Nvt
| | - Justin Penner
- Département de médecine de laboratoire et de pathobiologie (Burns), University of Toronto; Département de microbiologie (Burns), Mount Sinai Hospital, Toronto, Ont.; Département des maladies infectieuses pédiatriques (Mhapankar, Penner), Centre hospitalier pour enfants de l'est de l'Ontario, Département de pédiatrie (Mhapankar, Penner), Université d'Ottawa; Département de médecine interne (Kilabuk), L'Hôpital d'Ottawa, Ottawa, Ont. Départements de médecine (Kilabuk), et de pédiatrie (Penner), Hôpital général Qikiqtani, Iqaluit, Nvt.
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9
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Waly WR, Ismail MAGM, Ghieth MA, Abdel Gawad SS, El-Wakil ES, Abd El Wahab WM, Ahmed MM, Mousa AMA, Ali MI. Investigating therapeutic efficacy of silymarin on intestinal and muscular phases of trichinellosis: an experimental study. J Parasit Dis 2025; 49:111-120. [PMID: 39975605 PMCID: PMC11833028 DOI: 10.1007/s12639-024-01735-6] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/27/2024] [Accepted: 09/03/2024] [Indexed: 02/21/2025] Open
Abstract
Trichinellosis, one of the parasitic zoonoses, is treated with a benzimidazole derivative, primarily albendazole. However, this treatment has a lot of side effects and is not sufficiently effective in killing the encysted larvae. Silymarin, a polyphenolic flavonoid, has been proven to have anti-parasitic activities and various medical uses. The current study aimed to evaluate silymarin efficacy against intestinal and muscular phases of murine trichinellosis compared to the standard drug; albendazole. Forty-eight mice were divided into four discrete groups: healthy model; diseased model; silymarin treatment; and albendazole treatment. The assessment of therapy efficacy was conducted parasitologically through counting the adult worms and muscle larvae, histopathologically through examination of the intestinal and muscular tissues, and, immunohistochemically through muscular expression of the vascular endothelial growth factor. Both silymarin and albendazole-treated groups demonstrated a statistically significant decrease (P < 0.001) in the mean count of adult Trichinella and the encysted larvae when compared to the diseased model, with an improvement of intestinal and muscular inflammation, and degeneration of the encysted larvae in muscles. Also, vascular endothelial growth factor immunoreactivity was significantly reduced in both silymarin, and albendazole-treated groups compared to the diseased model. Silymarin recorded antiparasitic, anti-inflammatory, and antiangiogenic effects on experimental trichinellosis.
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Affiliation(s)
- Walaa Ramadan Waly
- Department of Medical Parasitology, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt
| | | | - Marwa Ahmed Ghieth
- Department of Medical Parasitology, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt
| | - Samah Sayed Abdel Gawad
- Department of Medical Parasitology, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt
| | - Eman Sayed El-Wakil
- Department of Parasitology, Theodor Bilharz Research Institute, Kornaish El-Nile St, Giza, 12411 Egypt
| | | | - Marwa Mohamed Ahmed
- Department of Pathology, College of Medicine, Beni-Suef University, Beni-Suef, Egypt
| | - Amr M. A. Mousa
- Department of Pathology, King Salman International University, Tur Sinai, Egypt
| | - Mona Ibrahim Ali
- Department of Medical Parasitology, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt
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10
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El-Saidy SA, El-Feki AS, El-Khodary GM, Hassan AAA, Elgendy DI, Gawaan YM. A potential therapeutic effect of sea cucumber Holothuria polii extract during the intestinal phase of experimental trichinellosis. J Parasit Dis 2025; 49:224-241. [PMID: 39975624 PMCID: PMC11832982 DOI: 10.1007/s12639-024-01737-4] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/26/2024] [Accepted: 09/11/2024] [Indexed: 02/21/2025] Open
Abstract
Trichinellosis is a severe parasitic disease transmitted by food, specifically caused by Trichinella spiralis, which exhibits great clinical importance worldwide. Albendazole (ABZ) is the main clinical treatment for trichinellosis but has some adverse effects and drug resistance. Sea cucumber Holothuria polii is an essential source of beneficial therapeutic metabolites. Hence, the purpose of the present study was to explore the potential therapeutic effectiveness of H. polii extract (HPE) during the intestinal phase of trichinellosis and the possibility of using it as a supplement to ABZ. For this purpose, mice were divided into a control group and four T. spiralis-infected groups: infected untreated, infected and ABZ-treated, infected and HPE-treated, and infected and combined therapy-treated groups. The treatment with the combined therapy decreased parasitic load by 96.76%, caused deleterious effects on the adult worm cuticle, improved jejunum histological architecture, diminished intestinal inflammatory cytokines, and decreased oxidative damage compared with the infected untreated group and ABZ-treated group. The ameliorating effect of HPE could be due to its total antioxidant capacity content and the presence of natural anti-inflammatory and antioxidant agents like saponins, phenolics, alkaloids, and flavonoids. In conclusion, HPE has a multifaceted, effective impact on trichinellosis and can be considered an ABZ-promising complementary treatment.
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Affiliation(s)
- Salwa A. El-Saidy
- Zoology Department, Faculty of Science, Damanhour University, Damanhour, 22511 Egypt
| | - Asmaa S. El-Feki
- Zoology Department, Faculty of Science, Damanhour University, Damanhour, 22511 Egypt
| | - Gihan M. El-Khodary
- Zoology Department, Faculty of Science, Damanhour University, Damanhour, 22511 Egypt
| | - Amal A. A. Hassan
- Zoology Department, Faculty of Science, Damanhour University, Damanhour, 22511 Egypt
| | - Dina I. Elgendy
- Medical Parasitology Department, Faculty of Medicine, Tanta University, Tanta, Egypt
| | - Yasmeen M. Gawaan
- Zoology Department, Faculty of Science, Damanhour University, Damanhour, 22511 Egypt
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11
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Mira NM, Henaish AM, Moussa EA, Helal IB, Kasem SM. Improved antiparasitic effects of mebendazole using chitosan and zinc oxide nanocomposites for drug delivery in Trichinella spiralis infected mice during the muscular phase. Acta Trop 2025; 263:107565. [PMID: 39986444 DOI: 10.1016/j.actatropica.2025.107565] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/08/2025] [Revised: 02/06/2025] [Accepted: 02/19/2025] [Indexed: 02/24/2025]
Abstract
This study was performed to assess the use of chitosan (Cs) and zinc oxide nanocomposites ZnO NCP with full and half dose mebendazole (MBZ) during the muscular phases of Trichinella spiralis infection. Sixty Swiss Albino male mice were divided into six groups: G1 (negative control), G2 (positive control), G3 (MBZ at 200 mg/kg/day), G4 (Cs@MBZ NCP at 400 mg/kg/day), G5 (Cs@MBZ400.ZnO NCP), and G6 (Cs@MBZ200.ZnO NCP). Mice were infected orally with 200 T. spiralis larvae and received treatments starting on day 35 post-infection for five consecutive days. Treatment outcomes were evaluated by counting total muscular larvae, conducting blood biochemical measurements, and performing histopathological examinations of the liver and hip joint muscles. ELISA was used to measure serum levels of transforming growth factor-beta1 (TGF-β1), tumor necrosis factor-alpha (TNF-α), and vascular endothelial growth factor (VEGF). Results indicated that both Cs@MBZ400.ZnO NCP and Cs@MBZ200.ZnO NCP groups exhibited significant reductions in muscular larval counts (96.4 % and 96.1 %, respectively). Treated mice also showed reduced AST and ALT levels, increased total protein and albumin, and decreased globulin levels compared to positive controls. Cytokines levels of TNF-α, TGF-β1, and VEGF were lower in treated groups. Histopathological examination revealed that Cs@MBZ400.ZnO and Cs@MBZ200.ZnO NCP restored up to 90 % of normal tissue architecture. In conclusion, chitosan and zinc oxide nanocomposites enhanced the therapeutic ability of mebendazole against T. spiralis muscular stage as these nanocomposites had the highest effect on reducing parasite burden, improving blood biochemical, decreasing cytokines levels and restoring normal histological architecture.
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Affiliation(s)
- Nabila M Mira
- Zoology Department, Faculty of Science, Kafrelsheikh University, Kafr Elsheikh 33516, Egypt
| | - Aya M Henaish
- Zoology Department, Faculty of Science, Kafrelsheikh University, Kafr Elsheikh 33516, Egypt
| | - Eman A Moussa
- Zoology Department, Faculty of Science, Kafrelsheikh University, Kafr Elsheikh 33516, Egypt
| | - Ibrahim B Helal
- Zoology Department, Faculty of Science, Tanta University, Tanta 31527, Egypt
| | - Shaimaa M Kasem
- Zoology Department, Faculty of Science, Kafrelsheikh University, Kafr Elsheikh 33516, Egypt.
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12
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Liu X, Zhang B, Zhang Z, Wang X, Zhang T, Huang H, Shi C, Yang W, Jiang Y, Cao X, Wang J, Zeng Y, Wang C, Wang N, Yang G. Interleukin-13 partly induced by the NLRP3 inflammasome promotes Trichinella spiralis encapsulation in infected mice. Vet Parasitol 2025; 334:110386. [PMID: 39732108 DOI: 10.1016/j.vetpar.2024.110386] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/26/2024] [Revised: 12/19/2024] [Accepted: 12/23/2024] [Indexed: 12/30/2024]
Abstract
Trichinella spiralis infection is a serious parasitic zoonosis in which a collagenous capsule surrounding the larva is developed in the striated muscle cells. However, the mechanism of T. spiralis encapsulation is currently poorly understood. It has been reported that T. spiralis infection can induce the production of IL-13 via the NLRP3 inflammasome, and it has also been suggested IL-13 thus produced may be involved in T. spiralis encapsulation. This research aimed to clarify the involvement of NLRP3 and IL-13 in the T. spiralis capsule formation process. IL-13 and NLRP3 inhibitors were used in a T. spiralis infected mouse model and in C2C12 cells to analyze the role of IL-13 and NLRP3 in encapsulation. The results showed that T. spiralis infection significantly increased the expression levels of IL-13 and collagen IV and VI. The production of collagen around the T. spiralis encapsulation zone was significantly inhibited when an IL-13 inhibitor was applied. Moreover, the expression levels of IL-13 and collagen IV and VI were significantly decreased by the NLRP3 inhibitor in vitro and in vivo. The above results indicated that NLRP3 can participate in the development of T. spiralis encapsulation by regulating IL-13 expression and stimulating collagen IV and VI synthesis during T. spiralis infection.
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Affiliation(s)
- Xuanrui Liu
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Bo Zhang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Zhiyuan Zhang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Xueting Wang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Tongxuan Zhang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Haibin Huang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Chunwei Shi
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Wentao Yang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Yanlong Jiang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Xin Cao
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Jianzhong Wang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Yan Zeng
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Chunfeng Wang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Nan Wang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
| | - Guilian Yang
- College of Veterinary Medicine, Jilin Agricultural University, Changchun 130118, China; Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Jilin Agricultural University, Changchun 130118, China; Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.
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13
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Thakker C, Warrell C, Barrett J, Booth HL, Chiodini PL, Defres S, Falconer J, Jacobs N, Jones J, Lambert J, Leong C, McBride A, Moore E, Moshiri T, Nabarro LE, O'Hara G, Stone N, van Halsema C, Checkley AM. UK guidelines for the investigation and management of eosinophilia in returning travellers and migrants. J Infect 2025; 90:106328. [PMID: 39537036 DOI: 10.1016/j.jinf.2024.106328] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/10/2024] [Accepted: 10/20/2024] [Indexed: 11/16/2024]
Abstract
Eosinophilia is a common finding in returning travellers, migrants and other travelling groups. In this setting, it often indicates an underlying helminth infection. Infections associated with eosinophilia are frequently either asymptomatic or associated with non-specific symptoms but some can cause severe disease. Here the British Infection Association guidelines group has comprehensively reviewed and updated the UK recommendations for the investigation and management of eosinophilia in returning travellers, migrants and other relevant groups, first published in 2010.1 Literature reviews have been undertaken to update the evidence on the prevalence and causes of eosinophilia in these groups and on the treatment of relevant pathogens and clinical conditions. Diagnostic tests available to UK-based clinicians are summarised. Changes made to the guidelines include updates in the sections on the investigation and empirical treatment of asymptomatic eosinophilia and on the treatment of trichuriasis, lymphatic filariasis, onchocerciasis, hookworm, fascioliasis and taeniasis. Pathogens which are rarely encountered in UK practice have been removed from the guidelines and others added, including an expanded section on fungal infection. A section on off-license and rarely used drugs has been included.
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Affiliation(s)
- Clare Thakker
- Hospital for Tropical Diseases, Capper Street, London, WC1E 6JB, UK; University College London, Gower Street, London, WC1E 6BT, UK.
| | - Clare Warrell
- Hospital for Tropical Diseases, Capper Street, London, WC1E 6JB, UK; Rare and Imported Pathogens Laboratory, UKHSA, Porton Down, SP4 0JG, UK; London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK
| | - Jessica Barrett
- North Bristol NHS Trust, Southmead Hospital, Southmead Road, Westbury-on-Trym, Bristol, BS10 5NB, UK
| | - Helen L Booth
- University College London Hospitals NHS Trust, 235 Euston Road, London, NW1 2BU, UK
| | - Peter L Chiodini
- Hospital for Tropical Diseases, Capper Street, London, WC1E 6JB, UK; London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK
| | - Sylviane Defres
- Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, UK; Liverpool University Hospitals NHS Foundation Trust, Mount Vernon Street, Liverpool, L7 8XP, UK; Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L69 7BE, UK
| | - Jane Falconer
- London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK
| | - Nathan Jacobs
- Regional Infectious Diseases Unit, North Manchester General Hospital, Manchester University NHS Foundation Trust, M8 5RB, UK
| | - Jayne Jones
- Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, UK
| | - Jonathan Lambert
- University College London Hospitals NHS Trust, 235 Euston Road, London, NW1 2BU, UK; UCL Cancer Institute, 72 Huntley St, London, WC1E 6DD, UK
| | - Clare Leong
- Cambridge University Hospitals, Addenbrookes Hospital, Hills Rd, Cambridge, CB2 0QQ, UK
| | - Angela McBride
- Kings College Hospital, Denmark Hill, London, SE5 9RS, UK; University of Oxford, Oxford, OX1 2JD, UK
| | - Elinor Moore
- Cambridge University Hospitals, Addenbrookes Hospital, Hills Rd, Cambridge, CB2 0QQ, UK
| | - Tara Moshiri
- Nottingham University Hospitals NHS Trust, Nottingham, NG5 1PB, UK
| | - Laura E Nabarro
- Hospital for Tropical Diseases, Capper Street, London, WC1E 6JB, UK
| | | | - Neil Stone
- University College London Hospitals NHS Trust, 235 Euston Road, London, NW1 2BU, UK
| | - Clare van Halsema
- Regional Infectious Diseases Unit, North Manchester General Hospital, Manchester University NHS Foundation Trust, M8 5RB, UK
| | - Anna M Checkley
- Hospital for Tropical Diseases, Capper Street, London, WC1E 6JB, UK; London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK.
