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For: Francesco VD, Zullo A, Hassan C, Giorgio F, Rosania R, Ierardi E. Mechanisms of Helicobacter pylori antibiotic resistance: An updated appraisal. World J Gastrointest Pathophysiol 2011; 2(3): 35-41 [PMID: 21860834 DOI: 10.4291/wjgp.v2.i3.35]
URL: https://www.wjgnet.com/2150-5330/full/v2/i3/35.htm
Number Citing Articles
1
Zeyneb Benramdane, Matteo Michelotti, Thamere Cheriet, Andrea Defant, Ines Mancini. Synthesis and In Silico Study of Pectolinarigenin–Metronidazole Hybrid Molecule as Anti-Helicobacter pylori. Molecules 2026; 31(12) doi: 10.3390/molecules31122089
2
Ramganesh Selvarajan, Chinedu Obize, Timothy Sibanda, Akebe Luther King Abia, Haijun Long. Evolution and Emergence of Antibiotic Resistance in Given Ecosystems: Possible Strategies for Addressing the Challenge of Antibiotic Resistance. Antibiotics 2022; 12(1) doi: 10.3390/antibiotics12010028
3
Paweł Krzyżek. Toxin-Antitoxin Systems - A New Player in Morphological Transformation of Antibiotic-Exposed Helicobacter pylori?. Frontiers in Cellular and Infection Microbiology 2021; 11 doi: 10.3389/fcimb.2021.670677
4
Luong Thi My Ngan, Joon-Kwan Moon, Takayuki Shibamoto, Young-Joon Ahn. Growth-Inhibiting, Bactericidal, and Urease Inhibitory Effects of Paeonia lactiflora Root Constituents and Related Compounds on Antibiotic-Susceptible and -Resistant Strains of Helicobacter pylori. Journal of Agricultural and Food Chemistry 2012; 60(36) doi: 10.1021/jf3035034
5
P. Bharathi, Kannaiyan Kavitha, V. Vinoth, Latha Ragunathan, Thiyagarajan Sanjeevi, Madiha Abdul Nazer, I. Deepika, Ravikumar Sambandam. Identification and Charcterization of Helicobacter pylori Isolated from Patients with Upper Gastrointestinal Disorders at a Tertiary Health Care Hospital. Biomedical and Biotechnology Research Journal 2023; 7(3) doi: 10.4103/bbrj.bbrj_136_23
6
Xiang Peng, Huang-wei Chen, Yu Wan, Pei-zhu Su, Jing Yu, Jun-jun Liu, Yi Lu, Min Zhang, Jia-Yin Yao, Min Zhi. Combination of vonoprazan and amoxicillin as the first-line Helicobacter pylori eradication therapy: a multicenter, prospective, randomized, parallel-controlled study. Clinical and Experimental Medicine 2023; 23(7) doi: 10.1007/s10238-023-01074-5
7
Camelia Quek, Son T. Pham, Kieu T. Tran, Binh T. Pham, Loc V. Huynh, Ngan B.L. Luu, Thao K.T. Le, Kelly Quek, Van H. Pham. Antimicrobial susceptibility and clarithromycin resistance patterns of Helicobacter pylori clinical isolates in Vietnam. F1000Research 2016; 5 doi: 10.12688/f1000research.8239.1
8
Anne Mlocek, Nadine Dietze-Jergus, Norman Lippmann, Gunter Matthias Christian Flemming, Jürgen Feisthammel, Albrecht Hoffmeister, Christoph Lübbert. Etablierung einer routinemäßigen Resistenzbestimmung von Helicobacter pylori am Universitätsklinikum Leipzig: Erste Ergebnisse lokaler Bemühungen zur Umsetzung des Prinzips einer resistenzbasierten Eradikationstherapie. Zeitschrift für Gastroenterologie 2026;  doi: 10.1055/a-2894-1917
9
Yong Hwan Kwon, Seong Woo Jeon, Su Youn Nam, Hyun Suk Lee, Ji Hey Park. Efficacy of tailored therapy for Helicobacter pylori eradication based on clarithromycin resistance and survey of previous antibiotic exposure: A single‐center prospective pilot study. Helicobacter 2019; 24(4) doi: 10.1111/hel.12585
10
Steven F. Moss, Long P. Dang, David Chua, Javier Sobrado, Yi Zhou, David Y. Graham. Comparable Results of Helicobacter pylori Antibiotic Resistance Testing of Stools vs Gastric Biopsies Using Next-Generation Sequencing. Gastroenterology 2022; 162(7) doi: 10.1053/j.gastro.2022.02.027
11
L.F. Garrido-Treviño, M. López-Martínez, J.A. Flores-Hinojosa, L. Tijerina-Rodríguez, F. Bosques-Padilla. Tratamiento empírico vs tratamiento basado en susceptibilidad para erradicar H.pylori: ¿es posible cambiar este paradigma usando métodos moleculares modernos?. Revista de Gastroenterología de México 2022; 87(3) doi: 10.1016/j.rgmx.2022.01.007
12
S. Yu. Serebrova, E. N. Kareva, N. N. Eremenko, A. B. Prokof’ev, D. O. Kurguzova, V. N. Drozdov, N. B. Lazareva, I. A. Komissarenko, A. K. Starodubtsev. Role of Drug – Drug Interactions in the Efficacy and Safety of Clarithromycin Treatment for Helicobacter Pylori Eradication. Pharmaceutical Chemistry Journal 2019; 53(8) doi: 10.1007/s11094-019-02061-5
13
