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Enterococci are commensals of the human and animal gastrointestinal tract and opportunistic pathogens that cause urinary tract infections (UTIs), endocarditis, and sepsis (1). Nosocomial infections caused by enterococci have increased; these pathogens are now the third most common at hospitals after Escherichia coli and Staphylococcus aureus (2); and enterococci are frequently recorded as the cause of UTIs, wound infections, bacteremia, and endocarditis (3–6). The sources of enterococcal infections in humans are not clear, but animal reservoirs have been suggested (2,4,7–9). A study comparing enterococcal isolates from 4 European countries and the United States demonstrated that E. faecalis isolated from pigs in Portugal had pulsed-field gel electrophoresis (PFGE) patterns identical to those of multidrug-resistant isolates at hospitals in Spain, Italy, and Portugal, all of which were shown by multilocus sequence typing (MLST) to belong to sequence type (ST) 6 (7). In Denmark, high-level gentamicin-resistant E. faecalis of ST16 with an identical PFGE pattern was isolated from pigs and from humans with endocarditis (9). Identical and closely related PFGE patterns were demonstrated by isolates from humans and from pork and chicken meat in the United States, all of which contained high-level gentamicin-resistant genes (4). Our objective was to characterize epidemiologically related E. faecalis isolated from humans with UTIs and from poultry living in the same households in Vietnam to evaluate the zoonotic potential of E. faecalis.

ork and chicken meat in the United States, all of which contained high-level gentamicin-resistant genes (4). Our objective was to characterize epidemiologically related E. faecalis isolated from humans with UTIs and from poultry living in the same households in Vietnam to evaluate the zoonotic potential of E. faecalis. Materials and Methods Recruitment of Patients, Urine Collection, and Bacterial Culture of Urine Urine samples were collected during January 2008–January 2010 at the Military Medical University, Hospital 103, in Ha Dong, Hanoi. Patients with clinical symptoms of UTI (i.e., >1 of the following symptoms: frequent urination; painful urination; hematuria; cloudy urine; or pain in pelvic area, flank, or low back) were referred from nearby pharmacies and informed about the project. A midstream urine sample was collected at the hospital under supervision of a nurse. Only patients with uncomplicated UTIs were included; patients reporting underlying diseases, such as hematologic disorders, respiratory infections, diarrhea, diabetes, cancer, HIV/AIDS, liver cirrhosis, alcoholism, anatomic malformations of urinary tract, nephrolithiasis, or urolithiasis were excluded, as were patients with hospital-acquired UTIs. The urine was cultured immediately after collection. Thirty-one UTI patients met the study criteria of having E. faecalis CFU >103/mL isolated from a urine sample in pure culture and were raising poultry in their households.

, nephrolithiasis, or urolithiasis were excluded, as were patients with hospital-acquired UTIs. The urine was cultured immediately after collection. Thirty-one UTI patients met the study criteria of having E. faecalis CFU >103/mL isolated from a urine sample in pure culture and were raising poultry in their households. The urine samples were cultured on Flexicult agar plates (Statens Serum Institut, Copenhagen, Denmark), where E. faecalis grows as small green/blue-green colonies and E. faecium as small green colonies (10). Three colonies were isolated from each UTI patient. All 31 participants were interviewed when urine samples were collected. Personal information recorded included age, sex, and underlying diseases. The following clinical symptoms were recorded: frequent urination, painful urination, cloudy urine, blood in urine, pain in pelvic area, flank pain, pain in low back, and fever. In addition, information about duration of symptoms; previous UTIs; and medical treatment before arrival at the hospital, including type of antimicrobial drug used, was recorded. Species identification of all 31 presumptive E. faecalis isolates from urine and 83 isolates from poultry were confirmed by species-specific PCR as described by Dutka-Malen et al. (11). Only isolates identified as E. faecalis by PCR were further characterized. All study participants were informed orally and in writing about the study and provided written consent. The ethics committee at Army Hospital 103 approved the study protocols.