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14
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Burns JE, Mhapankar G, Kilabuk E, Penner J. Zoonotic infections of the Canadian Arctic. CMAJ 2025; 197:E34-E43. [PMID: 39832930 PMCID: PMC11745538 DOI: 10.1503/cmaj.240541] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/22/2025] Open
Affiliation(s)
- James E Burns
- Department of Laboratory Medicine and Pathobiology (Burns), University of Toronto; Department of Microbiology (Burns), Mount Sinai Hospital, Toronto, Ont.; Department of Pediatric Infectious Diseases (Mhapankar, Penner), Children's Hospital of Eastern Ontario, Department of Pediatrics (Mhapankar, Penner), University of Ottawa; Department of Internal Medicine (Kilabuk), The Ottawa Hospital, Ottawa, Ont. Departments of Medicine (Kilabuk), and of Pediatrics (Penner), Qikiqtani General Hospital, Iqaluit, Nvt
| | - Gunjan Mhapankar
- Department of Laboratory Medicine and Pathobiology (Burns), University of Toronto; Department of Microbiology (Burns), Mount Sinai Hospital, Toronto, Ont.; Department of Pediatric Infectious Diseases (Mhapankar, Penner), Children's Hospital of Eastern Ontario, Department of Pediatrics (Mhapankar, Penner), University of Ottawa; Department of Internal Medicine (Kilabuk), The Ottawa Hospital, Ottawa, Ont. Departments of Medicine (Kilabuk), and of Pediatrics (Penner), Qikiqtani General Hospital, Iqaluit, Nvt
| | - Elaine Kilabuk
- Department of Laboratory Medicine and Pathobiology (Burns), University of Toronto; Department of Microbiology (Burns), Mount Sinai Hospital, Toronto, Ont.; Department of Pediatric Infectious Diseases (Mhapankar, Penner), Children's Hospital of Eastern Ontario, Department of Pediatrics (Mhapankar, Penner), University of Ottawa; Department of Internal Medicine (Kilabuk), The Ottawa Hospital, Ottawa, Ont. Departments of Medicine (Kilabuk), and of Pediatrics (Penner), Qikiqtani General Hospital, Iqaluit, Nvt
| | - Justin Penner
- Department of Laboratory Medicine and Pathobiology (Burns), University of Toronto; Department of Microbiology (Burns), Mount Sinai Hospital, Toronto, Ont.; Department of Pediatric Infectious Diseases (Mhapankar, Penner), Children's Hospital of Eastern Ontario, Department of Pediatrics (Mhapankar, Penner), University of Ottawa; Department of Internal Medicine (Kilabuk), The Ottawa Hospital, Ottawa, Ont. Departments of Medicine (Kilabuk), and of Pediatrics (Penner), Qikiqtani General Hospital, Iqaluit, Nvt.
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15
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Lu QQ, Zheng WW, Zhang ZY, Cong PK, Guo X, Zhang Y, Zhang XZ, Long SR, Liu RD, Wang ZQ, Cui J. Trichinella spiralis excretory/secretory proteins mediated larval invasion via inducing gut epithelial apoptosis and barrier disruption. PLoS Negl Trop Dis 2025; 19:e0012842. [PMID: 39847596 PMCID: PMC11793818 DOI: 10.1371/journal.pntd.0012842] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/01/2024] [Revised: 02/04/2025] [Accepted: 01/14/2025] [Indexed: 01/25/2025] Open
Abstract
BACKGROUND Intestinal larva invasion is a crucial step of Trichinella spiralis infection. Intestinal infective larvae (IIL) and their excretory/secretory proteins (ESP) interact with gut epithelium, which often results in gut epithelium barrier injuries. Previous studies showed when T. spiralis invaded intestinal epithelium cells, the IIL ESP disrupted the tight junctions (TJs) of Caco-2 monolayer, but the mechanism is not clear. The IIL ESP might cause gut epithelial apoptosis, weaken the gut barrier and aid the larval invasion. The aim of this study was to investigate whether T. spiralis IIL ESP participate in enterocyte apoptosis and disrupt gut epithelial barrier to promote the larval invasion. METHODOLOGY/PRINCIPAL FINDINGS Cell viability was assessed by CCK-8 assay and the results showed that 200 μg/ml of IIL ESP incubated with Caco-2 cells for 18 h inhibited the Caco-2 cell viability. The results of trans-epithelial electrical resistance (TEER) and FITC-dextran showed that IIL ESP decreased the TEER, increased FITC-dextran flux in Caco-2 monolayer. qPCR, Western blot and immunofluorescence test (IFT) showed that IIL ESP decreased the mRNA and protein expression of TJs (ZO-1, E-cad, Occludin and Claudin-1). The IIL ESP-induced Caco-2 cell apoptosis was observed by DAPI, Hoechst 33358, TUNEL and Annexin V/PI staining. Besides, flow cytometry revealed an increasing apoptosis rate in Caco-2 cells after the IIL ESP treatment. qPCR and Western blot analysis indicated that IIL ESP activated caspases (Caspase 3, Caspase 9 and Caspase 8), up-regulated the pro-apoptotic factors (Bax and Cytochrome c) and down-regulated the anti-apoptosis molecule Bcl-2. Interestingly, pretreatment of Caco-2 cells with apoptosis inhibitor Z-VAD-FMK abrogated and recovered the barrier function of Caco-2 monolayer destroyed by IIL ESP. Furthermore, the Z-VAD-FMK pretreatment also impeded the in vitro larva invasion of Caco-2 monolayer. CONCLUSIONS T. spiralis IIL ESP induced gut epithelial apoptosis, reduced the TJs expression, damaged gut epithelial integrity and barrier function, and promoted larval invasion. These findings provided a basis of further understanding the interaction mechanism between T. spiralis and host gut epithelium, and they were valuable to the development new prevention and therapeutic strategy of early T. spiralis infection.
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Affiliation(s)
- Qi Qi Lu
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Wen Wen Zheng
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Zhao Yu Zhang
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Pei Kun Cong
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Xin Guo
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Yao Zhang
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Xin Zhuo Zhang
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Shao Rong Long
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Ruo Dan Liu
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Zhong Quan Wang
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
| | - Jing Cui
- Department of Parasitology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China
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16
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Dupouy-Camet J, Bruschi F, Pozio E. Letter to the editor about "Pediatric trichinosis: A case report". Int J Surg Case Rep 2025; 126:110731. [PMID: 39667122 PMCID: PMC11697602 DOI: 10.1016/j.ijscr.2024.110731] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/06/2024] [Accepted: 12/09/2024] [Indexed: 12/14/2024] Open
Affiliation(s)
- Jean Dupouy-Camet
- Paris Cité Medical Faculty, French Veterinary Academy, Paris, France.
| | | | - Edoardo Pozio
- Department of Infectious Diseases, Istituto Superiore di Sanita, Rome, Italy
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17
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Johne A, Sachsenröder J, Richter M, Nöckler K. Trichinella findings in Germany from 2013 to 2023 indicate an increased prevalence in wild boar (Sus scrofa) population. Vet Parasitol 2025; 333:110316. [PMID: 39358070 DOI: 10.1016/j.vetpar.2024.110316] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/21/2024] [Revised: 09/06/2024] [Accepted: 09/09/2024] [Indexed: 10/04/2024]
Abstract
In Germany, Trichinella spp. are mainly detected in the sylvatic cycle. Here, the affected animal species are wild boar, fox, badger, raccoon dog, wolf, raccoon and golden jackal. The predominantly detected species are T. spiralis, followed by T. pseudospiralis and T. britovi. Due to legal requirements in Germany, all hunted wild boars and other susceptible animals must be examined for Trichinella spp. if their meat is intended for human consumption. In recent years, an increase in the number of Trichinella-positive wild boar shot in Germany has been registered and the prevalence of positive wild boar scaled up from 0.002 % to 0.005 % between 2013 and 2023. Regarding regional distribution, most Trichinella findings in wild boar have been registered in the North-Eastern part of Germany. Here, the federal states Western-Pomerania, Brandenburg and Saxony that are bordering to Poland are particularly affected. The increase in positive wild boar may be associated with the spread of raccoon dogs and wolves in these regions. Thus, measures are required to prevent the spread of Trichinella among wild animals and to follow the systematic meat inspection in susceptible wild animals intended for food especially wild boar.
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Affiliation(s)
- Annette Johne
- German Federal Institute for Risk Assessment (BfR), Department for Biological Safety, Max-Dohrn-Str. 8-10, Berlin 10589, Germany.
| | - Jana Sachsenröder
- German Federal Institute for Risk Assessment (BfR), Department for Biological Safety, Max-Dohrn-Str. 8-10, Berlin 10589, Germany.
| | - Martin Richter
- German Federal Institute for Risk Assessment (BfR), Department for Biological Safety, Max-Dohrn-Str. 8-10, Berlin 10589, Germany.
| | - Karsten Nöckler
- German Federal Institute for Risk Assessment (BfR), Department for Biological Safety, Max-Dohrn-Str. 8-10, Berlin 10589, Germany.
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18
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Krivokapich SJ, Degese MF, Gatti GM, Lopez L, Simonetti MA, Crescia MC, Calvo CD, Lapuyade CL, Cazaux N, D'Francisco FA. Molecular based confirmation of puma meat sausages implicated in trichinellosis outbreaks in Argentina. Int J Food Microbiol 2024; 425:110889. [PMID: 39214028 DOI: 10.1016/j.ijfoodmicro.2024.110889] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/22/2024] [Revised: 08/16/2024] [Accepted: 08/23/2024] [Indexed: 09/04/2024]
Abstract
Trichinellosis is a zoonotic disease caused by Trichinella, with the main source of infection being the consumption of pork and pork-derived products. However, it can also be acquired from eating the meat from wild animals targeted for sport hunting. The objectives of this study were: 1) to develop and implement a molecular method for the identification of Sus scrofa (pig and wild boar) and Puma concolor (Puma) meat in sausages eaten raw, which were linked to trichinellosis outbreaks occurring in Córdoba, Buenos Aires and La Pampa provinces, Argentina, in 2010, 2021, and 2022, respectively; and 2) to identify the Trichinella species present in the food. Specific primers were designed for PCR amplification and nucleotide sequencing of a region of the mitochondrial cytochrome b gene from both host species. Samples from the mentioned outbreaks were analysed, and the molecular identification of Trichinella spp. larvae was also performed. Results of the species identification system revealed that sausages from Córdoba and Buenos Aires had a mixed composition of pork and puma meat, while those from La Pampa contained puma meat only. Trichinella spiralis was implicated in all three outbreaks. The species identification system developed and implemented in this study revealed two host species of Trichinella related to human cases, and alerts about the risk of zoonotic transmission to humans through infected puma meat.
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Affiliation(s)
- Silvio J Krivokapich
- Departamento Parasitología, INEI, ANLIS, "Dr. Carlos G. Malbrán", CABA, Argentina.
| | - M Fernanda Degese
- Departamento Parasitología, INEI, ANLIS, "Dr. Carlos G. Malbrán", CABA, Argentina
| | - Graciana M Gatti
- Departamento Parasitología, INEI, ANLIS, "Dr. Carlos G. Malbrán", CABA, Argentina
| | - Laura Lopez
- Dirección de Jurisdicción de Epidemiología, Ministerio de Salud de Córdoba, Argentina
| | - María A Simonetti
- Secretaría de Salud, Municipalidad de Florentino Ameghino, Buenos Aires, Argentina
| | - María C Crescia
- Bromatología y Zoonosis, Municipalidad de Florentino Ameghino, Buenos Aires, Argentina
| | - Claudio D Calvo
- Cátedra de Parasitología y Enfermedades Parasitarias, Facultad de Ciencias Veterinarias, Universidad Nacional de La Pampa, Argentina
| | - Cecilia L Lapuyade
- Cátedra de Parasitología y Enfermedades Parasitarias, Facultad de Ciencias Veterinarias, Universidad Nacional de La Pampa, Argentina
| | - Natalia Cazaux
- Cátedra de Parasitología y Enfermedades Parasitarias, Facultad de Ciencias Veterinarias, Universidad Nacional de La Pampa, Argentina
| | - Florencia A D'Francisco
- Cátedra de Parasitología y Enfermedades Parasitarias, Facultad de Ciencias Veterinarias, Universidad Nacional de La Pampa, Argentina
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19
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Kindie EA, Sirak EH, Weyessa TG. Pediatric trichinosis: A case report. Int J Surg Case Rep 2024; 125:110607. [PMID: 39536674 PMCID: PMC11605389 DOI: 10.1016/j.ijscr.2024.110607] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/30/2024] [Revised: 11/09/2024] [Accepted: 11/11/2024] [Indexed: 11/16/2024] Open
Abstract
BACKGROUND Trichinellosis is a zoonosis, caused by roundworms of the genus Trichinella. Domestic pigs, wild boars, bears, rodents and horses are reservoir animals. We report a case of neck trichinosis presenting as lateral neck swelling. The diagnosis of trichinosis was confirmed by the presence of larvae on muscle biopsy. Furthermore, lateral neck swelling may provide a diagnostic challenge by clinically mimicking a lymphoma or other causes of lateral neck swelling. Due to its rarity and its tendency to pose a clinical diagnostic challenge, we decided to report it. CASE PRESENTATION A-10 yr old male patient presented with a 6 × 4 cm firm; non-tender left lateral neck swelling. Histopathology examination confirmed the diagnosis of trichinosis and the patient was started on albendazole 15 mg/kg/day, divided into two doses and prednisolone 20 mg by mouth, two times daily, for 14 days. Having completed his medication, he had a smooth course and was discharged with appointment scheduled for follow-up after 3 months. DISCUSSION Trichinella spp. occur worldwide, most frequently in regions with temperate climates. About 10,000 human infections occur annually worldwide. Cultural factors such as traditional dishes based on raw or undercooked meat or meat-derived products play an important role in the epidemiology of the disease. CONCLUSION In the clinical evaluation of a patient with lateral neck swelling, trichinosis must be considered as a differential diagnosis in subjects from endemic areas for early diagnostic workup and management.
