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Original Research Articles

Absence of vancomycin-resistant enterococci among highly ESBL-positive crows (Corvus splendens) foraging on hospital waste in Bangladesh

, DVM, PhD & , MD, PhD
Article: 29761 | Received 14 Sep 2015, Accepted 09 Nov 2015, Published online: 15 Dec 2015

Abstract

Background

Vancomycin-resistant enterococci (VRE) have emerged as a growing problem in hospitals; however, domesticated animals, poultry, and wild birds are acting as potential reservoirs. There is a knowledge gap in the Epidemiology of VRE from Bangladesh.

Methods

To study the prevalence of VRE and the mechanisms of resistance implicated among wild birds, 238 fecal samples were collected in 2010 from house crows (Corvus splendens) foraging on hospital waste in Bangladesh. Fecal samples were screened by analyzing color change in broth and screening for vanA and vanB resistant genes by PCR.

Results

Neither vanA nor vanB genes were detected from the fecal samples. The house crow does not seem to constitute a reservoir for VRE.

Conclusion

The zero prevalence is an indication that foraging on hospital waste does not constitute a major risk of VRE carriage in house crows and this is the first study to focus on the prevalence of VRE from wild birds in Bangladesh.

Different enterococci species are normally found as normal flora in human, mammals, birds, reptiles, and insects (Citation1). The emergence and rapid spread of antibiotic resistance in enterococcus has become a serious public health concern. Vancomycin is a glycopeptide antibiotic, which is considered as the last lines of defense against many multiresistant Gram-positive cocci. Vancomycin-resistant enterococci (VRE) are one of the organisms responsible for hospital-acquired infections with a high morbidity and mortality in humans (Citation2, Citation3). Resistance to vancomycin is caused by a series of genes (classified by the prefix van) that encode an enzyme important for the cell wall. There have been nine genes described in different species of enterococci: vanA, vanB, vanC, vanD, vanE, vanG, vanL, vanM, and vanN (Citation4Citation7). However, E. faecium and E. faecalis carrying vanA or vanB gene have received the most attention in relation to human health care because of their clinical importance, transferability potential, and abundance in clinical isolates (Citation8Citation10).

VRE have been reported in the hospitals of many countries throughout the world and spread is associated with poor hospital hygiene practice (Citation8, Citation11). Different livestock species in different countries have been reported as potential reservoirs for vancomycin-resistant determinants (Citation12, Citation13). VRE carrying the vanA gene were found in wild birds, including glaucous gulls (Larus hyperboreus) and wintering rooks (Corvus frugilegus) (Citation14, Citation15). Different livestock species and/or humans were thought to be sources of VRE in free-living wild bird populations (Citation15Citation17). Previously, we reported the house crow (Corvus splendens) and brown-headed gull (Chroicocephalus brunnicephalus) living close to human activities and hospital areas as potential carriers of clinically associated extended spectrum beta-lactamases (ESBL)-producing bacteria in Bangladesh (Citation18, Citation19). There is no information regarding carriage of VRE among these wild birds that were reported to be carriers of ESBL producers.

The aim of this study was to determine the prevalence of VRE in crows foraging in hospital areas of Bangladesh and to investigate whether this bird species constitutes a potential reservoir for VRE.

Materials and methods

In total, 238 fresh fecal samples from house crows (C. frugilegus) were collected during February 2010 from the ground areas of Rajshahi Medical College Hospital (n=200) and Chittagong Medical College Hospital of Bangladesh (n=38). Fresh fecal droppings were collected by sterile cotton swabs, which after collection were immediately stored at −80°C in bacterial freeze media containing Luria–Bertani broth (Becton, Dickinson and Company, Sparks, MD), phosphate-buffered saline, and 4.4% glycerol. Samples were shipped to Sweden for analysis and cold chain logistics were used for shipment. Fecal samples in bacterial freeze media were inoculated by sterile swabs. The swabs were immediately inoculated with the sample into 1 mL bile azide esculin broth and stored at −70°C for analysis.

