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Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes
Mayaro virus (MAYV) and chikungunya virus (CHIKV) are known for their arthrotropism, but accumulating evidence shows that CHIKV infections are occasionally associated with serious neurological complications. However, little is known about the capacity of MAYV to invade the central nervous system (CN...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001792/ https://www.ncbi.nlm.nih.gov/pubmed/33799906 http://dx.doi.org/10.3390/v13030465 |
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author | Bengue, Michèle Ferraris, Pauline Barthelemy, Jonathan Diagne, Cheikh Tidiane Hamel, Rodolphe Liégeois, Florian Nougairède, Antoine de Lamballerie, Xavier Simonin, Yannick Pompon, Julien Salinas, Sara Missé, Dorothée |
author_facet | Bengue, Michèle Ferraris, Pauline Barthelemy, Jonathan Diagne, Cheikh Tidiane Hamel, Rodolphe Liégeois, Florian Nougairède, Antoine de Lamballerie, Xavier Simonin, Yannick Pompon, Julien Salinas, Sara Missé, Dorothée |
author_sort | Bengue, Michèle |
collection | PubMed |
description | Mayaro virus (MAYV) and chikungunya virus (CHIKV) are known for their arthrotropism, but accumulating evidence shows that CHIKV infections are occasionally associated with serious neurological complications. However, little is known about the capacity of MAYV to invade the central nervous system (CNS). We show that human neural progenitors (hNPCs), pericytes and astrocytes are susceptible to MAYV infection, resulting in the production of infectious viral particles. In primary astrocytes, MAYV, and to a lesser extent CHIKV, elicited a strong antiviral response, as demonstrated by an increased expression of several interferon-stimulated genes, including ISG15, MX1 and OAS2. Infection with either virus led to an enhanced expression of inflammatory chemokines, such as CCL5, CXCL10 and CXCL11, whereas MAYV induced higher levels of IL-6, IL-12 and IL-15 in these cells. Moreover, MAYV was more susceptible than CHIKV to the antiviral effects of both type I and type II interferons. Taken together, this study shows that although MAYV and CHIKV are phylogenetically related, they induce different types of antiviral responses in astrocytes. This work is the first to evaluate the potential neurotropism of MAYV and shows that brain cells and particularly astrocytes and hNPCs are permissive to MAYV, which, consequently, could lead to MAYV-induced neuropathology. |
format | Online Article Text |
id | pubmed-8001792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80017922021-03-28 Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes Bengue, Michèle Ferraris, Pauline Barthelemy, Jonathan Diagne, Cheikh Tidiane Hamel, Rodolphe Liégeois, Florian Nougairède, Antoine de Lamballerie, Xavier Simonin, Yannick Pompon, Julien Salinas, Sara Missé, Dorothée Viruses Article Mayaro virus (MAYV) and chikungunya virus (CHIKV) are known for their arthrotropism, but accumulating evidence shows that CHIKV infections are occasionally associated with serious neurological complications. However, little is known about the capacity of MAYV to invade the central nervous system (CNS). We show that human neural progenitors (hNPCs), pericytes and astrocytes are susceptible to MAYV infection, resulting in the production of infectious viral particles. In primary astrocytes, MAYV, and to a lesser extent CHIKV, elicited a strong antiviral response, as demonstrated by an increased expression of several interferon-stimulated genes, including ISG15, MX1 and OAS2. Infection with either virus led to an enhanced expression of inflammatory chemokines, such as CCL5, CXCL10 and CXCL11, whereas MAYV induced higher levels of IL-6, IL-12 and IL-15 in these cells. Moreover, MAYV was more susceptible than CHIKV to the antiviral effects of both type I and type II interferons. Taken together, this study shows that although MAYV and CHIKV are phylogenetically related, they induce different types of antiviral responses in astrocytes. This work is the first to evaluate the potential neurotropism of MAYV and shows that brain cells and particularly astrocytes and hNPCs are permissive to MAYV, which, consequently, could lead to MAYV-induced neuropathology. MDPI 2021-03-11 /pmc/articles/PMC8001792/ /pubmed/33799906 http://dx.doi.org/10.3390/v13030465 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Bengue, Michèle Ferraris, Pauline Barthelemy, Jonathan Diagne, Cheikh Tidiane Hamel, Rodolphe Liégeois, Florian Nougairède, Antoine de Lamballerie, Xavier Simonin, Yannick Pompon, Julien Salinas, Sara Missé, Dorothée Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes |
title | Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes |
title_full | Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes |
title_fullStr | Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes |
title_full_unstemmed | Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes |
title_short | Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes |
title_sort | mayaro virus infects human brain cells and induces a potent antiviral response in human astrocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001792/ https://www.ncbi.nlm.nih.gov/pubmed/33799906 http://dx.doi.org/10.3390/v13030465 |
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