Species identification of all 31 presumptive E. faecalis isolates from urine and 83 isolates from poultry were confirmed by species-specific PCR as described by Dutka-Malen et al. (11). Only isolates identified as E. faecalis by PCR were further characterized. All study participants were informed orally and in writing about the study and provided written consent. The ethics committee at Army Hospital 103 approved the study protocols. Collection of Cloacal Swabs from Poultry When a urine sample was positive for E. faecalis, the patient’s household was visited within 1 week, and cloacal swabs were taken from 2–4 chickens in the household. Fecal samples were taken with a sterile cotton swab and immediately placed in Cary-Blair media (Oxoid, Basingstoke, Hampshire, UK) for transportation to the laboratory. Samples were then streaked on Slanetz and Bartley agar medium (Merck, Darmstadt, Germany) the same day and incubated for 24–48 h at 37°C. Subsequently, 2 individual colonies were randomly selected and subcultured on nonselective LB-agar, Lennox plates (Difco, Becton Dickinson, Sparks, MD, USA), which were incubated overnight at 37°C to obtain pure cultures. Colonies were then grown in brain–heart infusion broth (Oxoid) overnight at 37°C and stored for further characterization at –80°C in cryotubes containing 30% glycerol.

tured on nonselective LB-agar, Lennox plates (Difco, Becton Dickinson, Sparks, MD, USA), which were incubated overnight at 37°C to obtain pure cultures. Colonies were then grown in brain–heart infusion broth (Oxoid) overnight at 37°C and stored for further characterization at –80°C in cryotubes containing 30% glycerol. MLST and PFGE To investigate whether isolates of E. faecalis from urine and poultry belonged to identical STs, we characterized isolates from urine and poultry by MLST. Urine isolates were characterized by sequencing of all 7 housekeeping genes used in the MLST scheme: gdh, gyd, pstS, gki, aroE, xpt, and yqil. To confirm that the UTIs were caused by a single strain, 1 additional colony from 9 (29%) of 31 urine samples was characterized by sequencing the gki and yqil genes. Two isolates from each chicken were characterized by sequencing the gki and yqil genes. When sequences of both genes in 2 isolates corresponded to the sequence of the same genes in the urine isolate, which occurred in 11 cases, 1 of the 2 isolates from poultry was randomly selected and further characterized. When gene sequences in only 1 isolate from poultry were identical to the isolate from urine, the isolate was further characterized. Primers and PCR conditions are described on the E. faecalis MLST website (http://efaecalis.mlst.net/). Amplicons were sequenced in both directions by Macrogen (Seoul, South Korea). DNA sequences obtained were assembled using CLC Main Workbench 5.2 software (CLC bio, Aarhus, Denmark) and compared with published alleles, and an ST was assigned to each strain (http://efaecalis.mlst.net/). PFGE was performed as described (12) by using the restriction enzyme smaI (New England BioLabs, Ipswich, MA, USA).

A sequences obtained were assembled using CLC Main Workbench 5.2 software (CLC bio, Aarhus, Denmark) and compared with published alleles, and an ST was assigned to each strain (http://efaecalis.mlst.net/). PFGE was performed as described (12) by using the restriction enzyme smaI (New England BioLabs, Ipswich, MA, USA). Virulence Genes The presence and sequence of the following 6 virulence genes were used to further characterize the isolates from urine and poultry: asa1, CylA, efaA, Esp, gelE, and EF0591 (13). After detecting the virulence genes by PCR (13), we sequenced the genes in both directions using Macrogen. DNA sequences were compared, and possible nucleotide differences were calculated by using Smith-Waterman local alignment (EMBOSS) available online from the European Bioinformatics Institute: (www.ebi.ac.uk/). Antimicrobial Drug Susceptibility Testing MICs were determined for 16 antimicrobial drugs for comparison analyses by using the Sensititer system (Trek Diagnostics Systems, East Grindstead, UK) according to the manufacturer’s guidelines. These drugs were ampicillin (2–32 μg/mL), avilamycin (4–32 μg/mL), chloramphenicol (2–64 μg/mL), daptomycin (0.25–16 μg/mL), erythromycin (0.5–32 μg/mL), gentamicin (16–1,024 μg/mL), kanamicin (128–2,048 μg/mL), linezolid (0.5–8 μg/mL), moxifloxacin (0.25–8 μg/mL), penicillin (2–32 μg/mL), salinomycin (2–16 μg/mL), streptomycin (64–2,048 μg/mL), quinupristin-dalfopristin (0.25–16 μg/mL), tetracycline (1–32 μg/mL), tigecycline (0.015–2 μg/mL), and vancomycin (1–32 μg/mL).

