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Şahan Yapicier, O, Hesna Kandir, E, Öztürk, D. (1400). Antimicrobial Resistance of E. coli and Salmonella Isolated from Wild Birds in a Rehabilitation Center in Turkey. سامانه مدیریت نشریات علمی, 77(1), 257-267. doi: 10.22092/ari.2021.356322.1823
O Şahan Yapicier; E Hesna Kandir; D Öztürk. "Antimicrobial Resistance of E. coli and Salmonella Isolated from Wild Birds in a Rehabilitation Center in Turkey". سامانه مدیریت نشریات علمی, 77, 1, 1400, 257-267. doi: 10.22092/ari.2021.356322.1823
Şahan Yapicier, O, Hesna Kandir, E, Öztürk, D. (1400). 'Antimicrobial Resistance of E. coli and Salmonella Isolated from Wild Birds in a Rehabilitation Center in Turkey', سامانه مدیریت نشریات علمی, 77(1), pp. 257-267. doi: 10.22092/ari.2021.356322.1823
Şahan Yapicier, O, Hesna Kandir, E, Öztürk, D. Antimicrobial Resistance of E. coli and Salmonella Isolated from Wild Birds in a Rehabilitation Center in Turkey. سامانه مدیریت نشریات علمی, 1400; 77(1): 257-267. doi: 10.22092/ari.2021.356322.1823

Antimicrobial Resistance of E. coli and Salmonella Isolated from Wild Birds in a Rehabilitation Center in Turkey

Archives of Razi Institute
مقاله 35، دوره 77، شماره 1، فروردین و اردیبهشت 2022، صفحه 257-267    اصل مقاله (591.76 K)
نوع مقاله: Original Articles
شناسه دیجیتال (DOI): 10.22092/ari.2021.356322.1823
نویسندگان
O Şahan Yapicier* 1؛ E Hesna Kandir2؛ D Öztürk3
1Republic of Turkey Ministry of Agriculture and Forestry Veterinary Control Central Research Institute, Bacteriology Diagnostic Laboratory, Ankara, Turkey
2Afyon Kocatepe University, Veterinary Faculty, Department of Wild Animal Diseases and Ecology, Afyonkarahisar, Turkey
3Mehmet Akif Ersoy University, Faculty of Veterinary Medicine, Department of Microbiology, 15030, Burdur, Turkey
چکیده
Wildlife plays a critical role as a reservoir for zoonosis especially pathogenic enteric bacteria. In this study we evaluated the presence of E. coli and Salmonella isolates from wild birds and determined their antimicrobial resistance. Intestine and fecal samples from 82 dead wild birds obtained from rehabilitation centre, were examined by microbiological analysis, antibiotic susceptibilities against of 18 antimicrobials and presence of tetracycline resistance genes by multiplex and singleplex PCR were investigated. A total of 51 E. coli were identified as well as Salmonella Kentucky and Salmonella Bisberg. A majority of the E. coli isolates were resistant to lincomysin (100%), penicilline (96.1%), kanamycin (80.4%), tetracycline (68.6%), and oxytetracycline (64.7%). All Salmonella serotypes were resistant to lincomycin, nalidixic acid and penicilline.In addition, 58.82% of E. coli isolates had phenotypic resistance to at least three or more antimicrobials. Our results indicated that the high frequency of tetracycline resistance (68.62%) due to the tet (A), tet (B), and tet (D) genes. This is the first report isolating S. Bisberg and determining antibiotic susceptibility of E.coli and Salmonella isolates from wild birds in Turkey. These results will help providing better understand of the dissemination of antibiotic resistancy in the environment, which can be used to potentially decrease spread through bird migration. Moreover, these results help assess the risk of spread of resistance from wild birds to humans.
