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Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis
Fibrinous polyserositis in swine farming is a common pathological finding in nursery animals. The differential diagnosis of this finding should include Glaesserella parasuis (aetiological agent of Glässer’s disease) and Mycoplasma hyorhinis, among others. These microorganisms are early colonizers of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156107/ https://www.ncbi.nlm.nih.gov/pubmed/34069250 http://dx.doi.org/10.3390/pathogens10050603 |
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author | Blanco-Fuertes, Miguel Correa-Fiz, Florencia Fraile, Lorenzo Sibila, Marina Aragon, Virginia |
author_facet | Blanco-Fuertes, Miguel Correa-Fiz, Florencia Fraile, Lorenzo Sibila, Marina Aragon, Virginia |
author_sort | Blanco-Fuertes, Miguel |
collection | PubMed |
description | Fibrinous polyserositis in swine farming is a common pathological finding in nursery animals. The differential diagnosis of this finding should include Glaesserella parasuis (aetiological agent of Glässer’s disease) and Mycoplasma hyorhinis, among others. These microorganisms are early colonizers of the upper respiratory tract of piglets. The composition of the nasal microbiota at weaning was shown to constitute a predisposing factor for the development of Glässer’s disease. Here, we unravel the role of the nasal microbiota in the subsequent systemic infection by M. hyorhinis, and the similarities and differences with Glässer’s disease. Nasal samples from farms with recurrent problems with polyserositis associated with M. hyorhinis (MH) or Glässer’s disease (GD) were included in this study, together with healthy control farms (HC). Nasal swabs were taken from piglets in MH farms at weaning, before the onset of the clinical outbreaks, and were submitted to 16S rRNA gene amplicon sequencing (V3–V4 region). These sequences were analyzed together with sequences from similar samples previously obtained in GD and HC farms. Animals from farms with disease (MH and GD) had a nasal microbiota with lower diversity than those from the HC farms. However, the composition of the nasal microbiota of the piglets from these disease farms was different, suggesting that divergent microbiota imbalances may predispose the animals to the two systemic infections. We also found variants of the pathogens that were associated with the farms with the corresponding disease, highlighting the importance of studying the microbiome at strain-level resolution. |
format | Online Article Text |
id | pubmed-8156107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81561072021-05-28 Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis Blanco-Fuertes, Miguel Correa-Fiz, Florencia Fraile, Lorenzo Sibila, Marina Aragon, Virginia Pathogens Article Fibrinous polyserositis in swine farming is a common pathological finding in nursery animals. The differential diagnosis of this finding should include Glaesserella parasuis (aetiological agent of Glässer’s disease) and Mycoplasma hyorhinis, among others. These microorganisms are early colonizers of the upper respiratory tract of piglets. The composition of the nasal microbiota at weaning was shown to constitute a predisposing factor for the development of Glässer’s disease. Here, we unravel the role of the nasal microbiota in the subsequent systemic infection by M. hyorhinis, and the similarities and differences with Glässer’s disease. Nasal samples from farms with recurrent problems with polyserositis associated with M. hyorhinis (MH) or Glässer’s disease (GD) were included in this study, together with healthy control farms (HC). Nasal swabs were taken from piglets in MH farms at weaning, before the onset of the clinical outbreaks, and were submitted to 16S rRNA gene amplicon sequencing (V3–V4 region). These sequences were analyzed together with sequences from similar samples previously obtained in GD and HC farms. Animals from farms with disease (MH and GD) had a nasal microbiota with lower diversity than those from the HC farms. However, the composition of the nasal microbiota of the piglets from these disease farms was different, suggesting that divergent microbiota imbalances may predispose the animals to the two systemic infections. We also found variants of the pathogens that were associated with the farms with the corresponding disease, highlighting the importance of studying the microbiome at strain-level resolution. MDPI 2021-05-14 /pmc/articles/PMC8156107/ /pubmed/34069250 http://dx.doi.org/10.3390/pathogens10050603 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Blanco-Fuertes, Miguel Correa-Fiz, Florencia Fraile, Lorenzo Sibila, Marina Aragon, Virginia Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis |
title | Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis |
title_full | Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis |
title_fullStr | Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis |
title_full_unstemmed | Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis |
title_short | Altered Nasal Microbiota Composition Associated with Development of Polyserositis by Mycoplasma hyorhinis |
title_sort | altered nasal microbiota composition associated with development of polyserositis by mycoplasma hyorhinis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156107/ https://www.ncbi.nlm.nih.gov/pubmed/34069250 http://dx.doi.org/10.3390/pathogens10050603 |
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