Hong-xin Zhang, Yu-yu Qiu, Ying-hui Zhao, Xin-ting Liu, Ming Liu, Ai-lian Yu. Immunogenicity of oral vaccination with Lactococcus lactis derived vaccine candidate antigen (UreB) of Helicobacter pylori fused with the human interleukin 2 as adjuvant. Molecular and Cellular Probes 2014; 28(1) doi: 10.1016/j.mcp.2013.08.003
14
Katherine A. Lyseng-Williamson. Pylera® (bismuth subcitrate potassium/metronidazole/tetracycline hydrochloride) in the eradication of Helicobacter pylori infection: a profile of its use in Europe. Drugs & Therapy Perspectives 2017; 33(7) doi: 10.1007/s40267-017-0417-7
15
Helia Alavifard, Ali Nabavi-Rad, Kaveh Baghaei, Amir Sadeghi, Abbas Yadegar, Mohammad Reza Zali. Pyrosequencing analysis for rapid and accurate detection of clarithromycin resistance-associated mutations in Iranian Helicobacter pylori isolates. BMC Research Notes 2023; 16(1) doi: 10.1186/s13104-023-06420-0
16
Marwa S. Fathi, Runia Fouad EL-Folly, Rania Ahmed Hassan, Mohammed Ezz El-Arab. Genotypic and phenotypic patterns of antimicrobial susceptibility of Helicobacter pylori strains among Egyptian patients. Egyptian Journal of Medical Human Genetics 2013; 14(3) doi: 10.1016/j.ejmhg.2013.03.004
17
Isabella S. Sirit, Richard M. Peek. Decoding the Ability of Helicobacter pylori to Evade Immune Recognition and Cause Disease. Cellular and Molecular Gastroenterology and Hepatology 2025; 19(5) doi: 10.1016/j.jcmgh.2025.101470
18
John Jairo Aguilera-Correa, Pedro Urruzuno, Josefa Barrio, María José Martinez, Sonia Agudo, Angela Somodevilla, Laura Llorca, Teresa Alarcón. Detection of Helicobacter pylori and the genotypes of resistance to clarithromycin and the heterogeneous genotype to this antibiotic in biopsies obtained from symptomatic children. Diagnostic Microbiology and Infectious Disease 2017; 87(2) doi: 10.1016/j.diagmicrobio.2016.03.001
19
Reyhan Caliskan, Hrisi Bahar Tokman, Yusuf Erzin, Suat Saribas, Pelin Yuksel, Bora Kazim Bolek, Ecehan Ozge Sevuk, Mehmet Demirci, Ozge Yılmazli, Ozer Akgul, Fatma Kalayci, Huseyin Cakan, Barik Salih, Kadir Bal, Bekir Kocazeybek. Antimicrobial resistance of Helicobacter pylori strains to five antibiotics, including levofloxacin, in Northwestern Turkey. Revista da Sociedade Brasileira de Medicina Tropical 2015; 48(3) doi: 10.1590/0037-8682-0027-2015
20
Ji Hae Nahm, Won Kyu Kim, Yujin Kwon, Hyunki Kim. Detection of Helicobacter pylori with clarithromycin resistance‐associated mutations using peptide nucleic acid probe‐based melting point analysis. Helicobacter 2019; 24(5) doi: 10.1111/hel.12634
21
Amin Fath Tabar, Azar Nejati, Seyedeh Nasim Mirbahari, Mohammad Rahmanian, Ehsan Nazemalhosseini Mojarad, Zahra Sadeghloo, Hamideh Raeisi. Beyond Antibiotics: Alternative Strategies Targeting Helicobacter pylori Resistance. Expert Reviews in Molecular Medicine 2026; 28 doi: 10.1017/erm.2026.10040
22
Judit Alarcón-Millán, Gloria Fernández-Tilapa, Enoc Mariano Cortés-Malagón, Carlos Alberto Castañón-Sánchez, José De Sampedro-Reyes, Iván Cruz-del Carmen, Reyes Betancourt-Linares, Adolfo Román-Román. Clarithromycin resistance and prevalence of Helicobacter pylori virulent genotypes in patients from Southern México with chronic gastritis. Infection, Genetics and Evolution 2016; 44 doi: 10.1016/j.meegid.2016.06.044
23
Boram Cha, Byoung Wook Bang, Jong Beom Shin, Eun Jung Ko, Weonjin Ko, Kye Sook Kwon, Yong Woon Shin, Young Ju Suh, Hyungkil Kim. Bismuth containing quadruple therapy versus tailored therapy as first-line treatments for Helicobacter pylori infection in a high clarithromycin resistance area. Scandinavian Journal of Gastroenterology 2021; 56(9) doi: 10.1080/00365521.2021.1948606
24
Pratyusa Biswas, Laishram Pradeepkumar Singh. Global Trends in Health, Technology and Management II. 2026;  doi: 10.1007/978-3-032-12320-6_21
25
Jung Won Lee, Nayoung Kim, Ryoung Hee Nam, Ji Hyun Park, Yoon Jin Choi, Jung Mogg Kim, Joo Sung Kim, Hyun Chae Jung. GenoType HelicoDR test in the determination of antimicrobial resistance ofHelicobacter pyloriin Korea. Scandinavian Journal of Gastroenterology 2014; 49(9) doi: 10.3109/00365521.2014.894117
26
M.S. González-Huezo, A. Rojas-Sánchez, A.A. Rosales-Solís, R.M. Miranda-Cordero, A. Hinojosa-Ruiz, E. Mejía-García, E.G. Cruz-González. Frecuencia de erradicación del Helicobacter pylori con triple esquema convencional en pacientes adultos del Centro Médico Issemym. Revista de Gastroenterología de México 2012; 77(3) doi: 10.1016/j.rgmx.2012.05.001
