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Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma

Schistosomiasis, also called bilharziasis, is a neglected tropical disease induced by Schistosoma spp. that causes hundreds of millions of infections. Although Schistosoma ova-induced granulomas commonly cause inflammation, hyperplasia, ulceration, micro abscess formation, and polyposis, the role of...

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Autores principales: Zhao, Yanqing, Yang, Shuguo, Li, Bei, Li, Wei, Wang, Jue, Chen, Zongyun, Yang, Jing, Tan, Huabing, Li, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411663/
https://www.ncbi.nlm.nih.gov/pubmed/30891012
http://dx.doi.org/10.3389/fmicb.2019.00352
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author Zhao, Yanqing
Yang, Shuguo
Li, Bei
Li, Wei
Wang, Jue
Chen, Zongyun
Yang, Jing
Tan, Huabing
Li, Jian
author_facet Zhao, Yanqing
Yang, Shuguo
Li, Bei
Li, Wei
Wang, Jue
Chen, Zongyun
Yang, Jing
Tan, Huabing
Li, Jian
author_sort Zhao, Yanqing
collection PubMed
description Schistosomiasis, also called bilharziasis, is a neglected tropical disease induced by Schistosoma spp. that causes hundreds of millions of infections. Although Schistosoma ova-induced granulomas commonly cause inflammation, hyperplasia, ulceration, micro abscess formation, and polyposis, the role of the egg granuloma on the gut microbiome remains unclear. To explore the role, gut microbial communities in mice infected with Schistosoma japonicum were surveyed. Female C57BL/6 and BALB/c mice were exposed to cercariae of S. japonicum for 45 and 65 days and then sacrificed. Intestinal contents and feces were collected, DNA was extracted, and high-throughput 16S rRNA gene-based pyrosequencing was used to provide a comparative analysis of gut microbial diversity. The intestinal mucosal tissues were also examined. Histopathologic analysis demonstrated that the basic structure of the colonic mucosa was damaged by ova-induced granuloma. Regarding the gut microbiome, 2,578,303 good-quality sequences were studied and assigned to 25,278 Operational Taxonomic Units (OTUs) at a threshold of 97% similarity. The average number of OTUs for C57BL/6 and BALB/c were 545 and 530, respectively. At the phylum level, intestinal microbial communities were dominated by Firmicutes, Bacteroidetes, Proteobacteria, and Verrucomicrobia. Infection with S. japonicum modified bacterial richness in the fecal associated microbiota. Exposure significantly modified bacterial community composition among different groups. At the phylogenetic levels, LEfSe analysis revealed that several bacterial taxa were significantly associated with the S. japonicum-infected mice. The present results suggest that egg granulomas in the intestine influence differentiation of the gut microbial community under pathophysiological conditions. This result suggests that intestinal microbiome-based strategies should be considered for early diagnosis, clinical treatment, and prognosis evaluation of schistosomiasis.
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spelling pubmed-64116632019-03-19 Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma Zhao, Yanqing Yang, Shuguo Li, Bei Li, Wei Wang, Jue Chen, Zongyun Yang, Jing Tan, Huabing Li, Jian Front Microbiol Microbiology Schistosomiasis, also called bilharziasis, is a neglected tropical disease induced by Schistosoma spp. that causes hundreds of millions of infections. Although Schistosoma ova-induced granulomas commonly cause inflammation, hyperplasia, ulceration, micro abscess formation, and polyposis, the role of the egg granuloma on the gut microbiome remains unclear. To explore the role, gut microbial communities in mice infected with Schistosoma japonicum were surveyed. Female C57BL/6 and BALB/c mice were exposed to cercariae of S. japonicum for 45 and 65 days and then sacrificed. Intestinal contents and feces were collected, DNA was extracted, and high-throughput 16S rRNA gene-based pyrosequencing was used to provide a comparative analysis of gut microbial diversity. The intestinal mucosal tissues were also examined. Histopathologic analysis demonstrated that the basic structure of the colonic mucosa was damaged by ova-induced granuloma. Regarding the gut microbiome, 2,578,303 good-quality sequences were studied and assigned to 25,278 Operational Taxonomic Units (OTUs) at a threshold of 97% similarity. The average number of OTUs for C57BL/6 and BALB/c were 545 and 530, respectively. At the phylum level, intestinal microbial communities were dominated by Firmicutes, Bacteroidetes, Proteobacteria, and Verrucomicrobia. Infection with S. japonicum modified bacterial richness in the fecal associated microbiota. Exposure significantly modified bacterial community composition among different groups. At the phylogenetic levels, LEfSe analysis revealed that several bacterial taxa were significantly associated with the S. japonicum-infected mice. The present results suggest that egg granulomas in the intestine influence differentiation of the gut microbial community under pathophysiological conditions. This result suggests that intestinal microbiome-based strategies should be considered for early diagnosis, clinical treatment, and prognosis evaluation of schistosomiasis. Frontiers Media S.A. 2019-03-05 /pmc/articles/PMC6411663/ /pubmed/30891012 http://dx.doi.org/10.3389/fmicb.2019.00352 Text en Copyright © 2019 Zhao, Yang, Li, Li, Wang, Chen, Yang, Tan and Li. 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
Zhao, Yanqing
Yang, Shuguo
Li, Bei
Li, Wei
Wang, Jue
Chen, Zongyun
Yang, Jing
Tan, Huabing
Li, Jian
Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma
title Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma
title_full Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma
title_fullStr Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma
title_full_unstemmed Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma
title_short Alterations of the Mice Gut Microbiome via Schistosoma japonicum Ova-Induced Granuloma
title_sort alterations of the mice gut microbiome via schistosoma japonicum ova-induced granuloma
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411663/
https://www.ncbi.nlm.nih.gov/pubmed/30891012
http://dx.doi.org/10.3389/fmicb.2019.00352
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