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Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model

Clostridium difficile infection (CDI) is a major cause of infectious diarrhea among hospitalized patients. Probiotics could be instrumental in restoring the intestinal dysbiosis caused by CDI. Here, we examined the protective effect of Pediococcus pentosaceus LI05 in a mouse CDI model. C57BL/6 mice...

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Autores principales: Xu, Qiaomai, Gu, Silan, Chen, Yunbo, Quan, Jiazheng, Lv, Longxian, Chen, Dazhi, Zheng, Beiwen, Xu, Lichen, Li, Lanjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189400/
https://www.ncbi.nlm.nih.gov/pubmed/30356740
http://dx.doi.org/10.3389/fmicb.2018.02396
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author Xu, Qiaomai
Gu, Silan
Chen, Yunbo
Quan, Jiazheng
Lv, Longxian
Chen, Dazhi
Zheng, Beiwen
Xu, Lichen
Li, Lanjuan
author_facet Xu, Qiaomai
Gu, Silan
Chen, Yunbo
Quan, Jiazheng
Lv, Longxian
Chen, Dazhi
Zheng, Beiwen
Xu, Lichen
Li, Lanjuan
author_sort Xu, Qiaomai
collection PubMed
description Clostridium difficile infection (CDI) is a major cause of infectious diarrhea among hospitalized patients. Probiotics could be instrumental in restoring the intestinal dysbiosis caused by CDI. Here, we examined the protective effect of Pediococcus pentosaceus LI05 in a mouse CDI model. C57BL/6 mice were administrated P. pentosaceus LI05 (LI05 group) or sterile anaerobic PBS (CDI group) everyday for 14 days. Mice were exposed to antibiotics cocktail for 5 days; then challenged with C. difficile strain VPI10463. Mice were monitored daily for survival and weight loss. Colonic tissue and serum samples were assessed for intestinal histopathology, intestinal barrier function and systemic inflammation. The oral administration of P. pentosaceus LI05 improved the survival rate and alleviated the histopathological impact of C. difficile. Compared to the CDI group, the levels of inflammatory mediators in the colon as well as inflammatory cytokines and chemokines in serum were substantially attenuated in the LI05 group. P. pentosaceus LI05 alleviated the CDI-induced of disruption of ZO-1, occludin and claudin-1. Additionally, fecal microbiome analysis showed an enrichment in the abundance of the Porphyromonadaceae and Rikenellaceae, while, the relative abundance of Enterobacteriaceae were decreased. Our results demonstrated that the preventive effect of P. pentosaceus LI05 against CDI was mediated via improving tight junction proteins and down-regulating the inflammatory response. Therefore, P. pentosaceus LI05 could be a promising probiotic in CDI.
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spelling pubmed-61894002018-10-23 Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model Xu, Qiaomai Gu, Silan Chen, Yunbo Quan, Jiazheng Lv, Longxian Chen, Dazhi Zheng, Beiwen Xu, Lichen Li, Lanjuan Front Microbiol Microbiology Clostridium difficile infection (CDI) is a major cause of infectious diarrhea among hospitalized patients. Probiotics could be instrumental in restoring the intestinal dysbiosis caused by CDI. Here, we examined the protective effect of Pediococcus pentosaceus LI05 in a mouse CDI model. C57BL/6 mice were administrated P. pentosaceus LI05 (LI05 group) or sterile anaerobic PBS (CDI group) everyday for 14 days. Mice were exposed to antibiotics cocktail for 5 days; then challenged with C. difficile strain VPI10463. Mice were monitored daily for survival and weight loss. Colonic tissue and serum samples were assessed for intestinal histopathology, intestinal barrier function and systemic inflammation. The oral administration of P. pentosaceus LI05 improved the survival rate and alleviated the histopathological impact of C. difficile. Compared to the CDI group, the levels of inflammatory mediators in the colon as well as inflammatory cytokines and chemokines in serum were substantially attenuated in the LI05 group. P. pentosaceus LI05 alleviated the CDI-induced of disruption of ZO-1, occludin and claudin-1. Additionally, fecal microbiome analysis showed an enrichment in the abundance of the Porphyromonadaceae and Rikenellaceae, while, the relative abundance of Enterobacteriaceae were decreased. Our results demonstrated that the preventive effect of P. pentosaceus LI05 against CDI was mediated via improving tight junction proteins and down-regulating the inflammatory response. Therefore, P. pentosaceus LI05 could be a promising probiotic in CDI. Frontiers Media S.A. 2018-10-09 /pmc/articles/PMC6189400/ /pubmed/30356740 http://dx.doi.org/10.3389/fmicb.2018.02396 Text en Copyright © 2018 Xu, Gu, Chen, Quan, Lv, Chen, Zheng, Xu 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
Xu, Qiaomai
Gu, Silan
Chen, Yunbo
Quan, Jiazheng
Lv, Longxian
Chen, Dazhi
Zheng, Beiwen
Xu, Lichen
Li, Lanjuan
Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model
title Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model
title_full Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model
title_fullStr Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model
title_full_unstemmed Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model
title_short Protective Effect of Pediococcus pentosaceus LI05 Against Clostridium difficile Infection in a Mouse Model
title_sort protective effect of pediococcus pentosaceus li05 against clostridium difficile infection in a mouse model
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189400/
https://www.ncbi.nlm.nih.gov/pubmed/30356740
http://dx.doi.org/10.3389/fmicb.2018.02396
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