Identification and characterization of resistance and pathogenicity of Enterococcus spp. in samples of donor breast milk

Abstract

BACKGROUND

Breast milk is the primary source of nutrition for newborns. Hospitalized babies frequently need nutritional support from Human Milk Banks. As bacterial species of the genus Enterococcus are part of the microbiota of healthy donors, they may contaminate samples of pumped breast milk.

AIM

To identify and characterize the bacterial virulence and resistance in samples isolated from the nipple-areolar region, hands, and breast milk aliquots from donors at the Human Milk Bank of Municipal Hospital Esaú Matos in the city of Vitória da Conquista, Bahia State, Brazil.

METHODS

The personal hygiene and sanitation of donors were analyzed with the aim of identifying possible reasons for contamination of pumped milk. Cutaneous samples as well as aliquots of unpasteurized and pasteurized milk from 30 participants were obtained. Each Enterococcus spp. isolate underwent a disk diffusion susceptibility test and molecular biology techniques to determine resistance and virulence genes.

RESULTS

Enterococcus spp. were identified in 30% of donors (n = 9), and 11 specimens were isolated. Resistance to tetracycline was highly prevalent, being detectable in 63% of the isolates (n = 7) and followed by intermediate sensitivity to ciprofloxacin, observed in 27% of the specimens (n = 3). The efaA gene was found in 63% (n = 7) of the isolates, while the ace gene was detected in 27% (n = 3).

CONCLUSION

This study illustrates the importance of microbiological monitoring by Human Milk Banks and the need for alternatives to prevent the presence of Enterococcus spp. in hospital settings.

Key Words: Enterococcus spp., Breast milk, Virulence, Human milk, Pasteurization, Antimicrobial resistance

Core Tip: Human milk is the primary source of nutrition for newborns. Hospitalized newborns frequently require nutritional support from a Human Milk Bank. Enterococcus spp. can contaminate human milk, as they are part of the microbiota of healthy donors. This microbial genus is important in human diseases, mainly among newborns; therefore, this study aimed to identify and characterize the virulence and resistance of Enteroccocus spp. isolated from samples from the nipple-areolar region, hands, and raw and pasteurized milk aliquots from donors at a Brazilian Human Milk Bank.

INTRODUCTION

There is no ideal substitute for human milk (HM) during early life despite current technological advances in baby food production, processing, preservation, and preparation[1]. Unquestionably, HM supplies newborns (NBs) with all the nutrients that adequately meet the physiological and metabolic needs in this age group[2].

Premature births and hospitalizations in neonatal intensive care units as well as maternal illness, death, and low milk production can hinder the introduction and maintenance of breastfeeding. In this context, the use of donated HM has become an efficient alternative to breastfeeding[2] and allows NBs to be fed with milk obtained from Human Milk Banks (HMBs)[3]. This strategy involves the collection, processing, and quality control of colostrum, transition milk, and mature milk for later distribution to NBs under a doctor or nutritionist prescription[4].

Enterococcus species are associated with important infections in NBs and are potential contaminants of milked human milk (MHM) samples. Enterococcus spp. are part of the gastrointestinal tract microbiota in healthy humans[5] and may be present in significant numbers on the hands and utensils of milk donors. The presence of these bacteria in human milk indicates that they are due to direct or indirect contact with fecal material, compromising the quality of the MHM[6]. Some Enterococcus spp., especially Enterococcus faecalis (E. faecalis) and Enterococcus faecium (E. faecium), are highly pathogenic in NBs and must be effectively inactivated through pasteurization at HMBs.

To date, there are no published data on the isolation of enteric bacteria with hygienic-sanitary conditions of household collections performed by MHM donors. Considering the propensity of donated milk to be contaminated by these microorganisms, the clinical importance of such pathogens, and their ability to be dispersed through vectors such as health professionals and insects[7], it is important to investigate their virulence and dispersion capacity. Moreover, it is crucial to evaluate the quality of the collection, preservation, and processing of the HM offered to NBs. These procedures are essential for a better understanding of the pathogenicity of Enterococcus spp. present in raw and pasteurized human milk samples and in samples taken from the hands and nipple-areolar region of donors linked to HMBs.