کلیدواژه‌ها
E. coli؛ Salmonella؛ antibiotic susceptibility؛ tet genes wild birds
عنوان مقاله [English]
مقاومت ضد میکروبی E. coli و Salmonella جدا شده از پرندگان وحشی در یک مرکز توانبخشی در ترکیه
چکیده [English]
حیات وحش نقش مهمی را به عنوان مخزن زئونوز به ویژه باکتری های روده ای بیماری زا ایفا می کند. در این مطالعه حضور ایزوله های E. coli و Salmonella از پرندگان وحشی بررسی و مقاومت ضد میکروبی آنها تعیین شد. نمونه روده و مدفوع 82 پرنده وحشی مرده گرفته شده از مرکز توانبخشی، با استفاده از آنالیز میکروبیولوژیکی، حساسیت آنتی بیوتیکی در برابر 18 آنتی بیوتیک و وجود ژن های مقاومت به تتراسایکلین با روش Multiplex و singleplex PCR بررسی شد. در مجموع 51 E. coli و Salmonella Kentucky و Salmonella Bisberg شناسایی شدند. اکثر جدایه های E. coli به لینکومیسین (100٪)، پنی سیلین (96.1٪)، کانامایسین (80.4٪)، تتراسایکلین (68.6٪)، و اکسی تتراسایکلین (64.7٪) مقاوم بودند. همه سروتیپهای سالمونلا نسبت به لینکومایسین ، نالیدیکسیک اسید و پنی سیلین مقاوم بودند. علاوه بر این، 58.82 درصد از جدایه های E. coli دارای مقاومت فنوتیپی حداقل به سه یا بیشتر ضد میکروبی بودند. نتایج ما نشان داد که فراوانی بالای مقاومت به تتراسایکلین (62/68 درصد) ناشی از ژن‌های tet(A)، tet(B) و tet(D) است. این اولین گزارش جداسازی S. Bisberg و تعیین حساسیت آنتی بیوتیکی E.coli و سالمونلا جدا شده از پرندگان وحشی در ترکیه است. این نتایج به درک بهتر انتشار مقاومت آنتی بیوتیکی در محیط کمک می کند، که می تواند برای کاهش بالقوه انتشار از طریق مهاجرت پرندگان مورد استفاده قرار گیرد. علاوه بر این، این نتایج به ارزیابی خطر گسترش مقاومت از پرندگان وحشی به انسان کمک می کند.
کلیدواژه‌ها [English]
E. coli, Salmonella, حساسیت به آنتی بیوتیک, ژن tet پرندگان وحشی
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مراجع
  1. Barrowclough GF, Cracraft J, Klicka J, Zink RM. How Many Kinds of Birds Are There and Why Does It Matter? PLoS One. 2016;11(11):0166307.
  2. Benskin CM, Wilson K, Jones K, Hartley IR. Bacterial pathogens in wild birds: a review of the frequency and effects of infection. Biol Rev Camb Philos Soc. 2009;84(3):349-73.
  3. Gaukler SM, Linz GM, Sherwood JS, Dyer NW, Bleier WJ, Wannemuehler YM, et al. Escherichia coli, Salmonella, and Mycobacterium avium subsp. paratuberculosis in wild European starlings at a Kansas cattle feedlot. Avian Dis. 2009;53(4):544-51.
  4. Rahman MM, Talukder A, Chowdhury MMH, Talukder R, Akter R. Coronaviruses in wild birds - A potential and suitable vector for global distribution. Vet Med Sci. 2021;7(1):264-72.
  5. Lagerstrom KM, Hadly EA. The under-investigated wild side of Escherichia coli: genetic diversity, pathogenicity and antimicrobial resistance in wild animals. Proc Biol Sci. 2021;288(1948):20210399.
  6. Fogarty LR, Haack SK, Wolcott MJ, Whitman RL. Abundance and characteristics of the recreational water quality indicator bacteria Escherichia coli and enterococci in gull faeces. J Appl Microbiol. 2003;94(5):865-78.
  7. Kobayashi H, Kanazaki M, Shimizu Y, Nakajima H, Khatun MM, Hata E, et al. Salmonella isolates from cloacal swabs and footpads of wild birds in the immediate environment of Tokyo Bay. J Vet Med Sci. 2007;69(3):309-11.