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Mahgoub AMA, Ali MI, Abu-Sarea EY, Rady SA, Bayoumi Ali IR, Sayed DR. In vivo study of nano chitosan beads-based ELISA versus traditional sandwich ELISA for the early diagnosis of trichinosis. Exp Parasitol 2024; 268:108865. [PMID: 39613133 DOI: 10.1016/j.exppara.2024.108865] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/25/2024] [Revised: 11/13/2024] [Accepted: 11/26/2024] [Indexed: 12/01/2024]
Abstract
Human trichinosis is a serious foodborne parasitic zoonosis. Diagnosing human trichinosis is usually difficult due to the nonspecific clinical picture and the limited effectiveness of serological tests in acute infections. While ELISA can detect circulating Trichinella antigens, aiding in early diagnosis, its sensitivity may be low. The application of nanoparticles can improve the sensitivity of ELISA and allow a specific early diagnosis of the disease. This work compares the nano chitosan beads-based ELISA (NCSB-ELISA) and traditional sandwich ELISA for the detection of circulating Trichinella spiralis (T. spiralis) crude extract-antigen (CEA) in serum samples of experimentally infected mice. Fifty-seven mice included in this study were classified into 3 groups: T. spiralis infected group (Group I) (36 mice), which was equally subdivided into six subgroups according to the time of sacrifice (6, 8, 10, 12, 14 and 16) days post-infection (dpi), cross-reactivity group (Group II) (9 mice) and negative control group (Group III) (12 mice). T. spiralis AW-CEA prepared from the adult worms were used to produce anti- T. spiralis IgG-polyclonal antibodies in rabbits; these antibodies were utilized to detect AW-CEA in serum samples by traditional sandwich ELISA and NCSB-ELISA. Using NCSB-ELISA, T. spiralis AW-CEA was detected in sera collected at 8 dpi, with a sensitivity of 50% and a specificity of 100%. Meanwhile, traditional sandwich ELISA could not detect the antigen at the same time interval. Both ELISA were able to detect the antigen in samples collected at 10, 12, 14 and 16 dpi with a sensitivity of 16.67%, 50%, 67.67% and 83.67%, respectively, for traditional sandwich-ELISA and a specificity of 100% at 10, 12 and 14 dpi while at 16 dpi specificity was decreased to 90.91%. In contrast, the sensitivity of NCSB-sandwich ELISA on the same days was 66.67%, 83.34%, 100% and 100%, respectively, with a specificity of 100% at all days. False positive detection of T. spiralis AW-CEA in the serum of mice in GII was recorded on day 16 pi by only traditional sandwich ELISA. This study concluded that NCSB-ELISA is a promising and sensitive technique for the early and specific diagnosis of acute trichinosis in an animal model.
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Affiliation(s)
| | - Mona Ibrahim Ali
- Medical Parasitology, Faculty of Medicine, Beni-Suef University, Egypt.
| | | | - Sara Ahmed Rady
- Medical Parasitology, Faculty of Medicine, Nahda University, Egypt.
| | | | - Doaa Reda Sayed
- Medical Parasitology, Faculty of Medicine, Beni-Suef University, Egypt.
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Rashed HAEH, Albogami B, Alkhaldi AAM, Abuzinadah NY, Abuzahrah SS, Al-Salmi FA, Fayad E, Fouad RM, Fikry ME, ElSaey AAA, Abu Almaaty AH. Effect of vitamin C injections on exercise muscular performance and biochemical parameters in Trichinella spiralis-infected mice. PeerJ 2024; 12:e18381. [PMID: 39553708 PMCID: PMC11568815 DOI: 10.7717/peerj.18381] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/27/2024] [Accepted: 10/01/2024] [Indexed: 11/19/2024] Open
Abstract
Background Trichinella spiralis is a worldwide intestinal nematode that can parasitize the striated muscles of its hosts at the larval stage. This study aims to evaluate potential of vitamin C for treating trichinellosis-related pathological problems in the infected muscles of mice. Materials and Methods Thirty CD1 male Albino mice were divided into three groups (10 mice per group). Negative and positive control groups (0.9% NaCl) and the infected vitamin C group (10 mg/kg body weight). Two weeks post-infection, each group was intraperitoneally injected daily for two weeks with Vitamin C or saline. The performance of the muscles was assessed both before and after the treatment. After dissection, constant parts of striated muscles were removed for further assays. The scoring of the histological changes of infected muscles was carried out. In addition to muscle malondialdehyde levels, superoxide dismutase and catalase activities were measured for the oxidative and antioxidant states. Creatine kinase and aspartate aminotransferase were also measured in tissues to reflect the degree of muscular damage. Results Vitamin C enhances the weakness of the muscular performance resulting from the infection. Vitamin C was able to repair some of the histological lesions that resulted from the infection. Trichinellosis caused severe changes in the biochemical markers in positive control animals. Muscle damage biomarkers and, besides, oxidative and antioxidant conditions were greatly ameliorated in infected vitamin C animals. Summing up, vitamin C can be used as a complementary drug due to its efficiency in improving pathogenesis following a trichinellosis infection. The supplement also must be tested in the intestinal stage of infection after showing promising results in the muscular stage.
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Affiliation(s)
| | - Bander Albogami
- Department of Biology, College of Sciences, Taif University, Taif, Saudi Arabia
| | | | - Najlaa Y. Abuzinadah
- Department of Biological Sciences, College of Science, University of Jeddah, Jeddah, Saudi Arabia
| | - Samah S. Abuzahrah
- Department of Biological Sciences, College of Science, University of Jeddah, Jeddah, Saudi Arabia
| | - Fawziah A. Al-Salmi
- Department of Biology, College of Sciences, Taif University, Taif, Saudi Arabia
| | - Eman Fayad
- Department of Biotechnology, College of Sciences, Taif University, Taif, Saudi Arabia
| | - Rewan Mohamed Fouad
- Zoology Department, Faculty of Science, Port Said University, Port Said, Egypt
| | - Manar Elsayed Fikry
- Zoology Department, Faculty of Science, Port Said University, Port Said, Egypt
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22
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Gowler CD, Lee N, Morrison T, Mears V, Williams C, Fleischauer A, Wilson E. Notes from the Field: Suspected Outbreak of Trichinellosis Associated with Undercooked Bear Meat - North Carolina, November 2023. MMWR. MORBIDITY AND MORTALITY WEEKLY REPORT 2024; 73:906-907. [PMID: 39388384 PMCID: PMC11466378 DOI: 10.15585/mmwr.mm7340a4] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 10/12/2024]
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23
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El-kady AM, Altwaim SA, Wakid MH, Banjar AS, Mohammed K, Alfaifi MS, Elshazly H, Al-Megrin WAI, Alshehri EA, Sayed E, Elshabrawy HA. Prior Trichinella spiralis infection protects against Schistosoma mansoni induced hepatic fibrosis. Front Vet Sci 2024; 11:1443267. [PMID: 39439825 PMCID: PMC11494294 DOI: 10.3389/fvets.2024.1443267] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/03/2024] [Accepted: 09/23/2024] [Indexed: 10/25/2024] Open
Abstract
Background Schistosomiasis affects approximately 250 million people worldwide, with 200,000 deaths annually. It has been documented that the granulomatous response to Schistosoma mansoni (S. mansoni) oviposition is the root cause of progressive liver fibrosis in chronic infection, in 20% of the patients, and can lead to liver cirrhosis and/or liver cancer. The influence of helminths coinfection on schistosomiasis-induced liver pathological alterations remains poorly understood. Therefore, in this study, we investigated the effect of Trichinella spiralis (T. spiralis) infection on S. mansoni-induced hepatic fibrosis. Materials and methods Thirty adult male Balb-c mice were divided into three groups. Group 1 was left uninfected; group 2 was infected with S. mansoni cercariae and group 3 was orally infected with T. spiralis larvae, then 28 days later, this group was infected with S. mansoni cercariae. All groups were sacrificed at the end of the 8th week post infection with S. mansoni to evaluate the effect of pre-infection with T. spiralis on S. mansoni induced liver fibrosis was evaluated parasitologically (worm burden and egg count in tissues), biochemically (levels of alanine aminotransferase and aspartate aminotransferase), histopathologically (H&E and MT staining, and immunohistochemical staining for the expression of α-SMA, IL-6, IL-1β, IL-17, IL-23, TNF-α, and TGF-β). Results The results in the present study demonstrated marked protective effect of T. spiralis against S. mansoni induced liver pathology. We demonstrated that pre-infection with T. spirais caused marked reduction in the number of S. mansoni adult worms (3.17 ± 0.98 vs. 18 ± 2.16, P = 0.114) and egg count in both the intestine (207.2 ± 64.3 vs. 8,619.43 ± 727.52, P = 0.009) and liver tissues (279 ± 87.2 vs. 7,916.86 ± 771.34; P = 0.014). Consistently, we found significant reductions in both number (3.4 ± 1.1 vs. 11.8.3 ± 1.22; P = 0.007) and size (84 ± 11 vs. 294.3 ± 16.22; P = 0.001) of the hepatic granulomas in mice pre-infected with T. spiralis larvae compared to those infected with only S. mansoni. Furthermore, pre- infection with T. spiralis markedly reduced S. mansoni- induced hepatic fibrosis, as evidenced by decreased collagen deposition, low expression of α-SMA, and significantly reduced levels of IL-17, IL-1B, IL-6, TGF-B, IL-23, and TNF-α compared to mice infected with S. mansoni only. Conclusions Our data show that pre-infection with T. spiralis effectively protected mice from severe schistosomiasis and liver fibrosis. We believe that our findings support the potential utility of helminths for the preventing and ameliorating severe pathological alterations induced by schistosomiasis.
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Affiliation(s)
- Asmaa M. El-kady
- Department of Medical Parasitology, Faculty of Medicine, South Valley University, Qena, Egypt
| | - Sarah A. Altwaim
- Department of Clinical Microbiology and Immunology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
- Special Infectious Agents Unit, King Fahd Medical Research Center, Jeddah, Saudi Arabia
| | - Majed H. Wakid
- Special Infectious Agents Unit, King Fahd Medical Research Center, Jeddah, Saudi Arabia
- Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
| | - Alaa S. Banjar
- Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
- Center of Innovation in Personalized Medicine (CIPM), King Abdulaziz University, Jeddah, Saudi Arabia
| | - Khalil Mohammed
- Department of Epidemiology and Medical Statistics, Faculty of Public Health and Health Informatics, Umm Al-Qura University, Mecca, Saudi Arabia
| | - Mashael S. Alfaifi
- Department of Epidemiology and Medical Statistics, Faculty of Public Health and Health Informatics, Umm Al-Qura University, Mecca, Saudi Arabia
| | - Hayam Elshazly
- Department of Biology, Faculty of Sciences-Scientific Departments, Qassim University, Buraidah, Qassim, Saudi Arabia
- Department of Zoology, Faculty of Science, Beni-Suef University, Beni Suef, Egypt
| | - Wafa Abdullah I. Al-Megrin
- Department of Biology, College of Science, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia
| | | | - Eman Sayed
- Department of Parasitology, Faculty of Veterinary Medicine, South Valley University, Qena, Egypt
| | - Hatem A. Elshabrawy
- Department of Molecular and Cellular Biology, College of Osteopathic Medicine, Sam Houston State University, Conroe, TX, United States
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Villegas Pérez J, Navas González FJ, Serrano S, García Viejo F, Buffoni L. Evaluating Procedure-Linked Risk Determinants in Trichinella spp. Inspection under a Quality Management System in Southern Spain. Animals (Basel) 2024; 14:2802. [PMID: 39409751 PMCID: PMC11476041 DOI: 10.3390/ani14192802] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/02/2024] [Revised: 09/08/2024] [Accepted: 09/22/2024] [Indexed: 10/20/2024] Open
Abstract
Trichinellosis is a major foodborne zoonotic disease responsible for 41 human cases, according to the European Union One Health Zoonoses Report. In southern Spain, a quality management system (QMS) was applied to satellite laboratories (SLs) that conduct meat inspections of Trichinella spp. ensuring excellence practices. This study aimed to determine how eventual deviations from standard procedures may influence risk levels using Canonical Discriminant Analysis (CDA). Data were collected during slaughterhouses and game handling establishments' official audits in 18 SLs located in the provinces of Cordoba and Seville during a 6-year period. Technical requirement deviations regarding technique and trial information, such as performing tests or calculations incorrectly or not following technical procedures, significantly increased risk level differences. Imminent risk levels were detected if the above-mentioned deviations arose. Quality assurance compromising deviations were responsible for 1150 times risk level differences, suggesting finding such may be critical for risk determination. A lack of significant influence of records and documents compromising deviations (incomplete forms or missing-erroneous or illegible data) was found. These results strengthen Trichinella spp. control strategies by pinpointing crucial aspects within QMS that require improvement, particularly in addressing deviations related to technique, trial information, and quality assurance procedures to mitigate associated risks effectively.
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Affiliation(s)
| | | | - Salud Serrano
- Departamento de Bromatología y Tecnología de los Alimentos, Universidad de Córdoba, 14014 Córdoba, Spain;
| | | | - Leandro Buffoni
- Departamento de Sanidad Animal, Área de Parasitología, Universidad de Córdoba, 14014 Córdoba, Spain;
- UIC Zoonosis y Enfermedades Emergentes ENZOEM, Universidad de Córdoba, 14014 Córdoba, Spain
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25
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Abdel-Hakeem SS, Alnasser SM, Meshal A, Abdel-Samiee MAZ, Youssef MSE, Elsadek SHA, Abd-Elrahman SM. Pumpkin seed oil: unveiling its potential in controlling inflammation and pathogenicity during experimental trichinellosis. BMC Vet Res 2024; 20:419. [PMID: 39304848 DOI: 10.1186/s12917-024-04241-2] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/30/2024] [Accepted: 08/22/2024] [Indexed: 09/22/2024] Open
Abstract
BACKGROUND This study aimed to investigate the antiparasitic and anti-inflammatory potential of pumpkin seed oil in mice infected with Trichinella spiralis by demonstrating its impact on MMP-9 expression and pathogenesis during the intestinal and muscular phases. RESULTS In this study, 100 mice were divided into five groups: an infected group, a pumpkin seed oil-treated group (1.5 mg/kg BW, administered three times per week), an albendazole-treated group, a native control group, and a pumpkin oil control group. Gas chromatography-mass spectrometry analysis of the pumpkin seed oil revealed a broad spectrum of biologically active compounds. The pumpkin seed oil treatment led to a significant reduction in the parasite burden, with a 75% decrease in adult worms and a 66% decrease in encysted larvae. Additionally, the infected animals treated with pumpkin oil exhibited a marked reduction in intestinal inflammation, characterized by a progressive increase in goblet cells. The number of encysted larvae in the diaphragm and muscle tissues was also significantly decreased. Furthermore, pumpkin seed oil treatment significantly reduced MMP-9 levels in both intestinal and muscular tissues, highlighting its potential to attenuate inflammation. CONCLUSION These findings underscore the effectiveness of pumpkin seed oil as anti-inflammatory and antiparasitic agent.