27
Vincenzo De Francesco, Angelo Zullo, Floriana Giorgio, Ilaria Saracino, Cristina Zaccaro, Cesare Hassan, Enzo Ierardi, Alfredo Di Leo, Giulia Fiorini, Valentina Castelli, Giovanna Lo Re, Dino Vaira. Change of point mutations in Helicobacter pylori rRNA associated with clarithromycin resistance in Italy.  Journal of Medical Microbiology 2014; 63(3) doi: 10.1099/jmm.0.067942-0
28
Tarik Aanniz, Wissal Bakri, Safae El Mazouri, Hajar Wakrim, Ilham Kandoussi, Lahcen Belyamani, Mouna Ouadghiri, Azeddine Ibrahimi. Focus on Bacterial Biofilms. 2022;  doi: 10.5772/intechopen.104568
29
Nagendran Tharmalingam, Jenna Port, Dawilmer Castillo, Eleftherios Mylonakis. Repurposing the anthelmintic drug niclosamide to combat Helicobacter pylori. Scientific Reports 2018; 8(1) doi: 10.1038/s41598-018-22037-x
30
Jose Danilo Atehortua Rendon, Tania Liseth Pérez Cala, Alonso Martínez. Descripción de la resistencia de Helicobacter pylori a seis antibióticos de uso frecuente en Colombia. Revista Colombiana de Gastroenterología 2020; 35(3) doi: 10.22516/25007440.493
31
Animesh Tripathi, Anjali Jaiswal, Dinesh Kumar, Priyank Chavda, Ramesh Pandit, Madhvi Joshi, Damer P. Blake, Fiona M. Tomley, Chaitanya G. Joshi, Suresh Kumar Dubey. Antimicrobial resistance in plant endophytes associated with poultry-manure application revealed by selective culture and whole genome sequencing. Journal of Hazardous Materials 2024; 480 doi: 10.1016/j.jhazmat.2024.136166
32
I‐Fan Tu, Jiahn‐Haur Liao, Feng‐Ling Yang, Nien‐Tsung Lin, Hong‐Lin Chan, Shih‐Hsiung Wu. Lon Protease Affects the RdxA Nitroreductase Activity and Metronidazole Susceptibility in Helicobacter pylori. Helicobacter 2014; 19(5) doi: 10.1111/hel.12140
33
Meiliang Gong, Yingjie Han, Xuning Wang, Hongjin Tao, Fansen Meng, Baicun Hou, Benjamin B. Sun, Gangshi Wang. Effect of Temperature on Metronidazole Resistance in Helicobacter pylori. Frontiers in Microbiology 2021; 12 doi: 10.3389/fmicb.2021.681911
34
Wai Phyo Aung, Than Than Aye, Khin San Aye, Aye Mya Mya Kyaw. Levofloxacin‐based Helicobacter pylori eradication in chronic dyspepsia . GastroHep 2021; 3(6) doi: 10.1002/ygh2.478
35
Xiao-Juan Zhang, Shu-Ying Feng, Zhi-Tao Li, Yan-Ming Feng. Expression ofHelicobacter pylori hspAGene inLactococcus lactisNICE System and Experimental Study on Its Immunoreactivity. Gastroenterology Research and Practice 2015; 2015 doi: 10.1155/2015/750932
36
Tran Thanh Binh, Seiji Shiota, Rumiko Suzuki, Miyuki Matsuda, Tran Thi Huyen Trang, Dong Hyeon Kwon, Shun Iwatani, Yoshio Yamaoka. Discovery of novel mutations for clarithromycin resistance in Helicobacter pylori by using next-generation sequencing. Journal of Antimicrobial Chemotherapy 2014; 69(7) doi: 10.1093/jac/dku050
37
Naim Asyraf Rosli, Anis Rageh Al-Maleki, Mun Fai Loke, Sun Tee Tay, Mohd Salleh Rofiee, Lay Kek Teh, Mohd Zaki Salleh, Jamuna Vadivelu, Bashir Sajo Mienda. Exposure of Helicobacter pylori to clarithromycin in vitro resulting in the development of resistance and triggers metabolic reprogramming associated with virulence and pathogenicity. PLOS ONE 2024; 19(3) doi: 10.1371/journal.pone.0298434
38
Guillaume Pittie, Terry Laurent, Jean Radermacher, Sophie Herens, Anca Boeras, Giang Ho. Detection by Real-Time PCR of Helicobacter pylori and Clarithromycin Resistance Compared to Histology on Gastric Biopsies. Microorganisms 2024; 12(11) doi: 10.3390/microorganisms12112192
39
Ian H. Windham, D. Scott Merrell, George O’Toole. Interplay between Amoxicillin Resistance and Osmotic Stress in Helicobacter pylori. Journal of Bacteriology 2022; 204(5) doi: 10.1128/jb.00045-22
40
Meltem Ayaş, Yeşim Gürol. Antibiotic Resistance of Helicobacter pylori in Turkey: A Systematic Review and Meta-Analysis . Microbial Drug Resistance 2023; 29(3) doi: 10.1089/mdr.2022.0146
41
Tahereh Falsafi, Azadeh Ehsani, Bahareh Attaran, Vahid Niknam. Association of hp1181 and hp1184 Genes With the Active Efflux Phenotype in Multidrug-Resistant Isolates of Helicobacter pylori. Jundishapur Journal of Microbiology 2016; 9(4) doi: 10.5812/jjm.30726
42