  8. Moore JE, Gilpin D, Crothers E, Canney A, Kaneko A, Matsuda M. Occurrence of Campylobacter spp. and Cryptosporidium spp. in seagulls (Larus spp.). Vector Borne Zoonotic Dis. 2002;2(2):111-4.
  9. Greig J, Rajic A, Young I, Mascarenhas M, Waddell L, LeJeune J. A scoping review of the role of wildlife in the transmission of bacterial pathogens and antimicrobial resistance to the food Chain. Zoonoses Public Health. 2015;62(4):269-84.
  10. Hernandez J, Bonnedahl J, Eliasson I, Wallensten A, Comstedt P, Johansson A, et al. Globally disseminated human pathogenic Escherichia coli of O25b-ST131 clone, harbouring blaCTX-M-15 , found in Glaucous-winged gull at remote Commander Islands, Russia. Environ Microbiol Rep. 2010;2(2):329-32.
  11. Quinn P, Markey B, Lenonard F, FitzPatrick E, Fanning S, Hartigan P. Enterobactericeae. Veterinary Microbiology and Microbial Disease. 2nd ed. USA: Wiley-Blackwell Publication; 2011.
  12. International Organization for Standardization I. Microbiology of the food chain-Horizontal method for the detection, enumeration and serotyping of Salmonella - Part 1: Detection of Salmonella spp Geneva, Switzerland: International Organization for Standardization; 2017.
  13. Clinical and Laboratory Standards Institute C. Performance standards for antimicrobial susceptibility testing. CLSI supplement M100. 28th ed. Wayne, PA: Clinical and Laboratory Standards Institute; 2018.
  14. Chopra I, Roberts M. Tetracycline antibiotics: mode of action, applications, molecular biology, and epidemiology of bacterial resistance. Microbiol Mol Biol Rev. 2001;65(2):232-60.
  15. Ng LK, Martin I, Alfa M, Mulvey M. Multiplex PCR for the detection of tetracycline resistant genes. Mol Cell Probes. 2001;15(4):209-15.
  16. Roberts MC, Schwarz S, Aarts HJ. Erratum: Acquired antibiotic resistance genes: an overview. Front Microbiol. 2012;3:384.
  17. Bonnedahl J, Jarhult JD. Antibiotic resistance in wild birds. Ups J Med Sci. 2014;119(2):113-6.
  18. Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, Gittleman JL, et al. Global trends in emerging infectious diseases. Nature. 2008;451(7181):990-3.
  19. Maysa A, Abdallah M, Rehab E. Prevalence of zoonotic Escherichia coli and Salmonellae in wild birds and humans in Egypt with emphasis on RAPD-PCR fingerprinting of E. coli. Glob Vet J. 2013;11(6):781-8.
  20. Dolejska M, Papagiannitsis CC. Plasmid-mediated resistance is going wild. Plasmid. 2018;99:99-111.
  21. Okullu T, Onchweri A, Miruka C, Eilu E, Abimana J, Nyabayo M. Antibiotic resistant Escherichia coli isolates from barn swallow droppings in Ishaka Town, Uganda. J App Env Microbiol. 2016;4(2):34-8.
  22. Refsum T, Handeland K, Baggesen DL, Holstad G, Kapperud G. Salmonellae in avian wildlife in Norway from 1969 to 2000. Appl Environ Microbiol. 2002;68(11):5595-9.
  23. 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(10):1283-6.
  24. 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(2):134-9.
  25. Phalen DN, Drew ML, Simpson B, Roset K, Dubose K, Mora M. Salmonella enterica subsp. Enterica in Cattle Egret (Bubulcus ibis) chicks from central Texas: prevalence, serotypes, pathogenicity, and epizootic potential. J Wildl Dis. 2010;46(2):379-89.
  26. Awad-Alla ME, Abdien HM, Dessouki AA. Prevalence of bacteria and parasites in White Ibis in Egypt. Vet Ital. 2010;46(3):277-86.
  27. Brittingham MC, Temple SA, Duncan RM. A survey of the prevalence of selected bacteria in wild birds. J Wildl Dis. 1988;24(2):299-307.
