High Prevalence of Antimicrobial Resistance among Gram Negative Bacteria Isolated from Poultry
DOI:
https://doi.org/10.3823/824Keywords:
Multi-Drug resistance, Antimicrobial resistance, Poultry, Gaza, PalestineAbstract
Background: Multidrug resistant bacteria (MDR), such as Escherichia coli and Salmonella spp. are threat to the human health care system. In recent years, these MDR bacteria have been found increasingly inside and outside the hospital environment. Food animals (meat and poultry) are increasingly colonized with MDR bacteria, thus posing an additional concern. This study is intended to determine susceptibility and resistance pattern of pathogenic Gram negative bacteria isolated from rectal swabs of chicken against 16 antibiotics.
Methods: A total of 216 cloacal swab samples (Gaza strip poultry farms) and 87 frozen and fresh meat samples (from slaughter houses and retails) from June 2017 to June 2018 were collected. Isolation and identification of organisms were achieved using standard bacteriological techniques. Antimicrobial susceptibility test was performed according to standard protocols.
Results: 360 Enterobacteriaceae isolates, and 56 Gram-negative non fermenter were recovered. The predominant Enterobacteriaceae isolate was Citrobacter spp. (22.6%), followed by Enterobacter spp. (17.6%) and E. coli (16.5%). High rates of resistance against Ampicillin (85.4%) and Trimethoprim/ Sulfamethoxazole (80.1%) followed by Chloramphenicol (74%) were recorded. Six samples were positive for Salmonella spp. and Shigella spp. Of the tested Enterobacteriacae isolates, 94.7% were multidrug resistant (MDR), and 31.4% of None fermenting bacilli (NFB) were MDR. Carbapenem resistance was found to be high among isolates; 51.9% for imipenem and 1.8% for meropenem.
Conclusion: Isolated bacteria in the study area were MDR and this suggests that chickens may be important reservoir of antimicrobial resistant organisms which is a major public health concern.
References
References
Rabinowitz, P.M. and L.A. Conti, Human-Animal Medicine-E-Book: Clinical Approaches to Zoonoses, Toxicants and Other Shared Health Risks 2009; Elsevier Health Sciences.
Rwego, I.B., et al., Gastrointestinal bacterial transmission among humans, mountain gorillas, and livestock in Bwindi Impenetrable National Park, Uganda. Conservation Biology 2008; 22(6): p. 1600-1607.
Middleton, J. and A. Ambrose, Enumeration and antibiotic resistance patterns of fecal indicator organisms isolated from migratory Canada geese (Branta canadensis). Journal of wildlife diseases 2005; 41(2): p. 334-341.
Coque, T.M., et al., Dissemination of clonally related Escherichia coli strains expressing extended-spectrum β-lactamase CTX-M-15. Emerging infectious diseases 2008; 14(2): p. 195.
Martel, J.-L., et al., New trends in regulatory rules and surveillance of antimicrobial resistance in bacteria of animal origin. Veterinary research 2001; 32(3-4): p. 381-392.
Silva, N., et al., Molecular characterization of antimicrobial resistance in enterococci and Escherichia coli isolates from European wild rabbit (Oryctolagus cuniculus). Science of the total environment 2010; 408(20): p. 4871-4876.
Köhler, M., OIE Manual of Standards for Diagnostic Tests and Vaccines, Office International des Epizooties, Washington DC, USA (1997), XXXII, 723 pages, frF 800.-, US $160. 1998; Urban & Fischer.
Astal, Z., A. El-Manama, and F. Sharif, Antibiotic resistance of bacteria associated with community-acquired urinary tract infections in the southern area of the Gaza Strip. Journal of chemotherapy 2002; 14(3): p. 259-264.
Elmanama, A.A. and N. Abdelateef, Antimicrobial Resistance of Enteric Pathogens Isolated from Acute Gastroenteritis Patients in Gaza strip, Palestine. The International Arabic Journal of Antimicrobial Agents, 2013. 2(4).
Elmanama, A.A., Vancomycin Resistant Enterococci (VRE) among Non–Hospitalized Individuals in Gaza City, Palestine. Age 2008; 1(16): p. 17-40.
Krumperman, P.H., Multiple antibiotic resistance indexing of Escherichia coli to identify high-risk sources of fecal contamination of foods. Applied and environmental microbiology 1983; 46(1): p. 165-170.
STAMDARDS, A., Performance standards for antimicrobial susceptibility testing. Approved Standards CLSI 2010; p. M100-S20.
Russell, A., Similarities and differences in the responses of microorganisms to biocides. Journal of Antimicrobial Chemotherapy 2003; 52(5): p. 750-763.
