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Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points

Liver injury has caused significant illness in humans worldwide. The dynamics of intestinal bacterial communities associated with natural recovery and therapy for CCl(4)-treated liver injury remain poorly understood. This study was designed to determine the recovery dynamics of intestinal bacterial...

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Autores principales: Xu, Yanping, Zha, Hua, Chen, Wenyi, Cao, Hongcui, Li, Lanjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584945/
https://www.ncbi.nlm.nih.gov/pubmed/33123564
http://dx.doi.org/10.1155/2020/1673602
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author Xu, Yanping
Zha, Hua
Chen, Wenyi
Cao, Hongcui
Li, Lanjuan
author_facet Xu, Yanping
Zha, Hua
Chen, Wenyi
Cao, Hongcui
Li, Lanjuan
author_sort Xu, Yanping
collection PubMed
description Liver injury has caused significant illness in humans worldwide. The dynamics of intestinal bacterial communities associated with natural recovery and therapy for CCl(4)-treated liver injury remain poorly understood. This study was designed to determine the recovery dynamics of intestinal bacterial communities in CCl(4)-treated mice with or without mesenchymal stem cell transplantation (i.e., MSC and CCl(4) groups) at 48 h, 1 week (w), and 2 w. MSCs significantly improved the histopathology, survival rate, and intestinal structural integrity in the treated mice. The gut bacterial communities were determined with significant changes in both the MSC and CCl(4) groups over time, with the greatest difference between the MSC and CCl(4) groups at 48 h. The liver injury dysbiosis ratio experienced a decrease in the MSC groups and a rise in the CCl(4) groups over time, suggesting the mice in the MSC group at 48 h and the CCl(4) group at two weeks were at the least gut microbial dysbiosis status among the corresponding cohorts. Multiple OTUs and functional categories were associated with each of the bacterial communities in the MSC and CCl(4) groups over time. Among these gut phylotypes, OTU1352_S24-7 was determined as the vital member in MSC-treated mice at 48 h, while OTU453_S24-7, OTU1213_Ruminococcaceae, and OTU841_Ruminococcus were determined as the vital phylotypes in CCl(4)-treated mice at two weeks. The relevant findings could assist the diagnosis of the microbial dysbiosis status of intestinal bacterial communities in the CCl(4)-treated cohorts with or without MSC transplantation.
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spelling pubmed-75849452020-10-28 Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points Xu, Yanping Zha, Hua Chen, Wenyi Cao, Hongcui Li, Lanjuan Biomed Res Int Research Article Liver injury has caused significant illness in humans worldwide. The dynamics of intestinal bacterial communities associated with natural recovery and therapy for CCl(4)-treated liver injury remain poorly understood. This study was designed to determine the recovery dynamics of intestinal bacterial communities in CCl(4)-treated mice with or without mesenchymal stem cell transplantation (i.e., MSC and CCl(4) groups) at 48 h, 1 week (w), and 2 w. MSCs significantly improved the histopathology, survival rate, and intestinal structural integrity in the treated mice. The gut bacterial communities were determined with significant changes in both the MSC and CCl(4) groups over time, with the greatest difference between the MSC and CCl(4) groups at 48 h. The liver injury dysbiosis ratio experienced a decrease in the MSC groups and a rise in the CCl(4) groups over time, suggesting the mice in the MSC group at 48 h and the CCl(4) group at two weeks were at the least gut microbial dysbiosis status among the corresponding cohorts. Multiple OTUs and functional categories were associated with each of the bacterial communities in the MSC and CCl(4) groups over time. Among these gut phylotypes, OTU1352_S24-7 was determined as the vital member in MSC-treated mice at 48 h, while OTU453_S24-7, OTU1213_Ruminococcaceae, and OTU841_Ruminococcus were determined as the vital phylotypes in CCl(4)-treated mice at two weeks. The relevant findings could assist the diagnosis of the microbial dysbiosis status of intestinal bacterial communities in the CCl(4)-treated cohorts with or without MSC transplantation. Hindawi 2020-10-14 /pmc/articles/PMC7584945/ /pubmed/33123564 http://dx.doi.org/10.1155/2020/1673602 Text en Copyright © 2020 Yanping Xu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Xu, Yanping
Zha, Hua
Chen, Wenyi
Cao, Hongcui
Li, Lanjuan
Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points
title Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points
title_full Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points
title_fullStr Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points
title_full_unstemmed Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points
title_short Recovery Dynamics of Intestinal Bacterial Communities of CCl(4)-Treated Mice with or without Mesenchymal Stem Cell Transplantation over Different Time Points
title_sort recovery dynamics of intestinal bacterial communities of ccl(4)-treated mice with or without mesenchymal stem cell transplantation over different time points
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584945/
https://www.ncbi.nlm.nih.gov/pubmed/33123564
http://dx.doi.org/10.1155/2020/1673602
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