  28. Elsohaby I, Samy A, Elmoslemany A, Alorabi M, Alkafafy M, Aldoweriej A, et al. Migratory Wild Birds as a Potential Disseminator of Antimicrobial-Resistant Bacteria around Al-Asfar Lake, Eastern Saudi Arabia. Antibiotics (Basel). 2021;10(3).
  29. Gambino D, Vicari D, Vitale M, Schiro G, Mira F, Giglia M, et al. Study on Bacteria Isolates and Antimicrobial Resistance in Wildlife in Sicily, Southern Italy. Microorganisms. 2021;9(1).
  30. Suphoronski SA, Raso TdF, Weinert NC, Seki MC, Carrasco AdOT. Occurrence of Salmonella sp. and Escherichia coli in free-living and captive wild birds from 2010-2013 in Guarapuava, Paraná, Brazil. Afr J Microbiol Res. 2015;9(29):1778-82.
  31. Zurfluh K, Albini S, Mattmann P, Kindle P, Nuesch-Inderbinen M, Stephan R, et al. Antimicrobial resistant and extended-spectrum beta-lactamase producing Escherichia coli in common wild bird species in Switzerland. Microbiologyopen. 2019;8(11):e845.
  32. Matias CA, Pereira IA, de Araujo Mdos S, Santos AF, Lopes RP, Christakis S, et al. Characteristics of Salmonella spp. Isolated from Wild Birds Confiscated in Illegal Trade Markets, Rio de Janeiro, Brazil. Biomed Res Int. 2016;2016:3416864.
  33. Foti M, Mascetti A, Fisichella V, Fulco E, Orlandella BM, Lo Piccolo F. Antibiotic resistance assessment in bacteria isolated in migratory Passeriformes transiting through the Metaponto territory (Basilicata, Italy). Avian Res. 2017;8(1):26.
  34. Guenther S, Aschenbrenner K, Stamm I, Bethe A, Semmler T, Stubbe A, et al. Comparable high rates of extended-spectrum-beta-lactamase-producing Escherichia coli in birds of prey from Germany and Mongolia. PLoS One. 2012;7(12):e53039.
  35. Vlahović K, Matica B, Bata I, Pavlak M, Pavičić Ž, Popović M, et al. Campylobacter, salmonella and chlamydia in free-living birds of Croatia. Eur J Wildl Res. 2004;50(3):127-32.
  36. Sanches LA, Gomes MDS, Teixeira RHF, Cunha MPV, Oliveira MGX, Vieira MAM, et al. Captive wild birds as reservoirs of enteropathogenic E. coli (EPEC) and Shiga-toxin producing E. coli (STEC). Braz J Microbiol. 2017;48(4):760-3.
  37. Shelton DR, Karns JS, Coppock C, Patel J, Sharma M, Pachepsky YA. Relationship between eae and stx virulence genes and Escherichia coli in an agricultural watershed: implications for irrigation water standards and leafy green commodities. J Food Prot. 2011;74(1):18-23.
  38. Collignon PJ, Conly JM, Andremont A, McEwen SA, Aidara-Kane A, World Health Organization Advisory Group BMoISoAR, et al. World Health Organization Ranking of Antimicrobials According to Their Importance in Human Medicine: A Critical Step for Developing Risk Management Strategies to Control Antimicrobial Resistance From Food Animal Production. Clin Infect Dis. 2016;63(8):1087-93.
  39. Hasan B, Sandegren L, Melhus A, Drobni M, Hernandez J, Waldenstrom J, et al. Antimicrobial drug-resistant Escherichia coli in wild birds and free-range poultry, Bangladesh. Emerg Infect Dis. 2012;18(12):2055-8.
  40. Shobrak MY, Abo-Amer AE. Role of wild birds as carriers of multi-drug resistant Escherichia coli and Escherichia vulneris. Braz J Microbiol. 2014;45(4):1199-209.
  41. Dolejska M, Bierosova B, Kohoutova L, Literak I, Cizek A. Antibiotic-resistant Salmonella and Escherichia coli isolates with integrons and extended-spectrum beta-lactamases in surface water and sympatric black-headed gulls. J Appl Microbiol. 2009;106(6):1941-50.