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Affiliation(s)
- Sara Salah Abdel-Hakeem
- Parasitology Laboratory, Zoology and Entomology Department, Faculty of Science, Assiut University, Assiut, 71526, Egypt.
| | - Sulaiman Mohammed Alnasser
- Department of Pharmacology and Toxicology, College of Pharmacy, Qassim University, 52571, Buraydah, Saudi Arabia
| | - Alotaibi Meshal
- College of Pharmacy, University of Hafr Albatin, 39911, Hafr Albatin, Saudi Arabia
| | | | - Mohamed Salah Eldin Youssef
- Department of Pathology and Clinical Pathology, Faculty of Veterinary Medicine, Assiut University, Assiut, 71526, Egypt
| | - Shimaa Hamdi Abd Elsadek
- Department of Pathology and clinical pathology, Faculty of Veterinary Medicine, Sphinx University, Assiut University, Assiut, 71526, Egypt
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26
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Mandal S, Mondal C, Lyndem LM. Probiotics: an alternative anti-parasite therapy. J Parasit Dis 2024; 48:409-423. [PMID: 39145362 PMCID: PMC11319687 DOI: 10.1007/s12639-024-01680-4] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/07/2023] [Accepted: 04/27/2024] [Indexed: 08/16/2024] Open
Abstract
This paper review about probiotic effects and mechanism of action against the gut and non-gut helminths and protozoan parasites. Gastrointestinal parasitic infections are considered a serious health problem and are widely distributed globally. The disease process which emanates from this parasite infection provides some of the many public and veterinary health problems in the tropical and sub-tropical countries. Prevention and control of the parasite disease is through antihelmintic and anti-protozoan drugs, but, due to the increasing emergence of such drug resistance, eradication of parasite infestation in human and livestock still lingers a challenge, which requires the development of new alternative strategies. The use of beneficial microorganisms i.e. probiotics is becoming interesting due to their prophylactic application against several diseases including parasite infections. Recent studies on the interactions between probiotics, parasites and host immune cells using animal models and in vitro culture systems has increased considerably and draw much attention, yet the mechanisms of actions mediating the positive effects of these beneficial microorganisms on the hosts remain unexplored. Therefore, the aim of the present review is to summarize the latest findings on the probiotic research against the gut and non-gut parasites of significance.
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Affiliation(s)
- Sudeshna Mandal
- Visva-Bharati, Parasitology Research Laboratory, Department of Zoology, Santiniketan, 731235 West Bengal India
| | - Chandrani Mondal
- Visva-Bharati, Parasitology Research Laboratory, Department of Zoology, Santiniketan, 731235 West Bengal India
| | - Larisha M. Lyndem
- Visva-Bharati, Parasitology Research Laboratory, Department of Zoology, Santiniketan, 731235 West Bengal India
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Gamble HR, Hill DE, Fournet V, Adams B, Hawkins-Cooper D, Fredericks J, Aquino J, Agu S, Chehab N, Ankrah A, Antognoli MC, Remmenga MD, Kramer S, Gustafson L, Rosenthal BM. Surveillance for Trichinella infection in U.S. pigs raised under controlled management documents negligible risk for public health. Food Waterborne Parasitol 2024; 36:e00238. [PMID: 39193531 PMCID: PMC11347824 DOI: 10.1016/j.fawpar.2024.e00238] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/20/2024] [Revised: 07/10/2024] [Accepted: 07/20/2024] [Indexed: 08/29/2024] Open
Abstract
Biosecurity measures preventing exposure of pigs to rodents, wildlife, and contaminated feed or waste products reduce the risk of zoonotic Trichinella infection in pork. To understand the benefits of such measures in the United States, we conducted the first comprehensive survey of pigs produced under the Pork Quality Assurance Plus production standard, surveying 3,208,643 pork samples from twelve processing locations tested over a period of 54 months. We detected no Trichinella sp. positives in any of these pork samples, providing a 95% confidence in a Trichinella sp. prevalence of <1 in 1,000,000 for the processors represented by the study. These results are consistent with international guidelines for having a negligible risk to public health. Results obtained here should generalize to all PQA+ sources, as Trichinella sp. exposure risk is based on production guidelines that extend to the larger PQA+ population.
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Affiliation(s)
- H. Ray Gamble
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Dolores E. Hill
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Valsin Fournet
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Brandon Adams
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Diane Hawkins-Cooper
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Jorrell Fredericks
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Jovan Aquino
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Sonia Agu
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Nadya Chehab
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Ako Ankrah
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
| | - Maria C. Antognoli
- U.S. Department of Agriculture, Animal and Plant Health Inspection Service, Veterinary Services, Fort Collins, CO 80526, USA
| | - Marta D. Remmenga
- U.S. Department of Agriculture, Animal and Plant Health Inspection Service, Veterinary Services, Fort Collins, CO 80526, USA
| | - Scott Kramer
- U.S. Department of Agriculture, Animal and Plant Health Inspection Service, Veterinary Services, Riverdale, MD 20737, USA
| | - Lori Gustafson
- U.S. Department of Agriculture, Animal and Plant Health Inspection Service, Veterinary Services, Riverdale, MD 20737, USA
| | - Benjamin M. Rosenthal
- U.S. Department of Agriculture, Animal Parasitic Disease Laboratory, Beltsville, MD 20705, USA
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Briciu V, Kalmár Z, Ieremia A, Lupșe M, Flonta M, Muntean M, Cismaru C, Horvat M, Rădulescu A, Topan A, Jianu C, Ionică AM. Serological evidence of human exposure to foodborne zoonotic parasites in Romanian patients and possible association with food habits and hygiene. Food Waterborne Parasitol 2024; 36:e00240. [PMID: 39220615 PMCID: PMC11363570 DOI: 10.1016/j.fawpar.2024.e00240] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/20/2024] [Revised: 07/30/2024] [Accepted: 08/01/2024] [Indexed: 09/04/2024] Open
Abstract
Humans may become accidental dead-end hosts for a series of zoonotic foodborne parasites, of which Toxoplasma gondii, Echinococcus spp., Toxocara spp., and Trichinella spiralis are of major public health interest, due to their potential pathological implications. The aims of the study were to evaluate the exposure to these pathogens in north-western Romania, and to investigate their potential association to risk factors. From June 2022 to January 2024, 554 patients admitted to a tertiary hospital in north-western Romania were screened for the presence of IgG antibodies against T. gondii, Echinococcus spp., Toxocara canis, and T. spiralis by ELISA, and potential risks were assessed using a questionnaire. Overall, 225 samples (40.6%) were positive for at least one pathogen. The highest seroprevalence for IgG was found for T. gondii (33.9%), followed by Echinococcus spp. (9.1%), T. spiralis (2.9%), and T. canis (1.1%). For T. spiralis, raw meat consumption was associated with positivity. For T. gondii, increased age, rural environment, contact with cats, consumption of unwashed fruits/vegetables and drinking water from unverified sources were significantly associated to seropositivity. The present study provides new insights into the epidemiological status of zoonotic foodborne parasite in Romania, underlining the need to increase awareness on the importance of water, sanitation and food habits in relation with this neglected pathology.
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Affiliation(s)
- Violeta Briciu
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
| | - Zsuzsa Kalmár
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
- Department of Microbiology, Immunology, and Epidemiology, University of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca, 400372 Cluj-Napoca, Romania
| | - Anca Ieremia
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
| | - Mihaela Lupșe
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
| | - Mirela Flonta
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
| | - Monica Muntean
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
| | - Cristina Cismaru
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
| | - Melinda Horvat
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
| | - Amanda Rădulescu
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
| | - Adriana Topan
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
- Department of Infectious Diseases and Epidemiology, “Iuliu Hațieganu” University of Medicine and Pharmacy, 4000348 Cluj-Napoca, Romania
| | - Cristian Jianu
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
| | - Angela Monica Ionică
- Clinical Hospital of Infectious Diseases of Cluj-Napoca, 400348 Cluj-Napoca, Romania
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29
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Barnadas-Carceller B, Del Portillo HA, Fernandez-Becerra C. Extracellular vesicles as biomarkers in parasitic disease diagnosis. CURRENT TOPICS IN MEMBRANES 2024; 94:187-223. [PMID: 39370207 DOI: 10.1016/bs.ctm.2024.07.003] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 10/08/2024]
Abstract
Parasitic diseases constitute a major global health problem, affecting millions of people worldwide. Recent advances in the study of extracellular vesicles (EVs) have opened up new strategies for biomarker discovery in protozoan and helminth infections. Analyses of EVs in cultures and biological fluids have identified numerous potential biomarkers that could be useful for early and differential diagnosis, monitoring therapeutic responses, and the overall management and control of these diseases. Despite the potential of these biomarkers, several challenges must be addressed, including limited research, the need for standardized protocols, and the reproducibility of results across studies. In many parasitic infections, EVs have been obtained from various sample types, including plasma from human patients and mouse models, as well as cultures of the parasites at different stages. EVs were isolated by various methods and predominantly characterized through proteomic analysis or RNA sequencing to assess their cargo and identify potential biomarkers. These biomarker candidates were investigated and validated using different assays such as ELISA, Western Blot, and ROC curves. Overall, the use of EVs is considered a promising new diagnostic strategy for parasite infections, but further research with larger cohorts, standardized methods, and additional validation tests are essential for effective diagnosis and management of these diseases.
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Affiliation(s)
- Berta Barnadas-Carceller
- ISGlobal, Barcelona Institute for Global Health, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona (UB), Barcelona, Spain; IGTP Institut d'Investigació Germans Trias I Pujol, Badalona, Barcelona, Spain
| | - Hernando A Del Portillo
- ISGlobal, Barcelona Institute for Global Health, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona (UB), Barcelona, Spain; IGTP Institut d'Investigació Germans Trias I Pujol, Badalona, Barcelona, Spain; ICREA, Institució Catalana de Recerca i Estudis Avançats, Barcelona, Spain
| | - Carmen Fernandez-Becerra
- ISGlobal, Barcelona Institute for Global Health, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona (UB), Barcelona, Spain; IGTP Institut d'Investigació Germans Trias I Pujol, Badalona, Barcelona, Spain; CIBERINFEC, ISCIII-CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.
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Mukherjee B, Lalduhkimi C, Noronha V, Krishnakumar S. Double trouble: orbital rhabdomyoma with trichinellosis. Orbit 2024; 43:474-479. [PMID: 39083582 DOI: 10.1080/01676830.2023.2177679] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/06/2022] [Accepted: 02/01/2023] [Indexed: 08/02/2024]
Abstract
Rhabdomyoma of the orbit is a rare tumor with very few cases reported in the literature. We herein describe a 5-year-old boy who presented to us with a deviation of his left eye. Magnetic Resonance Imaging (MRI) showed a well-defined homogeneous intraconal mass in the superomedial aspect compressing the optic nerve. An excision biopsy was performed and the diagnosis of rhabdomyoma was confirmed on histopathology and immunohistochemistry with a coincidental finding of Trichinella spiralis larvae within the excised specimen. We report this phenomenon in two rare diseases with a predilection for striated muscle occurring simultaneously in a single patient.
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Affiliation(s)
- Bipasha Mukherjee
- Orbit, Oculoplasty, Reconstructive and Aesthetic services, Medical Research Foundation, Sankara Nethralaya, Chennai, India
| | - Chhakchhuak Lalduhkimi
- Orbit, Oculoplasty, Reconstructive and Aesthetic services, Medical Research Foundation, Sankara Nethralaya, Chennai, India
| | - Veena Noronha
- Department of Radiology, Consultant Radiologist, VRR Scans, Chennai, Tamil Nadu, India
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Bayaumy FEA, Rizk SA, Darwish AS. Superb bio-effectiveness of Cobalt (II) phthalocyanine and Ag NPs adorned Sm-doped ZnO nanorods/cuttlefish bone to annihilate Trichinella spiralis muscle larvae and adult worms: In-vitro evaluation. Parasitol Int 2024; 101:102899. [PMID: 38663799 DOI: 10.1016/j.parint.2024.102899] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/27/2024] [Revised: 04/08/2024] [Accepted: 04/21/2024] [Indexed: 04/28/2024]
Abstract
Herein, innovative biocides are designed for the treatment of Trichinella spiralis muscle larvae (ML) and adult worms. Samarium-doped ZnO nanorods (Sm-doped ZnO) are stabilized onto the laminar structure of cuttlefish bone (CB) matrix and adorned by either Ag NPs or cobalt phthalocyanine (CoPc) species. Physicochemical characteristics of such nanocomposites are scrutinised. Adorning of Sm-doped ZnO/CB with Ag NPs shortens rod-like shaped Sm-doped ZnO nanoparticles and accrues them, developing large-sized detached patches over CB moiety. Meanwhile, adorning of Sm-doped ZnO/CB by CoPc species degenerates CB lamellae forming semi-rounded platelets and encourages invading of Sm-doped ZnO nanorods deeply inside gallery spacings of CB. Both nanocomposites possess advanced parasiticidal activity, displaying quite intoxication for ML and adult worms (≥88% mortality) within an incubation period of <48 h at concentrations around 200 μg/ml. CoPc@Sm-doped ZnO/CB nanocomposite exhibits faster killing efficiency of adult worms than that of Ag@Sm-doped ZnO/CB at a concentration of ∼75 μg/ml showing entire destruction of parasite after 24 h incubation with the former nanocomposite and just 60% worm mortality after 36 h exposure to the later one. Morphological studies of the treated ML and adult worms show that CoPc@Sm-doped ZnO/CB exhibits a destructive impact on the parasite body, creating featureless and sloughed fragments enriched with intensive vacuoles. Hybridization of cuttlefish bone lamellae by CoPc species is considered a springboard for fabrication of futuristic aggressive drugs against various food- and water-borne parasites.
