University of Veterinary and Animal Sciences, Pakistan
* Corresponding author
University of Veterinary and Animal Sciences, Pakistan
University of Veterinary and Animal Sciences, Pakistan
Cholistan University of Veterinary and Animal Sciences, Pakistan
Quaid-E-Azam University Islamabad, Pakistan
University of Cambridge, UK

Article Main Content

Campylobacter, one of the most prevalent bacteria responsible for gastroenteritis in human worldwide. Campylobacter infections result from ingestion of contaminated food and water depending upon susceptibility of individuals and virulence of infecting strain. The prevalence of these bacteria is highly diverse and present worldwide. Increase in antibiotic resistance among these bacteria is recognized as emerging public health problem. Current study is designed to analyze the risk factors related with Campylobacteriosis, prevalence in meat (chicken, beef and mutton) and antimicrobial resistance profiles of these bacteria from district Okara, Pakistan. The time span for lab work was from October 2020 to March 2021including sampling and testing. A total of 300 swab samples were collected from poultry, beef and mutton. The ISO 10272-1:217(E) method for isolation through biochemical and molecular identification carried out. Disc diffusion method used for AMR calculation. The overall prevalence of campylobacter was only 2%, detected only in poultry meat out of 300 samples. Among the isolated strains, Campylobacter indicated highest resistance against Tetracycline 100%, followed by Cefotaxime, Tylocine 83%, Enrofloxacin 66%, Clindamycin and Nalidixic acid 50%, lowest resistance against Streptomycin and Doxycycline only 33% and 16% respectively. The significance relation was obtained for two variables that include eating during dealing meat and contact of excreta with meat. Prevalence of Campylobacter is very low as compared to study conducted earlier in Pakistan. The drug of choice for Campylobacter related infections is doxycycline and streptomycin. The results indicate that prevalence of Campylobacter is very low on meat in Okara region but higher microbial resistance.

References

  1. Ugboma, A.N., et al., Prevalence of Campylobacter species in ground water in Sokoto, Sokoto State, Nigeria. Veterinary world. 2013; 6(6): 285.
     Google Scholar
  2. Çiftçi, N., H. Türk-Dağı, and İ. Tuncer, Akut Gastroenterit Tanılı Hastalarda Campylobacter ve Salmonella Türlerinin Yeri ve Antimikrobiklere Duyarlılıkları. Klimik Dergisi. 2019; 32(2): 127–31. Turkish.
     Google Scholar
  3. Kanwal, S., et al., Variation in antibiotic susceptibility and presence of type VI secretion system (T6SS) in Campylobacter jejuni isolates from various sources. Comparative Immunology, Microbiology, and Infectious Diseases. 2019; 66: 101345.
     Google Scholar
  4. Andersen, S.R., et al. Antimicrobial resistance among Campylobacter jejuni isolated from raw poultry meat at retail level in Denmark. International journal of food microbiology. 2006; 107(3): 250–255.
     Google Scholar
  5. Hansson, I., et al. Knowledge gaps in control of Campylobacter for prevention of campylobacteriosis. Transboundary and emerging diseases. 2018; 65: 30–48.
     Google Scholar
  6. Nisar, M., et al., Occurrence of Campylobacter in retail meat in Lahore, Pakistan. Acta tropica. 2018; 185: 42–45.
     Google Scholar
  7. Gaulin, C., et al., Veal liver as food vehicle for human Campylobacter infections. Emerging infectious diseases. 2018; 24(6): 1130.
     Google Scholar
  8. Al-Banna, N.A., F. Cyprian, and M.J. Albert, Cytokine responses in campylobacteriosis: Linking pathogenesis to immunity. Cytokine & growth factor reviews. 2018; 41: 75–87.
     Google Scholar
  9. Oh, E., et al., Frequent implication of multistress-tolerant Campylobacter jejuni in human infections. Emerging infectious diseases. 2018; 24(6): 1037.
     Google Scholar
  10. Zhao, S., et al., antimicrobial resistance of Campylobacter isolates from retail meat in the United States between 2002 and 2007. Appl. Environ. Microbiol. 2010; 76(24): 7949–7956.
     Google Scholar
  11. Mohakud, N.K., et al., Detection and molecular typing of Campylobacter isolates from human and animal faeces in coastal belt of Odisha, India. Indian Journal of Medical Microbiology. 2019; 37(3): 2.
     Google Scholar
  12. Montgomery, M.P., et al., Multidrug-resistant Campylobacter jejuni outbreak linked to puppy exposure—United States, 2016–2018. Morbidity and Mortality Weekly Report. 2018; 67(37): 1032.
     Google Scholar
  13. Usha, M., et al., Occurrence and antibiotic resistance of Campylobacter jejuni and Campylobacter coli in retail broiler chicken. International Food Research Journal. 2010; 17(2): 247–255.
     Google Scholar
  14. Ibrahim, J.N., et al., Prevalence, antimicrobial resistance, and risk factors for campylobacteriosis in Lebanon. The Journal of Infection in Developing Countries. 2019; 13(01): 11–20.
     Google Scholar
  15. Tafa, B., et al., Isolation and antimicrobial susceptibility patterns of Campylobacter species among diarrheic children at Jimma, Ethiopia. International journal of bacteriology. 2014.
     Google Scholar
  16. García-Fernández, A., et al., Human campylobacteriosis in Italy: emergence of multi-drug resistance to ciprofloxacin, tetracycline, and erythromycin. Frontiers in microbiology. 2018; 9: 1906.
     Google Scholar
  17. Altekruse, S.F., et al., Campylobacter jejuni—an emerging foodborne pathogen. Emerging infectious diseases. 1999; 5(1): 28.
     Google Scholar
  18. Mohammed, A.N. and S.A.A.A. Aziz, the prevalence of Campylobacter species in broiler flocks and their environment: assessing the efficiency of chitosan/zinc oxide nanocomposite for adopting control strategy. Environmental Science and Pollution Research. 2019; 26(29): 30177–30187.
     Google Scholar
  19. Ammar, A., et al., Genotyping, and antimicrobial resistance of campylobacter Jejuni: A review. Adv. Anim. Vet. Sci. 2019; 7(s2): 129–136.
     Google Scholar
  20. Department of Agriculture, Water and the Environment Australia. Microbiological Manual for Sampling and Testing of Export Meat and Meat Products. Edition 1.05 July 2021.
     Google Scholar
  21. Refregier-Petton, J., et al., Risk factors for Campylobacter spp. contamination in French broiler-chicken flocks at the end of the rearing period. Preventive veterinary medicine. 2001; 50(1–2): 89–100.
     Google Scholar
  22. Boysen, L., H. Vigre, and H. Rosenquist, Seasonal influence on the prevalence of thermotolerant Campylobacter in retail broiler meat in Denmark. Food Microbiology. 2011; 28(5): 1028–1032.
     Google Scholar
  23. Yun, J., et al., Association between the ambient temperature and the occurrence of human Salmonella and Campylobacter infections. Scientific reports. 2016; 6(1): 1–7.
     Google Scholar