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Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome
Recent studies have suggested the existence of a blood microbiome in the healthy host. However, changes in the blood microbiome upon bloodstream infection are not known. Here, we analyzed the dynamics of the blood microbiome in a porcine model of polymicrobial bacteremia induced by fecal peritonitis...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435847/ https://www.ncbi.nlm.nih.gov/pubmed/34527598 http://dx.doi.org/10.3389/fcimb.2021.676650 |
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author | Hyun, Hwi Lee, Min Seok Park, Inwon Ko, Hwa Soo Yun, Seongmin Jang, Dong-Hyun Kim, Seonghye Kim, Hajin Kang, Joo H. Lee, Jae Hyuk Kwon, Taejoon |
author_facet | Hyun, Hwi Lee, Min Seok Park, Inwon Ko, Hwa Soo Yun, Seongmin Jang, Dong-Hyun Kim, Seonghye Kim, Hajin Kang, Joo H. Lee, Jae Hyuk Kwon, Taejoon |
author_sort | Hyun, Hwi |
collection | PubMed |
description | Recent studies have suggested the existence of a blood microbiome in the healthy host. However, changes in the blood microbiome upon bloodstream infection are not known. Here, we analyzed the dynamics of the blood microbiome in a porcine model of polymicrobial bacteremia induced by fecal peritonitis. Surprisingly, we detected bacterial populations in the bloodstream even before the infection, and these populations were maintained over time. The native blood microbiome was notably taxonomically different from the fecal microbiome that was used to induce peritonitis, reflecting microbial tropism for the blood. Although the population composition after the infection was similar to that of the native blood microbiome, new bacterial strains entered the bloodstream upon peritonitis induction as clinical symptoms relevant to sepsis developed. This indicates that the bacteria detected in the blood before peritonitis induction were derived from the blood rather than a contamination. Comparison of the functional pathways enriched in the blood and fecal microbiomes revealed that communication and stress management pathways are essential for the survival of the blood microbiome. |
format | Online Article Text |
id | pubmed-8435847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84358472021-09-14 Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome Hyun, Hwi Lee, Min Seok Park, Inwon Ko, Hwa Soo Yun, Seongmin Jang, Dong-Hyun Kim, Seonghye Kim, Hajin Kang, Joo H. Lee, Jae Hyuk Kwon, Taejoon Front Cell Infect Microbiol Cellular and Infection Microbiology Recent studies have suggested the existence of a blood microbiome in the healthy host. However, changes in the blood microbiome upon bloodstream infection are not known. Here, we analyzed the dynamics of the blood microbiome in a porcine model of polymicrobial bacteremia induced by fecal peritonitis. Surprisingly, we detected bacterial populations in the bloodstream even before the infection, and these populations were maintained over time. The native blood microbiome was notably taxonomically different from the fecal microbiome that was used to induce peritonitis, reflecting microbial tropism for the blood. Although the population composition after the infection was similar to that of the native blood microbiome, new bacterial strains entered the bloodstream upon peritonitis induction as clinical symptoms relevant to sepsis developed. This indicates that the bacteria detected in the blood before peritonitis induction were derived from the blood rather than a contamination. Comparison of the functional pathways enriched in the blood and fecal microbiomes revealed that communication and stress management pathways are essential for the survival of the blood microbiome. Frontiers Media S.A. 2021-08-30 /pmc/articles/PMC8435847/ /pubmed/34527598 http://dx.doi.org/10.3389/fcimb.2021.676650 Text en Copyright © 2021 Hyun, Lee, Park, Ko, Yun, Jang, Kim, Kim, Kang, Lee and Kwon 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 | Cellular and Infection Microbiology Hyun, Hwi Lee, Min Seok Park, Inwon Ko, Hwa Soo Yun, Seongmin Jang, Dong-Hyun Kim, Seonghye Kim, Hajin Kang, Joo H. Lee, Jae Hyuk Kwon, Taejoon Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome |
title | Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome |
title_full | Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome |
title_fullStr | Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome |
title_full_unstemmed | Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome |
title_short | Analysis of Porcine Model of Fecal-Induced Peritonitis Reveals the Tropism of Blood Microbiome |
title_sort | analysis of porcine model of fecal-induced peritonitis reveals the tropism of blood microbiome |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435847/ https://www.ncbi.nlm.nih.gov/pubmed/34527598 http://dx.doi.org/10.3389/fcimb.2021.676650 |
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