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Affiliation(s)
- Fatma E A Bayaumy
- Zoology Department, Faculty of Women for Arts, Science and Education, Ain Shams University, Cairo, Egypt.
| | - Sameh A Rizk
- Department of Chemistry, Faculty of Science, Ain Shams University, 11566 Cairo, Egypt
| | - Atef S Darwish
- Department of Chemistry, Faculty of Science, Ain Shams University, 11566 Cairo, Egypt
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Malone CJ, Oksanen A, Mukaratirwa S, Sharma R, Jenkins E. From wildlife to humans: The global distribution of Trichinella species and genotypes in wildlife and wildlife-associated human trichinellosis. Int J Parasitol Parasites Wildl 2024; 24:100934. [PMID: 38651034 PMCID: PMC11033181 DOI: 10.1016/j.ijppaw.2024.100934] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/28/2024] [Revised: 04/02/2024] [Accepted: 04/02/2024] [Indexed: 04/25/2024]
Abstract
Zoonotic nematodes of the genus Trichinella are foodborne parasites that have a global distribution in wild carnivores and omnivores, with spillover and spillback into domestic livestock and people, with concomitant trade and health consequences. Historically, most human cases were linked to domestic pigs infected with Trichinella spiralis, but under current high biosecurity swine production in many countries, wildlife have become a more important source of human trichinellosis. The aim of this review is to update the global distribution of Trichinella species and genotypes reported in wildlife, as well as reported human outbreaks from the consumption of wildlife. Using several online databases and by "snowballing" references, hundreds of reports of Trichinella spp. in wildlife published between January 1991 and December 2023 provide an important update to the host and geographic range for each of the recognized 13 species/genotypes, grouped by continent. Surveillance effort was highest in Europe and North America, while Africa, Asia, Oceania, Central and South America have had limited surveillance, in some instances with human cases serving as sentinels of transmission in a region. Dozens of human outbreaks are described, with wild boars (Sus scrofa) being the most frequently implicated wildlife species in human outbreaks globally. Bears are an important source of infection in North America, for wildlife tourism, and importation of bear meat has also been implicated in multicountry outbreaks. The largest study limitation was the dearth of molecular identification of larvae in both wildlife surveillance studies and human outbreaks, particulary in under-studied regions. We highlight the need for enhanced molecular epidemiological approaches to outbreaks of this important foodborne parasite, and emphasize the need for a One Health approach to manage Trichinella spp. which transmit among terrestrial and marine wildlife (including migratory birds), pigs, horses, and people, often across large geographic scales and borders.
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Affiliation(s)
- Cody J. Malone
- Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada
| | - Antti Oksanen
- Finnish Food Authority, (FINPAR), Elektroniikkatie 3, FI-90590, Oulu, Finland
| | - Samson Mukaratirwa
- One Health Center for Zoonoses and Tropical Veterinary Medicine, Ross University School of Veterinary Medicine, Basseterre, Saint Kitts and Nevis
- School of Life Sciences, University of KwaZulu-Natal, Durban, South Africa
| | - Rajnish Sharma
- Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada
- Centre for One Health, College of Veterinary Science, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana, Punjab, India
| | - Emily Jenkins
- Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada
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Elossily NA, Abd-ELrahman SM, Khedr AA, Dyab AK, Mahmoud AE, Mohamed SM, Abd Elrahman AM, Alsharif FM, Alsaadawy RM, Sayed RKA, Khalifa MM. Light microscopical and parasitological analyses revealed the beneficial effects of silver nanoparticles and various myrrh extracts against Trichinella spiralis infection in mice. Microsc Res Tech 2024; 87:1566-1575. [PMID: 38430198 DOI: 10.1002/jemt.24542] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/30/2023] [Revised: 01/19/2024] [Accepted: 02/22/2024] [Indexed: 03/03/2024]
Abstract
Trichinella spiralis infection is a food-borne zoonotic disease caused by nematodes that dwell in the tissues, presenting a significant public health concern. This study aimed to evaluate the effectiveness of different treatments including silver nanoparticles (AgNPs), myrrh biosynthesized AgNPs "AgNPs synthesized using plant-based green technologies", myrrh extract, and myrrh essential oil, as alternative treatments against T. spiralis infection. Parasitological, histopathological, and cytotoxicity assessments were conducted to investigate the effects of various concentrations of these treatments in reducing the populations of adult worms and larvae during both the intestinal and muscular phases of T. spiralis-infected mice. The results showed that the highest antihelminthic efficacy against the intestinal phase of T. spiralis was achieved by myrrh extract (86.66%), followed closely by AgNPs (84.96%) and myrrh AgNPs (82.51%) at higher concentrations (800 mg/kg for myrrh extract, 40 μg/mL for AgNPs, and 40 μg/mL for myrrh AgNPs). While the group treated with myrrh essential oil showed the lowest percentage of adult reduction (78.14%). However, all treatments demonstrated comparable effects in reducing the larvae population in the muscle phase. Histopathological examination of the tissues revealed compelling evidence of the effectiveness of AgNPs, particularly when prepared with myrrh. Additionally, a comprehensive assessment of the cytotoxicity of AgNPs indicated low toxicity levels. This study supports that AgNPs synthesized using plant-based green technologies hold therapeutic potential for the treatment of T. spiralis infection. These findings present a promising avenue for the development of novel antiparasitic drugs that are both effective and safe. RESEARCH HIGHLIGHTS: Myrrh extract has the highest antihelminthic efficacy against the intestinal phase of T. spiralis. Histopathological examination of the tissues revealed compelling evidence of the effectiveness of AgNPs, particularly when prepared with myrrh. During intestinal phase of T. spiralis, varying levels of nanoparticle precipitation were detected in the liver, brain, lung, and intestine. During the muscular phase, the highest amount of AgNPs precipitation was detected in the liver, followed by the brain, and lung.
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Affiliation(s)
- Nahed A Elossily
- Department of Medical Parasitology, Faculty of Medicine, Assiut University, Assiut, Egypt
| | - Salwa M Abd-ELrahman
- Department of Parasitology, Faculty of Veterinary Medicine, Assiut University, Assiut, Egypt
| | - Abeer A Khedr
- Department of Parasitology, Faculty of Veterinary Medicine, New Valley University, New Valley, Egypt
| | - Ahmed K Dyab
- Department of Medical Parasitology, Faculty of Medicine, Assiut University, Assiut, Egypt
| | - Abeer E Mahmoud
- Department of Medical Parasitology, Faculty of Medicine, Assiut University, Assiut, Egypt
| | - Shaymaa M Mohamed
- Department of Pharmacognosy, Faculty of Pharmacy, Assiut University, Assiut, Egypt
| | | | - Fahd M Alsharif
- Department of Pharmaceutics and Ind. Pharmacy, College of Pharmacy, Al-Azhar University, Assiut, Egypt
| | - Reem M Alsaadawy
- Department of Zoonoses, Faculty of Veterinary Medicine, Assiut University, Assiut, Egypt
| | - Ramy K A Sayed
- Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Sohag University, Sohag, Egypt
| | - Mervat M Khalifa
- Department of Medical Parasitology, Faculty of Medicine, Assiut University, Assiut, Egypt
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Intirach J, Shu C, Lv X, Gao S, Sutthanont N, Chen T, Lv Z. Human parasitic infections of the class Adenophorea: global epidemiology, pathogenesis, prevention and control. Infect Dis Poverty 2024; 13:48. [PMID: 38902844 PMCID: PMC11188577 DOI: 10.1186/s40249-024-01216-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/06/2024] [Accepted: 06/07/2024] [Indexed: 06/22/2024] Open
Abstract
BACKGROUND Human parasitic infections caused by Adenophorean nematodes encompass a range of diseases, including dioctophymiasis, trichuriasis, capillariasis, trichinellosis, and myositis. These infection can result in adverse impacts on human health and cause societal and economic concerns in tropical and subtropical regions. METHODS This review conducted searches in PubMed, Embase and Google Scholar for relevant studies that published in established databases up to April 26, 2024. Studies that focused on the common morphology, life cycle, disease distribution, clinical manifestations, and prevention and control strategies for Adenophorean parasitic diseases in humans were included. RESULTS Adenophorean nematodes exhibit shared morphological characteristics with a four-layered cuticle; uninucleate epidermal cells; pseudocoelom with six or more coelomocytes; generally three caudal glands; five esophageal glands; two testes in males with median-ventral supplementary glands in a single row; tail in males rarely possessing caudal alae; amphids always postlabial; presence of cephalic sensory organs; absence of phasmids; and a secretory-excretory system consisting of a single ventral gland cell, usually with a non-cuticularized terminal duct. Humans play two important roles in the life cycle of the nematode class, Adenophorea: 1) as a definitive host infected by ingesting undercooked paratenic hosts, embryonated eggs, infective larvae in fish tissue and meat contaminated with encysted or non-encysted larvae, and 2) as an accidental host infected by ingesting parasitic eggs in undercooked meat. Many organs are targeted by the Adenophorean nematode in humans such as the intestines, lungs, liver, kidneys, lymphatic circulation and blood vessels, resulting in gastrointestinal problems, excessive immunological responses, cell disruption, and even death. Most of these infections have significant incidence rates in the developing countries of Africa, Asia and Latin America; however, some parasitic diseases have restricted dissemination in outbreaks. To prevent these diseases, interventions together with education, sanitation, hygiene and animal control measures have been introduced in order to reduce and control parasite populations. CONCLUSIONS The common morphology, life cycle, global epidemiology and pathology of human Adenophorean nematode-borne parasitic diseases were highlighted, as well as their prevention and control. The findings of this review will contribute to improvement of monitoring and predicting human-parasitic infections, understanding the relationship between animals, humans and parasites, and preventing and controlling parasitic diseases.
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Affiliation(s)
- Jitrawadee Intirach
- Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 570100, China
| | - Chang Shu
- School of Basic Medical Sciences and Life Sciences, Hainan Medical University, Haikou, Hainan, 571199, China
| | - Xin Lv
- School of Public Health, Hainan Medical University, Haikou, Hainan, 571199, China
| | - Suzhen Gao
- School of Public Health, Hainan Medical University, Haikou, Hainan, 571199, China
| | - Nataya Sutthanont
- Department of Medical Entomology, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand
| | - Tao Chen
- Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 570100, China.
- Hainan Provincial Bureau of Disease Prevention and Control, Haikou, 570100, China.
| | - Zhiyue Lv
- Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 570100, China.
- Provincial Engineering Technology Research Center for Biological Vector Control, Guangzhou, Guangdong, 510080, China.
- Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou, Guangdong, 510080, China.
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El Saftawy EA, Aboulhoda BE, Hassan FE, Ismail MAM, Alghamdi MA, Hussein SM, Amin NM. ACV with/without IVM: a new talk on intestinal CDX2 and muscular CD34 and Cyclin D1 during Trichinella spiralis infection. Helminthologia 2024; 61:124-141. [PMID: 39040803 PMCID: PMC11260317 DOI: 10.2478/helm-2024-0013] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/04/2024] [Accepted: 03/25/2024] [Indexed: 07/24/2024] Open
Abstract
The current study assessed the efficacy of Acyclovir (ACV) and Ivermectin (IVM) as monotherapies and combined treatments for intestinal and muscular stages of Trichinella spiralis infection. One-hundred Swiss albino mice received orally 250 ± 50 infectious larvae and were divided into infected-untreated (Group-1), IVM-treated (Group-2), ACV-treated (Group-3), combined IVM+ACV (Group-4), and healthy controls (Group-5). Each group was subdivided into subgroup-A-enteric phase (10 mice, sacrificed day-7 p.i.) and subgroup-B-muscular phase (10 mice, sacrificed day-35 p.i.). Survival rate and body weight were recorded. Parasite burden and intestinal histopathology were assessed. In addition, immunohistochemical expression of epithelial CDX2 in the intestinal phase and CyclinD1 as well as CD34 in the muscular phase were evaluated. Compared, IVM and ACV monotherapies showed insignificant differences in the amelioration of enteric histopathology, except for lymphocytic counts. In the muscle phase, monotherapies showed variable disruptions in the encapsulated larvae. Compared with monotherapies, the combined treatment performed relatively better improvement of intestinal inflammation and reduction in the enteric and muscular parasite burden. CDX2 and CyclinD1 positively correlated with intestinal inflammation and parasite burden, while CD34 showed a negative correlation. CDX2 positively correlated with CyclinD1. CD34 negatively correlated with CDX2 and CyclinD1. IVM +ACV significantly ameliorated CDX2, CyclinD1, and CD34 expressions compared with monotherapies. Conclusion. T. spiralis infection-associated inflammation induced CDX2 and CyclinD1 expressions, whereas CD34 was reduced. The molecular tumorigenic effect of the nematode remains questionable. Nevertheless, IVM +ACV appeared to be a promising anthelminthic anti-inflammatory combination that, in parallel, rectified CDX2, CyclinD1, and CD34 expressions.
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Affiliation(s)
- E. A. El Saftawy
- Medical Parasitology Department, Faculty of Medicine, Cairo University, Cairo, Egypt
- Medical Parasitology Department, Armed Forces College of Medicine, Cairo, Egypt
| | - B. E. Aboulhoda
- Department of Anatomy and Embryology, Faculty of Medicine, Cairo University, Cairo, Egypt
| | - F. E. Hassan
- Medical Physiology Department, Kasr Alainy, Faculty of Medicine, Cairo University, Giza11562, Egypt
- General Medicine Practice Program, Department of Physiology, Batterjee Medical College, Jeddah21442, Saudi Arabia
| | - M. A. M. Ismail
- Medical Parasitology Department, Faculty of Medicine, Cairo University, Cairo, Egypt
| | - M. A. Alghamdi
- College of Medicine, King Khalid University, Abha62529, Saudi Arabia
- Genomics and Personalized Medicine Unit, College of Medicine, King Khalid University, Abha62529, Saudi Arabia
| | - S. M. Hussein
- Department of Anatomy and Embryology, Faculty of Medicine, Cairo University, Cairo, Egypt
| | - N. M. Amin
- Medical Parasitology Department, Faculty of Medicine, Cairo University, Cairo, Egypt
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Petrová M, Hurníková Z, Lauková A, Dvorožňáková E. Antiparasitic Activity of Enterocin M and Durancin-like from Beneficial Enterococci in Mice Experimentally Infected with Trichinella spiralis. Microorganisms 2024; 12:923. [PMID: 38792753 PMCID: PMC11123709 DOI: 10.3390/microorganisms12050923] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/28/2024] [Revised: 04/26/2024] [Accepted: 04/29/2024] [Indexed: 05/26/2024] Open
Abstract
Beneficial/probiotic strains protect the host from pathogens by competitive displacement and production of antibacterial substances, i.e., bacteriocins. The antiparasitic potential of bacteriocins/enterocins and their producing strains in experimental murine trichinellosis were tested as a new therapeutic strategy. Enterocin M and Durancin-like and their producers Enterococcus faecium CCM8558 and Enterococcus durans ED26E/7 were administered daily to mice that were challenged with Trichinella spiralis. Our study confirmed the antiparasitic effect of enterocins/enterococci, which reduced the number of adults in the intestine (Enterocin M-43.8%, E. faecium CCM8558-54.5%, Durancin-like-16.4%, E. durans ED26E/7-35.7%), suppressed the Trichinella reproductive capacity ex vivo (Enterocin M-61%, E. faecium CCM8558-74%, Durancin-like-38%, E. durans ED26E/7-66%), and reduced the number of muscle larvae (Enterocin M-39.6%, E. faecium CCM8558-55.7%, Durancin-like-15%, E. durans ED26E/7-36.3%). The direct effect of enterocins on Trichinella fecundity was documented by an in vitro test in which Durancin-like showed a comparable reducing effect to Enterocin M (40-60%) in contrast to the ex vivo test. The reducing activity of T.spiralis infection induced by Enterocin M was comparable to its strain E. faecium CCM8558; Durancin-like showed lower antiparasitic activity than its producer E. durans ED26E/7.
