Antimicrobial resistance profiles and virulence factors of Escherichia coli O157 collected from a poultry processing plant

The aims of this study were to investigate the presence of Escherichia coli O157 and to determine the antibiotic susceptibility of isolates in different poultry-originated materials. In total 300 samples of chicken carcass swabs (n = 50), chicken feces (n = 50), gizzard (n = 50), liver (n = 50), water in the final scald tank (n = 50), and equipment such as tables, conveyers, and knives (n = 50) were used as materials. Overall, 45 E. coli isolates were obtained from the 300 poultry samples. However, 13 (4.3%) of the samples were identified as E. coli O157 including 3 liver, 3 carcass, and 7 fecal samples. All 13 isolates were positive for O157 but negative for H7 using PCR. Only intimin (encoded by eaeA gene) was detected in 10 E. coli O157 isolates while no other virulence factors (enterohemolysin A, shiga toxin 1 and 2) were detected. All E. coli O157 isolates were susceptible to gentamicin (100%). In conclusion, the presence of E. coli O157 in poultry is of utmost significance (4.3%) and our results demonstrated that poultry carcasses and giblets may be contaminated by E. coli O157 with feces during evisceration. To prevent E. coli O157 infections, hygiene rules must be tightly observed. In addition, antibiotic use must be controlled for avoiding increased antibiotic resistance.

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  • Coia JE. Clinical, microbiological and epidemiological aspects of Escherichia coli O157 infection. FEMS Immunol Med Mic 1998; 20: 1-9.
  • Coia JE, Johnston Y, Steers NJ, Hanson MF. A survey of the prevalence of Escherichia coli O157 in raw meats, raw cow’s milk and raw-milk cheeses in south-east Scotland. Int J Food Microbiol. 2001; 66: 63-69.
  • Mather AE, Innocent GT, McEwen SA, Reilly WJ, Taylor DJ, Steele WB, Gunn GJ, Ternent HE, Reid SW, Mellor DJ. Risk factors for hide contamination of Scottish cattle at slaughter with Escherichia coli O157. Prev Vet Med 2007; 80: 257-270.
  • Dontorou A, Papadopoulou C, Filioussis G, Economou V, Apostolou I, Zakkas G, Salamoura A, Kansouzidou A, Levidiotou S. Isolation of Escherichia coli O157:H7 from foods in Greece. Int J Food Microbiol 2003; 82: 273-279.
  • De Giusti M, Tufi D, Aurigemma C, Del Cimmuto A, Trinti F, Mannocci A, Boccia A. Detection of Escherichia coli O157 in raw and cooked meat: comparison of conventional direct culture method and Enzyme Linked Fluorescent Assay (ELFA). Ital J Public Health 2011; 8: 22-28.
  • Farrokh, C, Jordan K, Auvray F, Glass K, Oppegaard H, Raynaud S, Thevenot D, Condron R, De Reu K, Govaris A et al. Review of Shiga-toxin-producing Escherichia coli (STEC) and their significance in dairy production. Int J Food Microbiol 2013; 162: 190-212.
  • Cornick NA, Booher SL, Moon HW. Intimin facilitates colonization by Escherichia coli O157:H7 in adult ruminants. Infect Immun 2002; 70: 2704-2707.
  • Akbar A, Sitara U, Ali I, Iftikhar Khan M, Phadungchob T, Anal AK. Presence of Escherichia coli in poultry meat: a potential food safety threat. Int Food Res J 2014; 21: 941-945.
  • Sarimehmetoglu B, Aksoy MH, Ayaz ND, Ayaz Y, Kuplulu O, Kaplan YZ. Detection of Escherichia coli O157:H7 in ground beef using immunomagnetic separation and multiplex PCR. Food Control 2009; 20: 357-361.
  • Maurer JJ, Schmidt D, Petrosko P, Sanchez S, Bolton L, Lee MD. Development of primers to O-antigen biosynthesis genes for specific detection of Escherichia coli O157 by PCR. Appl Environ Microbiol 1999; 65: 2954-2960.
  • Fratamico PM, Bagi LK, Pepe T. A multiplex polymerase chain reaction assay for rapid detection and identification of Escherichia coli O157:H7 in foods and bovine feces. J Food Protect 2000; 63: 1032-1037.
  • Clinical and Laboratory Standards Institute (CLSI). Clinical and Laboratory Standards Institute Performance standards for antimicrobial susceptibility testing; Twenty-Fourth Informational Supplement. 2014. CLSI document M100-S24. Wayne, PA: Clinical and Laboratory Standards Institute.
