A cross-sectional study was conducted to assess the prevalence, molecular detection, and antimicrobial resistance of isolates within 162 poultry farms in selected urban and peri-urban areas of central Ethiopia. A total of 1515 samples, including cloacal swabs (n = 763), fresh fecal droppings (n = 188), litter (n = 188), feed (n = 188), and water (n = 188), were bacteriologically tested. The molecular detection of some culture-positive isolates was performed via polymerase chain reaction (PCR) by targeting spy and sdfl genes for Typhimurium and Enteritidis, respectively. Risk factors for the occurrence of the bacterial isolates were assessed. Antimicrobial susceptibility testing of PCR-confirmed isolates was conducted using 12 antibiotics. In this study, it was observed that 50.6% of the farms were positive for . The overall sample-level prevalence of was 14.4%. Among the analyzed risk factors, the type of production, breed, and sample type demonstrated a statistically significant association ( < 0.05) with the bacteriological prevalence of . The PCR test disclosed that 45.5% (15/33) and 23.3% (10/43) of the isolates were positive for genes of Typhimurium and Enteritidis, respectively. The antimicrobial susceptibility test disclosed multi-drug resistance to ten of the tested antibiotics that belong to different classes. Substantial isolation of Typhimurium and Enteritidis in poultry and on poultry farms, along with the existence of multi-drug resistant isolates, poses an alarming risk of zoonotic and food safety issues. Hence, routine flock testing, farm surveillance, biosecurity intervention, stringent antimicrobial use regulations, and policy support for the sector are highly needed.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11051739 | PMC |
http://dx.doi.org/10.3390/microorganisms12040767 | DOI Listing |
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