Sandhu, R., S. Dahiya, and P. Sayal, Evaluation of multiple antibiotic resistance (MAR) index and Doxycycline susceptibility of Acinetobacter species among inpatients. International Journal of Infectious Diseases 2016; 45: p. 327.
Rahman, M., et al., ANTIMICROBIAL RESISTANCE OF ESCHERICHIA COLI ISOLATED FROM MILK, BEEF AND CHICKEN MEAT IN BANGLADESH. Bangladesh Journal of Veterinary Medicine 2017; 15(2): p. 141-146.
Rahman, M., et al., Bacterio-pathological studies on salmonellosis, colibacillosis and pasteurellosis in natural and experimental infections in chickens. Bangladesh Journal of Veterinary Medicine 2004; 2(1): p. 1-8.
Barua, R., et al., Prevalence and rapid detection of shiga toxin producing E. coli (STEC) in water and ready-to-eat (RTE) foods. Journal of Veterinary Public Health 2007; 5(2): p. 75-83.
Jakaria, A., M.A. Islam, and M.M. Khatun, Prevalence, characteristics and antibiogram profiles of Escherichia coli isolated from apparently healthy chickens in Mymensingh, Bangladesh. Microbes and Health 2012; 1(1): p. 27-29.
Arya, G., et al., Serogroups, atypical biochemical characters, colicinogeny and antibiotic resistance pattern of Shiga toxinâ€producing Escherichia coli isolated from diarrhoeic calves in Gujarat, India. Zoonoses and public health 2008; 55(2): p. 89-98.
Yulistiani, R., et al. Prevalence of Antibiotic-resistance Enterobacteriaceae strains Isolated from Chicken Meat at Traditional Markets in Surabaya, Indonesia. in IOP Conference Series: Materials Science and Engineering 2017; IOP Publishing.
Azevedo, I., et al., Antibiotic resistance of Enterobacteriaceae isolated from the domestic food related environments. Journal of food quality and hazards control, 2015. 2(2): p. 51-55.
Alsan, M., et al., Out-of-pocket health expenditures and antimicrobial resistance in low-income and middle-income countries: an economic analysis. The Lancet infectious diseases 2015; 15(10): p. 1203-1210.
Nguyen, F., et al., Tetracycline antibiotics and resistance mechanisms. Biological chemistry, 2014. 395(5): p. 559-575.
Elmanama, A.A. and M.A. Albayoumi, High Prevalence of Antibiotic Residues among Broiler Chickens in Gaza Strip. Food and Public Health 2016; 6(4): p. 93-98.
Abraham, S., et al., Isolation and plasmid characterization of carbapenemase (IMP-4) producing Salmonella enterica Typhimurium from cats. Scientific reports 2016; 6: p. 35527.
Webb, H.E., et al., Carbapenem-resistant bacteria recovered from faeces of dairy cattle in the high plains region of the USA. PloS one 2016; 11(1): p. e0147363.
Wang, Y., et al., Identification of New Delhi metallo-β-lactamase 1 in Acinetobacter lwoffii of food animal origin. PloS one 2012; 7(5): p. e37152.
Stolle, I., et al., Emergence of OXA-48 carbapenemase-producing Escherichia coli and Klebsiella pneumoniae in dogs. Journal of Antimicrobial Chemotherapy 2013; 68(12): p. 2802-2808.
Abraham, S., et al., Carbapenemase-producing bacteria in companion animals: a public health concern on the horizon. Journal of Antimicrobial Chemotherapy 2014; 69(5): p. 1155-1157.
Rubin, J.E., S. Ekanayake, and C. Fernando, Carbapenemase-producing organism in food, 2014. Emerging infectious diseases 2014; 20(7): p. 1264-1265.
Poirel, L., et al., Carbapenemase-producing Acinetobacter spp. in cattle, France. Emerging infectious diseases, 2012. 18(3): p. 523.
Laube, H., et al., Longitudinal monitoring of Esbl/Ampc-Producing Escherichia coli in German broiler chicken fattening farms. Applied and environmental microbiology 2013; p. AEM. 00856-13.
Hazards, E.P.o.B., Scientific Opinion on Carbapenem resistance in food animal ecosystems. EFSA Journal 2013; 11(12): p. 3501.
Downloads
Published
Issue
Section
License
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access and Benefits of Publishing Open Access).
This journal provides immediate open access to its content on the principle that making research freely available to the public supports a greater global exchange of knowledge.
Articles are published Under License of Creative Commons Attribution 3.0 License ©
Copyright policies & self-archiving
This is our Copyright Policy. We are a RoMEO green journal.
Author's Pre-print: | ![]() |
Author's Post-print: | ![]() |
Publisher's Version/PDF: | ![]() |