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LAMR1 restricts Zika virus infection by attenuating the envelope protein ubiquitination.

Dingwen HuYingchong WangAixin LiQin LiCaifeng WuMuhammad Adnan ShereenShanyu HuangKailang WuYing ZhuWenbiao WangJian-Guo Wu
Published in: Virulence (2022)
Zika virus (ZIKV) infection can cause severe neurological disorders, including Guillain-Barre syndrome and meningoencephalitis in adults and microcephaly in fetuses. Here, we reveal that laminin receptor 1 (LAMR1) is a novel host resistance factor against ZIKV infection. Mechanistically, we found that LAMR1 binds to ZIKV envelope (E) protein via its intracellular region and attenuates E protein ubiquitination through recruiting the deubiquitinase eukaryotic translation initiation factor 3 subunit 5 (EIF3S5). We further found that the conserved G282 residue of E protein is essential for its interaction with LAMR1. Moreover, a G282A substitution abolished the binding of E protein to LAMR1 and inhibited LAMR1-mediated E protein deubiquitination. Together, our results indicated that LAMR1 represses ZIKV infection through binding to E protein and attenuating its ubiquitination.
Keyphrases
  • zika virus
  • protein protein
  • binding protein
  • amino acid
  • dengue virus
  • small molecule
  • case report
  • intellectual disability
  • preterm birth