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Affiliation(s)
- Miroslava Petrová
- Institute of Parasitology, Slovak Academy of Sciences, 040 01 Kosice, Slovakia; (M.P.); (Z.H.)
| | - Zuzana Hurníková
- Institute of Parasitology, Slovak Academy of Sciences, 040 01 Kosice, Slovakia; (M.P.); (Z.H.)
| | - Andrea Lauková
- Institute of Animal Physiology, Centre of Biosciences, Slovak Academy of Sciences, 040 01 Kosice, Slovakia;
| | - Emília Dvorožňáková
- Institute of Parasitology, Slovak Academy of Sciences, 040 01 Kosice, Slovakia; (M.P.); (Z.H.)
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Abdel-Hakeem SS, Abdel-Samiee MAZ, Youssef MSE, Abd-Elsadek SH, Abd-Elrahman SM, Abdel-Hakeem SS. Nanocurcumin: A Promising Therapeutic Candidate for Experimental Trichinellosis. MICROSCOPY AND MICROANALYSIS : THE OFFICIAL JOURNAL OF MICROSCOPY SOCIETY OF AMERICA, MICROBEAM ANALYSIS SOCIETY, MICROSCOPICAL SOCIETY OF CANADA 2024; 30:368-381. [PMID: 38323506 DOI: 10.1093/micmic/ozae007] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 08/19/2023] [Revised: 12/18/2023] [Accepted: 01/18/2024] [Indexed: 02/08/2024]
Abstract
In our pursuit of an alternative drug against Trichinella spiralis, we assessed the effectiveness of nanocurcumin in alleviating pathogenesis, parasitological factors, MMP-9 levels, and its expression in the enteral and parenteral phases of infection. The nanocurcumin particles, with a spherical shape and a size of 100 ± 20 nm, were used in the study. Eighty mice were divided into four groups: the control group, the untreated infected group, the nanocurcumin-treated group, and the albendazole-treated group. The nanocurcumin-treated group exhibited a statistically significant increase in the percentage of lymphocytes, along with a reduction in neutrophils, monocytes, and eosinophils compared to the untreated, infected group. Both the nanocurcumin (87.2 and 97.3%) and the albendazole-treated groups (99.8 and 98.2%) showed a significant reduction in the mean number of intestinal worms and encysted larvae, respectively. The treated groups exhibited normal intestinal villi, suppression of the inflammatory process, and fewer instances of degenerated larvae in the diaphragm and muscle compared to the untreated, infected group. Immunohistochemistry and ELISA analyses revealed a significant downregulation of MMP-9 levels in the intestines and muscles of the treated groups. Our data demonstrate that nanocurcumin contains highly versatile molecules capable of modulating biological activity against inflammation and its pathway markers.
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Affiliation(s)
- Sara Salah Abdel-Hakeem
- Zoology and Entomology Department, Faculty of Science, Assiut University, Assiut 71526, Egypt
| | | | - Mohamed Salah Eldin Youssef
- Department of Pathology and Clinical Pathology, Faculty of Veterinary Medicine, Assiut University, Assiut 71526, Egypt
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Tammone Santos A, Riva E, Condorí WE, Fernández V, Rodriguez MG, Rivero MA, Faraco M, Aguirre P, Loyza L, Caselli AE, Uhart MM, Estein SM. Trichinella Infection in Culled Wild Boar (Sus scrofa) from El Palmar National Park, Argentina, and Exposure Risk in Humans and Dogs Consuming Wild Boar Meat. J Wildl Dis 2024; 60:401-412. [PMID: 38314854 DOI: 10.7589/jwd-d-23-00027] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/24/2023] [Accepted: 10/31/2023] [Indexed: 02/07/2024]
Abstract
Trichinellosis is a foodborne disease caused by ingestion of raw or undercooked meat containing Trichinella spp. larvae. Consumption of wild boar (Sus scrofa) meat represents an important source of human trichinellosis worldwide. In El Palmar National Park (EPNP), Argentina, invasive alien wild boars are controlled and meat from culled animals is released for public consumption following on-site artificial digestion (AD) testing. Meat trimmings and offal from the control program are often used as food for dogs (Canis familiaris). We evaluated infection and exposure to Trichinella spp. in wild boars from EPNP, as well as exposure to Trichinella spp. and associated risk factors in dogs and human consumers of wild boar meat. Trichinella spp. larvae were detected in muscle samples from 5/49 wild boars by AD (10.2%; 95% confidence interval [CI], 3.8%-23%), with a mean burden of 0.24 larvae per gram (lpg; range, 0.06-0.95 lpg). Anti-Trichinella antibodies were not detected in wild boar serum samples (n=42). In dogs, 12/34 were seropositive to Trichinella spp. (35.29%; 95%, CI, 20.3%-53.5%). Immunoglobulin (Ig) G antibodies were not detected in human serum samples (n=63). Our results reveal the presence, albeit at low prevalence, of Trichinella spp. in wild boars and exposure in dogs fed game offal. These findings suggest that the low prevalence and parasitic load in wild boars, together with the best practices applied by EPNP culling program personnel, contribute to keeping the risk of infection in people low. The dog results highlight that the parasite is circulating in the area, and therefore the risk of infection is not negligible. We recommend the implementation of an animal surveillance strategy in order to monitor the evolution of this zoonosis in the study area.
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Affiliation(s)
- Agostina Tammone Santos
- Centro de Investigación Veterinaria de Tandil, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
- Programa de Conservación Comunitaria del Territorio, Departamento de Ciencias Biológicas, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Eliana Riva
- Centro de Investigación Veterinaria de Tandil, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
- Área de Parasitología y Enfermedades Parasitarias, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Walter E Condorí
- Centro de Investigación Veterinaria de Tandil, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
- Programa de Conservación Comunitaria del Territorio, Departamento de Ciencias Biológicas, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Valentina Fernández
- Programa de Conservación Comunitaria del Territorio, Departamento de Ciencias Biológicas, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Marcelo G Rodriguez
- Área de Epidemiología, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Mariana A Rivero
- Centro de Investigación Veterinaria de Tandil, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
- Área de Epidemiología, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Matias Faraco
- Programa de Conservación Comunitaria del Territorio, Departamento de Ciencias Biológicas, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Pablo Aguirre
- Departamento de Zoonosis Rurales, Ministerio de Salud de la Provincia de Buenos Aires, España 770, Azul, 7300, Buenos Aires, Argentina
| | - Lorena Loyza
- Programa de Conservación Comunitaria del Territorio, Departamento de Ciencias Biológicas, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
- Administración de Parques Nacionales, Av. Rivadavia 1475, C1009ABM, Ciudad Autónoma de Buenos Aires, Argentina
| | - Andrea E Caselli
- Programa de Conservación Comunitaria del Territorio, Departamento de Ciencias Biológicas, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
| | - Marcela M Uhart
- One Health Institute, School of Veterinary Medicine, University of California Davis, 1089 Veterinary Medicine Dr., VM3B ground floor, Davis, California 95616, USA
| | - Silvia M Estein
- Centro de Investigación Veterinaria de Tandil, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
- Laboratorio de Inmunología, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires, Campus Universitario, Paraje Arroyo Seco s/n, Tandil, 7000, Buenos Aires, Argentina
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Langner T, Otranto D, Bezerra-Santos MA, Franzen J, Johne A, Tonanzi D, Pfeffer M, Birka S. Detection of Spirocerca lupi and an unknown Trichinella-like nematode in raccoon ( Procyon lotor). Int J Parasitol Parasites Wildl 2024; 23:100911. [PMID: 38352914 PMCID: PMC10862008 DOI: 10.1016/j.ijppaw.2024.100911] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/05/2023] [Revised: 01/26/2024] [Accepted: 01/26/2024] [Indexed: 02/16/2024]
Abstract
The raccoon Procyon lotor (Carnivora: Procyonidae) is an invasive species of growing importance for the introduction of alien pathogens or as additional hosts for autochthonous pathogens in Europe, including zoonotic parasites. As the population is steadily increasing and outcompeting the red fox (Vulpes vulpes) in Germany, the consumption of raccoon meat raises concerns about pathogens they may transmit. Therefore the presence of Trichinella larvae was here investigated in muscle samples (n = 904) of raccoons from northern Germany. No Trichinella larvae were found, thus confirming the general low occurrence of this parasite in Germany. However, Spirocerca lupi (n = 12) and an unidentified Trichinella-like nematode (n = 1) were accidently detected in the examined samples. The first is not a zoonotic parasite but has a high veterinary relevance as it can cause severe diseases in dogs. It is the first documented autochthonous infection of this nematode in Germany. The larvae of an unidentified Trichinella-like nematode were found in high abundance in all examined muscles of one raccoon, though they could not be identified to species level. Histological investigation revealed intramuscular cystic structures. This is the largest study investigating muscular parasites of raccoons in Europe so far, which suggests that this invasive animal species is infected by S. lupi and by a yet unknown Trichinella -like parasite.
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Affiliation(s)
- Torsten Langner
- Leipzig University, Faculty of Veterinary Medicine, Institute of Food Hygiene, Germany
| | - Domenico Otranto
- Department of Veterinary Medicine, University of Bari Aldo Moro, Str. prov. per Casamassima km 3, Valenzano, Bari, 70010, Italy
| | - Marcos Antonio Bezerra-Santos
- Department of Veterinary Medicine, University of Bari Aldo Moro, Str. prov. per Casamassima km 3, Valenzano, Bari, 70010, Italy
| | - Jan Franzen
- Institute of Animal Pathology, University of Bern, Bern, Switzerland
| | - Annette Johne
- German Federal Institute for Risk Assessment, NRL for Trichinella, Max-Dohrn-Str. 8-10, 10589, Berlin, Germany
| | - Daniele Tonanzi
- European Union Reference Laboratory for Parasites, Istituto Superiore Di Sanità, Rome, Italy
| | - Martin Pfeffer
- Institute of Animal Hygiene and Veterinary Public Health, Faculty of Veterinary Medicine, University of Leipzig, An den Tierkliniken 1, 04103, Leipzig, Germany
| | - Stefan Birka
- Leipzig University, Faculty of Veterinary Medicine, Institute of Food Hygiene, Germany
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Omeragić J, Kapo N, Škapur V, Crnkić Ć, Goletić Š, Softić A, Goletić T. Diversity of Trichinella species in carnivores from Bosnia and Herzegovina. BMC Vet Res 2024; 20:117. [PMID: 38521906 PMCID: PMC10960444 DOI: 10.1186/s12917-024-03964-6] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/14/2023] [Accepted: 03/03/2024] [Indexed: 03/25/2024] Open
Abstract
BACKGROUND In Bosnia and Herzegovina, domestic and wild carnivores represent a significant driver for the transmission and ecology of zoonotic pathogens, especially those of parasitic aetiology. Nevertheless, there is no systematic research of Trichinella species in animals that have been conducted in Bosnia and Herzegovina, even though trichinellosis is considered the most important parasitic zoonosis. The available results of the few studies carried out in Bosnia and Herzegovina are mainly related to the confirmation of parasitic larvae in the musculature of domestic pigs and wild boars or data related to trichinellosis in humans. The objective of our study was to present the findings of a comprehensive investigation into the species composition of Trichinella among 11 carnivorous species within the territory of Bosnia and Herzegovina, as follows: red fox (Vulpes vulpes), grey wolf (Canis lupus), brown bear (Ursus arctos), wildcat (Felis silvestris), pine marten (Martes martes), European badger (Meles meles), weasel (Mustela nivalis), European polecat (Mustela putorius), Eurasian lynx (Lynx lynx), but also dog (Canis lupus familiaris) and cat (Felis catus). RESULTS In the period 2013-2023, carnivore musculature samples (n = 629), each consisting of 10 g of muscle tissue, were taken post-mortem and individually examined using the artificial digestion method. In the positive samples (n = 128), molecular genotyping and identification of parasitic larvae of Trichinella spp. were performed using a PCR-based technique up to the species/genotype level. Positive samples were used for basic PCR detection of the genus Trichinella (rrnS rt-PCR technique) and genotyping (rrnl-EVS rt-PCR technique). The Trichinella infection was documented for the first time in Bosnia and Herzegovina among red foxes, grey wolves, brown bears, dogs, badgers and Eurasian lynx, with a frequency rate of 20.3%. Additionally, the presence of T. britovi infection was newly confirmed in Bosnia and Herzegovina, marking the initial documented cases. Furthermore, both T. britovi and T. pseudospiralis infections were observed in the wildcat population, whereas T. britovi and T. spiralis infections were detected in pine martens. Consistent with previous research, our findings align particularly regarding carnivores, with data from other countries such as Germany, Finland, Romania, Poland and Spain, where T. britovi exhibits a wider distribution (62.5-100%) compared to T. spiralis (0.0-37.5%). T. britovi is more common among sylvatic carnivores (89.0%), while T. spiralis prevails in wild boars (62.0%), domestic swine (82.0%) and rodents (75.0%). CONCLUSION The results of our study represent the first molecular identification of species of the genus Trichinella in Bosnia and Herzegovina. Additionally, our findings underscore the necessity for targeted epidemiological studies to thoroughly assess trichinellosis prevalence across diverse animal populations. Considering the relatively high frequency of trichinellosis infection in investigated animal species and its public health implications, there is an evident need for establishing an effective trichinellosis surveillance system in Bosnia and Herzegovina.