Screening for VRE was performed in a selective bile azide esculin broth supplemented with 4 mg/L vancomycin and 60 mg/L aztreonam (ICN Biomedicals, Inc., Aurora, OH), and PCR for vanA and vanB, according to the methods described previously (Citation20, Citation21). Briefly, this real-time PCR protocol was used to detect the vanA and vanB gene. Amplification was conducted in a total volume of 20 µL containing 12.1 µL of PCR water, 4 µL of LC480 M-Mix (2×), 0.4 µL of vanA F (10 µM) (5′-CGGCAAGACAATATGACAGCAA-3′), 0.4 µL of vanA R (10 µM) (5′-TCAGTACAATGCGGCCGTTA-3′), 0.4 µL of vanB F (10 µM) (5′-GGGAGGATGGTGCGATACA-3′), 0.4 µL of vanB R (10 µM) (5′-CCGAAATCGCTTGCTCAA-3′), 0.15 µL of vanA prob (10 µM) (5′-HEX-CAGTTATAACCGTTCCCGCAGACCTT-BHQ1-3′), 0.15 µL of vanB prob (10 µM) (5′-FAM-CTTTGTGAAGCCGGCACGGTCAGGTT-BHQ1-3′), and 2 µL of the samples. The following cycling parameters were used in the PCR run: 95°C for 5 min (95°C for 10 s, 60°C for 30 s) for 45 cycles. Finally, the amplified PCR product was analyzed.

Results, discussion, and conclusion

All together 238 fecal samples were analyzed. Surprisingly, none of them demonstrated a color change after testing in the bile azide esculin broth meaning no growth of enterococci was demonstrated. Neither vanA nor vanB were confirmed through PCR screening. These results indicate that there was no VRE carriage by the house crows in Bangladesh. As the testing in bile azide esculin broth did not demonstrate growth of any enterococci, the findings may be interpreted as a low propensity of crows to carry enterococci in general, and thus also to carry VRE. However, previous findings of VRE among birds of the genus Corvus (Citation15, Citation17) indicate that carriage of VRE is indeed possible, and that crows therefore can be used as sentinels. VRE also reported in different wild bird species like European robins (Erithacus rubecula), quail (Coturnix coturnix conturbans), Common chaffinch (Fringilla coelebs), Blackcap (Sylvia atricapilla) and buzzards (Buteo buteo) (Citation16, Citation22). More interestingly, wild birds very close to contact with human activities, for example crows and gulls, are potential carriers of clinically important VRE (Citation14, Citation17). A study from Bangladeshi hospitals showed a low prevalence (3%) of E. faecalis among patients with urinary tract infections (Citation23). Another study from Bangladesh showed that E. faecalis is the dominant species among patients with Enterococcus infection and all E. faecalis and E. facium strains isolated from patients were resistant to vancomycin (Citation24). Thus, VRE is a serious challenge for hospitals; however, there are no reports about the prevalence of VRE from livestock, poultry, or wild birds in Bangladesh.

The house crow (C. splendens) has a widespread distribution in South Asian countries like Bangladesh and India, and it lives close to humans. It occupies different ecological niches, including household areas, city dumps, hospital dumps, and water sources like lakes, ponds, and rivers. The house crow has been shown to carry several human pathogenic bacteria in its intestines (Citation25, Citation26). A study on these samples demonstrated that 59% of the crows living on hospital waste were potential carriers of clinically relevant ESBL-producing E. coli and Klebsiella (Citation19), and hospital waste has been reported as a potential source of antibiotic-resistant bacteria (Citation19, Citation27). These crows were reported as potential carriers of clinical relevant human-associated ESBL-producing E. coli ST13-O25b clones, likely because of their foraging behaviors in hospital waste dumps (Citation28). It has also been documented that wild birds can carry VRE and ESBL-producing bacteria simultaneously (Citation16). Thus, the high prevalence of ESBL-producing bacteria among crows living in hospital areas has increased our suspicion about the possible carriage and spread of VRE as well, like in Azores, Portugal (Citation16).

