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Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2

Respiratory syncytial virus (RSV) is a major pathogen that infects lower respiratory tract and causes a common respiratory disease. Despite serious pathological consequences with this virus, effective treatments for controlling RSV infection remain unsolved, along with poor innate immune responses i...

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Autores principales: Hong, Ji Eun, Kye, Yoon-Chul, Park, Sung-Moo, Cheon, In Su, Chu, Hyuk, Park, Byung-Chul, Park, Yeong-Min, Chang, Jun, Cho, Jae-Ho, Song, Man Ki, Han, Seung Hyun, Yun, Cheol-Heui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423497/
https://www.ncbi.nlm.nih.gov/pubmed/30930867
http://dx.doi.org/10.3389/fmicb.2019.00447
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author Hong, Ji Eun
Kye, Yoon-Chul
Park, Sung-Moo
Cheon, In Su
Chu, Hyuk
Park, Byung-Chul
Park, Yeong-Min
Chang, Jun
Cho, Jae-Ho
Song, Man Ki
Han, Seung Hyun
Yun, Cheol-Heui
author_facet Hong, Ji Eun
Kye, Yoon-Chul
Park, Sung-Moo
Cheon, In Su
Chu, Hyuk
Park, Byung-Chul
Park, Yeong-Min
Chang, Jun
Cho, Jae-Ho
Song, Man Ki
Han, Seung Hyun
Yun, Cheol-Heui
author_sort Hong, Ji Eun
collection PubMed
description Respiratory syncytial virus (RSV) is a major pathogen that infects lower respiratory tract and causes a common respiratory disease. Despite serious pathological consequences with this virus, effective treatments for controlling RSV infection remain unsolved, along with poor innate immune responses induced at the initial stage of RSV infection. Such a poor innate defense mechanism against RSV leads us to study the role of alveolar macrophage (AM) that is one of the primary innate immune cell types in the respiratory tract and may contribute to protective responses against RSV infection. As an effective strategy for enhancing anti-viral function of AM, this study suggests the intranasal administration of Bacillus subtilis spore which induces expansion of AM in the lung with activation and enhanced production of inflammatory cytokines along with several genes associated with M1 macrophage differentiation. Such effect by spore on AM was largely dependent on TLR-MyD88 signaling and, most importantly, resulted in a profound reduction of viral titers and pathological lung injury upon RSV infection. Taken together, our results suggest a protective role of AM in RSV infection and its functional modulation by B. subtilis spore, which may be a useful and potential therapeutic approach against RSV.
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spelling pubmed-64234972019-03-29 Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2 Hong, Ji Eun Kye, Yoon-Chul Park, Sung-Moo Cheon, In Su Chu, Hyuk Park, Byung-Chul Park, Yeong-Min Chang, Jun Cho, Jae-Ho Song, Man Ki Han, Seung Hyun Yun, Cheol-Heui Front Microbiol Microbiology Respiratory syncytial virus (RSV) is a major pathogen that infects lower respiratory tract and causes a common respiratory disease. Despite serious pathological consequences with this virus, effective treatments for controlling RSV infection remain unsolved, along with poor innate immune responses induced at the initial stage of RSV infection. Such a poor innate defense mechanism against RSV leads us to study the role of alveolar macrophage (AM) that is one of the primary innate immune cell types in the respiratory tract and may contribute to protective responses against RSV infection. As an effective strategy for enhancing anti-viral function of AM, this study suggests the intranasal administration of Bacillus subtilis spore which induces expansion of AM in the lung with activation and enhanced production of inflammatory cytokines along with several genes associated with M1 macrophage differentiation. Such effect by spore on AM was largely dependent on TLR-MyD88 signaling and, most importantly, resulted in a profound reduction of viral titers and pathological lung injury upon RSV infection. Taken together, our results suggest a protective role of AM in RSV infection and its functional modulation by B. subtilis spore, which may be a useful and potential therapeutic approach against RSV. Frontiers Media S.A. 2019-03-12 /pmc/articles/PMC6423497/ /pubmed/30930867 http://dx.doi.org/10.3389/fmicb.2019.00447 Text en Copyright © 2019 Hong, Kye, Park, Cheon, Chu, Park, Park, Chang, Cho, Song, Han and Yun. 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
Hong, Ji Eun
Kye, Yoon-Chul
Park, Sung-Moo
Cheon, In Su
Chu, Hyuk
Park, Byung-Chul
Park, Yeong-Min
Chang, Jun
Cho, Jae-Ho
Song, Man Ki
Han, Seung Hyun
Yun, Cheol-Heui
Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2
title Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2
title_full Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2
title_fullStr Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2
title_full_unstemmed Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2
title_short Alveolar Macrophages Treated With Bacillus subtilis Spore Protect Mice Infected With Respiratory Syncytial Virus A2
title_sort alveolar macrophages treated with bacillus subtilis spore protect mice infected with respiratory syncytial virus a2
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423497/
https://www.ncbi.nlm.nih.gov/pubmed/30930867
http://dx.doi.org/10.3389/fmicb.2019.00447
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