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Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility

This study investigated the influence of gut microbiome composition in modulating susceptibility to Mycoplasma hyopneumoniae in pigs. Thirty-two conventional M. hyopneumoniae free piglets were randomly selected from six different litters at 3 weeks of age and were experimentally inoculated with M. h...

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Autores principales: Surendran Nair, Meera, Eucker, Tyson, Martinson, Brian, Neubauer, Axel, Victoria, Joseph, Nicholson, Bryon, Pieters, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819593/
https://www.ncbi.nlm.nih.gov/pubmed/31661027
http://dx.doi.org/10.1186/s13567-019-0701-8
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author Surendran Nair, Meera
Eucker, Tyson
Martinson, Brian
Neubauer, Axel
Victoria, Joseph
Nicholson, Bryon
Pieters, Maria
author_facet Surendran Nair, Meera
Eucker, Tyson
Martinson, Brian
Neubauer, Axel
Victoria, Joseph
Nicholson, Bryon
Pieters, Maria
author_sort Surendran Nair, Meera
collection PubMed
description This study investigated the influence of gut microbiome composition in modulating susceptibility to Mycoplasma hyopneumoniae in pigs. Thirty-two conventional M. hyopneumoniae free piglets were randomly selected from six different litters at 3 weeks of age and were experimentally inoculated with M. hyopneumoniae at 8 weeks of age. Lung lesion scores (LS) were recorded 4 weeks post-inoculation (12 weeks of age) from piglet lungs at necropsy. Fecal bacterial community composition of piglets at 3, 8 and 12 weeks of age were targeted by amplifying the V3–V4 region of the 16S rRNA gene. The LS ranged from 0.3 to 43% with an evident clustering of the scores observed in piglets within litters. There were significant differences in species richness and alpha diversity in fecal microbiomes among piglets within litters at different time points (p < 0.05). The dissimilarity matrices indicated that at 3 weeks of age, the fecal microbiota of piglets was more dissimilar compared to those from 8 to 12 weeks of age. Specific groups of bacteria in the gut that might predict the decreased severity of M. hyopneumoniae associated lesions were identified. The microbial shift at 3 weeks of age was observed to be driven by the increase in abundance of the indicator family, Ruminococcaceae in piglets with low LS (p < 0.05). The taxa, Ruminococcus_2 having the highest richness scores, correlated significantly between litters showing stronger associations with the lowest LS (r = −0.49, p = 0.005). These findings suggest that early life gut microbiota can be a potential determinant for M. hyopneumoniae susceptibility in pigs.
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spelling pubmed-68195932019-10-31 Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility Surendran Nair, Meera Eucker, Tyson Martinson, Brian Neubauer, Axel Victoria, Joseph Nicholson, Bryon Pieters, Maria Vet Res Research Article This study investigated the influence of gut microbiome composition in modulating susceptibility to Mycoplasma hyopneumoniae in pigs. Thirty-two conventional M. hyopneumoniae free piglets were randomly selected from six different litters at 3 weeks of age and were experimentally inoculated with M. hyopneumoniae at 8 weeks of age. Lung lesion scores (LS) were recorded 4 weeks post-inoculation (12 weeks of age) from piglet lungs at necropsy. Fecal bacterial community composition of piglets at 3, 8 and 12 weeks of age were targeted by amplifying the V3–V4 region of the 16S rRNA gene. The LS ranged from 0.3 to 43% with an evident clustering of the scores observed in piglets within litters. There were significant differences in species richness and alpha diversity in fecal microbiomes among piglets within litters at different time points (p < 0.05). The dissimilarity matrices indicated that at 3 weeks of age, the fecal microbiota of piglets was more dissimilar compared to those from 8 to 12 weeks of age. Specific groups of bacteria in the gut that might predict the decreased severity of M. hyopneumoniae associated lesions were identified. The microbial shift at 3 weeks of age was observed to be driven by the increase in abundance of the indicator family, Ruminococcaceae in piglets with low LS (p < 0.05). The taxa, Ruminococcus_2 having the highest richness scores, correlated significantly between litters showing stronger associations with the lowest LS (r = −0.49, p = 0.005). These findings suggest that early life gut microbiota can be a potential determinant for M. hyopneumoniae susceptibility in pigs. BioMed Central 2019-10-28 2019 /pmc/articles/PMC6819593/ /pubmed/31661027 http://dx.doi.org/10.1186/s13567-019-0701-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Surendran Nair, Meera
Eucker, Tyson
Martinson, Brian
Neubauer, Axel
Victoria, Joseph
Nicholson, Bryon
Pieters, Maria
Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility
title Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility
title_full Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility
title_fullStr Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility
title_full_unstemmed Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility
title_short Influence of pig gut microbiota on Mycoplasma hyopneumoniae susceptibility
title_sort influence of pig gut microbiota on mycoplasma hyopneumoniae susceptibility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819593/
https://www.ncbi.nlm.nih.gov/pubmed/31661027
http://dx.doi.org/10.1186/s13567-019-0701-8
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