IFITMs exhibit antiviral activity against Chikungunya and Zika virus infection via the alteration of TLRs and RLRs signaling pathways
1
Issued Date
2025-12-01
Resource Type
eISSN
20452322
Scopus ID
2-s2.0-105004312464
Journal Title
Scientific Reports
Volume
15
Issue
1
Rights Holder(s)
SCOPUS
Bibliographic Citation
Scientific Reports Vol.15 No.1 (2025)
Suggested Citation
Gumpangseth N., Villarroel P.M.S., Diack A., Songhong T., Yainoy S., Hamel R., Khanom W., Koomhin P., Punsawad C., Srikiatkhachorn A., Missé D., Saetear P., Wichit S. IFITMs exhibit antiviral activity against Chikungunya and Zika virus infection via the alteration of TLRs and RLRs signaling pathways. Scientific Reports Vol.15 No.1 (2025). doi:10.1038/s41598-025-00663-6 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/110089
Title
IFITMs exhibit antiviral activity against Chikungunya and Zika virus infection via the alteration of TLRs and RLRs signaling pathways
Author's Affiliation
Faculty of Science, Mahidol University
Maladies Infectieuses et Vecteurs : Écologie, Génétique, Évolution et Contrôle
Walailak University
University of Rhode Island Feinstein Providence Campus
King Mongkut's Institute of Technology Ladkrabang
Mahidol University
Flow Innovation-Research for Science and Technology Laboratories (FIRST Labs)
Maladies Infectieuses et Vecteurs : Écologie, Génétique, Évolution et Contrôle
Walailak University
University of Rhode Island Feinstein Providence Campus
King Mongkut's Institute of Technology Ladkrabang
Mahidol University
Flow Innovation-Research for Science and Technology Laboratories (FIRST Labs)
Corresponding Author(s)
Other Contributor(s)
Abstract
Chikungunya virus (CHIKV) poses a significant challenge as there are currently no targeted antiviral drugs or vaccines to combat this infection. Here, we demonstrate that interferon-induced transmembrane proteins (IFITMs), including IFITM1, IFITM2, and IFITM3, which are interferon-stimulated genes (ISGs), inhibit CHIKV infection in human skin fibroblasts. Overexpression of IFITMs in cells restricts viral infection, whereas knockdown of IFITMs enhances viral infection. IFITMs overexpression causes a substantial upregulation of antiviral genes, namely TLR3, TLR7, TLR8, and TLR9, and their downstream signaling molecules such as TRADD, IRAK1, TRAF6, and MAP3K7, involved in TLRs signaling pathways. Furthermore, the DHX58 gene encoding the LGP2 protein, a negative regulator of RIG-I in RLRs signaling pathways, was downregulated in the overexpressed cells. Transcription factors including interferon regulatory factors (IRF) 3/5/7, which are downstream signaling components of both TLR and RLR signaling pathways, were also upregulated, resulting in enhanced IFNs signaling. IFITMs not only inhibits the early and late stages of viral infection but can also alter the antiviral innate-immune response to restrict CHIKV infection in human skin fibroblasts. Additionally, IFITMs exhibit their antiviral activity against Zika virus (ZIKV). Altogether, these results show the broad-spectrum antiviral property of IFITMs against arboviruses in foreskin cells.