4.3 Article

Antimicrobial resistance in Escherichia coli isolated from on-farm and conventional hatching broiler farms in Ireland

Journal

IRISH VETERINARY JOURNAL
Volume 75, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13620-022-00214-9

Keywords

Antimicrobial resistance; beta-lactamases; Broiler; Hatching system; E. coli; Poultry

Funding

  1. Department of Agriculture, Food, & the Marine (DAFM) [15 S 676]

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There was no difference in E. coil isolation rates or prevalence of AMR found between on-farm hatching systems and conventional hatching systems. Hatcheries could be a reservoir and major contributor to the transmission of AMR bacteria to broilers after entry to the rearing farms.
Background: On-farm hatching (OH) systems are becoming more common in broiler production. Hatching conditions differ from conventional farms as OH chicks avoid exposure to handling, transport, post-hatch water and feed deprivation. In contrast, chicks in conventional hatching conditions (CH) are exposed to standard hatchery procedures and transported post hatching. The objectives of this pilot study were to investigate the prevalence and frequency of Escherichia coil resistant to antimicrobials, including presumptive ESBL/AmpC-producing E. coil, isolated from environmental and faecal samples from OH versus CH hatching systems, and to investigate the presence of ESBL/AmpC-producing encoding genes. Results: Environmental samples were collected from one flock in 10 poultry farms (5 OH farms, 5 CH farms) on day 0 post disinfection of the facilities to assess hygiene standards. On D10 and D21 post egg/chick arrival onto the farm, samples of faeces, boot swabs and water drinker lines were collected. E. coli were isolated on MacConkey agar (MC) and MacConkey supplemented with cefotaxime (MC+). Few E. coil were detected on DO. However, on D10 and D21 E. coli isolates were recovered from faeces and boot swabs. Water samples had minimal contamination. In this study, 100% of cefotaxime resistant E. coli isolates (n=33) detected on selective media and 44% of E. coil isolates (84/192) detected on nonselective media were multidrug resistant (MDR). The antimicrobial resistance (AMR) genotype for the 15 ESBL/AmpC producing isolates was determined using multiplex PCR. Six of these were selected for Sanger sequencing of which two were positive for bla(CMY-)(2), two for bla(TEM-1) and two were positive for both genes. Conclusions: There was no difference in E. coil isolation rates or prevalence of AMR found between the OH versus CH systems, suggesting that the OH system may not be an additional risk of resistant E. coil dissemination to broilers compared to the CH systems. The frequency of beta-lactam resistant E. coil in boot swab and faeces samples across both OH (24/33 (73%)) and CH (9/33 (27%)) systems may indicate that hatcheries could be a reservoir and major contributor to the transmission of AMR bacteria to flocks after entry to the rearing farms.

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