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Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model

The association of the lower respiratory tract microbiome in pigs with that of other tissues and environment is still unclear. This study aimed to describe the microbiome of tracheal and oral fluids, air, and feces in the late stage of Mycoplasma hyopneumoniae infection in pigs, and assess the assoc...

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Autores principales: Valeris-Chacin, Robert, Sponheim, Amanda, Fano, Eduardo, Isaacson, Richard, Singer, Randall S., Nerem, Joel, Leite, Fernando L., Pieters, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912642/
https://www.ncbi.nlm.nih.gov/pubmed/33513772
http://dx.doi.org/10.3390/microorganisms9020252
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author Valeris-Chacin, Robert
Sponheim, Amanda
Fano, Eduardo
Isaacson, Richard
Singer, Randall S.
Nerem, Joel
Leite, Fernando L.
Pieters, Maria
author_facet Valeris-Chacin, Robert
Sponheim, Amanda
Fano, Eduardo
Isaacson, Richard
Singer, Randall S.
Nerem, Joel
Leite, Fernando L.
Pieters, Maria
author_sort Valeris-Chacin, Robert
collection PubMed
description The association of the lower respiratory tract microbiome in pigs with that of other tissues and environment is still unclear. This study aimed to describe the microbiome of tracheal and oral fluids, air, and feces in the late stage of Mycoplasma hyopneumoniae infection in pigs, and assess the association between the tracheal microbiome and those from air, feces, and oral fluids. Tracheal fluids (n = 73), feces (n = 71), oropharyngeal fluids (n = 8), and air (n = 12) were collected in seeder pigs (inoculated with M. hyopneumoniae) and contact pigs (113 days post exposure to seeder pigs). After DNA extraction, the V4 region from 16S rRNA gene was sequenced and reads were processed using Divisive Amplicon Denoising Algorithm (DADA2). Clostridium and Streptococcus were among the top five genera identified in all sample types. Mycoplasma hyopneumoniae in tracheal fluids was associated with a reduction of diversity and increment of M. hyorhinis, Glaesserella parasuis, and Pasteurella multocida in tracheal fluids, as well as a reduction of Ruminiclostridium, Barnesiella, and Lactobacillus in feces. Air contributed in a greater proportion to bacteria in the trachea compared with feces and oral fluids. In conclusion, evidence suggests the existence of complex interactions between bacterial communities from distant and distinct niches.
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spelling pubmed-79126422021-02-28 Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model Valeris-Chacin, Robert Sponheim, Amanda Fano, Eduardo Isaacson, Richard Singer, Randall S. Nerem, Joel Leite, Fernando L. Pieters, Maria Microorganisms Article The association of the lower respiratory tract microbiome in pigs with that of other tissues and environment is still unclear. This study aimed to describe the microbiome of tracheal and oral fluids, air, and feces in the late stage of Mycoplasma hyopneumoniae infection in pigs, and assess the association between the tracheal microbiome and those from air, feces, and oral fluids. Tracheal fluids (n = 73), feces (n = 71), oropharyngeal fluids (n = 8), and air (n = 12) were collected in seeder pigs (inoculated with M. hyopneumoniae) and contact pigs (113 days post exposure to seeder pigs). After DNA extraction, the V4 region from 16S rRNA gene was sequenced and reads were processed using Divisive Amplicon Denoising Algorithm (DADA2). Clostridium and Streptococcus were among the top five genera identified in all sample types. Mycoplasma hyopneumoniae in tracheal fluids was associated with a reduction of diversity and increment of M. hyorhinis, Glaesserella parasuis, and Pasteurella multocida in tracheal fluids, as well as a reduction of Ruminiclostridium, Barnesiella, and Lactobacillus in feces. Air contributed in a greater proportion to bacteria in the trachea compared with feces and oral fluids. In conclusion, evidence suggests the existence of complex interactions between bacterial communities from distant and distinct niches. MDPI 2021-01-27 /pmc/articles/PMC7912642/ /pubmed/33513772 http://dx.doi.org/10.3390/microorganisms9020252 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Valeris-Chacin, Robert
Sponheim, Amanda
Fano, Eduardo
Isaacson, Richard
Singer, Randall S.
Nerem, Joel
Leite, Fernando L.
Pieters, Maria
Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model
title Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model
title_full Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model
title_fullStr Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model
title_full_unstemmed Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model
title_short Relationships among Fecal, Air, Oral, and Tracheal Microbial Communities in Pigs in a Respiratory Infection Disease Model
title_sort relationships among fecal, air, oral, and tracheal microbial communities in pigs in a respiratory infection disease model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912642/
https://www.ncbi.nlm.nih.gov/pubmed/33513772
http://dx.doi.org/10.3390/microorganisms9020252
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