Literature DB >> 28866137

Aedes Aegypti saliva enhances chikungunya virus replication in human skin fibroblasts via inhibition of the type I interferon signaling pathway.

Sineewanlaya Wichit1, Fodé Diop1, Rodolphe Hamel1, Loïc Talignani1, Pauline Ferraris1, Sylvie Cornelie1, Florian Liegeois1, Frédéric Thomas1, Hans Yssel2, Dorothée Missé3.   

Abstract

Chikungunya virus (CHIKV) transmission occurs through the bite of an infected Aedes mosquito which injects virus-containing saliva into the skin of the human host during blood feeding. In the present study, we have determined the effect of Aedes aegypti saliva on CHIKV replication in human skin fibroblasts, a major cell type for viral entry, which mimics the events that occur during natural transmission. A significant increase in the expression of viral transcripts and infectious viral particles was observed in fibroblasts infected with CHIKV in the presence of saliva, as compared with those infected with virus alone. CHIKV-infected human fibroblasts were found to express significantly increased levels of various type I IFN-responsive genes, as demonstrated by specific PCR array analysis. In contrast, the expression of these genes was markedly decreased in cells infected with CHIKV in the presence of mosquito saliva. Moreover, Western blotting analysis revealed that STAT2 and its phosphorylated form were down-regulated in the presence of mosquito saliva. Our data demonstrate for the first time the significance of Aedes aegypti saliva in promoting CHIKV infection via down-regulation of several type I IFN-responsive genes in infected human skin fibroblasts via the JAK-STAT signaling pathway.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Aedes aegypti; Arbovirus; Chikungunya; Human skin fibroblasts; Saliva; Type I IFN

Mesh:

Substances:

Year:  2017        PMID: 28866137     DOI: 10.1016/j.meegid.2017.08.032

Source DB:  PubMed          Journal:  Infect Genet Evol        ISSN: 1567-1348            Impact factor:   3.342


  11 in total

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