| Literature DB >> 29917090 |
Temet M McMichael1,2, Yu Zhang3, Adam D Kenney1,2, Lizhi Zhang1,2, Ashley Zani1,2, Mijia Lu3,2, Mahesh Chemudupati1,2, Jianrong Li3,2, Jacob S Yount1,2.
Abstract
Human metapneumovirus (hMPV) utilizes a bifurcated cellular entry strategy, fusing either with the plasma membrane or, after endocytosis, with the endosome membrane. Whether cellular factors restrict or enhance either entry pathway is largely unknown. We found that the interferon-induced transmembrane protein 3 (IFITM3) inhibits hMPV infection to an extent similar to endocytosis-inhibiting drugs, and an IFITM3 variant that accumulates at the plasma membrane in addition to its endosome localization provided increased virus restriction. Mechanistically, IFITM3 blocks hMPV F protein-mediated membrane fusion, and inhibition of infection was reversed by the membrane destabilizing drug amphotericin B. Conversely, we found that infection by some hMPV strains is enhanced by the endosomal protein toll-like receptor 7 (TLR7), and that IFITM3 retains the ability to restrict hMPV infection even in cells expressing TLR7. Overall, our results identify IFITM3 as an endosomal restriction factor that limits hMPV infection of cells.Entities:
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Year: 2018 PMID: 29917090 PMCID: PMC6173576 DOI: 10.1093/infdis/jiy361
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226