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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
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.
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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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