Occurrence and antimicrobial resistance of Campylobacter jejuni isolates from poultry in Casablanca-Settat, Morocco

Submitted: 18 November 2019
Accepted: 4 February 2020
Published: 6 April 2020
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Campylobacteriosis and Campylobacter spp. resistance to antibiotics represents a serious worldwide public health problem thermophilic Campylobacters, in particular, are major causes of gastroenteritis in humans. The aim of this study was to determine the prevalence and antimicrobial resistance of Campylobacter jejuni isolated from chicken droppings, of commercial poultry in the city of Casablanca, Morocco. Between February and September 2017, 140 samples of chicken droppings were collected and analyzed by classical bacteriology methods for isolation and identification according to Moroccan Standard NM ISO/TS 10272-3 (2013), followed by molecular identification (PCR: polymerase chain reaction). Among the 140 samples, 102 (73%) were positive by Campylobacter spp. tests and 38 (27.14 %) were negative to Campylobacter spp. Among the positive colonies, 41 (40, 2%) were C. jejuni. Of the 41 C. jejuni isolates, resistance was detected to tetracycline (100%), erythromycin (97%), ampicillin (85%), ciprofloxacin (77%), amoxicillin/ clavulanic acid (61.4%), and gentamicin (12.0%). In conclusion, the data obtained in the current study demonstrate that the majority of C. jejuni isolates evaluated were resistant to antimicrobials of the cycline, macrolide, and fluoroquinolone families, and all of the isolates were susceptible to gentamicin. Fluoroquinolone is the drug of choice for treating Campylobacter infections. These results underline the need for prudent use of antibiotics in poultry production to minimize the spread of antibioticresistant Campylobacter spp.

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Bsteer. L.A., Essack, S.Y., 2008. Prevalence of antibiotic resistance in Campylobacter isolates from commercial poultry suppliers in KwaZulu-Natal, South Africa. Antimicrob. Chemother. 62, 1298– 1300. DOI: https://doi.org/10.1093/jac/dkn408
Bûttner S, Bruhn S, Danuser J, Overesch G &Schûpbach G. 2008 “Baseline study on the prevalence of Campylobacter in broiler flocks and the prevalence of Campylobacter / Salmonella on broiler carcasses in”. FederalVeterinary Office. Suisse 45 pages.
Campagnolo ER, Philipp LM, Long JM, Hanshaw NL 2017 .Pet-associated Campylobacteriosis: A persisting public health concern. Zoonoses Public Health. . doi: 10.1111/zph.12389 DOI: https://doi.org/10.1111/zph.12389
Chen. Z. and Jiang. X., 2014 “Microbiological safety of chicken litter or chicken litter-based organic fertilizers: a review,” Agriculture, vol. 4, no. 1, pp. 1–29. DOI: https://doi.org/10.3390/agriculture4010001
European Food Safety Authority (EFSA), 2019.
European Food Safety Authority (EFSA), 2010 “’The community summary report on trends and sources of zoonoses’. Zoonotic agents and foodborne outbreaks in the European Union (2008),” EFSA Journal, 8 (3):1496–1906. DOI: https://doi.org/10.2903/j.efsa.2010.1496
Food Administration. FDA 2014. Annual summary report on antimicrobials sold or distributed in 2012 for use in food-producing animals. https://www.fda.gov/media/94906/download
Giacomelli. M, Salata. C, Martini. M, Montesissa. C, and Piccirillo. A, 2014 “Antimicrobial resistance of Campylobacter jejuni and Campylobacter coli from poultry in Italy,” Microbial Drug Resistance, 20(2): 181–188. DOI: https://doi.org/10.1089/mdr.2013.0110
Giannatale. Di, E., Di Serafino, G., Zilli, K., Alessiani, A., Sacchini, L., Garofolo, G., Aprea, G., Marotta, F. 2014, Characterization of antimicrobial resistance patterns and detection of virulence genes in Campylobacter isolates in Italy. Sensors (Basel), 14: 3308-3322. doi:10.3390/s140203308. DOI: https://doi.org/10.3390/s140203308
Giombelli A. and M. B. A. Gloria, 2014 “Prevalence of Salmonella and Campylobacter on broiler chickens from farm to slaughter and efficiency of methods to remove visible fecal contamination,” Journal of Food Protection, vol. 77, no. 11, pp. 1851–1859. DOI: https://doi.org/10.4315/0362-028X.JFP-14-200
Goualie. G.B., G.T. karou, S. bakayoko, K.J. coulibaly, K.E. coulibaly, S.L. niamke et M. dosso raspa 2010 “Prevalence of Campylobacter in chickens sold in Abidjan markets: Pilot study conducted in Adjamé commune in 2005” Vol.8 N0S.
