1. Mayaro Virus Infects Human Brain Cells and Induces a Potent Antiviral Response in Human Astrocytes.
- Author
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Bengue M, Ferraris P, Barthelemy J, Diagne CT, Hamel R, Liégeois F, Nougairède A, de Lamballerie X, Simonin Y, Pompon J, Salinas S, and Missé D
- Subjects
- 2',5'-Oligoadenylate Synthetase metabolism, Alphavirus Infections pathology, Animals, Brain virology, Cell Line, Chemokine CCL5 metabolism, Chemokine CXCL10 metabolism, Chemokine CXCL11 metabolism, Chikungunya Fever immunology, Chikungunya virus immunology, Chlorocebus aethiops, Cytokines metabolism, Humans, Interferon Type I immunology, Interferon-gamma immunology, Myxovirus Resistance Proteins metabolism, Neural Stem Cells virology, Pericytes virology, Ubiquitins metabolism, Vero Cells, Alphavirus immunology, Alphavirus Infections immunology, Astrocytes immunology, Astrocytes virology, Brain immunology
- Abstract
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.
- Published
- 2021
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