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Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens
Avibacterium paragallinarum-associated infectious coryza (IC) is an important threat in commercial poultry. Previous studies about the characteristics of A. paragallinarum are succeeded in revealing the course of IC disease, but whether and how resident microbes contribute to the infection remains u...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672371/ https://www.ncbi.nlm.nih.gov/pubmed/36406434 http://dx.doi.org/10.3389/fmicb.2022.1010584 |
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author | Zhu, Jiajia Chen, Yunsheng Wu, Yifan Wang, Yongqiang Zhu, Kui |
author_facet | Zhu, Jiajia Chen, Yunsheng Wu, Yifan Wang, Yongqiang Zhu, Kui |
author_sort | Zhu, Jiajia |
collection | PubMed |
description | Avibacterium paragallinarum-associated infectious coryza (IC) is an important threat in commercial poultry. Previous studies about the characteristics of A. paragallinarum are succeeded in revealing the course of IC disease, but whether and how resident microbes contribute to the infection remains unclear. To understand the role of commensal bacteria, we isolated 467 commensal bacteria, including 38 A. paragallinarum, from the respiratory tract of IC chicken. The predominant commensal isolates were Gram-positive bacteria belonging to Staphylococcus spp. [33.19%, 95% confidence interval (CI): 28.93–37.66%], Enterococcus spp. (16.49%, 95% CI: 13.23–20.17%), and Bacillus spp. (16.27%, 95% CI: 13.04–19.94%). These isolates were closely correlated with the survival of A. paragallinarum. We examined and found that commensal bacteria aggravate A. paragallinarum-associated infections because certain commensal species (28.57%, 95% CI: 15.72–44.58%) induced hemolysis and promoted the growth of A. paragallinarum in vitro. Notably, A. paragallinarum showed high resistance to routine antibiotics such as erythromycin (84.21%, 95% CI: 68.75–93.98%), tetracycline (73.68%, 95% CI: 56.90–86.60%) and carried diverse mobile resistance gene clusters. Overall, we found commensal bacteria especially Gram-positive bacteria facilitate the survival of multidrug-resistant A. paragallinarum to exacerbate infections, suggesting that novel strategies may diminish A. paragallinarum-associated infections by modulating the population dynamics of commensal bacteria. |
format | Online Article Text |
id | pubmed-9672371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96723712022-11-19 Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens Zhu, Jiajia Chen, Yunsheng Wu, Yifan Wang, Yongqiang Zhu, Kui Front Microbiol Microbiology Avibacterium paragallinarum-associated infectious coryza (IC) is an important threat in commercial poultry. Previous studies about the characteristics of A. paragallinarum are succeeded in revealing the course of IC disease, but whether and how resident microbes contribute to the infection remains unclear. To understand the role of commensal bacteria, we isolated 467 commensal bacteria, including 38 A. paragallinarum, from the respiratory tract of IC chicken. The predominant commensal isolates were Gram-positive bacteria belonging to Staphylococcus spp. [33.19%, 95% confidence interval (CI): 28.93–37.66%], Enterococcus spp. (16.49%, 95% CI: 13.23–20.17%), and Bacillus spp. (16.27%, 95% CI: 13.04–19.94%). These isolates were closely correlated with the survival of A. paragallinarum. We examined and found that commensal bacteria aggravate A. paragallinarum-associated infections because certain commensal species (28.57%, 95% CI: 15.72–44.58%) induced hemolysis and promoted the growth of A. paragallinarum in vitro. Notably, A. paragallinarum showed high resistance to routine antibiotics such as erythromycin (84.21%, 95% CI: 68.75–93.98%), tetracycline (73.68%, 95% CI: 56.90–86.60%) and carried diverse mobile resistance gene clusters. Overall, we found commensal bacteria especially Gram-positive bacteria facilitate the survival of multidrug-resistant A. paragallinarum to exacerbate infections, suggesting that novel strategies may diminish A. paragallinarum-associated infections by modulating the population dynamics of commensal bacteria. Frontiers Media S.A. 2022-11-04 /pmc/articles/PMC9672371/ /pubmed/36406434 http://dx.doi.org/10.3389/fmicb.2022.1010584 Text en Copyright © 2022 Zhu, Chen, Wu, Wang and Zhu. 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 Zhu, Jiajia Chen, Yunsheng Wu, Yifan Wang, Yongqiang Zhu, Kui Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens |
title | Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens |
title_full | Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens |
title_fullStr | Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens |
title_full_unstemmed | Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens |
title_short | Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens |
title_sort | commensal bacteria contribute to the growth of multidrug-resistant avibacterium paragallinarum in chickens |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672371/ https://www.ncbi.nlm.nih.gov/pubmed/36406434 http://dx.doi.org/10.3389/fmicb.2022.1010584 |
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