Hariharan. H, Sharma. S, Chikweto. A, Matthew. V, DeAllie. C, 2009. Antimicrobial drug resistance as determined by the E-test in Campylobacter jejuni, C. coli, and C. lari isolates from the ceca of broiler and layer chickens in Grenada. Comp. Immun. Microbiol. Infect. Dis. 32: 21–28. DOI: https://doi.org/10.1016/j.cimid.2008.01.010
Jain. D, Sinha. S., Prasad. K.N, Pandey, C.M., 2005 Campylobacter species and drug resistance in a north Indian rural community. Trans. R. Soc. Trop. Med. Hyg. 99:207–214. DOI: https://doi.org/10.1016/j.trstmh.2004.09.006
Johnson T.J., Shank J.M., Johnson J.G. 2017. Current and Potential Treatments for Reducing Campylobacter Colonization in Animal Hosts and Disease in Humans. Front. Microbiol. 8:487. doi: 10.3389/fmicb.2017.00487. DOI: https://doi.org/10.3389/fmicb.2017.00487
Kaakoush. N. O, Castaño-Rodríguez. N, Mitchell. H. M, and Man. S. M. 2015 Global epidemiology of campylobacter infection. Clin. Microbiol. Rev. 28: 687–720. doi: 10.1128/CMR.00006-15. DOI: https://doi.org/10.1128/CMR.00006-15
Kalupahana. R. S, Mughini-Gras. L, Kottawatta. S. A, Somarathne. S, Gamage. C., and Wagenaar. J. A, 2018 “Weather correlates of Campylobacter prevalence in broilers at slaughter under tropical conditions in Sri Lanka,” Epidemiology and Infection, 146 (08): 972–979. DOI: https://doi.org/10.1017/S0950268818000894
Kim. H. J., Kim. J. H., Kim Y. I. and al., 2010 “Prevalence and characterization of Campylobacter spp. isolated from domestic and imported poultry meat in Korea, 2004–2008,” Foodborne Pathogens and Disease, 7(10): 1203–1209. DOI: https://doi.org/10.1089/fpd.2010.0553
Leahy. AM, Cummings KJ, Rodriguez-Rivera LD, Hamer SA and Lawhon SD. 2017 Faecal Campylobacter shedding among dogs in animal shelters across Texas. Zoonoses Public Health. doi: 10.1111/zph.12356 DOI: https://doi.org/10.1111/zph.12356
Ma. SM. 2011 The clinical importance of emerging Campylobacter species. Nat Rev Gastroenterol Hepatol.; 8(12):669-85. DOI: https://doi.org/10.1038/nrgastro.2011.191
Manel G. et al. 2018. Prevalence and Antibiotic Resistance Patterns of Campylobacter spp. Isolated from Broiler Chickens in the North of Tunisia. BioMed Research International 2018, Article ID 7943786. DOI: 10.1155/2018/7943786 DOI: https://doi.org/10.1155/2018/7943786
Manfreda. G, A. Parisi, A. De Cesare, D. Mion, S. Piva, and R. G. Zanoni, 2016 “Typing of Campylobacter jejuni Isolated from Turkey by genotypic methods, antimicrobial susceptibility, and virulence gene patterns: a retrospective study,” Foodborne Pathogens and Disease, 13(2):93–100. DOI: https://doi.org/10.1089/fpd.2015.2048
Mattheus W, Botteldoorn N, Heylen K, Pochet B, Dierick K.. 2012 Trend analysis of antimicrobial resistance in Campylobacter jejuni and Campylobacter coli isolated from belgian pork and poultry meat products using surveillance data of 2004-2009. Foodborn Pathog Dis; 9: 465- 472. DOI: https://doi.org/10.1089/fpd.2011.1042
Merle. R, Hajek. P, Käsbohrer. A, Hegger-Gravenhorst. C, Mollenhauer. Y, Robanus. M, et al. 2012. Monitoring of antibiotic consumption in livestock: a German feasibility study. Preventive veterinary medicine. 104(1-2):34-43. DOI: https://doi.org/10.1016/j.prevetmed.2011.10.013
Moore. J. E, Corcoran. D, Dooby. S. G, Lucey. B, Matsuda. M, McDowell. A, Megraud. F, Millar. B .O, Mahony. R., Riordan. L, O’Rourke. M, Rao. J, Rooney. P, Sails. A. and Whyte, P. 2005 Campylobacter. Veterinary Research, 36:351-382.
Migura-Garcia. L and R. Ramos , 2017 “Antimicrobial resistance of salmonella serovars and Campylobacter spp. isolated from an opportunistic gull species, yellow-legged gull (Larusmichahellis),” Journal of Wildlife Diseases, 53(1):148–152, DOI: https://doi.org/10.7589/2016-03-051
Norstro. M., Johnsen. G, Hofshagen., Tharaldsen. H, Kruse. H. 2007 Antimicrobial resistance in Campylobacter jejuni from broilers and broiler house environments in Norway. J. Food Prot. 70:736–738. DOI: https://doi.org/10.4315/0362-028X-70.3.736
Nylen. G, Dunstan. F, Palmer. S et al 2002, “The seasonal distribution of campylobacter infection in nine European countries and New Zealand,” Epidemiology and Infection, 128 (03):383– 390. DOI: https://doi.org/10.1017/S0950268802006830
ONSSA. Requirements for poultry production. 10 March 2015.