Kimberly Sánchez-Alonzo, Libnny Belmar, Cristian Parra-Sepúlveda, Humberto Bernasconi, Víctor L. Campos, Carlos T. Smith, Katia Sáez, Apolinaria García-Cancino. Antibiotics as a Stressing Factor Triggering the Harboring of Helicobacter pylori J99 within Candida albicans ATCC10231. Pathogens 2021; 10(3) doi: 10.3390/pathogens10030382
43
Se-Won Lee, Jeong Ho Lee. Anti-inflammatory and anti-Helicobacter effects of the Aralia elata hot-water extract. Korean Journal of Food Preservation 2021; 28(2) doi: 10.11002/kjfp.2021.28.2.279
44
Ilaria Maria Saracino, Giulia Fiorini, Angelo Zullo, Matteo Pavoni, Laura Saccomanno, Dino Vaira. Trends in Primary Antibiotic Resistance in H. pylori Strains Isolated in Italy between 2009 and 2019. Antibiotics 2020; 9(1) doi: 10.3390/antibiotics9010026
45
Ana Bačić, Vladimir Milivojević, Isidora Petković, Dušan Kekić, Ina Gajić, Branislava Medić Brkić, Dušan Popadić, Tomica Milosavljević, Mirjana Rajilić-Stojanović. In Search for Reasons behind Helicobacter pylori Eradication Failure–Assessment of the Antibiotics Resistance Rate and Co-Existence of Helicobacter pylori with Candida Species. Journal of Fungi 2023; 9(3) doi: 10.3390/jof9030328
46
L.F. Garrido-Treviño, M. López-Martínez, J.A. Flores-Hinojosa, L. Tijerina-Rodríguez, F. Bosques-Padilla. Empiric treatment vs susceptibility-guided treatment for eradicating H. pylori: Is it possible to change that paradigm using modern molecular methods?. Revista de Gastroenterología de México (English Edition) 2022; 87(3) doi: 10.1016/j.rgmxen.2022.06.003
47
Nazlı Arslan, Özlem Yılmaz, Ebru Demiray-Gürbüz. Importance of antimicrobial susceptibility testing for the management of eradication in <i>Helicobacter pylori</i> infection. World Journal of Gastroenterology 2017; 23(16): 2854-2869 doi: 10.3748/wjg.v23.i16.2854
48
Joana S. Vital, Luís Tanoeiro, Ricardo Lopes-Oliveira, Filipa F. Vale. Biomarker Characterization and Prediction of Virulence and Antibiotic Resistance from Helicobacter pylori Next Generation Sequencing Data. Biomolecules 2022; 12(5) doi: 10.3390/biom12050691
49
Yakun Zhao, Lihua He, Lu Sun, Wentao Liu, Hairui Wang, Jianzhong Zhang, Yanan Gong, Xiaohui Wang. RdxA-independent mechanism of Helicobacter pylori metronidazole metabolism. Frontiers in Microbiology 2025; 16 doi: 10.3389/fmicb.2025.1553734
50
Nuno Almeida, José M. Romãozinho, Maria M. Donato, Cristina Luxo, Olga Cardoso, Maria A. Cipriano, Carol Marinho, Carlos Sofia. Triple Therapy with High‐Dose Proton‐Pump Inhibitor, Amoxicillin, and Doxycycline Is Useless for Helicobacter pylori Eradication: A Proof‐of‐Concept Study. Helicobacter 2014; 19(2) doi: 10.1111/hel.12106
51
Ayla Debraekeleer, Han Remaut. Future Perspective for Potential Helicobacter Pylori Eradication Therapies . Future Microbiology 2018; 13(6) doi: 10.2217/fmb-2017-0115
52
Shamshul Ansari, Yoshio Yamaoka. Helicobacter pylori Infection, Its Laboratory Diagnosis, and Antimicrobial Resistance: a Perspective of Clinical Relevance. Clinical Microbiology Reviews 2022; 35(3) doi: 10.1128/cmr.00258-21
53
Bradd Mendoza-Guido, Juan D Romero-Carpio, Silvia Molina-Castro. Comprehensive plasmidomic analysis of Helicobacter pylori reveals the potential role of plasmids in pathogenic adaptation and a novel putative toxin-antitoxin system. FEMS Microbiology Letters 2025; 372 doi: 10.1093/femsle/fnaf092
54
Fayaz Ahmad Wani, Gulnaz Bashir, Mushtaq Ahmad Khan, Showkat Ali Zargar, Zubaida Rasool, Qurteeba Qadri. Antibiotic Resistance in Helicobacter pylori: A Mutational Analysis from a Tertiary Care Hospital in Kashmir, India. Indian Journal of Medical Microbiology 2018; 36(2) doi: 10.4103/ijmm.IJMM_18_19
55
A.J. Matta, D.C. Zambrano, Y.C. Martínez, F.F. Fernández. Point mutations in the glycosyltransferase domain of the pbp1a gene in amoxicillin-resistant Helicobacter pylori isolates. Revista de Gastroenterología de México (English Edition) 2023; 88(2) doi: 10.1016/j.rgmxen.2021.05.015
56
A.J. Matta, D.C. Zambrano, Y.C. Martínez, F.F. Fernández. Mutaciones puntuales en el dominio transglicosilasa del gen pbp1a en aislados de Helicobacter pylori resistentes a amoxicilina. Revista de Gastroenterología de México 2023; 88(2) doi: 10.1016/j.rgmx.2021.05.008
57
Mutita Wongsuwanlert, Rawee Teanpaisan, Praphansri Ruangsri, Apichat Kaewdech, Somkiat Sunpaweravong, Nuntiya Pahumunto. Effect of mouthwash containing poly l-Lysine and glycerol monolaurate on oral Helicobacter pylori relating to biofilm eradication, anti-adhesion, and pro-inflammatory cytokine suppression. Journal of Dental Sciences 2024; 19(3) doi: 10.1016/j.jds.2023.10.010
