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Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83

The purpose of this study was to determine whether administration of the microorganism Eubacterium rectale (E. rectale) could regulate dendritic cell (DC) activation and systemic inflammation in herpes simplex virus type 1-induced Behçet’s disease (BD). E. rectale, butyrate-producing bacteria, was a...

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Autores principales: Islam, S. M. Shamsul, Ryu, Hye-Myung, Sayeed, Hasan M., Byun, Hae-Ok, Jung, Ju-Yang, Kim, Hyoun-Ah, Suh, Chang-Hee, Sohn, Seonghyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438521/
https://www.ncbi.nlm.nih.gov/pubmed/34531862
http://dx.doi.org/10.3389/fimmu.2021.712312
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author Islam, S. M. Shamsul
Ryu, Hye-Myung
Sayeed, Hasan M.
Byun, Hae-Ok
Jung, Ju-Yang
Kim, Hyoun-Ah
Suh, Chang-Hee
Sohn, Seonghyang
author_facet Islam, S. M. Shamsul
Ryu, Hye-Myung
Sayeed, Hasan M.
Byun, Hae-Ok
Jung, Ju-Yang
Kim, Hyoun-Ah
Suh, Chang-Hee
Sohn, Seonghyang
author_sort Islam, S. M. Shamsul
collection PubMed
description The purpose of this study was to determine whether administration of the microorganism Eubacterium rectale (E. rectale) could regulate dendritic cell (DC) activation and systemic inflammation in herpes simplex virus type 1-induced Behçet’s disease (BD). E. rectale, butyrate-producing bacteria, was administered to BD mice. Peripheral blood leukocytes (PBL) and lymph node cells were isolated and analyzed by flow cytometry. 16S rRNA metagenomic analysis was performed in the feces of mice to determine the differences in the composition of the microbial population between normal and BD mice. Serum cytokine levels were measured by enzyme-linked immunosorbent assay. The frequency of DC activation marker CD83 positive cells was significantly increased in PBL of BD mice. Frequencies of CD83+ cells were also significantly increased in patients with active BD. 16S rRNA metagenomic analysis revealed different gut microbiota composition between normal and BD mice. The administration of E. rectale to BD mice reduced the frequency of CD83+ cells and significantly increased the frequency of NK1.1+ cells with the improvement of symptoms. The co-administration of colchicine and E. rectale also significantly reduced the frequency of CD83+ cells. Differences in gut microbiota were observed between normal mice and BD mice, and the administration of E. rectale downregulated the frequency of CD83, which was associated with BD deterioration. These data indicate that E. rectale could be a new therapeutic adjuvant for BD management.
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spelling pubmed-84385212021-09-15 Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83 Islam, S. M. Shamsul Ryu, Hye-Myung Sayeed, Hasan M. Byun, Hae-Ok Jung, Ju-Yang Kim, Hyoun-Ah Suh, Chang-Hee Sohn, Seonghyang Front Immunol Immunology The purpose of this study was to determine whether administration of the microorganism Eubacterium rectale (E. rectale) could regulate dendritic cell (DC) activation and systemic inflammation in herpes simplex virus type 1-induced Behçet’s disease (BD). E. rectale, butyrate-producing bacteria, was administered to BD mice. Peripheral blood leukocytes (PBL) and lymph node cells were isolated and analyzed by flow cytometry. 16S rRNA metagenomic analysis was performed in the feces of mice to determine the differences in the composition of the microbial population between normal and BD mice. Serum cytokine levels were measured by enzyme-linked immunosorbent assay. The frequency of DC activation marker CD83 positive cells was significantly increased in PBL of BD mice. Frequencies of CD83+ cells were also significantly increased in patients with active BD. 16S rRNA metagenomic analysis revealed different gut microbiota composition between normal and BD mice. The administration of E. rectale to BD mice reduced the frequency of CD83+ cells and significantly increased the frequency of NK1.1+ cells with the improvement of symptoms. The co-administration of colchicine and E. rectale also significantly reduced the frequency of CD83+ cells. Differences in gut microbiota were observed between normal mice and BD mice, and the administration of E. rectale downregulated the frequency of CD83, which was associated with BD deterioration. These data indicate that E. rectale could be a new therapeutic adjuvant for BD management. Frontiers Media S.A. 2021-08-31 /pmc/articles/PMC8438521/ /pubmed/34531862 http://dx.doi.org/10.3389/fimmu.2021.712312 Text en Copyright © 2021 Islam, Ryu, Sayeed, Byun, Jung, Kim, Suh and Sohn https://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 Immunology
Islam, S. M. Shamsul
Ryu, Hye-Myung
Sayeed, Hasan M.
Byun, Hae-Ok
Jung, Ju-Yang
Kim, Hyoun-Ah
Suh, Chang-Hee
Sohn, Seonghyang
Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83
title Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83
title_full Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83
title_fullStr Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83
title_full_unstemmed Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83
title_short Eubacterium rectale Attenuates HSV-1 Induced Systemic Inflammation in Mice by Inhibiting CD83
title_sort eubacterium rectale attenuates hsv-1 induced systemic inflammation in mice by inhibiting cd83
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438521/
https://www.ncbi.nlm.nih.gov/pubmed/34531862
http://dx.doi.org/10.3389/fimmu.2021.712312
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