Oporto. B, Juste. R, Hurtado. A. 2009 Phenotypic and genotypic antimicrobial resistance profiles of Campylobacter jejuni isolated from cattle, sheep, and free-range poultry faeces. Int J Microbiol. [Online]. Available from: DOI: 10.1155/2009/456573. DOI: https://doi.org/10.1155/2009/456573
Parsons. B. N., Porter. C. J, Ryvar. R., Stavisky. J., Williams. N. J, Pinchbeck. G. L, Birtles. R.J, Christley. R. M, German. A. J, Radford. A. D, Hart. C.A, Gaskell. R. M, Dawson. S. 2010 Prevalence of Campylobacter spp. in a cross-sectional study of dogs attending veterinary practices in the UK and risk indicators associated with shedding. The Veterinary Journal. 184: 66–70. DOI: https://doi.org/10.1016/j.tvjl.2009.01.009
Rahmatallah. N, El Rhaffouli. H, Lahlou Amine. I, Sekhsokh Y, Fassi Fihri. O, El Houadfi. M. 2018. Consumption of antibacterial molecules in broiler production in Morocco. Veterinary medicine and science. 4(2):80-90. DOI: https://doi.org/10.1002/vms3.89
Ravel A., Pintar K., Nesbitt A., Pollari F. 2016. Non food-related risk factors of campylobacteriosis in Canada: A matched case-control study. BMC Public Health. 16:1016. DOI: https://doi.org/10.1186/s12889-016-3679-4
Rosenberg Goldstein .R.E., Cruz-Cano R., Jiang C., Palmer A., Blythe D., Ryan P., Hogan B., White B., Dunn J.R., Libby T., et al. 2016. Association between community socioeconomic factors, animal feeding operations, and campylobacteriosis incidence rates: Foodborne Diseases Active Surveillance Network (FoodNet), 2004–2010. BMC Infect. Dis.;16:354.
Sahin. O, Kassem. I. I., Shen. Z, Lin. J, Rajashekara. G., and Zhang. Q., 2015 Campylobacter in poultry: ecology and potential interventions,” Avian Diseases, 59(2):185–200. DOI: https://doi.org/10.1637/11072-032315-Review
Sanders P, Bousquet-Mélou A, Chauvin C, Toutain P-L. 2011. Utilisation des antibiotiques en élevage et enjeux de santé publique. INRA Productions Animales. 24(2):199-204. DOI: https://doi.org/10.20870/productions-animales.2011.24.2.3254
Skarp. C. P. A, Anninen M.-L. H¨, and Rautelin H. I. K., 2016 “Campylobacteriosis: The role of poultry meat,” Clinical Microbiology and Infection, 22 (2): 103–109. DOI: https://doi.org/10.1016/j.cmi.2015.11.019
Sonnevend. A., Rotimi, V.O., Kolodziejek, J., Usmani, A., Nowotny, N., Pal, T., 2006 High level of ciprofloxacin resistance and its molecular background among Campylobacter jejuni strains isolated in the United Arab Emirates. J. Med. Microbiol. 55:1533–1538. DOI: https://doi.org/10.1099/jmm.0.46744-0
Stonnet V, Guesdon JL, 1993 Campylobacter jejuni: specific oligonucleotides and DNA probes for use in polymerase chain reaction-based diagnosis. FEMS Immunology and Medical Microbiology. 7: 337- 344. DOI: https://doi.org/10.1111/j.1574-695X.1993.tb00415.x
Suzuki. H. and Yamamoto. S., 2009 “Campylobacter contamination in retail poultry meats and by-products in the world: a literature survey,” Journal of Veterinary Medical Science, 71(3): 255–261. DOI: https://doi.org/10.1292/jvms.71.255
Thai TH, Hirai T, Lan NT, Yamaguchi R. 2012. Antibiotic resistance profiles of Salmonella serovars isolated from retail pork and chicken meat in North Vietnam. International journal of food microbiology. 156(2):147-51.
Verma, A.K., Kumar, A., Singh, S.K., Rahal, A., Ahmed, I., Singh, D., Singh, A.P., and Singh, L. 2014 Prevalence and resistance to antimicrobial agents of Campylobacter spp. isolated from dogs in India. Journal of Biological Sciences, 14(2):142- 148.
Wang. Ge. B, Sjolund-Karlsson, M., and McDermott, 2013, P. F. Antimicrobial resistance in campylobacter: susceptibility testing methods and resistance trends. J. Microbiol. Methods. 95:57–67. DOI: https://doi.org/10.1016/j.mimet.2013.06.021
WHO: WHO 2001 global strategy for containment of antimicrobial resistance. World Health organization, 99 pages.

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1.
Es-soucratti K, Hammoumi A, Bouchrif B, Asmai R, En-nassiri H, Karraouan B. Occurrence and antimicrobial resistance of Campylobacter jejuni isolates from poultry in Casablanca-Settat, Morocco. Ital J Food Safety [Internet]. 2020 Apr. 6 [cited 2024 Dec. 12];9(1). Available from: https://www.pagepressjournals.org/ijfs/article/view/8692