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Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria

Mycobacterium avium is the most common nontuberculous mycobacterium (NTM) species causing infectious disease. Here, we characterized a M. avium infection model in zebrafish larvae, and compared it to M. marinum infection, a model of tuberculosis. M. avium bacteria are efficiently phagocytosed and fr...

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Autores principales: Hu, Wanbin, Koch, Bjørn E. V., Lamers, Gerda E. M., Forn-Cuní, Gabriel, Spaink, Herman P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890051/
https://www.ncbi.nlm.nih.gov/pubmed/36741407
http://dx.doi.org/10.3389/fimmu.2022.1075473
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author Hu, Wanbin
Koch, Bjørn E. V.
Lamers, Gerda E. M.
Forn-Cuní, Gabriel
Spaink, Herman P.
author_facet Hu, Wanbin
Koch, Bjørn E. V.
Lamers, Gerda E. M.
Forn-Cuní, Gabriel
Spaink, Herman P.
author_sort Hu, Wanbin
collection PubMed
description Mycobacterium avium is the most common nontuberculous mycobacterium (NTM) species causing infectious disease. Here, we characterized a M. avium infection model in zebrafish larvae, and compared it to M. marinum infection, a model of tuberculosis. M. avium bacteria are efficiently phagocytosed and frequently induce granuloma-like structures in zebrafish larvae. Although macrophages can respond to both mycobacterial infections, their migration speed is faster in infections caused by M. marinum. Tlr2 is conservatively involved in most aspects of the defense against both mycobacterial infections. However, Tlr2 has a function in the migration speed of macrophages and neutrophils to infection sites with M. marinum that is not observed with M. avium. Using RNAseq analysis, we found a distinct transcriptome response in cytokine-cytokine receptor interaction for M. avium and M. marinum infection. In addition, we found differences in gene expression in metabolic pathways, phagosome formation, matrix remodeling, and apoptosis in response to these mycobacterial infections. In conclusion, we characterized a new M. avium infection model in zebrafish that can be further used in studying pathological mechanisms for NTM-caused diseases.
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spelling pubmed-98900512023-02-02 Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria Hu, Wanbin Koch, Bjørn E. V. Lamers, Gerda E. M. Forn-Cuní, Gabriel Spaink, Herman P. Front Immunol Immunology Mycobacterium avium is the most common nontuberculous mycobacterium (NTM) species causing infectious disease. Here, we characterized a M. avium infection model in zebrafish larvae, and compared it to M. marinum infection, a model of tuberculosis. M. avium bacteria are efficiently phagocytosed and frequently induce granuloma-like structures in zebrafish larvae. Although macrophages can respond to both mycobacterial infections, their migration speed is faster in infections caused by M. marinum. Tlr2 is conservatively involved in most aspects of the defense against both mycobacterial infections. However, Tlr2 has a function in the migration speed of macrophages and neutrophils to infection sites with M. marinum that is not observed with M. avium. Using RNAseq analysis, we found a distinct transcriptome response in cytokine-cytokine receptor interaction for M. avium and M. marinum infection. In addition, we found differences in gene expression in metabolic pathways, phagosome formation, matrix remodeling, and apoptosis in response to these mycobacterial infections. In conclusion, we characterized a new M. avium infection model in zebrafish that can be further used in studying pathological mechanisms for NTM-caused diseases. Frontiers Media S.A. 2023-01-18 /pmc/articles/PMC9890051/ /pubmed/36741407 http://dx.doi.org/10.3389/fimmu.2022.1075473 Text en Copyright © 2023 Hu, Koch, Lamers, Forn-Cuní and Spaink 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
Hu, Wanbin
Koch, Bjørn E. V.
Lamers, Gerda E. M.
Forn-Cuní, Gabriel
Spaink, Herman P.
Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria
title Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria
title_full Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria
title_fullStr Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria
title_full_unstemmed Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria
title_short Specificity of the innate immune responses to different classes of non-tuberculous mycobacteria
title_sort specificity of the innate immune responses to different classes of non-tuberculous mycobacteria
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890051/
https://www.ncbi.nlm.nih.gov/pubmed/36741407
http://dx.doi.org/10.3389/fimmu.2022.1075473
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