Publication:
Interferon-inducible protein (IFI) 16 regulates chikungunya and zika virus infection in human skin fibroblasts

dc.contributor.authorSineewanlaya Wichiten_US
dc.contributor.authorRodolphe Hamelen_US
dc.contributor.authorSakda Yainoyen_US
dc.contributor.authorNuttamonpat Gumpangsethen_US
dc.contributor.authorSuchawadee Panichen_US
dc.contributor.authorThanawat Phuadraksaen_US
dc.contributor.authorPhoonthawee Saetearen_US
dc.contributor.authorArnaud Monteilen_US
dc.contributor.authorRonald Morales Vargasen_US
dc.contributor.authorDorothée Misséen_US
dc.contributor.otherMaladies Infectieuses et Vecteurs : Écologie, Génétique, Évolution et Contrôleen_US
dc.contributor.otherUniversité de Montpellieren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-01-27T07:31:13Z
dc.date.available2020-01-27T07:31:13Z
dc.date.issued2019-01-01en_US
dc.description.abstract© 2019, Leibniz Research Centre for Working Environment and Human Factors. All rights reserved. Chikungunya virus (CHIKV), a re-emerging infectious arbovirus, causes Chikungunya fever that is characterized by fever, skin rash, joint pain, arthralgia and occasionally death. Despite it has been described for 66 years already, neither potential vaccine nor a specific drug is available yet. During CHIKV infection, interferon type I signaling pathway is stimulated and releases hundreds of interferon stimulated genes (ISGs). Our previous study reported that IFI16, a member of ISGs, is up-regulated during CHIKV virus infection and the suppression of the gene resulted in increased virus replication. Furthermore, our group also found that inflammasome activation can inhibit CHIKV infection in human foreskin cells (HFF1). Concomitantly, it has been reported that IFI16 activates the inflammasome to suppress virus infection. Therefore, we have hypothesized that IFI16 could be involved in CHIKV infection. In this study, we confirmed the expression level of IFI16 by Western blotting analysis and found that IFI16 was up-regulated following CHIKV infection in both HFF1 and human embryonic kidney cells. We next investigated its antiviral activity and found that forced expression of IFI16 completely restricted CHIKV infection while endogenous silencing of the gene markedly increased virus replication. Furthermore, we have discovered that IFI16 inhibited CHIKV replication, at least, in cell-to-cell transmission as well as the diffusion step. Interestingly, IFI16 also exerted its antiviral activity against Zika virus (ZIKV) infection, the global threat reemerging virus can cause microcephaly in humans. Taken together, this study provides the first evidence of an antivirus activity of IFI16 during in vitro arbovirus infection, thus expanding its antiviral spectrum that paves the way to further development of antiviral drugs and vaccines.en_US
dc.identifier.citationEXCLI Journal. Vol.18, (2019), 467-476en_US
dc.identifier.doi10.17179/excli2019-1271en_US
dc.identifier.issn16112156en_US
dc.identifier.other2-s2.0-85068764507en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/49926
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85068764507&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleInterferon-inducible protein (IFI) 16 regulates chikungunya and zika virus infection in human skin fibroblastsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85068764507&origin=inwarden_US

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