m6A modification associated with YTHDF1 is involved in Japanese encephalitis virus infection

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Author(s)

  • Xiao-han Li
  • Jing Chen
  • Yu-da Ou
  • Xiang Zhong
  • Jia-huan Hu
  • Rui-cong Sun
  • Ying-jun Lv
  • Jian-chao Wei
  • Bin Zhou

Detail(s)

Original languageEnglish
Article number109887
Journal / PublicationVeterinary Microbiology
Volume287
Online published31 Oct 2023
Publication statusPublished - Dec 2023

Abstract

N6-methyladenosine (m6A), the most common modification in mammalian mRNA and viral RNA, regulates mRNA structure, stability, translation, and nuclear export. The Japanese encephalitis virus (JEV) is a mosquito-borne flavivirus causing severe neurologic disease in humans. To date, the role of m6A modification in JEV infection remains unclear. Herein, we aimed to determine the impact of m6A methylation modification on JEV replication in vitro and in vivo. Our results demonstrated that the overexpression of the m6A reader protein YTHDF1 in vitro significantly inhibits JEV proliferation. Additionally, YTHDF1 negatively regulates JEV proliferation in YTHDF1 knockdown cells and YTHDF1 knockout mice. MeRIP-seq analysis indicated that YTHDF1 interacts with several interferon-stimulated genes (ISGs), especially in IFIT3. Overall, our data showed that YTHDF1 played a vital role in inhibiting JEV replication. These findings bring novel insights into the specific mechanisms involved in the innate immune response to infection with JEV. They can be used in the development of novel therapeutics for controlling JEV infection. © 2023 Elsevier B.V.

Research Area(s)

  • Antiviral, ISGs, Japanese encephalitis virus, N6-methyladenosine, YTHDF1

Citation Format(s)

m6A modification associated with YTHDF1 is involved in Japanese encephalitis virus infection. / Li, Xiao-han; Chen, Jing; Ou, Yu-da et al.
In: Veterinary Microbiology, Vol. 287, 109887, 12.2023.

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review