entamicin (16–1,024 μg/mL), kanamicin (128–2,048 μg/mL), linezolid (0.5–8 μg/mL), moxifloxacin (0.25–8 μg/mL), penicillin (2–32 μg/mL), salinomycin (2–16 μg/mL), streptomycin (64–2,048 μg/mL), quinupristin-dalfopristin (0.25–16 μg/mL), tetracycline (1–32 μg/mL), tigecycline (0.015–2 μg/mL), and vancomycin (1–32 μg/mL). Results In 7 (23%) of 31 UTI cases, E. faecalis isolated from patient urine and poultry demonstrated identical STs and an indistinguishable (4 pairs) or closely related PFGE pattern (3 pairs, defined as showing <3 fragment difference) (Figure). In addition, antimicrobial drug susceptibility patterns were similar, and only 1 variation was found in the virulence gene profiles (Table 1, Table 2). Five of these 7 patients reportedly had a profession where they worked with poultry. A total of 22 patients who did not share a clone of E. faecalis found in poultry in their household reported working with poultry. Figure Pulsed-field gel electrophoresis of SmaI-digested Enterococcus faecalis isolated from humans with urinary tract infections and from poultry in the same houselhold, Vietnam, January 2008–January 2010. Lanes A and P are molecular weight markers. Lane B, isolate 90U; lane C, isolate 90P; lane D, 122U; lane E, 122P; lane F, 186U; lane G, 186P; lane H, 191U; lane I, 191P; lane J, 204U; lane K, 204P; lane L, 217U; lane M, 217P; lane N, 221U; and lane O, 221P.

ry in the same houselhold, Vietnam, January 2008–January 2010. Lanes A and P are molecular weight markers. Lane B, isolate 90U; lane C, isolate 90P; lane D, 122U; lane E, 122P; lane F, 186U; lane G, 186P; lane H, 191U; lane I, 191P; lane J, 204U; lane K, 204P; lane L, 217U; lane M, 217P; lane N, 221U; and lane O, 221P. Table 1 MLST, PFGE, and virulence gene profiles for Enterococcus faecalis isolated from humans with urinary tract infections and poultry from the same households, Vietnam, January 2008–January 2010* Strain† Source MLST type PFGE pattern Virulence genes Duration of symptoms, mo asa1 CylA efaA Esp gelE EF0591 90U Urine 16 A1 – + + + – + 1 90P Poultry 16 A2 + + + + – + NA 122U Urine 16 A2 + + + + – + 7 122P Poultry 16 A1 + + + + – + NA 186U Urine 93 A3 – – + – – – 24 186P Poultry 93 A3 – – + – – – NA 191U Urine 413 A3 – + + + – + 24 191P Poultry 413 A1 – + + + – + NA 204U Urine 16 A1 – + + + – + 2 204P Poultry 16 A1 – + + + – + NA 217U Urine 415 A3 + – + – + – 0.5 217P Poultry 415 A3 + – + – + – NA 221U Urine 141 A6 – – + – + – 120 221P Poultry 141 A6 – – + – + – NA *MLST, multilocus sequence typing; PFGE, pulsed-field gel electrophoresis; +, positive; –, negative; NA, not applicable. †All isolates except 221U were recovered from female patients. Strains isolated from patients with urinary tract infections are designated as U and strains isolated from poultry as P.

