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Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice
Cystic echinococcosis (CE) is a chronic infectious disease caused by Echinococcus granulosus. To confirm whether the infection impacts on the gut microbiota, we established a mouse model of E. granulosus infection in this study whereby BALB/c mice were infected with micro-cysts of E. granulosus. Aft...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281689/ https://www.ncbi.nlm.nih.gov/pubmed/30555437 http://dx.doi.org/10.3389/fmicb.2018.02890 |
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author | Bao, Jianling Zheng, Huajun Wang, Yuezhu Zheng, Xueting He, Li Qi, Wenjing Wang, Tian Guo, Baoping Guo, Gang Zhang, Zhaoxia Zhang, Wenbao Li, Jun McManus, Donald P. |
author_facet | Bao, Jianling Zheng, Huajun Wang, Yuezhu Zheng, Xueting He, Li Qi, Wenjing Wang, Tian Guo, Baoping Guo, Gang Zhang, Zhaoxia Zhang, Wenbao Li, Jun McManus, Donald P. |
author_sort | Bao, Jianling |
collection | PubMed |
description | Cystic echinococcosis (CE) is a chronic infectious disease caused by Echinococcus granulosus. To confirm whether the infection impacts on the gut microbiota, we established a mouse model of E. granulosus infection in this study whereby BALB/c mice were infected with micro-cysts of E. granulosus. After 4 months of infection, fecal samples were collected for high-throughput sequencing of the hypervariable regions of the 16S rRNA gene. Sequence analysis revealed a total of 13,353 operational taxonomic units (OTUs) with only 40.6% of the OTUs having genera reference information and 101 of the OTUs were significantly increased in infected mice. Bioinformatics analysis showed that the common core microbiota were not significantly changed at family level. However, two genera (Eisenbergiella and Parabacteroides) were enriched in the infected mice (P(AMOV A) < 0.05) at genus level. Functional analysis indicated that seven pathways were altered in the E. granulosus Infection Group compared with the Uninfected Group. Spearman correlation analysis showed strong correlations of IgG, IgG1 and IgG2a with nine major genera. E. granulosus cyst infection may change the gut microbiota which may be associated with metabolic pathways. |
format | Online Article Text |
id | pubmed-6281689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62816892018-12-14 Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice Bao, Jianling Zheng, Huajun Wang, Yuezhu Zheng, Xueting He, Li Qi, Wenjing Wang, Tian Guo, Baoping Guo, Gang Zhang, Zhaoxia Zhang, Wenbao Li, Jun McManus, Donald P. Front Microbiol Microbiology Cystic echinococcosis (CE) is a chronic infectious disease caused by Echinococcus granulosus. To confirm whether the infection impacts on the gut microbiota, we established a mouse model of E. granulosus infection in this study whereby BALB/c mice were infected with micro-cysts of E. granulosus. After 4 months of infection, fecal samples were collected for high-throughput sequencing of the hypervariable regions of the 16S rRNA gene. Sequence analysis revealed a total of 13,353 operational taxonomic units (OTUs) with only 40.6% of the OTUs having genera reference information and 101 of the OTUs were significantly increased in infected mice. Bioinformatics analysis showed that the common core microbiota were not significantly changed at family level. However, two genera (Eisenbergiella and Parabacteroides) were enriched in the infected mice (P(AMOV A) < 0.05) at genus level. Functional analysis indicated that seven pathways were altered in the E. granulosus Infection Group compared with the Uninfected Group. Spearman correlation analysis showed strong correlations of IgG, IgG1 and IgG2a with nine major genera. E. granulosus cyst infection may change the gut microbiota which may be associated with metabolic pathways. Frontiers Media S.A. 2018-11-29 /pmc/articles/PMC6281689/ /pubmed/30555437 http://dx.doi.org/10.3389/fmicb.2018.02890 Text en Copyright © 2018 Bao, Zheng, Wang, Zheng, He, Qi, Wang, Guo, Guo, Zhang, Zhang, Li and McManus. http://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 | Microbiology Bao, Jianling Zheng, Huajun Wang, Yuezhu Zheng, Xueting He, Li Qi, Wenjing Wang, Tian Guo, Baoping Guo, Gang Zhang, Zhaoxia Zhang, Wenbao Li, Jun McManus, Donald P. Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice |
title | Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice |
title_full | Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice |
title_fullStr | Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice |
title_full_unstemmed | Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice |
title_short | Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice |
title_sort | echinococcus granulosus infection results in an increase in eisenbergiella and parabacteroides genera in the gut of mice |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281689/ https://www.ncbi.nlm.nih.gov/pubmed/30555437 http://dx.doi.org/10.3389/fmicb.2018.02890 |
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