This study indicates the absence of VRE harboring vanA and vanB genes among crows foraging on hospital wastes even though they were potential carriers of ESBL-producing Enterobacteriaceae (Citation28). Thus, spread through hospital waste via house crows does not seem to be a major mechanism for dissemination of VRE in Bangladesh. However, proper steps should be taken to stop the possible future environmental spread of VRE, as well as other resistant microorganisms, through hospital waste and from hospitals settings in Bangladesh.

Conflict of interest and funding

No competing financial interests exist.

Acknowledgements

This work was financially supported by Emil & Ragna Börjeson Foundation, Åke Wibergs Foundation, and Medicine Faculty of Uppsala University. I am also thankful to Mr. Justin Makii from Uppsala University, Sweden, for his contribution as English proof-reader.

References

  • Lebreton F, Willems RJL, Gilmore MS, Gilmore MS, Clewell DB, Ike Y, Shankar N. Enterococcus diversity, origins in nature, and gut colonization. Enterococci: from commensals to leading causes of drug resistant infection . 2014; Boston, MA: Massachusetts Eye and Ear Infirmary. 1–45.
  • DiazGranados CA, Zimmer SM, Klein M, Jernigan JA. Comparison of mortality associated with vancomycin-resistant and vancomycin-susceptible enterococcal bloodstream infections: a meta-analysis. Clin Infect Dis. 2005; 41: 327–33.
  • Graham M, Ballard SA, Grabsch EA, Johnson PD, Grayson ML. High rates of fecal carriage of nonenterococcal vanB in both children and adults. Antimicrob Agents Chemother. 2008; 52: 1195–7.
  • Courvalin P. Vancomycin resistance in Gram-positive cocci. Clin Infect Dis. 2006; 42(Suppl 1): S25–34.
  • Withey JC, Marzluff JM. Dispersal by juvenile American crows affects population dynamics across a gradient of urbanization. Auk. 2005; 122: 205–21.
  • Xu X, Lin D, Yan G, Ye X, Wu S, Guo Y, etal. vanM, a new glycopeptide resistance gene cluster found in Enterococcus faecium. Antimicrob Agents Chemother. 2010; 54: 4643–7.
  • Nomura T, Tanimoto K, Shibayama K, Arakawa Y, Fujimoto S, Ike Y, etal. Identification of VanN-type vancomycin resistance in an Enterococcus faecium isolate from chicken meat in Japan. Antimicrob Agents Chemother. 2012; 56: 6389–92.
  • Willems RJ, Top J, van Santen M, Robinson DA, Coque TM, Baquero F, etal. Global spread of vancomycin-resistant Enterococcus faecium from distinct nosocomial genetic complex. Emerg Infect Dis. 2005; 11: 821–8.
  • Dahl KH, Mater DD, Flores MJ, Johnsen PJ, Midtvedt T, Corthier G, etal. Transfer of plasmid and chromosomal glycopeptide resistance determinants occurs more readily in the digestive tract of mice than in vitro and exconjugants can persist stably in vivo in the absence of glycopeptide selection. J Antimicrob Chemother. 2007; 59: 478–86.
  • Rice LB, Carias LL, Donskey CL, Rudin SD. Transferable, plasmid-mediated vanB-type glycopeptide resistance in Enterococcus faecium. Antimicrob Agents Chemother. 1998; 42: 963–4.
  • Armeanu E, Bonten MJ. Control of vancomycin-resistant enterococci: one size fits all?. Clin Infect Dis. 2005; 41: 210–16.
  • Kruse H, Johansen BK, Rorvik LM, Schaller G. The use of avoparcin as a growth promoter and the occurrence of vancomycin-resistant Enterococcus species in Norwegian poultry and swine production. Microb Drug Resist. 1999; 5: 135–9.