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Affiliation(s)
- Jasmin Omeragić
- University of Sarajevo - Veterinary Faculty, Zmaja od Bosne 90, Sarajevo, 71 000, Bosnia and Herzegovina
| | - Naida Kapo
- University of Sarajevo - Veterinary Faculty, Zmaja od Bosne 90, Sarajevo, 71 000, Bosnia and Herzegovina.
| | - Vedad Škapur
- University of Sarajevo - Faculty of Agriculture and Food Science, Zmaja od Bosne 8, Sarajevo, 71 000, Bosnia and Herzegovina
| | - Ćazim Crnkić
- University of Sarajevo - Veterinary Faculty, Zmaja od Bosne 90, Sarajevo, 71 000, Bosnia and Herzegovina
| | - Šejla Goletić
- University of Sarajevo - Veterinary Faculty, Zmaja od Bosne 90, Sarajevo, 71 000, Bosnia and Herzegovina
| | - Adis Softić
- University of Sarajevo - Veterinary Faculty, Zmaja od Bosne 90, Sarajevo, 71 000, Bosnia and Herzegovina
| | - Teufik Goletić
- University of Sarajevo - Veterinary Faculty, Zmaja od Bosne 90, Sarajevo, 71 000, Bosnia and Herzegovina
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Mahgoub AA, Shoeb RA, Negm MS, Ibrahim HM, El-Sayed SH, Khater MM. Nematocidal activity of chitosan nanoparticles conjugated with albendazole against the enteral and parenteral phases of trichinosis in experimentally infected mice. J Parasit Dis 2024; 48:141-149. [PMID: 38440755 PMCID: PMC10909009 DOI: 10.1007/s12639-024-01648-4] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/07/2023] [Accepted: 01/06/2024] [Indexed: 03/06/2024] Open
Abstract
Trichinosis is a serious parasitic zoonotic disease caused mainly by Trichinella spiralis. The used drugs for treatment of trichinosis showed limited bioavailability and high degree of resistance. Moreover, they have a very poor effect in treatment of encysted larvae. Therefore, there is a need for development of new agents which help in improving the bioavailability of the used drugs and enable them to reach different tissues. This study was designed to assess the use of chitosan nanoparticles (CSNPs) in conjugation with full and half dose albendazole (ABZ) in treatment of intestinal and muscular trichinosis. Albino mice (84 mice) were used to evaluate the efficacy of drugs and divided into seven groups; I: control, II: ABZ (50 mg/kg) treated, III: ABZ (25 mg/kg) treated, IV: ABZ (50 mg/kg) conjugated CSNPs treated, V: ABZ (25 mg/kg) conjugated CSNPs treated, VI: CS treated and VII: CSNPs treated. Parasitological and histopathological examinations were used to evaluate the therapeutic efficacy of the used drugs. Results showed significant reduction of adult Trichinella extracted from intestine of all ABZ treated groups either conjugated or not with the highest reduction rate in group IV followed by group V with percentage of reduction of 99.33% and 98.11%, respectively and marked improvement of histopathological examination. Also, results showed significant reduction of Trichinella larvae extracted from muscles of group IV, V and VII with the highest reduction rate in group IV with percentage of reduction of 100% in muscle larvae and marked improvement of histopathological examination. It was concluded that albendazole full dose conjugated chitosan nanoparticles can be a good candidate drug for treating both intestinal and muscular trichinosis.
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Affiliation(s)
- Abeer A. Mahgoub
- Medical Parasitology Department, Faculty of Medicine, Kasr Al-Ainy, Cairo University, Cairo, Egypt
| | - Ragaa A. Shoeb
- Medical Parasitology Department, Faculty of Medicine, Helwan University, Cairo, Egypt
| | | | | | - Shaimaa H. El-Sayed
- Medical Parasitology Department, Faculty of Medicine, Helwan University, Cairo, Egypt
| | - Mona M. Khater
- Medical Parasitology Department, Faculty of Medicine, Kasr Al-Ainy, Cairo University, Cairo, Egypt
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Abdeltawab MS, Abdel-Shafi IR, Aboulhoda BE, Mahfoz AM, Hamed AM. The neuroprotective potential of curcumin on T. Spiralis infected mice. BMC Complement Med Ther 2024; 24:99. [PMID: 38388410 PMCID: PMC10882799 DOI: 10.1186/s12906-024-04399-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/30/2023] [Accepted: 02/13/2024] [Indexed: 02/24/2024] Open
Abstract
BACKGROUND Trichinella spiralis can affect the brain by inducing inflammatory and vascular changes. Drug management with the antiparasitic drug albendazole can be enhanced by natural compounds such as curcumin. The potential benefit of curcumin as an adjuvant to albendazole in the management of cerebral affection during experimental T. spiralis infection was evaluated. Animals received either curcumin 150 mg/Kg, albendazole 50 mg/Kg or a combination of both drugs. Animal groups receiving treatment were compared with infected and non-infected control groups. Blood levels of reduced glutathione (GSH) and dopamine were measured, and brain tissue expression of cyclooxygenase-2 enzyme (COX-2) and CD34 was assessed by immunohistochemistry. RESULTS T. spiralis infection resulted in a state of oxidative stress, which was improved by albendazole and curcumin. Also, both drugs restored the peripheral dopamine level, which was decreased in infected non-treated mice. Curcumin was also found to be efficient in improving brain pathology and reducing local COX-2 and CD 34 expression. CONCLUSIONS Inflammatory and pathological changes during neurotrichinosis can be improved by the addition of curcumin to conventional anti-parasitic drugs.
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Affiliation(s)
- Magda Sa Abdeltawab
- Department of Medical Parasitology, Faculty of Medicine, Cairo University, Cairo, Egypt
| | - Iman R Abdel-Shafi
- Department of Medical Parasitology, Faculty of Medicine, Cairo University, Cairo, Egypt
| | - Basma Emad Aboulhoda
- Anatomy and Embryology Department, Faculty of Medicine, Cairo University, Cairo, Egypt
| | - Amal M Mahfoz
- Department of Pharmacology and Toxicology, Faculty of Pharmacy, Modern University for Technology and Information, Cairo, Egypt.
| | - Alshaimaa Mr Hamed
- Department of Medical Parasitology, Faculty of Medicine, Cairo University, Cairo, Egypt
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Milton AAP, Das S, Ghatak S, Srinivas K, Priya GB, Angappan M, Prasad MCB, Wahlang L, Sailo B, Lalhruaipuii L, Singh M, Garam GB, Sen A. Seroepidemological investigation of Toxoplasma gondii and Trichinella spp. in pigs reared by tribal communities and small-holder livestock farmers in Northeastern India. PLoS One 2024; 19:e0298357. [PMID: 38377066 PMCID: PMC10878514 DOI: 10.1371/journal.pone.0298357] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/06/2023] [Accepted: 01/22/2024] [Indexed: 02/22/2024] Open
Abstract
Toxoplasma gondii and Trichinella spp. are critical tissue-dwelling foodborne zoonotic parasites associated with pork consumption and pig rearing. Despite being a major pig-rearing region in the country, Northeastern India has not undergone any investigation regarding the presence of T. gondii and Trichinella spp. in pigs. Therefore, this study aims to determine the seroprevalence of T. gondii and Trichinella spp. and identify associated risk factors in pigs reared by tribal communities and small-holder livestock farmers in the northeastern region of India. In a cross-sectional serological survey, 400 pigs from 400 households across five northeastern states of India underwent testing for the seroprevalence of porcine toxoplasmosis and trichinellosis. Serum samples (80 from each state) were analyzed using commercially available ELISA assays. Data on backyard farm characteristics and various management aspects were collected, and risk factors linked with prevalence were analyzed through univariate and multivariate logistic regression analysis. The findings revealed that the apparent and true prevalence of anti-T. gondii antibodies were 45% (40.12-49.88, 95% CI) and 45.7% (40.7-50.69, 95% CI), respectively. As for anti- Trichinella antibodies, both the apparent and true prevalence were 0.75% (-0.1-1.6, 95% CI). The univariate and multivariate analyses indicated that age above 24 months (OR 7.20, 95% CI 2.45-23.71), exposure to cats (OR = 5.87, 95% CI 2.55-14.05), and farms operating for breeding purposes (OR = 5.60, 95% CI 3.01-11.04) were significant risk factors associated with the seroprevalence of T. gondii. This study marks the initial documentation of the seroprevalence of T. gondii and Trichinella spp. in pigs reared by tribal communities in Northeastern India. The results emphasize the significance of these parasites as foodborne zoonotic threats in the region, potentially posing substantial public health risks, especially within tribal and rural communities. The insights derived from this research could be valuable in formulating targeted preventive and control strategies against T. gondii and Trichinella spp. in pigs, not only in this region but also in areas with similar rearing practices.
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Affiliation(s)
- A. A. P. Milton
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - Samir Das
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - S. Ghatak
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - K. Srinivas
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - G. Bhuvana Priya
- College of Agriculture, Central Agricultural University (Imphal), Kyrdemkulai, Meghalaya, India
| | - M. Angappan
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - M. C. B. Prasad
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - L. Wahlang
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - Blessa Sailo
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | | | - Mahak Singh
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
| | - G. B. Garam
- Department of Animal Husbandry, Veterinary & Dairy Development, Nirjuli, Arunachal Pradesh, India
| | - A. Sen
- ICAR Research Complex for NEH Region, Umiam, Meghalaya, India
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Juozaitytė-Ngugu E, Maziliauskaitė E, Kirjušina M, Prakas P, Vaitkevičiūtė R, Stankevičiūtė J, Butkauskas D. Identification of Sarcocystis and Trichinella Species in Muscles of Gray Wolf ( Canis lupus) from Lithuania. Vet Sci 2024; 11:85. [PMID: 38393103 PMCID: PMC10892562 DOI: 10.3390/vetsci11020085] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/28/2023] [Revised: 02/07/2024] [Accepted: 02/08/2024] [Indexed: 02/25/2024] Open
Abstract
Apicomplexan Sarcocystis and Trichinella nematodes are food-borne parasites whose life cycle is carried-out in various wildlife and domestic animals. The gray wolf (Canis lupus) is an apex predator acting as an ecosystem engineer. This study aimed to identify the species of Sarcocystis and Trichinella found in the muscles of gray wolves in Lithuania. During the 2017-2022 period, diaphragm, heart, and hind leg samples of 15 animals were examined. Microscopical analysis showed the presence of two types of Sarcocystis parasites in 26.7% of the analyzed muscle samples. Based on the sequencing of five loci, nuclear 18S rDNA, 28S rDNA, ITS1, mitochondrial cox1, and apicoplast rpoB, S. arctica, and S. svanai were identified. The current work presents the first report of S. svanai in gray wolf. Phylogenetically, S. svanai clustered together with S. lutrae, infecting various carnivorans, and S. arctica was most closely related to S. felis from domestic cats. Trichinella spp. were found in 12 gray wolves (80%). For the first time, Trichinella species were molecularly identified in gray wolves from Lithuania. Trichinella britovi was confirmed in all of the isolated Trichinella larvae using a multiplex PCR. Gray wolves in Lithuania may serve as a major source of zoonotic pathogens due to the presence of these parasites.
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Affiliation(s)
| | | | - Muza Kirjušina
- Department of Ecology, Institute of Life Sciences and Technology, Daugavpils University, Parādes 1, 5401 Daugavpils, Latvia
| | - Petras Prakas
- Nature Research Centre, Akademijos 2, 08412 Vilnius, Lithuania
| | - Rasa Vaitkevičiūtė
- Agriculture Academy, Vytautas Magnus University, Studentų 11, Akademija, 53361 Kaunas, Lithuania
| | - Jolanta Stankevičiūtė
- Agriculture Academy, Vytautas Magnus University, Studentų 11, Akademija, 53361 Kaunas, Lithuania
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Khedr SI, Gomaa MM, Mogahed NMFH, Gamea GA, Khodear GAM, Sheta E, Soliman NAH, El Saadany AA, Salama AM. Trichinella spiralis: A new parasitic target for curcumin nanoformulas in mice models. Parasitol Int 2024; 98:102810. [PMID: 37730195 DOI: 10.1016/j.parint.2023.102810] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/11/2023] [Revised: 08/28/2023] [Accepted: 09/14/2023] [Indexed: 09/22/2023]
Abstract
Trichinosis spiralis is a global disease with significant economic impact. Albendazole is the current-treatment. Yet, the world-widely emerging antimicrobial resistance necessitates search for therapeutic substitutes. Curcumin is a natural compound with abundant therapeutic benefits. This study aimed to evaluate the potential of crude-curcumin, chitosan and for the first time curcumin-nano-emulsion and curcumin-loaded-chitosan-nanoparticles against Trichinella spiralis adults and larvae in acute and chronic trichinosis models. Trichinosis spiralis was induced in 96 Swiss-albino mice. Infected mice were divided into 2 groups. Group I constituted the acute model, where treatment started 2 h after infection for 5 successive days. Group II constituted the chronic model, where treatment started at the 30th day-post-infection and continued for 10 successive days (Refer to graphical abstract). Each group contained 8 subgroups that were designated Ia-Ih and IIa-IIh and included; a; Untreated-control, b; Albendazole-treated (Alb-treated), c; Crude-curcumin-treated (Cur-treated), d; Curcumin-nanoemulsion-treated (Cur-NE-treated), e; Albendazole and crude-curcumin-treated (Alb-Cur-treated), f; Albendazole and curcumin-nanoemulsion-treated (Alb-Cur-NE-treated), g; Chitosan-nanoparticles-treated (CS-NPs-treated) and h; Curcumin-loaded-chitosan-nanoparticles-treated (Cur-CS-NPs-treated). Additionally, six mice constituted control-uninfected group III. The effects of the used compounds on the parasite tegument, in-vivo parasitic load-worm burden, local pathology and MDA concentration in small intestines of acutely-infected and skeletal muscle of chronically-infected mice were studied. Results showed that albendazole was effective, yet, its combination with Cur-NE showed significant potentiation against adult worms and muscle larvae and alleviated the pathology in both models. Cur-CS-NPs exhibited promising results in both models. Crude-curcumin showed encouraging results especially against muscle larvae on long-term use. Treatments effectively reduced parasite load, local MDA level and CD31 expression with anti-inflammatory effect in intestine and muscle sections.
