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MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota

The gut microbiota and microRNAs play important roles in the defense against infection. However, the role of miR-146a in L. monocytogenes infection and gut microbiota remains unclear. We tried to determine whether miR-146a controlled L. monocytogenes infection by regulating the gut microbiota. Wild-...

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Autores principales: Du, Chong-Tao, Gao, Wei, Ma, Ke, Yu, Shui-Xing, Li, Na, Yan, Shi-Qing, Zhou, Feng-Hua, Liu, Zhen-Zhen, Chen, Wei, Lei, Lian-Cheng, Yang, Yong-Jun, Han, Wen-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979314/
https://www.ncbi.nlm.nih.gov/pubmed/29587465
http://dx.doi.org/10.3390/ijms19040993
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author Du, Chong-Tao
Gao, Wei
Ma, Ke
Yu, Shui-Xing
Li, Na
Yan, Shi-Qing
Zhou, Feng-Hua
Liu, Zhen-Zhen
Chen, Wei
Lei, Lian-Cheng
Yang, Yong-Jun
Han, Wen-Yu
author_facet Du, Chong-Tao
Gao, Wei
Ma, Ke
Yu, Shui-Xing
Li, Na
Yan, Shi-Qing
Zhou, Feng-Hua
Liu, Zhen-Zhen
Chen, Wei
Lei, Lian-Cheng
Yang, Yong-Jun
Han, Wen-Yu
author_sort Du, Chong-Tao
collection PubMed
description The gut microbiota and microRNAs play important roles in the defense against infection. However, the role of miR-146a in L. monocytogenes infection and gut microbiota remains unclear. We tried to determine whether miR-146a controlled L. monocytogenes infection by regulating the gut microbiota. Wild-type and miR-146a-deficient mice or macrophages were used to characterize the impact of miR-146a on animal survival, cell death, bacterial clearance, and gut microbiota following L. monocytogenes challenge. We found that L. monocytogenes infection induced miR-146a expression both in vitro and in vivo. When compared to wild-type mice, miR-146a-deficient mice were more resistant to L. monocytogenes infection. MiR-146a deficiency in macrophages resulted in reduced invasion and intracellular survival of L. monocytogenes. High-throughput sequencing of 16S rRNA revealed that the gut microbiota composition differed between miR-146a-deficient and wild-type mice. Relative to wild-type mice, miR-146a-deficient mice had decreased levels of the Proteobacteria phylum, Prevotellaceae family, and Parasutterella genus, and significantly increased short-chain fatty acid producing bacteria, including the genera Alistipes, Blautia, Coprococcus_1, and Ruminococcus_1. Wild-type mice co-housed with miR-146a-deficient mice had increased resistance to L. monocytogenes, indicating that miR-146a deficiency guides the gut microbiota to alleviate infection. Together, these results suggest that miR-146a deficiency protects against L. monocytogenes infection by regulating the gut microbiota.
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spelling pubmed-59793142018-06-10 MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota Du, Chong-Tao Gao, Wei Ma, Ke Yu, Shui-Xing Li, Na Yan, Shi-Qing Zhou, Feng-Hua Liu, Zhen-Zhen Chen, Wei Lei, Lian-Cheng Yang, Yong-Jun Han, Wen-Yu Int J Mol Sci Article The gut microbiota and microRNAs play important roles in the defense against infection. However, the role of miR-146a in L. monocytogenes infection and gut microbiota remains unclear. We tried to determine whether miR-146a controlled L. monocytogenes infection by regulating the gut microbiota. Wild-type and miR-146a-deficient mice or macrophages were used to characterize the impact of miR-146a on animal survival, cell death, bacterial clearance, and gut microbiota following L. monocytogenes challenge. We found that L. monocytogenes infection induced miR-146a expression both in vitro and in vivo. When compared to wild-type mice, miR-146a-deficient mice were more resistant to L. monocytogenes infection. MiR-146a deficiency in macrophages resulted in reduced invasion and intracellular survival of L. monocytogenes. High-throughput sequencing of 16S rRNA revealed that the gut microbiota composition differed between miR-146a-deficient and wild-type mice. Relative to wild-type mice, miR-146a-deficient mice had decreased levels of the Proteobacteria phylum, Prevotellaceae family, and Parasutterella genus, and significantly increased short-chain fatty acid producing bacteria, including the genera Alistipes, Blautia, Coprococcus_1, and Ruminococcus_1. Wild-type mice co-housed with miR-146a-deficient mice had increased resistance to L. monocytogenes, indicating that miR-146a deficiency guides the gut microbiota to alleviate infection. Together, these results suggest that miR-146a deficiency protects against L. monocytogenes infection by regulating the gut microbiota. MDPI 2018-03-26 /pmc/articles/PMC5979314/ /pubmed/29587465 http://dx.doi.org/10.3390/ijms19040993 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Du, Chong-Tao
Gao, Wei
Ma, Ke
Yu, Shui-Xing
Li, Na
Yan, Shi-Qing
Zhou, Feng-Hua
Liu, Zhen-Zhen
Chen, Wei
Lei, Lian-Cheng
Yang, Yong-Jun
Han, Wen-Yu
MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota
title MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota
title_full MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota
title_fullStr MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota
title_full_unstemmed MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota
title_short MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota
title_sort microrna-146a deficiency protects against listeria monocytogenes infection by modulating the gut microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979314/
https://www.ncbi.nlm.nih.gov/pubmed/29587465
http://dx.doi.org/10.3390/ijms19040993
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