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Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China

This study was carried out to investigate the resistance phenotypes and resistance genes of Escherichia coli from swine in Guizhou, China. A total of 47 E. coli strains isolated between 2013 and 2018 were tested using the Kirby–Bauer (K–B) method to verify their resistance to 19 common clinical anti...

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Autores principales: Yu, Bo, Zhang, Yanan, Yang, Li, Xu, Jinge, Bu, Shijin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008041/
https://www.ncbi.nlm.nih.gov/pubmed/33764151
http://dx.doi.org/10.4102/ojvr.v88i1.1880
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author Yu, Bo
Zhang, Yanan
Yang, Li
Xu, Jinge
Bu, Shijin
author_facet Yu, Bo
Zhang, Yanan
Yang, Li
Xu, Jinge
Bu, Shijin
author_sort Yu, Bo
collection PubMed
description This study was carried out to investigate the resistance phenotypes and resistance genes of Escherichia coli from swine in Guizhou, China. A total of 47 E. coli strains isolated between 2013 and 2018 were tested using the Kirby–Bauer (K–B) method to verify their resistance to 19 common clinical antimicrobials. Five classes consisting of 29 resistance genes were detected using polymerase chain reaction. The status regarding extended-spectrum β-lactamase (ESBL) and the relationship between ESBL CTX-M-type β-lactamase genes and plasmid-mediated quinolone resistance (PMQR) genes were analysed. A total of 46 strains (97.9%) were found to be multidrug resistant. Amongst them, 27 strains (57.4%) were resistant to more than eight antimicrobials, and the maximum number of resistant antimicrobial agents was 16. Twenty antibiotic resistance genes were detected, including six β-lactamase genes blaTEM (74.5%), blaCTX-M-9G (29.8%), blaDHA (17.0%), blaCTX-M-1G (10.6%), blaSHV (8.5%), blaOXA (2.1%), five aminoglycoside-modifying enzyme genes aac(3′)-IV (93.6%), aadA1 (78.7%), aadA2 (76.6%), aac(3′)-II c (55.3%), aac(6′)-Ib (2.1%) and five amphenicol resistance genes floR (70.2%), cmlA (53.2%), cat2 (10.6%), cat1 (6.4%), cmlB (2.1%), three PMQR genes qnrS (55.3%), oqxA (53.2%), qepA (27.7%) and polypeptide resistance gene mcr-1 (40.4%). The detection rate of ESBL-positive strains was 80.9% (38/47) and ESBL TEM-type was the most abundant ESBLs. The percentage of the PMQR gene in blaCTX-M-positive strains was high, and the detection rate of blaCTX-M-9G was the highest in CTX-M type. It is clear that multiple drug resistant E. coli is common in healthy swine in this study. Extended-spectrum β-lactamase is very abundant in the E. coli strains isolated from swine and most of them are multiple compound genotypes.
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spelling pubmed-80080412021-04-05 Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China Yu, Bo Zhang, Yanan Yang, Li Xu, Jinge Bu, Shijin Onderstepoort J Vet Res Original Research This study was carried out to investigate the resistance phenotypes and resistance genes of Escherichia coli from swine in Guizhou, China. A total of 47 E. coli strains isolated between 2013 and 2018 were tested using the Kirby–Bauer (K–B) method to verify their resistance to 19 common clinical antimicrobials. Five classes consisting of 29 resistance genes were detected using polymerase chain reaction. The status regarding extended-spectrum β-lactamase (ESBL) and the relationship between ESBL CTX-M-type β-lactamase genes and plasmid-mediated quinolone resistance (PMQR) genes were analysed. A total of 46 strains (97.9%) were found to be multidrug resistant. Amongst them, 27 strains (57.4%) were resistant to more than eight antimicrobials, and the maximum number of resistant antimicrobial agents was 16. Twenty antibiotic resistance genes were detected, including six β-lactamase genes blaTEM (74.5%), blaCTX-M-9G (29.8%), blaDHA (17.0%), blaCTX-M-1G (10.6%), blaSHV (8.5%), blaOXA (2.1%), five aminoglycoside-modifying enzyme genes aac(3′)-IV (93.6%), aadA1 (78.7%), aadA2 (76.6%), aac(3′)-II c (55.3%), aac(6′)-Ib (2.1%) and five amphenicol resistance genes floR (70.2%), cmlA (53.2%), cat2 (10.6%), cat1 (6.4%), cmlB (2.1%), three PMQR genes qnrS (55.3%), oqxA (53.2%), qepA (27.7%) and polypeptide resistance gene mcr-1 (40.4%). The detection rate of ESBL-positive strains was 80.9% (38/47) and ESBL TEM-type was the most abundant ESBLs. The percentage of the PMQR gene in blaCTX-M-positive strains was high, and the detection rate of blaCTX-M-9G was the highest in CTX-M type. It is clear that multiple drug resistant E. coli is common in healthy swine in this study. Extended-spectrum β-lactamase is very abundant in the E. coli strains isolated from swine and most of them are multiple compound genotypes. AOSIS 2021-02-24 /pmc/articles/PMC8008041/ /pubmed/33764151 http://dx.doi.org/10.4102/ojvr.v88i1.1880 Text en © 2021. The Authors https://creativecommons.org/licenses/by/4.0/ Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Yu, Bo
Zhang, Yanan
Yang, Li
Xu, Jinge
Bu, Shijin
Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China
title Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China
title_full Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China
title_fullStr Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China
title_full_unstemmed Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China
title_short Analysis of antibiotic resistance phenotypes and genes of Escherichia coli from healthy swine in Guizhou, China
title_sort analysis of antibiotic resistance phenotypes and genes of escherichia coli from healthy swine in guizhou, china
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008041/
https://www.ncbi.nlm.nih.gov/pubmed/33764151
http://dx.doi.org/10.4102/ojvr.v88i1.1880
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