  • Ramos S, Igrejas G, Rodrigues J, Capelo-Martinez JL, Poeta P. Genetic characterisation of antibiotic resistance and virulence factors in vanA-containing enterococci from cattle, sheep and pigs subsequent to the discontinuation of the use of avoparcin. Vet J. 2012; 193: 301–3.
  • Drobni M, Bonnedahl J, Hernandez J, Haemig P, Olsen B. Vancomycin-resistant enterococci, Point Barrow, Alaska, USA. Emerg Infect Dis. 2009; 15: 838–9.
  • Oravcova V, Ghosh A, Zurek L, Bardon J, Guenther S, Cizek A, etal. Vancomycin-resistant enterococci in rooks (Corvus frugilegus) wintering throughout Europe. Environ Microbiol. 2013; 15: 548–56.
  • Silva N, Igrejas G, Rodrigues P, Rodrigues T, Goncalves A, Felgar AC, etal. Molecular characterization of vancomycin-resistant enterococci and extended-spectrum beta-lactamase-containing Escherichia coli isolates in wild birds from the Azores Archipelago. Avian Pathol. 2011; 40: 473–9.
  • Oravcova V, Zurek L, Townsend A, Clark AB, Ellis JC, Cizek A, etal. American crows as carriers of vancomycin-resistant enterococci with vanA gene. Environ Microbiol. 2014; 16: 939–49.
  • Hasan B, Melhus A, Sandegren L, Alam M, Olsen B. The gull (Chroicocephalus brunnicephalus) as an environmental bioindicator and reservoir for antibiotic resistance on the coastlines of the Bay of Bengal. Microb Drug Resist. 2014; 20: 466–71.
  • Hasan B, Drobni P, Drobni M, Alam M, Olsen B. Dissemination of NDM-1. Lancet Infect Dis. 2012; 12: 99.
  • Palladino S, Kay ID, Costa AM, Lambert EJ, Flexman JP. Real-time PCR for the rapid detection of vanA and vanB genes. Diagn Microbiol Infect Dis. 2003; 45: 81–4.
  • Kaarme J, Hasan B, Rashid M, Olsen B. Zero prevalence of vancomycin-resistant enterococci among Swedish preschool children. Microb Drug Resist. 2015; 21: 65–8.
  • Radhouani H, Pinto L, Coelho C, Sargo R, Araujo C, Lopez M, etal. MLST and a genetic study of antibiotic resistance and virulence factors in vanA-containing Enterococcus from buzzards (Buteo buteo). Lett Appl Microbiol. 2010; 50: 537–41.
  • Rahman SR, Ahmed MF, Begum A. Occurrence of urinary tract infection in adolescent and adult women of shanty town in Dhaka City, Bangladesh. Ethiop J Health Sci. 2014; 24: 145–52.
  • Akhter S, Asna ZH, Rahman MM. Prevalence and antimicrobial susceptibility of enterococcus species isolated from clinical specimens. Mymensingh Med J. 2011; 20: 694–9.
  • Aruji Y, Tamura K, Sugita S, Adachi Y. Intestinal microflora in 45 crows in Ueno Zoo and the in vitro susceptibilities of 29 Escherichia coli isolates to 14 antimicrobial agents. J Vet Med Sci. 2004; 66: 1283–6.
  • Lee HY, Stephen A, Sushela D, Mala M. Detection of protozoan and bacterial pathogens of public health importance in faeces of Corvus spp. (large-billed crow). Trop Biomed. 2008; 25: 134–9.
  • Sharpe M. High on pollution: drugs as environmental contaminants. J Environ Monit. 2003; 5: 42n–6n.
  • Hasan B, Olsen B, Alam A, Akter L, Melhus A. Dissemination of multidrug resistant ESBL-producing E. coli O25b-ST131 clone and role of house crow (Corvus splendens) foraging on hospital waste in Bangladesh. Clin Microbiol Infect. 2015; 21: 1000.e1–4.