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Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection

The tropism of Zika virus (ZIKV) has been described in the nervous system, blood, placenta, thymus, and skeletal muscle. We investigated the mechanisms of skeletal muscle susceptibility to ZIKV using an in vitro model of human skeletal muscle myogenesis, in which myoblasts differentiate into myotube...

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Autores principales: Riederer, Ingo, Mendes-da-Cruz, Daniella Arêas, da Fonseca, Guilherme Cordenonsi, González, Mariela Natacha, Brustolini, Otavio, Rocha, Cássia, Loss, Guilherme, de Carvalho, Joseane Biso, Menezes, Mariane Talon, Raphael, Lidiane Menezes Souza, Gerber, Alexandra, Bonaldo, Myrna Cristina, Butler-Browne, Gillian, Mouly, Vincent, Cotta-de-Almeida, Vinicius, Savino, Wilson, Ribeiro de Vasconcelos, Ana Tereza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923442/
https://www.ncbi.nlm.nih.gov/pubmed/35171909
http://dx.doi.org/10.1371/journal.pntd.0010166
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author Riederer, Ingo
Mendes-da-Cruz, Daniella Arêas
da Fonseca, Guilherme Cordenonsi
González, Mariela Natacha
Brustolini, Otavio
Rocha, Cássia
Loss, Guilherme
de Carvalho, Joseane Biso
Menezes, Mariane Talon
Raphael, Lidiane Menezes Souza
Gerber, Alexandra
Bonaldo, Myrna Cristina
Butler-Browne, Gillian
Mouly, Vincent
Cotta-de-Almeida, Vinicius
Savino, Wilson
Ribeiro de Vasconcelos, Ana Tereza
author_facet Riederer, Ingo
Mendes-da-Cruz, Daniella Arêas
da Fonseca, Guilherme Cordenonsi
González, Mariela Natacha
Brustolini, Otavio
Rocha, Cássia
Loss, Guilherme
de Carvalho, Joseane Biso
Menezes, Mariane Talon
Raphael, Lidiane Menezes Souza
Gerber, Alexandra
Bonaldo, Myrna Cristina
Butler-Browne, Gillian
Mouly, Vincent
Cotta-de-Almeida, Vinicius
Savino, Wilson
Ribeiro de Vasconcelos, Ana Tereza
author_sort Riederer, Ingo
collection PubMed
description The tropism of Zika virus (ZIKV) has been described in the nervous system, blood, placenta, thymus, and skeletal muscle. We investigated the mechanisms of skeletal muscle susceptibility to ZIKV using an in vitro model of human skeletal muscle myogenesis, in which myoblasts differentiate into myotubes. Myoblasts were permissive to ZIKV infection, generating productive viral particles, while myotubes controlled ZIKV replication. To investigate the underlying mechanisms, we used gene expression profiling. First, we assessed gene changes in myotubes compared with myoblasts in the model without infection. As expected, we observed an increase in genes and pathways related to the contractile muscle system in the myotubes, a reduction in processes linked to proliferation, migration and cytokine production, among others, confirming the myogenic capacity of our system in vitro. A comparison between non-infected and infected myoblasts revealed more than 500 differentially expressed genes (DEGs). In contrast, infected myotubes showed almost 2,000 DEGs, among which we detected genes and pathways highly or exclusively expressed in myotubes, including those related to antiviral and innate immune responses. Such gene modulation could explain our findings showing that ZIKV also invades myotubes but does not replicate in these differentiated cells. In conclusion, we showed that ZIKV largely (but differentially) disrupts gene expression in human myoblasts and myotubes. Identifying genes involved in myotube resistance can shed light on potential antiviral mechanisms against ZIKV infection.
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spelling pubmed-89234422022-03-16 Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection Riederer, Ingo Mendes-da-Cruz, Daniella Arêas da Fonseca, Guilherme Cordenonsi González, Mariela Natacha Brustolini, Otavio Rocha, Cássia Loss, Guilherme de Carvalho, Joseane Biso Menezes, Mariane Talon Raphael, Lidiane Menezes Souza Gerber, Alexandra Bonaldo, Myrna Cristina Butler-Browne, Gillian Mouly, Vincent Cotta-de-Almeida, Vinicius Savino, Wilson Ribeiro de Vasconcelos, Ana Tereza PLoS Negl Trop Dis Research Article The tropism of Zika virus (ZIKV) has been described in the nervous system, blood, placenta, thymus, and skeletal muscle. We investigated the mechanisms of skeletal muscle susceptibility to ZIKV using an in vitro model of human skeletal muscle myogenesis, in which myoblasts differentiate into myotubes. Myoblasts were permissive to ZIKV infection, generating productive viral particles, while myotubes controlled ZIKV replication. To investigate the underlying mechanisms, we used gene expression profiling. First, we assessed gene changes in myotubes compared with myoblasts in the model without infection. As expected, we observed an increase in genes and pathways related to the contractile muscle system in the myotubes, a reduction in processes linked to proliferation, migration and cytokine production, among others, confirming the myogenic capacity of our system in vitro. A comparison between non-infected and infected myoblasts revealed more than 500 differentially expressed genes (DEGs). In contrast, infected myotubes showed almost 2,000 DEGs, among which we detected genes and pathways highly or exclusively expressed in myotubes, including those related to antiviral and innate immune responses. Such gene modulation could explain our findings showing that ZIKV also invades myotubes but does not replicate in these differentiated cells. In conclusion, we showed that ZIKV largely (but differentially) disrupts gene expression in human myoblasts and myotubes. Identifying genes involved in myotube resistance can shed light on potential antiviral mechanisms against ZIKV infection. Public Library of Science 2022-02-16 /pmc/articles/PMC8923442/ /pubmed/35171909 http://dx.doi.org/10.1371/journal.pntd.0010166 Text en © 2022 Riederer et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Riederer, Ingo
Mendes-da-Cruz, Daniella Arêas
da Fonseca, Guilherme Cordenonsi
González, Mariela Natacha
Brustolini, Otavio
Rocha, Cássia
Loss, Guilherme
de Carvalho, Joseane Biso
Menezes, Mariane Talon
Raphael, Lidiane Menezes Souza
Gerber, Alexandra
Bonaldo, Myrna Cristina
Butler-Browne, Gillian
Mouly, Vincent
Cotta-de-Almeida, Vinicius
Savino, Wilson
Ribeiro de Vasconcelos, Ana Tereza
Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection
title Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection
title_full Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection
title_fullStr Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection
title_full_unstemmed Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection
title_short Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection
title_sort zika virus disrupts gene expression in human myoblasts and myotubes: relationship with susceptibility to infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923442/
https://www.ncbi.nlm.nih.gov/pubmed/35171909
http://dx.doi.org/10.1371/journal.pntd.0010166
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