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Affiliation(s)
- Safaa Ibrahim Khedr
- Medical Parasitology Department, Faculty of Medicine, Alexandria University, Egypt.
| | - Maha Mohamed Gomaa
- Medical Parasitology Department, Faculty of Medicine, Alexandria University, Egypt
| | | | - Ghada A Gamea
- Medical Parasitology Department, Faculty of Medicine, Tanta University, Egypt
| | - Gehan A M Khodear
- Medical technology center, Medical Research Institute, Alexandria University, Egypt
| | - Eman Sheta
- Pathology Department, Faculty of Medicine, Alexandria University, Egypt
| | - Nada A H Soliman
- Medical Biochemistry Department, Faculty of Medicine, Alexandria University, Egypt
| | | | - Amina M Salama
- Medical Parasitology Department, Faculty of Medicine, Tanta University, Egypt
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Saleh AS, El-Newary SA, Mohamed WA, Elgamal AM, Farah MA. Pumpkin seeds (Cucurbita pepo subsp. ovifera) decoction promotes Trichinella spiralis expulsion during intestinal phase via "Weep and Sweep" mechanism. Sci Rep 2024; 14:1548. [PMID: 38233460 PMCID: PMC10794180 DOI: 10.1038/s41598-024-51616-4] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/27/2023] [Accepted: 01/07/2024] [Indexed: 01/19/2024] Open
Abstract
Trichinosis is a zoonotic disease of communal health concern as it instigated human outbreaks in several countries. Besides, the development of resistance, traditional therapy has numerous antagonistic effects. Thereby, finding efficient natural alternatives is required. In comparison to albendazole, this study evaluated the impact of pumpkin decoction on Trichinella spiralis in experimentally infected mice. The anthelmintic action of pumpkin decoction (500 mg/kg) was determined using T. spiralis infected mice in enteric phase for 5 days. Pumpkin decoction anthelmintic activity fortified by mixing with honey (1:1). Pumpkin decoction and Pumpkin decoction-honey mixture were evaluated by comprising with reference drug, albendazole (50 mg/kg). The T. spiralis adult count was significantly lower in all treated groups, with the pumpkin decoction-honey mixture showing the largest reduction (83.2%) when compared to the infected group (P ≤ 0.001). The intestinal histological changes and the level of COX-2 expression in the intestinal tissue were both significantly reduced in the same group. The pumpkin decoction improved the immune response, as evidenced by a significant decrease in nitric oxide (NO) and tumor necrosis factor (TNF-α) and a significant increase in the expression of the transforming growth factor (TGF-1β) and interleukin-17 (IL-17). The pumpkin decoction's anthelmintic action was facilitated by the TGF-1β and IL-17-driven Weep and Sweep mechanism. Both administration of pumpkin decoction beside honey showed the best treatment group that resulted in high infection reduction besides amelioration of biochemical markers and restoration of histological to normal state. In conclusion, pumpkin decoction is highly effective against T. spiralis which could be a promising alternative herbal drug and the pumpkin decoction effect was higher in the case of combination with honey.
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Affiliation(s)
- Aml S Saleh
- Zoology Department, Faculty of Women for Arts, Science and Education, Ain Shams University, Cairo, Egypt.
| | - Samah A El-Newary
- Medicinal and Aromatic Plants Research Department, Pharmaceutical and Drug Industries Research Institute, National Research Centre, 33 El Bohouth St. (Former EL Tahrir St.), Dokki, P.O. 12622, Giza, Egypt
| | - Walaa A Mohamed
- Zoology Department, Faculty of Women for Arts, Science and Education, Ain Shams University, Cairo, Egypt
| | - Abdelbaset M Elgamal
- Department of Chemistry of Microbial and Natural Products, Pharmaceutical and Drug Industries Research Division, National Research Centre, Giza, Egypt
| | - Mona A Farah
- Zoology Department, Faculty of Women for Arts, Science and Education, Ain Shams University, Cairo, Egypt
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Han LL, Lu QQ, Li YL, Zheng WW, Ren P, Liu RD, Cui J, Wang ZQ. Application of a recombinant novel trypsin from Trichinella spiralis for serodiagnosis of trichinellosis. Parasit Vectors 2024; 17:9. [PMID: 38178167 PMCID: PMC10768479 DOI: 10.1186/s13071-023-06067-7] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/27/2023] [Accepted: 11/26/2023] [Indexed: 01/06/2024] Open
Abstract
BACKGROUND The excretory/secretory (ES) antigen of Trichinella spiralis muscle larvae (ML) is currently the most widely used diagnostic antigen to detect T. spiralis infection. However, this antigen has certain drawbacks, such as a complicated ES antigen preparation process and lower sensitivity during the early phase of infection. The aim of this study was to investigate the features of a novel T. spiralis trypsin (TsTryp) and evaluate its potential diagnostic value for trichinellosis. METHODS The TsTryp gene was cloned and recombinant TsTryp (rTsTryp) expressed. Western blotting and an enzyme-linked immunosorbent assay (ELISA) were performed to confirm the antigenicity of rTsTryp. The expression pattern and distribution signature of TsTryp at various life-cycle stages of T. spiralis were analyzed by quantitative PCR, western blotting and the immunofluorescence test. An ELISA with rTsTryp and ML ES antigens was used to detect immunoglobulins G and M (IgG, IgM) in serum samples of infected mice, swine and humans. The seropositive results were further confirmed by western blot with rTsTryp and ML ES antigens. RESULTS TsTryp expression was observed in diverse T. spiralis life-cycle phases, with particularly high expression in the early developmental phase (intestinal infectious larvae and adults), with distribution observed mainly at the nematode outer cuticle and stichosome. rTsTryp was identified by T. spiralis-infected mouse sera and anti-rTsTryp sera. Natural TsTryp protease was detected in somatic soluble and ES antigens of the nematode. In mice infected with 200 T. spiralis ML, serum-specific IgG was first detected by rTsTryp-ELISA at 8 days post-infection (dpi), reaching 100% positivity at 12 dpi, and first detected by ES-ELISA at 10 dpi, reaching 100% positivity at 14 dpi. Specific IgG was detected by rTsTryp 2 days earlier than by ES antigens. When specific IgG was determined in serum samples from trichinellosis patients, the sensitivity of rTsTryp-ELISA and ES antigens-ELISA was 98.1% (51/52 samples) and 94.2% (49/52 samples), respectively (P = 0.308), but the specificity of rTsTryp was significantly higher than that of ES antigens (98.7% vs. 95.4%; P = 0.030). Additionally, rTsTryp conferred a lower cross-reaction, with only three serum samples in total testing positive from 11 clonorchiasis, 20 cysticercosis and 24 echinococcosis patients (1 sample from each patient group). CONCLUSIONS TsTryp was shown to be an early and highly expressed antigen at intestinal T. spiralis stages, indicating that rTsTryp represents a valuable diagnostic antigen for the serodiagnosis of early Trichinella infection.
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Affiliation(s)
- Lu Lu Han
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China
| | - Qi Qi Lu
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China
| | - Yang Li Li
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China
| | - Wen Wen Zheng
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China
| | - Pian Ren
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China
| | - Ruo Dan Liu
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China
| | - Jing Cui
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China.
| | - Zhong Quan Wang
- Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, 450001, China.
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Malone CJ, Kolapo TU, Whitney H, Callahan C, Hann S, Keefe D, Jenkins E. New Geographic Records for Trichinella nativa and Echinococcus canadensis in Coyotes (Canis latrans) from Insular Newfoundland, Canada. J Wildl Dis 2024; 60:211-215. [PMID: 37972642 DOI: 10.7589/jwd-d-23-00084] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/08/2023] [Accepted: 08/14/2023] [Indexed: 11/19/2023]
Abstract
Coyotes (Canis latrans) rapidly expanded across North America during the 20th century and in 1987 colonized insular Newfoundland, Canada. Their arrival brought the potential for new predator-prey interactions and the potential for transmission of parasites to naïve populations. Trichinella spp. and Echinococcus spp. are zoonotic parasites not previously reported from the island of Newfoundland, Canada. Muscle samples (diaphragm and tongue) from 153 coyotes and feces from 35/153 coyotes were collected. Larvae of Trichinella spp. were recovered by muscle digestion from 6/153 coyotes (3.9%) and identified using multiplex PCR and Sanger sequencing as T. nativa. Fecal samples were screened for DNA of Echinococcus spp. using qPCR, and intestines from positive animals were examined for adult cestodes. No fecal samples were positive for DNA of E. multilocularis, and 2/35 (5.7%) samples were positive for E. canadensis, of which one was successfully genotyped as the G10 cervid strain. Echinococcus canadensis has not previously been reported on the island of Newfoundland, historically the only region of Canada where Echinococcus spp. was not known to occur. No species of Trichinella have previously been reported on the island. Both parasites are zoonotic, and hunters, trappers, dog owners, and the general public should be aware of these new risks for public health.
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Affiliation(s)
- Cody J Malone
- Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, Saskatchewan, S7N 5B4, Canada
| | - Temitope U Kolapo
- Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, Saskatchewan, S7N 5B4, Canada
| | - Hugh Whitney
- Department of Biology, Memorial University of Newfoundland, 45 Arctic Avenue, St. John's, Newfoundland and Labrador, A1C 5S7, Canada
| | - Chris Callahan
- Fisheries, Forestry and Agriculture, Government of Newfoundland and Labrador, 192 Wheeler's Road, Corner Brook, P.O. Box 2006, Newfoundland and Labrador, A2H 0J1, Canada
| | - Shane Hann
- Fisheries, Forestry and Agriculture, Government of Newfoundland and Labrador, 192 Wheeler's Road, Corner Brook, P.O. Box 2006, Newfoundland and Labrador, A2H 0J1, Canada
| | - Don Keefe
- Fisheries, Forestry and Agriculture, Government of Newfoundland and Labrador, 192 Wheeler's Road, Corner Brook, P.O. Box 2006, Newfoundland and Labrador, A2H 0J1, Canada
| | - Emily Jenkins
- Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, Saskatchewan, S7N 5B4, Canada
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49
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Cleveland CA, Haynes E, Callaghan KC, Fojtik A, Coker S, Doub E, Brown VR, Majewska AA, Yabsley MJ. Distribution and prevalence of antibodies to Trichinella spp. and Toxoplasma gondii in wild pigs (Sus scrofa) in the United States. Vet Parasitol 2024; 325:110090. [PMID: 38043480 DOI: 10.1016/j.vetpar.2023.110090] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/30/2023] [Revised: 11/21/2023] [Accepted: 11/24/2023] [Indexed: 12/05/2023]
Abstract
Invasive wild pigs (Sus scrofa) are a reservoir for over 100 viral, bacterial, and parasitic pathogens that are transmissible to humans, livestock, domestic animals, and wildlife in North America. Numerous historical local surveys and results from a nation-wide survey (2006-2010) indicated that wild pigs in the United States act as reservoirs for Trichinella spp. and Toxoplasma gondii, two zoonotic pathogens of importance for human and animal health. Since that time, wild pig populations have expanded and increased in density in many areas. Population expansion of wild pigs creates opportunities for the introduction of pathogens to new areas of the country, increasing health risks. The goal of this study was to investigate the current geographic distribution and prevalence of Trichinella spp. and T. gondii antibodies in wild pigs using serum samples collected from 2014 to 2020. Serum samples from 36 states were tested for antibodies to Trichinella spp. (n = 7467) and T. gondii (n = 5984) using commercially available enzyme-linked immunosorbent assays. Seroprevalence for Trichinella spp. (12.4%, 927/7467) and T. gondii (40.8%, 2444/5984) are significantly higher compared to a previous 2006-2010 study across all regions. Results from this study also showed a lower seroprevalence (4.8%) for Trichinella spp. in the West region compared to the other regions (South: 13.4%; Midwest: 18.4%; Northeast: 19.1%). There were new detection records for antibodies to Trichinella spp. in 11 states, mostly in the West, Midwest, and Northeast regions compared to a previous study in 2014. Males and juveniles were less likely to be positive for Trichinella spp. antibodies, compared to females and older animals, respectively. Seroprevalence was similar for T. gondii across the regions (31.8-56%) with some states having particularly high seroprevalence (e.g., Hawaii 79.4% and Pennsylvania 68%). There were new T. gondii antibody detection records for 12 states, mostly in the West, Midwest, and Northeast regions. Adults were more likely than juveniles and subadults to be seropositive. These data confirm that the distribution and prevalence of antibodies for Trichinella spp. and T. gondii are increasing in the United States, likely driven by wild pig population growth and range expansion.
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Affiliation(s)
- Christopher A Cleveland
- Southeastern Cooperative Wildlife Disease Study, University of Georgia, Athens, GA 30602, USA; Center for Ecology of Infectious Diseases, University of Georgia, Athens, GA 30602, USA.
| | - Ellen Haynes
- Southeastern Cooperative Wildlife Disease Study, University of Georgia, Athens, GA 30602, USA.
| | - Katherine C Callaghan
- Warnell School of Forestry and Natural Resources, University of Georgia, Athens, GA 30602, USA
| | - Alinde Fojtik
- Southeastern Cooperative Wildlife Disease Study, University of Georgia, Athens, GA 30602, USA
| | - Sarah Coker
- Southeastern Cooperative Wildlife Disease Study, University of Georgia, Athens, GA 30602, USA
| | - Emily Doub
- Southeastern Cooperative Wildlife Disease Study, University of Georgia, Athens, GA 30602, USA
| | - Vienna R Brown
- USDA APHIS Wildlife Services, National Feral Swine Damage Management Program, Fort Collins, CO 80521, USA
| | - Ania A Majewska
- Center for Ecology of Infectious Diseases, University of Georgia, Athens, GA 30602, USA; Department of Physiology and Pharmacology, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA
| | - Michael J Yabsley
- Southeastern Cooperative Wildlife Disease Study, University of Georgia, Athens, GA 30602, USA; Center for Ecology of Infectious Diseases, University of Georgia, Athens, GA 30602, USA.
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50
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Liblik K, Florica IT, Baranchuk A. Original algorithms for the detection of cardiovascular involvement of neglected tropical diseases. Expert Rev Cardiovasc Ther 2024; 22:59-74. [PMID: 38308590 DOI: 10.1080/14779072.2024.2315090] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 08/29/2023] [Accepted: 02/02/2024] [Indexed: 02/05/2024]
Abstract
INTRODUCTION Neglected tropical diseases (NTDs) introduce considerable morbidity and mortality on a global scale, directly impacting over 1 billion individuals as well as their families and communities. Afflicted individuals may have limited access to resources and care in these regions, contributing to a high proportion of chronic, progressive, and systemic disease. The cardiovascular system is at particular risk of demise for several NTDs, yet remains largely unstudied due in part to the lack of robust data collection mechanisms in the most impacted regions. AREAS COVERED The present review is a part of the Neglected Tropical Diseases and other Infectious Diseases affecting the Heart (NET-Heart) Project, aiming at summarizing the current knowledge on cardiovascular implications of NTDs and providing diagnostic as well as management recommendations which can be tailored to low-resource settings. The diagnostic and management algorithms of 13 unique NTDs are presented and summarized. EXPERT OPINION Recognizing cardiac manifestations of NTDs can significantly alter disease trajectory and all physicians benefit from improved knowledge about NTDs. Great potential exists to advance patient care by improving data collection, communication, and international collaboration.
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Affiliation(s)
- Kiera Liblik
- Department of Medicine, Kingston Health Science Center, Queen's University, Kingston, Ontario, Canada
| | - Ioana Tereza Florica
- Department of Medicine, Kingston Health Science Center, Queen's University, Kingston, Ontario, Canada
| | - Adrian Baranchuk
- Division of Cardiology, Kingston Health Science Center, Queen's University, Kingston, Ontario, Canada
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