MATERIALS AND METHODS

Study design, period, region, and population

This is a cross-sectional study performed using samples from the nipple-areolar region, hands, and aliquots of raw and pasteurized MHM from healthy donors registered at the HMB of the Municipal Hospital Esaú Matos in the city of Vitória da Conquista, State of Bahia, Brazil.

The present study recruited donors registered at the above-mentioned HMB who had a donation history with a mean weekly volume of donated milk greater than or equal to 400 mL. Donated samples of raw milk with a volume less than 400 mL were pooled with milk samples from other donors for pasteurization, thus losing the traceability and specificity of the sample from a specific donor. The exclusion criteria were: donors with wounds on the hand or nipple-areolar region and donation of raw milk samples with a milk volume lower than that required for individual pasteurization.

The microbial isolates analyzed in the present study were obtained by the single collection of samples from the nipple-areolar region and hands as well as aliquots of MHM before and after pasteurization from 30 donors between March and August 2018. The collections were carried out at the donors’ residences during scheduled visits. In addition to microbiological evaluation of the above-mentioned biological samples, questionnaires on hygienic-sanitary issues regarding the collection, packaging, and preservation of the donated milk were completed by the participants.

Ethical considerations

The study was approved by the Ethics Committee on Research with Human Beings of the Multidisciplinary Institute of Health of the Universidade Federal da Bahia, under the Certificate of Presentation for Ethics Apprehension number 80800717.8.0000.5556 and committee opinion number 2.475.023. The study followed all the conditions established by the Resolution 466/2012 of the Brazilian National Health Council.

Isolation, identification, evaluation of antimicrobial activity, and detection of constitutive, virulence, and resistance genes in Enterococcus spp.

After collection, the biological samples were immediately inoculated into enrichment brain heart infusion broth (HIMEDIA^®) and incubated at 35-37ºC for 24 h. After that, they were placed in Petri dishes with 5% Blood Agar Medium (Base Agar, HIMEDIA^®) and Chromagar Orientation (BD™ CHROMagar™ Orientation) in a bacteriological oven at 35-37ºC for 24 h. Both methods were important for increasing the isolation and identification of microorganisms of interest in the present study.

The colonies with presumptive characteristics of Enterococcus spp. selected in both media underwent Gram staining to evaluate the morphological characteristics as well as to perform the catalase test and subsequent tests to identify the genus Enterococcus, namely: hydrolysis of esculin in the presence of bile and growth in sodium chloride (NaCl) 6.5% media.

All Enterococcus spp. isolates underwent evaluation of antimicrobial activity using the agar diffusion method[8-10], according to the recommendations of the Clinical and Laboratory Standards Institute (2017)[11].

With the aim of detecting the constitutive[12], virulence[13-16], and resistance[17,18] genes in Enterococcus spp., all samples that were positive in the identification step underwent polymerase chain reaction (PCR) after reactivation in brain heart infusion medium.

Statistical analysis

A descriptive analysis of the study variables was carried out from a database constituted in Microsoft Excel through the Statistical Program EPI INFO (version 7.2.2.6). For the frequency comparison, the chi-square test was used, with values of P < 0.05 (95% confidence interval) considered statistically significant.

RESULTS

Milk samples were collected from 30 donors registered at the HMB of the Municipal Hospital Esaú Matos, in Vitória da Conquista, Bahia State, Brazil. A total of 81 samples were collected: 30 samples from swabs containing skin samples from the nipple-areolar region and donors’ hands, 30 samples of raw MHM, and 21 samples of pasteurized MHM. Following the methodological criteria, it was not possible to obtain an appropriate aliquot of pasteurized milk from 9 (30%) participants as they did not donate enough milk volume to perform pasteurization in a single bottle.

