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Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter

BACKGROUND: Linezolid is a critically important oxazolidinone antibiotic used in human medicine. Although linezolid is not licensed for use in food-producing animals, the use of florfenicol in veterinary medicine co-selects for oxazolidinone resistance genes. OBJECTIVE: This study aimed to assess th...

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Autores principales: Nüesch-Inderbinen, Magdalena, Biggel, Michael, Haussmann, Adrian, Treier, Andrea, Heyvaert, Lore, Cernela, Nicole, Stephan, Roger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301837/
https://www.ncbi.nlm.nih.gov/pubmed/37389336
http://dx.doi.org/10.3389/fmicb.2023.1150070
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author Nüesch-Inderbinen, Magdalena
Biggel, Michael
Haussmann, Adrian
Treier, Andrea
Heyvaert, Lore
Cernela, Nicole
Stephan, Roger
author_facet Nüesch-Inderbinen, Magdalena
Biggel, Michael
Haussmann, Adrian
Treier, Andrea
Heyvaert, Lore
Cernela, Nicole
Stephan, Roger
author_sort Nüesch-Inderbinen, Magdalena
collection PubMed
description BACKGROUND: Linezolid is a critically important oxazolidinone antibiotic used in human medicine. Although linezolid is not licensed for use in food-producing animals, the use of florfenicol in veterinary medicine co-selects for oxazolidinone resistance genes. OBJECTIVE: This study aimed to assess the occurrence of cfr, optrA, and poxtA in florfenicol-resistant isolates from beef cattle and veal calves from different herds in Switzerland. METHODS: A total of 618 cecal samples taken from beef cattle and veal calves at slaughter originating from 199 herds were cultured after an enrichment step on a selective medium containing 10 mg/L florfenicol. Isolates were screened by PCR for cfr, optrA, and poxtA which are genes known to confer resistance to oxazolidinones and phenicols. One isolate per PCR-positive species and herd was selected for antimicrobial susceptibility testing (AST) and whole-genome sequencing (WGS). RESULTS: Overall, 105 florfenicol-resistant isolates were obtained from 99 (16%) of the samples, corresponding to 4% of the beef cattle herds and 24% of the veal calf herds. Screening by PCR revealed the presence of optrA in 95 (90%) and poxtA in 22 (21%) of the isolates. None of the isolates contained cfr. Isolates included for AST and WGS analysis were Enterococcus (E.) faecalis (n = 14), E. faecium (n = 12), E. dispar (n = 1), E. durans (n = 2), E. gallinarum (n = 1), Vagococcus (V.) lutrae (n = 2), Aerococcus (A.) urinaeequi (n = 1), and Companilactobacillus (C.) farciminis (n = 1). Thirteen isolates exhibited phenotypic linezolid resistance. Three novel OptrA variants were identified. Multilocus sequence typing identified four E. faecium ST18 belonging to hospital-associated clade A1. There was a difference in the replicon profile among optrA- and poxtA-harboring plasmids, with rep9 (RepA_N) plasmids dominating in optrA-harboring E. faecalis and rep2 (Inc18) and rep29 (Rep_3) plasmids in poxtA-carrying E. faecium. CONCLUSION: Beef cattle and veal calves are reservoirs for enterococci with acquired linezolid resistance genes optrA and poxtA. The presence of E. faecium ST18 highlights the zoonotic potential of some bovine isolates. The dispersal of clinically relevant oxazolidinone resistance genes throughout a wide variety of species including Enterococcus spp., V. lutrae, A. urinaeequi, and the probiotic C. farciminis in food-producing animals is a public health concern.
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spelling pubmed-103018372023-06-29 Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter Nüesch-Inderbinen, Magdalena Biggel, Michael Haussmann, Adrian Treier, Andrea Heyvaert, Lore Cernela, Nicole Stephan, Roger Front Microbiol Microbiology BACKGROUND: Linezolid is a critically important oxazolidinone antibiotic used in human medicine. Although linezolid is not licensed for use in food-producing animals, the use of florfenicol in veterinary medicine co-selects for oxazolidinone resistance genes. OBJECTIVE: This study aimed to assess the occurrence of cfr, optrA, and poxtA in florfenicol-resistant isolates from beef cattle and veal calves from different herds in Switzerland. METHODS: A total of 618 cecal samples taken from beef cattle and veal calves at slaughter originating from 199 herds were cultured after an enrichment step on a selective medium containing 10 mg/L florfenicol. Isolates were screened by PCR for cfr, optrA, and poxtA which are genes known to confer resistance to oxazolidinones and phenicols. One isolate per PCR-positive species and herd was selected for antimicrobial susceptibility testing (AST) and whole-genome sequencing (WGS). RESULTS: Overall, 105 florfenicol-resistant isolates were obtained from 99 (16%) of the samples, corresponding to 4% of the beef cattle herds and 24% of the veal calf herds. Screening by PCR revealed the presence of optrA in 95 (90%) and poxtA in 22 (21%) of the isolates. None of the isolates contained cfr. Isolates included for AST and WGS analysis were Enterococcus (E.) faecalis (n = 14), E. faecium (n = 12), E. dispar (n = 1), E. durans (n = 2), E. gallinarum (n = 1), Vagococcus (V.) lutrae (n = 2), Aerococcus (A.) urinaeequi (n = 1), and Companilactobacillus (C.) farciminis (n = 1). Thirteen isolates exhibited phenotypic linezolid resistance. Three novel OptrA variants were identified. Multilocus sequence typing identified four E. faecium ST18 belonging to hospital-associated clade A1. There was a difference in the replicon profile among optrA- and poxtA-harboring plasmids, with rep9 (RepA_N) plasmids dominating in optrA-harboring E. faecalis and rep2 (Inc18) and rep29 (Rep_3) plasmids in poxtA-carrying E. faecium. CONCLUSION: Beef cattle and veal calves are reservoirs for enterococci with acquired linezolid resistance genes optrA and poxtA. The presence of E. faecium ST18 highlights the zoonotic potential of some bovine isolates. The dispersal of clinically relevant oxazolidinone resistance genes throughout a wide variety of species including Enterococcus spp., V. lutrae, A. urinaeequi, and the probiotic C. farciminis in food-producing animals is a public health concern. Frontiers Media S.A. 2023-06-14 /pmc/articles/PMC10301837/ /pubmed/37389336 http://dx.doi.org/10.3389/fmicb.2023.1150070 Text en Copyright © 2023 Nüesch-Inderbinen, Biggel, Haussmann, Treier, Heyvaert, Cernela and Stephan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Nüesch-Inderbinen, Magdalena
Biggel, Michael
Haussmann, Adrian
Treier, Andrea
Heyvaert, Lore
Cernela, Nicole
Stephan, Roger
Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter
title Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter
title_full Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter
title_fullStr Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter
title_full_unstemmed Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter
title_short Oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter
title_sort oxazolidinone resistance genes in florfenicol-resistant enterococci from beef cattle and veal calves at slaughter
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301837/
https://www.ncbi.nlm.nih.gov/pubmed/37389336
http://dx.doi.org/10.3389/fmicb.2023.1150070
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