– – + – + – NA *MLST, multilocus sequence typing; PFGE, pulsed-field gel electrophoresis; +, positive; –, negative; NA, not applicable. †All isolates except 221U were recovered from female patients. Strains isolated from patients with urinary tract infections are designated as U and strains isolated from poultry as P. Table 2 Antimicrobial drug susceptibility (MIC) testing of Enterococcus faecalis isolated from humans with urinary tract infections and poultry in the same household, Vietnam, January 2008–January 2010* Strain Antimicrobial drug and test interval, µg/mL CHL, 2–64 DAP, 0.25–16 ERY, 0.5–32 GEN, 16–1,024 KAN, 128–2,048 MXF, 0.25–8 STR, 64–2048 Q-D, 0.25–16 TET, 1–32 90U 64 4† >32 >1,024 >2,048 <0.25 >2,048† 16 >32 90P >64 >16† 32 512 >2,048 <0.25 128† 16 >32 122U 64 4 >32 64† >2,048 <0.25 128† 16 >32 122P >64 4 >32 1,024† >2,048 <0.25 >2,048† 16 >32 186U 4 4 >32† <16 <128 <0.25 <64 16 >32† 186P 4 8 <0.5† <16 <128 <0.25 <64 16 <1† 191U 32 4 >32 >1,024 >2,048 <0.25 >2,048 16 32† 191P 64 8 >32 512 >2,048 <0.25 >2,048 16 <1† 204U 64† 4 >32† >1,024† >2,048† <0.25† >2,048† 16† 32 204P 4† 8 4† <16† <128† 2† <64† 0.5† 32 217U 4 4 <0.5 32 <128 <0.25 256 8 <1 217P 4 4 <0.5 <16 <128 <0.25 256 8 <1 221U 64 4 <0.5 <16† <128 <0.25 128 8 >32 221P 64 4 1 64† <128 <0.25 128 8 >32 *CHL, chloramphenicol; DAP, daptomycin; ERY, erythromycin; GEN, gentamicin; KAN, kanamicin; MXF, moxifloxacin; STR, streptomycin; Q-D, quinupristin-dalfopristin; TET, tetracycline. †>1 dilution difference between urine and poultry strain.

<1 221U 64 4 <0.5 <16† <128 <0.25 128 8 >32 221P 64 4 1 64† <128 <0.25 128 8 >32 *CHL, chloramphenicol; DAP, daptomycin; ERY, erythromycin; GEN, gentamicin; KAN, kanamicin; MXF, moxifloxacin; STR, streptomycin; Q-D, quinupristin-dalfopristin; TET, tetracycline. †>1 dilution difference between urine and poultry strain. MLST Sequencing the 7 housekeeping genes in the 31 E. faecalis strains showed the following 14 STs: 4, 16, 17, 93, 116, 136, 141, 314, 410, 411, 412, 413, 415, and 417, with ST16 shown by 16 (51.6%) isolates. Three isolates belonged to ST4, and each of the remaining STs was represented by only 1 isolate. In 7 of 31 households, the same ST was obtained from poultry and urine (Table 1). In 3 households, ST16 was isolated from urine and poultry. In the remaining 4 households, STs 93, 141, 413, and 415 were identified (Table 1). Because each pair of isolates from all selected patients (28%) showed identical gki and yqil gene sequences, we concluded that the UTI cases were associated with 1 E. faecalis strain. PFGE We detected 6 PFGE patterns (A1–A6). Of these, 4 pairs from urine and poultry from the same households showed indistinguishable patterns (Table 1; Figure).

MLST Sequencing the 7 housekeeping genes in the 31 E. faecalis strains showed the following 14 STs: 4, 16, 17, 93, 116, 136, 141, 314, 410, 411, 412, 413, 415, and 417, with ST16 shown by 16 (51.6%) isolates. Three isolates belonged to ST4, and each of the remaining STs was represented by only 1 isolate. In 7 of 31 households, the same ST was obtained from poultry and urine (Table 1). In 3 households, ST16 was isolated from urine and poultry. In the remaining 4 households, STs 93, 141, 413, and 415 were identified (Table 1). Because each pair of isolates from all selected patients (28%) showed identical gki and yqil gene sequences, we concluded that the UTI cases were associated with 1 E. faecalis strain. PFGE We detected 6 PFGE patterns (A1–A6). Of these, 4 pairs from urine and poultry from the same households showed indistinguishable patterns (Table 1; Figure). Antimicrobial Drug Susceptibility Testing When we compared isolates from urine and poultry from individual households, we detected similar MICs of each tested antimicrobial drug, showing a 1-dilution factor deviation (Table 2). For several isolates, an MIC could not be established because the MIC fell outside the test intervals. We detected different MICs for 7 antimicrobial drugs when we compared strains 204U and 204P. All isolates were fully susceptible (lowest or second lowest MIC tested) to ampicillin, avilamycin, linezolid, penicillin, salinomycin, tigecycline, and vancomycin (results not shown in Table 2).