Enterococcus spp. strains were isolated from 9 donors (30%), and a total of 11 strains were identified: 7 strains (63.6%) from skin samples and 4 strains (36.4%) from raw MHM samples. Although Enterococcus spp. were not detected in the pasteurized MHM samples, in 38% (n = 8) of these samples other microorganisms, mainly Staphylococcus aureus, were isolated.

The study participants were questioned about socioeconomic aspects and hygienic-sanitary conditions in order to link selected variables to the route of human milk contamination by Enterococcus spp. In this context, most participants were aged 30 years or less, were married or living with a partner, had a family income above two minimum wages, had one child, and were educated to high school level.

With regard to the hygienic-sanitary procedures performed by the donors for milk collection, most participants reported that they always performed the following procedures: hand washing before the collection of milk (96%); held back hair before milking (80%); breast washing before milking (86.7%); used a mask while milking (86.7%); avoided talking during milking (60%); discarded the first jet of milk (53.3%); milk obtained using a manual/electric pump (80%). However, only 12 (80%) participants declared that they checked the size of their nails and trimmed them when necessary before milking (Table 1).

Table 1 Descriptive analysis of the socioeconomic aspects and hygienic-sanitary conditions related to the collection of human milk and to human milk donors (n = 30) registered in the Human Milk Bank of the Municipal Hospital Esaú Matos in Vitória da Conquista, Bahia State, Brazil.

Descriptive analysis of socioeconomic aspects of HM donors
Variable	n	(%)
Age group
Age less than 30 yr	19	63.3
Over 30 yr of age	11	36.7
Marital status/Conjugal state
Married/living with spouse	20	66.7
Single or divorced/without a partner	10	33.3
Family income
Less than 2 minimum wages1	9	30.0
Above 2 minimum wages	21	70.0
Number of children
One child	16	53.3
Two or more children	14	36.7
Schooling
High school	21	70.0
Graduate	9	30.0
Total	30	100.0
Descriptive analysis of hygienic-sanitary conditions of HM donors
Variable	n	(%)
Hand washing prior to collection
Sometimes/never	1	3.3
Always	29	96.7
Nail size check/trim before collection
Sometimes/never	18	60.0
Always	12	40.0
Hair holding habit before collection
Sometimes/never	6	20.0
Always	24	80.0
Breast lavage before collection
Sometimes/never	4	13.3
Always	26	86.7
Use of mask during collection
Sometimes/never	4	13.3
Always	26	86.7
Avoid talking during collection
Sometimes/never	12	40.0
Always	18	60.0
Discard first jet of milk at the beginning of collection
Sometimes/never	14	46.7
Always	16	53.3
Milk collection
Manual/electric pump	24	80.0
Manual milking	6	20.0
Cleaning frequency of the pump2
Sometimes/never	0	0
Always before using	241	100.01
Total	30	100.0

¹Minimum wage in the period: BRL954,00. ²Question applied only to donors who reported performing milking by hand and using an electric pump.

Socioeconomic variables of HM donors such as age (above or below 30 years), marital status (single or living as a couple), family income (higher or lower than 2 minimum wages), number of children (one or more than one), and educational level (high school or graduate) as well as variables related to hygienic-sanitary procedures including hand washing before milking, talking during milking, and discarding the first milk jet at the beginning of collection were not significantly associated with the detection of Enterococcus spp. in samples (P < 0.05) (Table 1).

Among the 11 isolates of Enterococcus spp., antimicrobial resistance was found in 10 isolates (91%). Resistance to tetracycline was most common (63% of isolates, n = 7), and intermediate sensitivity to ciprofloxacin was found in 27% of the isolates (n = 3). Resistance to quinolones (ciprofloxacin, norfloxacin, and levofloxacin) was observed in 9% of the isolates (n = 1) (Table 2). All isolates were sensitive to vancomycin. All specimens were analyzed by PCR to detect quinolone resistance genes (gyrA and parC genes), but no positive results were obtained.

Table 2 Sensitivity profile of the isolates (n = 11) of Enterococcus spp. found in relation to the list of antimicrobials evaluated following the recommendations of the Clinical and Laboratory Standards Institute (2017).

