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Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application

Fluoroquinolone agents are considered critical for human medicine by the World Health Organization (WHO). However, they are often used for the treatment of avian colibacillosis in poultry production, creating considerable concern regarding the potential spread of fluoroquinolone resistance genes fro...

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Autores principales: Temmerman, Robin, Ghanbari, Mahdi, Antonissen, Gunther, Schatzmayr, Gerd, Duchateau, Luc, Haesebrouck, Freddy, Garmyn, An, Devreese, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386515/
https://www.ncbi.nlm.nih.gov/pubmed/35992659
http://dx.doi.org/10.3389/fmicb.2022.869538
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author Temmerman, Robin
Ghanbari, Mahdi
Antonissen, Gunther
Schatzmayr, Gerd
Duchateau, Luc
Haesebrouck, Freddy
Garmyn, An
Devreese, Mathias
author_facet Temmerman, Robin
Ghanbari, Mahdi
Antonissen, Gunther
Schatzmayr, Gerd
Duchateau, Luc
Haesebrouck, Freddy
Garmyn, An
Devreese, Mathias
author_sort Temmerman, Robin
collection PubMed
description Fluoroquinolone agents are considered critical for human medicine by the World Health Organization (WHO). However, they are often used for the treatment of avian colibacillosis in poultry production, creating considerable concern regarding the potential spread of fluoroquinolone resistance genes from commensals to pathogens. Therefore, there is a need to understand the impact of fluoroquinolone application on the reservoir of ARGs in poultry gut and devise means to circumvent potential resistome expansion. Building upon a recent dose optimization effort, we used shotgun metagenomics to investigate the time-course change in the cecal microbiome and resistome of broiler chickens receiving an optimized dosage [12.5 mg/kg body weight (bw)/day], with or without synbiotic supplementation (PoultryStar(®), BIOMIN GmbH), and a high dosage of enrofloxacin (50 mg/kg bw/day). Compared to the high dose treatment, the low (optimized) dose of enrofloxacin caused the most significant perturbations in the cecal microbiota and resistome of the broiler chickens, demonstrated by a lower cecal microbiota diversity while substantially increasing the antibiotic resistance genes (ARGs) resistome diversity. Withdrawal of antibiotics resulted in a pronounced reduction in ARG diversity. Chickens receiving the synbiotic treatment had the lowest diversity and number of enriched ARGs, suggesting an alleviating impact on the burden of the gut resistome. Some Proteobacteria were significantly increased in the cecal metagenome of chickens receiving enrofloxacin and showed a positive association with increased ARG burden. Differential abundance (DA) analysis revealed a significant increase in the abundance of ARGs encoding resistance to macrolides-lincosamides-streptogramins (MLS), aminoglycosides, and tetracyclines over the period of enrofloxacin application, with the optimized dosage application resulting in a twofold higher number of affected ARG compared to high dosage application. Our results provide novel insights into the dose-dependent effects of clinically important enrofloxacin application in shaping the broiler gut resistome, which was mitigated by a synbiotic application. The contribution to ameliorating the adverse effects of antimicrobial agents, that is, lowering the spread of antimicrobial resistance genes, on the poultry and potentially other livestock gastrointestinal microbiomes and resistomes merits further study.
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spelling pubmed-93865152022-08-19 Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application Temmerman, Robin Ghanbari, Mahdi Antonissen, Gunther Schatzmayr, Gerd Duchateau, Luc Haesebrouck, Freddy Garmyn, An Devreese, Mathias Front Microbiol Microbiology Fluoroquinolone agents are considered critical for human medicine by the World Health Organization (WHO). However, they are often used for the treatment of avian colibacillosis in poultry production, creating considerable concern regarding the potential spread of fluoroquinolone resistance genes from commensals to pathogens. Therefore, there is a need to understand the impact of fluoroquinolone application on the reservoir of ARGs in poultry gut and devise means to circumvent potential resistome expansion. Building upon a recent dose optimization effort, we used shotgun metagenomics to investigate the time-course change in the cecal microbiome and resistome of broiler chickens receiving an optimized dosage [12.5 mg/kg body weight (bw)/day], with or without synbiotic supplementation (PoultryStar(®), BIOMIN GmbH), and a high dosage of enrofloxacin (50 mg/kg bw/day). Compared to the high dose treatment, the low (optimized) dose of enrofloxacin caused the most significant perturbations in the cecal microbiota and resistome of the broiler chickens, demonstrated by a lower cecal microbiota diversity while substantially increasing the antibiotic resistance genes (ARGs) resistome diversity. Withdrawal of antibiotics resulted in a pronounced reduction in ARG diversity. Chickens receiving the synbiotic treatment had the lowest diversity and number of enriched ARGs, suggesting an alleviating impact on the burden of the gut resistome. Some Proteobacteria were significantly increased in the cecal metagenome of chickens receiving enrofloxacin and showed a positive association with increased ARG burden. Differential abundance (DA) analysis revealed a significant increase in the abundance of ARGs encoding resistance to macrolides-lincosamides-streptogramins (MLS), aminoglycosides, and tetracyclines over the period of enrofloxacin application, with the optimized dosage application resulting in a twofold higher number of affected ARG compared to high dosage application. Our results provide novel insights into the dose-dependent effects of clinically important enrofloxacin application in shaping the broiler gut resistome, which was mitigated by a synbiotic application. The contribution to ameliorating the adverse effects of antimicrobial agents, that is, lowering the spread of antimicrobial resistance genes, on the poultry and potentially other livestock gastrointestinal microbiomes and resistomes merits further study. Frontiers Media S.A. 2022-08-04 /pmc/articles/PMC9386515/ /pubmed/35992659 http://dx.doi.org/10.3389/fmicb.2022.869538 Text en Copyright © 2022 Temmerman, Ghanbari, Antonissen, Schatzmayr, Duchateau, Haesebrouck, Garmyn and Devreese. 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
Temmerman, Robin
Ghanbari, Mahdi
Antonissen, Gunther
Schatzmayr, Gerd
Duchateau, Luc
Haesebrouck, Freddy
Garmyn, An
Devreese, Mathias
Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application
title Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application
title_full Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application
title_fullStr Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application
title_full_unstemmed Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application
title_short Dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application
title_sort dose-dependent impact of enrofloxacin on broiler chicken gut resistome is mitigated by synbiotic application
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386515/
https://www.ncbi.nlm.nih.gov/pubmed/35992659
http://dx.doi.org/10.3389/fmicb.2022.869538
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