ell outside the test intervals. We detected different MICs for 7 antimicrobial drugs when we compared strains 204U and 204P. All isolates were fully susceptible (lowest or second lowest MIC tested) to ampicillin, avilamycin, linezolid, penicillin, salinomycin, tigecycline, and vancomycin (results not shown in Table 2). Virulence Genes PCR for the 6 virulence genes showed that the isolates from urine and poultry from an individual household contained identical virulence genes that varied from 1 to 5 genes, except for 1 household in which the isolate from urine (90U) did not contain the asa1 gene (Table 1). When we compared the DNA sequences from the epidemiologically related urine and poultry strains, we found that all 23 sequenced gene pairs showed 100% similarity. Discussion We document isolation of the same clone of E. faecalis in urine and poultry from the same households in which patients had close contact with the poultry. The potential for zoonotic transmission of E. faecalis has been suggested, but to our knowledge, only epidemiologically unrelated isolates have been investigated (3,4,7–9,14). Most of the isolates in our study belonged to ST16, which has been isolated from animals and humans, including clinical and nonclinical isolates (14). ST93 was isolated from a patient with an ulcer in Poland and from an unknown source in the United States, and ST141 was isolated from chickens in Denmark and from a blood sample of a hospitalized person in Poland (http://efaecalis.mlst.net/).

ed from animals and humans, including clinical and nonclinical isolates (14). ST93 was isolated from a patient with an ulcer in Poland and from an unknown source in the United States, and ST141 was isolated from chickens in Denmark and from a blood sample of a hospitalized person in Poland (http://efaecalis.mlst.net/). When we interpreted PFGE patterns for their relatedness using criteria suggested by Tenover et al. (15), we found 4 pairs of E. faecalis strains with indistinguishable band patterns that could be “considered to represent the same strain” (15). From 3 individual households, isolates from urine and poultry showed PFGE patterns with 1 or 2 band differences and thus can be considered closely related (15). These identical or closely related PFGE patterns, together with the supporting findings by MLST and virulence gene profiling, suggest that E. faecalis might be transmitted from poultry to humans, causing UTIs. However, the finding of similar isolates from humans and poultry also could result from sharing a common clone of E. faecalis. ST16 has been reported from various epidemiologically unrelated human and animal sources (14), which could indicate a common clone in humans and animals. Because no data about ST16 in the environment are available, an environmental reservoir cannot be ruled out. Because 27 of the 31 patients reported having contact with poultry through their work, contact with poultry outside the household environment cannot be excluded as the source of E. faecalis. Epidemiologic risk factor studies are needed to document actual transmission routes.