58
Hyun-Kyung Lee, Ha Eun Song, Haeng-Byung Lee, Cheol-Soo Kim, Mamoru Koketsu, Luong Thi My Ngan, Young-Joon Ahn, Dipshikha Chakravortty. Growth Inhibitory, Bactericidal, and Morphostructural Effects of Dehydrocostus Lactone from Magnolia sieboldii Leaves on Antibiotic-Susceptible and -Resistant Strains of Helicobacter pylori. PLoS ONE 2014; 9(4) doi: 10.1371/journal.pone.0095530
59
Ali Baradaran Moghaddam, Nour Amirmozafari, Shahla Mansouri, Nastaran Farzi, Naser Ebrahimi-Daryani, Masoud Alebouyeh, Mohammad Reza Zali. Nitazoxanide and Doxycycline Sensitivity Among Metronidazole Resistant Helicobacter pylori Isolates from Patients with Gastritis. Archives of Clinical Infectious Diseases 2018; 13(1) doi: 10.5812/archcid.66693
60
Francis Lauener, Frank Imkamp, Philippe Lehours, Alice Buissonnière, Lucie Benejat, Reinhard Zbinden, Peter Keller, Karoline Wagner. Genetic Determinants and Prediction of Antibiotic Resistance Phenotypes in Helicobacter pylori. Journal of Clinical Medicine 2019; 8(1) doi: 10.3390/jcm8010053
61
Divya S. Raj, Dinesh Kumar Kesavan, Natarajan Muthusamy, S. Umamaheswari. Efflux pumps potential drug targets to circumvent drug Resistance – Multi drug efflux pumps of Helicobacter pylori. Materials Today: Proceedings 2021; 45 doi: 10.1016/j.matpr.2020.11.955
62
Dalia Hamza, Rehab Elhelw, Mahmoud Elhariri, Eman Ragab. Genotyping and antimicrobial resistance patterns of Helicobacter pylori in human and dogs associated with A2142G and A2143G point mutations in clarithromycin resistance. Microbial Pathogenesis 2018; 123 doi: 10.1016/j.micpath.2018.07.016
63
Sandra Salillas, Juan José Galano-Frutos, Alejandro Mahía, Ritwik Maity, María Conde-Giménez, Ernesto Anoz-Carbonell, Helena Berlamont, Adrian Velazquez-Campoy, Eliette Touati, Uwe Mamat, Ulrich E. Schaible, José A. Gálvez, María D. Díaz-de-Villegas, Freddy Haesebrouck, José A. Aínsa, Javier Sancho. Selective Targeting of Human and Animal Pathogens of the Helicobacter Genus by Flavodoxin Inhibitors: Efficacy, Synergy, Resistance and Mechanistic Studies. International Journal of Molecular Sciences 2021; 22(18) doi: 10.3390/ijms221810137
64
Dana Binyamin, Nina Pastukh, Avi On, Maya Paritsky, Avi Peretz. Phenotypic and genotypic correlation as expressed in Helicobacter pylori resistance to clarithromycin and fluoroquinolones. Gut Pathogens 2017; 9(1) doi: 10.1186/s13099-017-0198-5
65
Dusan Kekic, Milos Jovicevic, Jovana Kabic, Iva Lolic, Ina Gajic, Stefan Stojkovic, Lazar Ranin, Tomica Milosavljevic, Natasa Opavski, Ivan Rankovic, Vladimir Milivojevic. Genetic Determinants of Clarithromycin and Fluoroquinolones Resistance in Helicobacter pylori in Serbia. Antibiotics 2024; 13(10) doi: 10.3390/antibiotics13100933
66
Alain Cimuanga-Mukanya, Evariste Tshibangu-Kabamba, Patrick de Jesus Ngoma Kisoko, Kartika Afrida Fauzia, Fabien Mbaya Tshibangu, Antoine Tshimpi Wola, Pascal Tshiamala Kashala, Dieudonné Mumba Ngoyi, Steve Ahuka-Mundeke, Gunturu Revathi, Ghislain Disashi-Tumba, Yasutoshi Kido, Takashi Matsumoto, Junko Akada, Yoshio Yamaoka, Paul D. Fey. Synergistic effects of novel penicillin-binding protein 1A amino acid substitutions contribute to high-level amoxicillin resistance of Helicobacter pylori . mSphere 2024; 9(8) doi: 10.1128/msphere.00089-24
67
Saracino I.M., Pavoni M., Zullo A., Fiorini G., Saccomanno L., Lazzarotto T., Cavallo R., Antonelli G., Vaira D.. Antibiotic Resistance and Therapy Outcome in H. pylori Eradication Failure Patients. Antibiotics 2020; 9(3) doi: 10.3390/antibiotics9030121
68
Jiaoe Chen, Liping Ye, Liangmin Jin, Xuehua Xu, Peisong Xu, Xianjun Wang, Hongzhang Li. Application of next-generation sequencing to characterize novel mutations in clarithromycin-susceptible Helicobacter pylori strains with A2143G of 23S rRNA gene. Annals of Clinical Microbiology and Antimicrobials 2018; 17(1) doi: 10.1186/s12941-018-0259-8
69
Éva Kocsmár, György Miklós Buzás, Ildikó Szirtes, Ildikó Kocsmár, Zsófia Kramer, Attila Szijártó, Petra Fadgyas-Freyler, Kató Szénás, Massimo Rugge, Matteo Fassan, András Kiss, Zsuzsa Schaff, Gergely Röst, Gábor Lotz. Primary and secondary clarithromycin resistance in Helicobacter pylori and mathematical modeling of the role of macrolides. Nature Communications 2021; 12(1) doi: 10.1038/s41467-021-22557-7