Antimicrobials	Sensitive, n (%)	Intermediate, n (%)	Resistant, n (%)
Ampicillin 10 µg	11 (100.0)	0 (0)	0 (0)
Penicillin 10 un	9 (81.8)	0 (0)	2 (18.2)
Tetracycline 30 µg	4 (36.4)	0 (0)	7 (63.6)
Ciprofloxacin 5 µg	7 (63.6)	3 (27.3)	1 (9.1)
Norfloxacin 10 µg	9 (81.8)	0 (0%)	2 (18.2)
Levofloxacin 5 µg	10 (90.9)	0 (0)	1 (9.1)
Nitrofurantoin 300 µg	9 (81.8)	0 (0)	2 (18.2)
Linezolid 30 µg	11 (100.0)	0 (0)	0 (0)
Vancomycin 30 µg	11 (100.0)	0 (0)	0 (0)

un: Units.

The Enterococcus spp. isolates were analyzed by PCR for detection of the constitutive ddl gene encoding the D-alanine ligases, which are species-specific for E. faecalis and E. faecium. This analysis showed that among the 11 enterococcal strains from 9 participants, 6 isolates were identified as Enterococcus spp. and 5 isolates were identified as E. faecalis. However, three E. faecalis isolates were found to be simultaneously colonized by E. faecium strains. Thus, three donors had E. faecalis and E. faecium strains. Such detection was possible because, after the initial identification of the Enterococcus genus, the stored colonies were collected from the CHROMagar Orientation medium (BD™ CHROMagar™ Orientation), which identified the genus and not the species of Enterococcus; thus, colonies of both species were collected.

All isolates of Enterococcus spp. underwent PCR for detection of the virulence genes ace, efaA, gelE, as, cylA, hyl, esp, as, cylA, hyl, and esp (Table 3). Among the 11 isolates, 7 isolates (63%) had the efaA gene that encodes the surface antigen A, which is commonly associated with biofilm formation and endocarditis, and 3 isolates (27%) had the ace gene, which encodes the protein that adheres to collagen and laminin, favoring bacterial adhesion commonly associated with endocarditis. The following enterocin genes were also genotypically investigated by PCR in Enterococcus spp.: Enterocin A, Enterocin B, Enterocin P, and Enterocin 31, also known as Bacteriocin. However, none of the isolates were positive for these genes.

Table 3 Distribution of the virulence genes of Enterococcus faecium, Enterococcus faecalis, and Enterococcus spp..

Virulence genes	E. faecalis		E. faecium		Enterococcus spp.		Total
	N (isolated )	%	N (isolated )	%	N (isolated )	%	N (isolated )	%
Ace	1a	33	1a	33	2	67	3	27
efaA	3b	43	2b	28	3	43	7	63
gelE	0	-	0	-	0	-	0	-
As	0	-	0	-	0	-	0	-
cylA	0	-	0	-	0	-	0	-
Hyl	0	-	0	-	0	-	0	-
Esp	0	-	0	-	0	-	0	-

^aace gene found in 1 isolate (containing strains of Enterococcus faecalis and Enterococcus faecium). ^befaA gene found in three Enterococcus faecalis isolates (being a single isolate of Enterococcus faecalis and two isolates of Enterococcus faecalis and Enterococcus faecium). E. faecalis: Enterococcus faecalis; E. faecium: Enterococcus faecium.

DISCUSSION

Enterococcus spp. are present in the human microbiota and are associated with important infections in NBs, and are potential contaminants of HM samples[8]. To date, there are no studies correlating NB infections and infant colonization with Enterococcus spp. in the city where this study was carried out. Moreover, there are no data associating socioeconomic aspects and hygienic-sanitary conditions regarding HM donors with the isolation of enteric bacteria. In the present study, Enterococcus spp. were isolated from 30% of the participants. Similarly, Enterococcus ssp. were isolated from raw MHM samples within four[19] and seven[20] days after delivery. In such studies, gram-positive bacteria, including E. faecalis[21], E. faecium[21,22], Staphylococcus spp[23] and fecal coliforms[2] were identified in MHM[19], but they were not detected after milk pasteurization; however, other microorganisms continued to be detected after pasteurization.