  42. Sacristan C, Esperon F, Herrera-Leon S, Iglesias I, Neves E, Nogal V, et al. Virulence genes, antibiotic resistance and integrons in Escherichia coli strains isolated from synanthropic birds from Spain. Avian Pathol. 2014;43(2):172-5.
  43. Stedt J, Bonnedahl J, Hernandez J, McMahon BJ, Hasan B, Olsen B, et al. Antibiotic resistance patterns in Escherichia coli from gulls in nine European countries. Infect Ecol Epidemiol. 2014;4.
  44. Radhouani H, Poeta P, Goncalves A, Pacheco R, Sargo R, Igrejas G. Wild birds as biological indicators of environmental pollution: antimicrobial resistance patterns of Escherichia coli and enterococci isolated from common buzzards (Buteo buteo). J Med Microbiol. 2012;61(Pt 6):837-43.
  45. Mohsin M, Raza S, Schaufler K, Roschanski N, Sarwar F, Semmler T, et al. High Prevalence of CTX-M-15-Type ESBL-Producing E. coli from Migratory Avian Species in Pakistan. Front Microbiol. 2017;8:2476.
  46. Blyton MD, Pi H, Vangchhia B, Abraham S, Trott DJ, Johnson JR, et al. Genetic Structure and Antimicrobial Resistance of Escherichia coli and Cryptic Clades in Birds with Diverse Human Associations. Appl Environ Microbiol. 2015;81(15):5123-33.
  1. Ong KH, Khor WC, Quek JY, Low ZX, Arivalan S, Humaidi M, et al. Occurrence and Antimicrobial Resistance Traits of Escherichia coli from Wild Birds and Rodents in Singapore. Int J Environ Res Public Health. 2020;17(15).
  2. Allen HK, Donato J, Wang HH, Cloud-Hansen KA, Davies J, Handelsman J. Call of the wild: antibiotic resistance genes in natural environments. Nat Rev Microbiol. 2010;8(4):251-9.
  3. Karkman A, Parnanen K, Larsson DGJ. Fecal pollution can explain antibiotic resistance gene abundances in anthropogenically impacted environments. Nat Commun. 2019;10(1):80.
  4. Smith S, Wang J, Fanning S, McMahon BJ. Antimicrobial resistant bacteria in wild mammals and birds: a coincidence or cause for concern? Ir Vet J. 2014;67(1):8.
  5. Arabzadeh F, Aeini F, Keshavarzi F, Behrvash S. Resistance to Tetracycline and Vancomycin of Staphylococcus aureus Isolates from Sanandaj Patients by Molecular Genotyping. Ann Clin Lab Res. 2018;06.
  6. Santos T, Silva N, Igrejas G, Rodrigues P, Micael J, Rodrigues T, et al. Dissemination of antibiotic resistant Enterococcus spp. and Escherichia coli from wild birds of Azores Archipelago. Anaerobe. 2013;24:25-31.
  7. Botti V, Navillod FV, Domenis L, Orusa R, Pepe E, Robetto S, et al. Salmonella spp. and antibiotic-resistant strains in wild mammals and birds in north-western Italy from 2002 to 2010. Vet Ital. 2013;49(2):195-202.
  8. Forte Beleza A, Cardoso Maciel W, Souza Lopes E, de Albuquerque Á, Silva Carreira A, Guedes Nogueira C, et al. Evidence of the role of free-living birds as disseminators of Salmonella spp. Arq Inst Biol. 2020;87.
  9. Tizard I. Salmonellosis in wild birds. Semin Avian Exot Pet Med. 2004;13(2):50-66.
  10. Üniversitesi MAE, Fakültesi V, Dam1 MA, editors. First Isolation of Salmonella Hessarek from Sturnus vulgaris in Turkey : A Case Report. Kafkas Univ Vet Fak Derg. 2017; 23 (2): 343-346.
  11. Daoust P-Y, Prescott JF. Salmonellosis. Infectious Diseases of Wild Birds 2007. p. 270-88.
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