70
Hye Yoon Park, Eun Jeong Kang, Dong Gun Kim, Ki Ju Kim, Jin Woo Choi, Su Youn Nam, Yong Hwan Kwon, Hyun Seok Lee, Seong Woo Jeon. High and Frequent Dose of Dexlansoprazole and Amoxicillin Dual Therapy for Helicobacter pylori Infections: A Single Arm Prospective Study. Korean Journal of Gastroenterology 2017; 70(4) doi: 10.4166/kjg.2017.70.4.176
71
Judit Alarcón-Millán, José Bonilla-Delgado, Gloria Fernández-Tilapa, Nayeli Goreti Nieto-Velázquez, Mónica Sierra-Martínez, Víctor Manuel Alvarado-Castro, Enoc Mariano Cortés-Malagón. Helicobacter pylori Virulence Factors and Clarithromycin Resistance-Associated Mutations in Mexican Patients. Pathogens 2023; 12(2) doi: 10.3390/pathogens12020234
72
Jung Won Lee, Nayoung Kim, Ryoung Hee Nam, Jeong Eun Yu, Joo Hee Son, Sun Min Lee, Dong Ho Lee. Efficacy of Tegoprazan for Improving the Susceptibility of Antimicrobial Agents against Antibiotic-Resistant Helicobacter pylori. Gut and Liver 2021; 15(1) doi: 10.5009/gnl20247
73
Kimberly Sánchez-Alonzo, Luciano Arellano-Arriagada, Susana Castro-Seriche, Cristian Parra-Sepúlveda, Humberto Bernasconi, Héctor Benavidez-Hernández, Víctor L. Campos, Katia Sáez, Carlos T. Smith, Apolinaria García-Cancino. Temperatures Outside the Optimal Range for Helicobacter pylori Increase Its Harboring within Candida Yeast Cells. Biology 2021; 10(9) doi: 10.3390/biology10090915
74
Urszula Zarzecka, Aileen Harrer, Anna Zawilak-Pawlik, Joanna Skorko-Glonek, Steffen Backert. Chaperone activity of serine protease HtrA of Helicobacter pylori as a crucial survival factor under stress conditions. Cell Communication and Signaling 2019; 17(1) doi: 10.1186/s12964-019-0481-9
75
Shahrbanoo Keshavarz Azizi Raftar, Rezvan Moniri, Mahmood Saffari, Mohsen Razavi Zadeh, Abbas Arj, Seyed Gholam Abbas Mousavi, Hamed Mirzaei Ghazi Kalayeh, Kamran Dastehgoli. The Helicobacter pylori Resistance Rate to Clarithromycin in Iran . Microbial Drug Resistance 2015; 21(1) doi: 10.1089/mdr.2014.0104
76
Asif Sukri, Alfizah Hanafiah, Hamidah Yusoff, Nur Atiqah Shamsul Nizam, Zarith Nameyrra, Zhiqin Wong, Raja Affendi Raja Ali. Multidrug-Resistant Helicobacter pylori Strains: A Five-Year Surveillance Study and Its Genome Characteristics. Antibiotics 2022; 11(10) doi: 10.3390/antibiotics11101391
77
Shaza Azlin Razak, Alfizah Hanafiah, Asif Sukri, Hui-min Neoh, Noraziah Mohamad Zin. Analysis of antibiotic resistance and cagPAI variability in Helicobacter pylori strains from Malaysian patients. International Microbiology 2025; 28(8) doi: 10.1007/s10123-025-00741-9
78
Ilaria Maria Saracino, Matteo Pavoni, Angelo Zullo, Giulia Fiorini, Tiziana Lazzarotto, Claudio Borghi, Dino Vaira. Next Generation Sequencing for the Prediction of the Antibiotic Resistance in Helicobacter pylori: A Literature Review. Antibiotics 2021; 10(4) doi: 10.3390/antibiotics10040437
79
Van Huy Tran, Thi Minh Thi Ha, Phan Tuong Quynh Le, Trung Nam Phan, Thi Nhu Hoa Tran. Characterisation of point mutations in domain V of the 23S rRNA gene of clinical Helicobacter pylori strains and clarithromycin-resistant phenotype in central Vietnam. Journal of Global Antimicrobial Resistance 2019; 16 doi: 10.1016/j.jgar.2018.09.012
80
L. B. Lazebnik, N. N. Dekhnich, S. I. Sitkin, V. G. Atrushevich, E. B. Avalueva, I. G. Bakulin, N. V. Bakulina, N. V. Baryshnikova, L. N. Belousova, D. S. Bordin, A. V. Veselov, V. B. Grinevich, M. M. Gurova, E. Yu. Eremina, N. V. Ivanchik, R. S. Kozlov, I. V. Kozlova, E. A. Kornienko, Yu. A. Kravchuk, I. N. Kupriyanova, Yu. A. Kucheryavy, B. N. Levitan, M. A. Livzan, E. V. Luzina, E. A. Lyalyukova, V. P. Novikova, O. D. Ostroumova, T. L. Pilat, A. S. Sarsenbaeva, D. A. Sychev, A. A. Tryapyshko, D. I. Trukhan, S. V. Turkina, Yu. P. Uspensky, Yu. L. Fedorchenko, Yu. A. Fominykh, A. I. Khavkin, O. V. Khlynova, S. G. Khomeriki, N. M. Khomeriki, M. A. Shevyakov. Helicobacter pylori, helicobacteriosis and associated diseases (VIII Moscow Agreements on the diagnosis and treatment of helicobacteriosis in adults and children) A Clinical Guide for Physicians. Experimental and Clinical Gastroenterology 2024; (12) doi: 10.31146/1682-8658-ecg-232-12-49-145
81
82