Similar findings were observed in other HMBs in which the isolation rates were 2%[2], 6%[2], 7.5%[21], and even 70.4%[3] in non-pasteurized MHM samples and was 50.7% in pasteurized MHM[3] samples. These data reinforce the importance of strict hygienic-sanitary procedures in HMBs as well as the microbiological control of HM samples.

Among the 11 Enterococcus spp. isolated in this study, different types of resistance to antibiotics were found in 91% of the isolates (n = 10). In the phenotypical analysis of antimicrobial resistance, most isolates were susceptible to ampicillin, linezolid, and vancomycin, but resistance to tetracycline (63%), ciprofloxacin (27%), norfloxacin, levofloxacin, nitrofurantoin (9%), and penicillin was detected. Enterococcus spp. resistance has been previously reported in samples from miscellaneous clinical materials[22], food, and clinical samples[23], with resistance rates of 5% to tetracycline[22] and of 3%[22] and 70.5%[23] to ciprofloxacin.

Despite the identification of quinolone resistance, the resistance genes gyrA and parC were not detected. This phenomenon may be associated with interferences, including differences in the pH of the Mueller Hinton media, in mean temperature, and in the density of the inoculum applied. Due to Enterococcus spp. resistance to antimicrobials such as penicillin, ampicillin, aminoglycosides, tetracycline, and vancomycin and its association with nosocomial infections[24], it is crucial to identify these bacteria in different types of biological samples, including HM.

In this study, the presence of virulence factors in the isolated strains was also evaluated, and the genes efaA and ace were found in 63% and 27% of the isolates, respectively. These genes are associated with enterococcal biofilm formation and endocarditis, making the treatment of infections caused by these microorganisms difficult. With regard to species identification, of the three isolates with the ace gene, two were Enteroccocus spp. and one had E. faecium and E. faecalis strains. Among the seven isolates carrying the efaA gene, three were Enterococcus spp., two were E. faecalis, and two had E. faecalis and E. faecium strains.

The genes ace and efaA have been previously detected in E. faecalis and E. faecium[22] hospital strains and the ace gene has also been found in Enterococcus spp. of clinical origin[23]. The pathogenicity mechanisms of Enterococcus spp. are not yet fully understood. It is known that these microorganisms have virulence factors that are associated with the severity and duration of human infections as well as with the dissemination of these microorganisms in the hospital environment, where they mainly cause urinary infections, endocarditis, and bacteremia. The most frequently reported virulence factors are related to the adhesion to host tissues, invasion, abscess formation, modulation of the host inflammatory responses, and secretion of toxic products[25].

The high percentage of Enterococcus spp. isolates in HM samples associated with the high antimicrobial resistance rate (mainly to tetracycline and ciprofloxacin) and the positivity of virulence factors (detection of the genes ace and efaA) found in this study confirm the importance of carrying out strict control from the collection to the distribution of MHM. In this context, it is necessary to take utmost care during milk processing in order to avoid the dispersion of microorganisms, as the entry of these microorganisms into the hospital environment can increase the risk of infection in hospitalized patients, mainly in those with a weakened immune system.

CONCLUSION

The present study demonstrates the necessity for microbiological control in HMBs and the requirement to develop alternatives to avoid the entry of Enterococcus spp. species into the hospital environment, which can potentially lead to important NB infections that increase the length of hospitalizations and, consequently, health service costs. Considering that most premature NBs are transferred to intensive care units, thereby requiring food supplementation with MHM, and that the consumption of contaminated MHM can lead to mild-to-severe infections, the accurate identification of bacterial pathogens is an essential requirement for the detection of microorganism reservoirs, infection sources, HM distribution monitoring, and decision taking aiming to reduce health risks in NBs. Moreover, strict control from the collection to the distribution of donated HM may reduce the dispersion rates of virulent and multidrug-resistant microorganisms that can cause several problems in a hospital environment, leading to increases in morbidity, mortality, and costs related to health care.