  • Dursun SG, Kaya O. The identification and antibiotic sensibility of E. coli O157:H7 in broiler chickens. Pendik Veteriner Mikrobiyoloji Dergisi 2010; 37: 19-31 (article in Turkish with a summary in English).
  • Jo MY, Kim JH, Lim JH, Kang MY, Koh HB, Park YH, Yoon DY, Chae JS, Eo SK, Lee JH. Prevalence and characteristics of Escherichia coli O157 from major food animals in Korea. Int J Food Microbiol 2004; 95: 41-49.
  • Abay S, Aydin F, Ertaş N, Hizlisoy H, Erdogdu S, Gönülalan Z. Kanatlılardan Escherichia coli O157 izolasyonu üzerine çalışmalar. Erciyes Üniv Vet Fak Derg 2014; 11: 1-6 (in Turkish).
  • Abdul-Raouf UM, Ammar MS, Beuchat LR. Isolation of Escherichia coli O157:H7 from some Egyptian foods. Int J Food Microbiol 1996; 29: 423-426.
  • Chinen I, Tanoro JD, Miliwebsky E, Lound LH, Chillemi G, Ledri S. Isolation and characterisation of Escherichia coli O157:H7 from retail meats in Argentina. J Food Prot 2001; 64: 1346-1351.
  • Alonso MZ, Lucchesi PMA, Rodriguez EM, Parma AE, Padola NL. Enteropathogenic (EPEC) and shigatoxigenic Escherichia coli (STEC) in broiler chickens and derived products at different retail stores. Food Control 2012; 23: 351-355.
  • Darwish WS, Eldin WFS, Eldesoky KI. Prevalence, molecular characterization and antibiotic susceptibility of Escherichia coli isolated from duck meat and giblets. J Food Safety 2015; 35: 410-415.
  • Arias ML, Monge-Rojas R, Chaves C, Antillon F. Effect of storage temperatures on growth and survival of Escherichia coli O157:H7 inoculated in foods from a neotropical environment. Rev Biol Trop 2001; 49: 517-524.
  • Tabatabaei M, Mokarizade A, Foad-Marashi N. Detection and molecular characterization of sorbitol negative shiga toxigenic Escherichia coli in chicken from northwest of Iran. Vet Res Forum 2011; 2: 183-188.
  • Kobayashi H, Pohjanvirta T, Pelkonen S. Prevalence and characteristics of intimin- and Shiga toxin-producing Escherichia coli from gulls, pigeons and broilers in Finland. J Vet Med Sci 2002; 64: 1071-1073.
  • Oh JY, Kang MS, An BK, Shin EG, Kim MJ, Kim YJ, Kwon YK. Prevalence and characteristics of intimin-producing Escherichia coli strains isolated from healthy chickens in Korea. Poultry Sci 2012; 91: 2438-2443.
  • Karadal F, Ertas N, Hizlisoy H, Abay S, Al S. Prevalence of Escherichia coli O157:H7 and their verotoxins and Salmonella spp. in processed poultry products. J Food Safety 2013; 33: 313- 318.
  • Dipineto L, Santaniello A, Fontanella M, Lagos K, Fioretti A, Menna LF. Presence of Shiga toxin-producing Escherichia coli O157:H7 in living layer hens. Lett Appl Microbiol 2006; 43: 293-295.
  • Momtaz H, Jamshidi A. Shiga toxin-producing Escherichia coli isolated from chicken meat in Iran: serogroups, virulence factors, and antimicrobial resistance properties. Poultry Sci 2013; 92: 1305-1313.
  • Mainil JG, Daube G. Verotoxigenic Escherichia coli from animals, humans and foods: who’s who? J Appl Microbiol 2005; 98: 1322-1344.
  • Benshaban M, Dahmani K, Elouzi A. Antimicrobial resistance patterns of pathogenic bacteria isolated from chicken’s liver. Am J Microbiol Biotechn 2014; 1: 88-93.
  • Schroeder CM, Zhao C, Debroy C, Torcolini J, Zhao S, White DG, Wagner DD, Mcdermott PF, Walker RD, Meng J. Antimicrobial resistance of Escherichia coli O157 isolated from humans, cattle, swine, and food. Appl Environ Microbiol 2002; 68: 576-581.
  • Miles TD, McLaughlin W, Brown PD. Antimicrobial resistance of Escherichia coli isolates from broiler chickens and humans. BMC Vet Res 2006; 2: 1-7.