Luong Thi My Ngan, Pham Phuong Dung, Nguyen Vang Thi Yen Nhi, Nguyen van Minh Hoang, Tran Trung Hieu. Antibacterial activity of ethanolic extracts of some Vietnamese medicinal plants against Helicobacter pylori. 2017; 1878 doi: 10.1063/1.5000198
83
Bekir Kocazeybek, Merve Kutlu Sakli, Pelin Yuksel, Mehmet Demirci, Reyhan Caliskan, Tevhide Ziver Sarp, Suat Saribas, Suleyman Demiryas, Fatma Kalayci, Huseyin Cakan, Hayriye Kirkoyun Uysal, Nesrin Gareayaghi, Sevgi Ergin, Yusuf Ziya Erzin, Kadir Bal, İhsan Tascı, Hrisi Bahar Tokman. Comparison of new and classical point mutations associated with clarithromycin resistance in Helicobacter pylori strains isolated from dyspeptic patients and their effects on phenotypic clarithromycin resistance.  Journal of Medical Microbiology 2019; 68(4) doi: 10.1099/jmm.0.000944
84
Yuji Morita, Junko Tomida, Yoshiaki Kawamura. Multidrug Efflux Systems in Helicobacter cinaedi. Antibiotics 2012; 1(1) doi: 10.3390/antibiotics1010029
85
Meltem Ayaş, Sinem Oktem-Okullu, Orhan Özcan, Tanıl Kocagöz, Yeşim Gürol. Exploring the Molecular Mechanisms of Macrolide Resistance in Laboratory Mutant Helicobacter pylori. Antibiotics 2024; 13(5) doi: 10.3390/antibiotics13050396
86
I V Maev, D N Andreev. Molecular genetic predictors of resistance to anti-Helicobacter pylori therapy. Terapevticheskii arkhiv 2017; 89(8) doi: 10.17116/terarkh20178985-12
87
Nina Pastukh, Dana Binyamin, Avi On, Maya Paritsky, Avi Peretz. GenoType® HelicoDR test in comparison with histology and culture for Helicobacter pylori detection and identification of resistance mutations to clarithromycin and fluoroquinolones. Helicobacter 2017; 22(6) doi: 10.1111/hel.12447
88
Alicia C Marín, Adrian G McNicholl, Vincenzo Savarino, Xavier Calvet, Grigorios I Leontiadis, Lori Fischbach, Yuhong Yuan, Javier P Gisbert. Optimum second-line regimens for Helicobacter pylori eradication. Cochrane Database of Systematic Reviews 2014;  doi: 10.1002/14651858.CD011363
89
Vincenzo De Francesco, Cesare Hassan, Lorenzo Ridola, Floriana Giorgio, Enzo Ierardi, Angelo Zullo. Sequential, concomitant and hybrid first-line therapies for Helicobacter pylori eradication: a prospective randomized study.  Journal of Medical Microbiology 2014; 63(5) doi: 10.1099/jmm.0.072322-0
90
N. Almeida, J.M. Romãozinho, M.M. Donato, C. Luxo, O. Cardoso, M.A. Cipriano, C. Marinho, A. Fernandes, C. Calhau, C. Sofia. Helicobacter pylori antimicrobial resistance rates in the central region of Portugal. Clinical Microbiology and Infection 2014; 20(11) doi: 10.1111/1469-0691.12701
91
Vignesh Shetty, Binit Lamichhane, Chin Yen Tay, Ganesh C. Pai, Ramachandra Lingadakai, Girisha Balaraju, Shiran Shetty, Mamatha Ballal, Eng Guan Chua. High primary resistance to metronidazole and levofloxacin, and a moderate resistance to clarithromycin in Helicobacter pylori isolated from Karnataka patients. Gut Pathogens 2019; 11(1) doi: 10.1186/s13099-019-0305-x
92
I.A. Egorov, T.A. Egorova, E.A. Yildirim, K.A. Kalitkina, L.A. Ilina, V.G. Frolov, S. Eliseeva, E.A. Vatskel. Effect of chitosan complexes on the bacterial community of cecum and productivity of broiler chickens. BIO Web of Conferences 2022; 48 doi: 10.1051/bioconf/20224803007
93
L. G. Vologzanina, O. A. Igumnova, I. V. Petuhova. Effectiveness of eradication therapy for Hp infection of residents of Perm and the Perm region. Experimental and Clinical Gastroenterology 2023; (6) doi: 10.31146/1682-8658-ecg-214-6-14-21
94
Ian H. Windham, D. Scott Merrell. Analysis of fitness costs associated with metronidazole and amoxicillin resistance in Helicobacter pylori. Helicobacter 2020; 25(5) doi: 10.1111/hel.12724
95
Angelo Zullo, Giuseppe Scaccianoce, Vincenzo De Francesco, Valentina Ruggiero, Pasquale D’Ambrosio, Luigi Castorani, Leonilde Bonfrate, Lucy Vannella, Cesare Hassan, Piero Portincasa. Concomitant, sequential, and hybrid therapy for H. pylori eradication: A pilot study. Clinics and Research in Hepatology and Gastroenterology 2013; 37(6) doi: 10.1016/j.clinre.2013.04.003
96
Lingling Wang, Haobin Yao, Teresa Tong, KamShing Lau, Suet Yi Leung, Joshua W. K. Ho, Wai K. Leung. Dynamic changes in antibiotic resistance genes and gut microbiota afterHelicobacter pylorieradication therapies. Helicobacter 2022; 27(2) doi: 10.1111/hel.12871
97