ARTICLE HIGHLIGHTS

Research background

Human milk is the primary source of nutrition for newborns. Hospitalized babies often require nutritional support from Human Milk Banks. As Enterococcus spp. are part of the microbiota of healthy donors, they are potential contaminants of pumped breast milk.

Research motivation

Donor Human Milk is an important alternative that allows the appropriate feeding of hospitalized newborns. A number of steps are needed to ensure the safe collection, processing, and quality control of colostrum, transition milk, and mature milk for subsequent distribution to newborns under a doctor or nutritionist prescription. However, such milk can be contaminated by Enterococcus spp. species that are highly pathogenic in newborns, and can increase morbidity, hospitalization time, and mortality among neonates.

Research objectives

The present study intended to identify and describe the bacterial virulence and resistance in samples obtained from the nipple-areolar region, hands, and breast milk aliquots of donors at the HMB of Municipal Hospital Esaú Matos in the city of Vitória da Conquista, Bahia State, Brazil.

Research methods

This cross-sectional study used samples from the nipple-areolar region, hands, and aliquots of raw and pasteurized milked human milk from healthy human milk donors. The study recruited donors who had a donation history of a mean weekly volume of donated milk equal to or higher than 400 mL. The microbial isolates from milk samples were analyzed before and after pasteurization. A total of 30 donors were assessed between March and August 2018.

The samples were immediately inoculated into enrichment brain heart infusion broth (HIMEDIA^®) and incubated at 35-37ºC for 24 h after collection. Thereafter, they were placed in Petri dishes with 5% Blood Agar Medium (Base Agar, HIMEDIA^®) and Chromagar Orientation (BD™ CHROMagar™ Orientation) in an incubator at 35-37ºC for 24 h.

Colonies in which Enterococcus spp. were observed were selected from both media and underwent Gram staining to evaluate the morphological characteristics and to perform the catalase test and subsequent tests to identify the genus Enterococcus.

All Enterococcus spp. isolates underwent evaluation of antimicrobial activity by the agar diffusion method, according to the recommendations of the Clinical and Laboratory Standards Institute (2017).

To detect the constitutive, virulence, and resistance genes in Enterococcus spp., all samples that were positive in the identification step underwent polymerase chain reaction after reactivation in brain heart infusion media.

A descriptive analysis of the study variables was carried out from a database constituted in Microsoft Excel through the Statistical Program EPI INFO (version 7.2.2.6). For the frequency comparison, the chi-square test was used, with values of P < 0.05 (95% confidence interval) considered statistically significant.

Research results

Eighty-one samples were collected, with 30 samples from swabs containing nipple-areolar region skin samples and donors’ hands, 30 samples of raw milked human milk, and 21 samples of pasteurized milked human milk. Enterococcus spp. strains were isolated from 30% of the donors and 11 strains were identified: 7 strains (63.6%) from skin samples and 4 strains (36.4%) from raw MHM samples.

The majority of participants declared that they washed their hands before the collection of milk (96%), held back hair before milking (80%, washed the breasts before milking (86.7%), used a mask while milking (86.7%), avoided talking during milking (60%), discarded the first jet of milk (53.3%), and obtained milk using a manual/electric pump (80%).

No statistically significant associations between demographic and hygienic characteristics and the detection of Enterococcus spp. were observed. Antimicrobial resistance was identified in 10 isolates (91%), mainly to tetracycline.

Research conclusions

Here we demonstrate the importance of appropriate microbiological control in Human Milk Banks in order to prevent Enterococcus spp. in hospitals as these bacteria can lead to important newborn infections that increase morbidity, mortality, and hospitalizations among these patients, and increase health service costs.

Research perspectives

This study adds information to the microbiological control of donated milk, which, if well-performed from human milk collection to its distribution, may reduce the dispersion rates of virulent and multidrug-resistant microorganisms in a hospital environment, avoiding unwanted clinical outcomes among newborns. Putting such measures into practice may improve the health of children around the world.