Occurrence of Escherichia coli producing extended spectrum beta-lactamases in food-producing animals

Balázs, Bence and Nagy, József Bálint and Tóth, Zoltán and Nagy, Fruzsina and Károlyi, Sándor and Kecskemétiné Turcsányi, Ibolya and Tóthné Bistyák, Andrea Tünde and Sárközi, Rita and Kardos, Gábor (2021) Occurrence of Escherichia coli producing extended spectrum beta-lactamases in food-producing animals. ACTA VETERINARIA HUNGARICA, 69 (3). pp. 211-215. ISSN 0236-6290

Preview

Text 15882705-ActaVeterinariaHungaricaOccurrenceofEscherichiacoliproducingextendedspectrum-lactamasesinfood-producinganimals1.pdf Download (442kB) | Preview

Abstract

Multidrug resistance due to the production of extended-spectrum beta-lactamases (ESBLs) is a major problem in human as well as in veterinary medicine. These strains appear in animal and human microbiomes and can be the source of infection both in animal and in human healthcare, in accordance with the One Health theorem. In this study we examined the prevalence of ESBL: producing bacteria in food-producing animals. We collected 100 porcine and 114 poultry samples to examine the prevalence of ESBL producers. Isolates were identified using the MALDI-TOF system and their antibiotic susceptibility was tested using the disk diffusion method. ESBL gene families and phylogroups were detected by polymerase chain reactions. The prevalence of ESBL producers was relatively high in both sample groups: 72 (72.0%) porcine and 39 (34.2%) poultry isolates were ESBL producers. Escherichia coli isolates were chosen for further investigations. The most common ESBL gene was CTX-M-1 (79.3%). Most of the isolates belong to the commensal E. coli phylogroups. The porcine isolates could be divided into three phylogroups, while the distribution of the poultry isolates was more varied. In summary, ESBL-producing bacteria are prevalent in the faecal samples of the examined food-producing animals, with a dominance of the CTX-M-1 group enzymes and commensal E. coli phylogroups.

Actions (login required)

Edit Item