Tran Thanh Binh, Rumiko Suzuki, Tran Thi Huyen Trang, Dong Hyeon Kwon, Yoshio Yamaoka. Search for Novel Candidate Mutations for Metronidazole Resistance in Helicobacter pylori Using Next-Generation Sequencing. Antimicrobial Agents and Chemotherapy 2015; 59(4) doi: 10.1128/AAC.04852-14
98
Le Guo, Dantong Hong, Shue Wang, Fan Zhang, Feng Tang, Tao Wu, Yuankui Chu, Hongpeng Liu, Meng He, Hua Yang, Runting Yin, Kunmei Liu. Therapeutic Protection Against H. pylori Infection in Mongolian Gerbils by Oral Immunization With a Tetravalent Epitope-Based Vaccine With Polysaccharide Adjuvant. Frontiers in Immunology 2019; 10 doi: 10.3389/fimmu.2019.01185
99
Carol Thomas, Christopher D. Gwenin. The Role of Nitroreductases in Resistance to Nitroimidazoles. Biology 2021; 10(5) doi: 10.3390/biology10050388
100
Arshid Yousefi-Avarvand, Hamid Vaez, Mohsen Tafaghodi, Amir Hossein Sahebkar, Mohsen Arzanlou, Farzad Khademi. Antibiotic Resistance of Helicobacter pylori in Iranian Children: A Systematic Review and Meta-Analysis. Microbial Drug Resistance 2018; 24(7) doi: 10.1089/mdr.2017.0292
101
Amin Talebi Bezmin Abadi. Helicobacter pylori treatment: New perspectives using current experience. Journal of Global Antimicrobial Resistance 2017; 8 doi: 10.1016/j.jgar.2016.11.008
102
103
Surveillance of Helicobacter pylori Antibiotic Susceptibility in Indonesia: Different Resistance Types among Regions and with Novel Genetic Mutations. PLOS ONE 2016; 11(12) doi: 10.1371/journal.pone.0166199
104
Bahareh Attaran, Tahereh Falsafi, Nassim Ghorbanmehr. Effect of biofilm formation by clinical isolates of <i>Helicobacter pylori</i> on the efflux-mediated resistance to commonly used antibiotics. World Journal of Gastroenterology 2017; 23(7): 1163-1170 doi: 10.3748/wjg.v23.i7.1163
105
Ilaria Maria Saracino, Matteo Pavoni, Laura Saccomanno, Giulia Fiorini, Valeria Pesci, Claudio Foschi, Giulia Piccirilli, Giulia Bernardini, John Holton, Natale Figura, Tiziana Lazzarotto, Claudio Borghi, Berardino Vaira. Antimicrobial Efficacy of Five Probiotic Strains Against Helicobacter pylori. Antibiotics 2020; 9(5) doi: 10.3390/antibiotics9050244
106
Monika Maria Biernat, Aldona Bińkowska, Łukasz Łaczmański, Paweł Biernat, Paweł Krzyżek, Grażyna Gościniak. Phenotypic and Genotypic Analysis of Resistant Helicobacter pylori Strains Isolated from Children with Gastrointestinal Diseases. Diagnostics 2020; 10(10) doi: 10.3390/diagnostics10100759
107
Bahgat Fayed, Jayalakshmi Jagal, Roberta Cagliani, Reena A. Kedia, Amr Elsherbeny, Hulya Bayraktutan, Ghalia Khoder, Mohamed Haider. Co-administration of amoxicillin-loaded chitosan nanoparticles and inulin: A novel strategy for mitigating antibiotic resistance and preserving microbiota balance in Helicobacter pylori treatment. International Journal of Biological Macromolecules 2023; 253 doi: 10.1016/j.ijbiomac.2023.126706
108
Farideh Siavoshi, Parastoo Saniee, Reza Malekzadeh. Effective antimicrobial activity of rifabutin against multidrug‐resistant Helicobacter pylori. Helicobacter 2018; 23(6) doi: 10.1111/hel.12531
109
Toshihiro Nishizawa, Hidekazu Suzuki. Mechanisms of Helicobacter pylori antibiotic resistance and molecular testing. Frontiers in Molecular Biosciences 2014; 1 doi: 10.3389/fmolb.2014.00019
110
Thejaswi Bhat, Manish Kumar, Tamizh Selvan Gnanasekaran, Pavan Gollapalli. Targeting methyl-accepting chemotaxis transmembrane sensory protein inhibits Helicobacter pylori autoinducer-2 quorum sensing system. Biologia 2026; 81(8) doi: 10.1007/s11756-026-02302-5
111
Tran Thanh Binh, Rumiko Suzuki, Dong Hyeon Kwon, Yoshio Yamaoka. Complete Genome Sequence of a Metronidazole-Resistant Helicobacter pylori Strain. Genome Announcements 2015; 3(2) doi: 10.1128/genomeA.00051-15
112
Masumi Okuda, Yingsong Lin, Chaochen Wang, Toshihiko Kakiuchi, Shogo Kikuchi. Metronidazole for Helicobacter pylori eradication therapy among children and adolescents in Japan: Overcoming controversies and concerns. Helicobacter 2019; 24(3) doi: 10.1111/hel.12575
113
Jennifer Li, Xian-Zhi Li. Efflux-Mediated Antimicrobial Resistance in Bacteria. 2016;  doi: 10.1007/978-3-319-39658-3_19
114
Nicoline F. Tanih, Roland N. Ndip. Molecular Detection of Antibiotic Resistance in South African Isolates ofHelicobacter pylori. Gastroenterology Research and Practice 2013; 2013 doi: 10.1155/2013/259457