When we interpreted PFGE patterns for their relatedness using criteria suggested by Tenover et al. (15), we found 4 pairs of E. faecalis strains with indistinguishable band patterns that could be “considered to represent the same strain” (15). From 3 individual households, isolates from urine and poultry showed PFGE patterns with 1 or 2 band differences and thus can be considered closely related (15). These identical or closely related PFGE patterns, together with the supporting findings by MLST and virulence gene profiling, suggest that E. faecalis might be transmitted from poultry to humans, causing UTIs. However, the finding of similar isolates from humans and poultry also could result from sharing a common clone of E. faecalis. ST16 has been reported from various epidemiologically unrelated human and animal sources (14), which could indicate a common clone in humans and animals. Because no data about ST16 in the environment are available, an environmental reservoir cannot be ruled out. Because 27 of the 31 patients reported having contact with poultry through their work, contact with poultry outside the household environment cannot be excluded as the source of E. faecalis. Epidemiologic risk factor studies are needed to document actual transmission routes. The variation found in resistance patterns might have resulted from exposure to different antimicrobial drugs, resulting in different selection pressure on E. faecalis in the human and poultry hosts. The 7 patients studied had UTI symptoms for an average of 514 days (range 5 days–10 years), which is unusually long for UTI (Table 1). Although self-medication is well established to be a common practice in Vietnam (16), only 2 of the 7 patients acknowledged use of antimicrobial drugs to treat their UTI symptoms before they participated in the study (data not shown). Over time, patients tend to forget what kind of medication they received. Furthermore, the questionnaire asked only whether antimicrobial drugs were used against UTI, not whether they were used to treat other diseases. In addition, poultry might have been exposed to antimicrobial drugs through growth promoters added in the feedstuff and during therapeutic or preventive treatments, but information about such use was not available.

ly whether antimicrobial drugs were used against UTI, not whether they were used to treat other diseases. In addition, poultry might have been exposed to antimicrobial drugs through growth promoters added in the feedstuff and during therapeutic or preventive treatments, but information about such use was not available. In most Western countries, contact with poultry occurs mainly through handling and consumption of poultry meat. However, the risk for zoonotic transmission of E. faecalis from poultry meat remains to be investigated. Thus, similar studies and risk factor studies should be conducted in more countries to evaluate the effect on zoonotic transmission of differences in human habits of poultry consumption and contact with poultry. In addition, animals other than pigs and poultry should be investigated as sources of zoonotic E. faecalis transmission. Finally, we cannot exclude the possibility that E. faecalis pathotypes found in poultry might represent transmission from humans, e.g., in this study, from UTI patients. However, poultry as carriers of ST16 has been documented (17), and it seems more likely that humans are exposed to poultry litter than that poultry are exposed to human feces.

e the possibility that E. faecalis pathotypes found in poultry might represent transmission from humans, e.g., in this study, from UTI patients. However, poultry as carriers of ST16 has been documented (17), and it seems more likely that humans are exposed to poultry litter than that poultry are exposed to human feces. We did not investigate the route of E. faecalis transmission, but the route could be colonization of the human intestine and subsequently ascending the urethra as reported for E. coli (18). Further studies are required to explain routes of transmission. The emergence of enterococci as causes of human infections and their resistance to some of the crucial antimicrobial drugs used for human treatment emphasizes the need to elucidate transmission routes and reservoirs for the enterococci and their resistance genes (5,6,19–21). Suggested citation for this article: Poulsen LL, Bisgaard M, Son NT, Trung NV, An HM, Dalsgaard A. Enterococcus faecalis clones in poultry and in humans with urinary tract infections, Vietnam. Emerg Infect Dis [serial on the Internet]. 2012 Jul [date cited]. http://dx.doi.org/10.3201/eid1807.111754 Acknowledgments We thank all patients for their participation in the study; Flemming Scheutz for his involvement and advice during the development of the protocols; staff at the Army Hospital 103, Ha Dong, Hanoi; and Nina Flint and Gitte Petersen for their excellent technical and laboratory support.

Suggested citation for this article: Poulsen LL, Bisgaard M, Son NT, Trung NV, An HM, Dalsgaard A. Enterococcus faecalis clones in poultry and in humans with urinary tract infections, Vietnam. Emerg Infect Dis [serial on the Internet]. 2012 Jul [date cited]. http://dx.doi.org/10.3201/eid1807.111754 Acknowledgments We thank all patients for their participation in the study; Flemming Scheutz for his involvement and advice during the development of the protocols; staff at the Army Hospital 103, Ha Dong, Hanoi; and Nina Flint and Gitte Petersen for their excellent technical and laboratory support. This study was supported by the University of Copenhagen through an ordinary PhD stipend to L.L.P. The Danish International Development Assistance (Danida) provided financial support through the project “Chickens as a possible reservoir for urinary tract infections in humans.” Dr Poulsen is a PhD student in the Department of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen. Her primary research interests include zoonotic diseases and transmission routes.