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Gut microbiome diversity of porcine peritonitis model of sepsis

Animal models are essential in understanding of the mechanisms of sepsis moreover the development and the assessment of emerging therapies. In clinically relevant porcine model, however, a significant variability in the host response has been observed among animals. Thus, there is a strong demand to...

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Autores principales: Chalupova, Miroslava, Horak, Jan, Kramna, Lenka, Nalos, Lukas, Stengl, Milan, Chudejova, Katerina, Kraftova, Lucie, Cinek, Ondrej, Klein, Pavel, Matejovic, Martin, Hrabak, Jaroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581925/
https://www.ncbi.nlm.nih.gov/pubmed/36261543
http://dx.doi.org/10.1038/s41598-022-21079-6
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author Chalupova, Miroslava
Horak, Jan
Kramna, Lenka
Nalos, Lukas
Stengl, Milan
Chudejova, Katerina
Kraftova, Lucie
Cinek, Ondrej
Klein, Pavel
Matejovic, Martin
Hrabak, Jaroslav
author_facet Chalupova, Miroslava
Horak, Jan
Kramna, Lenka
Nalos, Lukas
Stengl, Milan
Chudejova, Katerina
Kraftova, Lucie
Cinek, Ondrej
Klein, Pavel
Matejovic, Martin
Hrabak, Jaroslav
author_sort Chalupova, Miroslava
collection PubMed
description Animal models are essential in understanding of the mechanisms of sepsis moreover the development and the assessment of emerging therapies. In clinically relevant porcine model, however, a significant variability in the host response has been observed among animals. Thus, there is a strong demand to better understand the potential sources of this heterogeneity. In this study, we compared faecal microbiome composition of 12 animals. Three samples were collected at different time points from each animal. Bacteriome was subjected to 16S rDNA profiling. A significant difference in bacterial composition was associated with the season (p < 0.001) but not with the sex of the pig (p = 0.28), the timing of sample collection (p = 0.59), or interactions thereof (all p > 0.3). The season batch explained 55% of the total variance in the bacteriome diversity. The season term was highly significant from the high-resolution level of the bacterial amplicon sequencing variants up to the level of phylum. The diversity of the microbiome composition could significantly influence experimental model of sepsis, and studies are warranted to demonstrate the effects of gut microbiome diversity on the host-response. If confirmed, control of the gut microbiome should become a standard part of the pre-clinical sepsis experiments.
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spelling pubmed-95819252022-10-21 Gut microbiome diversity of porcine peritonitis model of sepsis Chalupova, Miroslava Horak, Jan Kramna, Lenka Nalos, Lukas Stengl, Milan Chudejova, Katerina Kraftova, Lucie Cinek, Ondrej Klein, Pavel Matejovic, Martin Hrabak, Jaroslav Sci Rep Article Animal models are essential in understanding of the mechanisms of sepsis moreover the development and the assessment of emerging therapies. In clinically relevant porcine model, however, a significant variability in the host response has been observed among animals. Thus, there is a strong demand to better understand the potential sources of this heterogeneity. In this study, we compared faecal microbiome composition of 12 animals. Three samples were collected at different time points from each animal. Bacteriome was subjected to 16S rDNA profiling. A significant difference in bacterial composition was associated with the season (p < 0.001) but not with the sex of the pig (p = 0.28), the timing of sample collection (p = 0.59), or interactions thereof (all p > 0.3). The season batch explained 55% of the total variance in the bacteriome diversity. The season term was highly significant from the high-resolution level of the bacterial amplicon sequencing variants up to the level of phylum. The diversity of the microbiome composition could significantly influence experimental model of sepsis, and studies are warranted to demonstrate the effects of gut microbiome diversity on the host-response. If confirmed, control of the gut microbiome should become a standard part of the pre-clinical sepsis experiments. Nature Publishing Group UK 2022-10-19 /pmc/articles/PMC9581925/ /pubmed/36261543 http://dx.doi.org/10.1038/s41598-022-21079-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chalupova, Miroslava
Horak, Jan
Kramna, Lenka
Nalos, Lukas
Stengl, Milan
Chudejova, Katerina
Kraftova, Lucie
Cinek, Ondrej
Klein, Pavel
Matejovic, Martin
Hrabak, Jaroslav
Gut microbiome diversity of porcine peritonitis model of sepsis
title Gut microbiome diversity of porcine peritonitis model of sepsis
title_full Gut microbiome diversity of porcine peritonitis model of sepsis
title_fullStr Gut microbiome diversity of porcine peritonitis model of sepsis
title_full_unstemmed Gut microbiome diversity of porcine peritonitis model of sepsis
title_short Gut microbiome diversity of porcine peritonitis model of sepsis
title_sort gut microbiome diversity of porcine peritonitis model of sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581925/
https://www.ncbi.nlm.nih.gov/pubmed/36261543
http://dx.doi.org/10.1038/s41598-022-21079-6
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