Scientific article
Open access

Influenza A virus exploits transferrin receptor recycling to enter host cells

Publication date2023-05-16
First online date2023-05-16

Influenza A virus (IAV) enters host cells mostly through clathrin-dependent receptor-mediated endocytosis. A single bona fide entry receptor protein supporting this entry mechanism remains elusive. Here we performed proximity ligation of biotin to host cell surface proteins in the vicinity of attached trimeric hemagglutinin-HRP and characterized biotinylated targets using mass spectrometry. This approach identified transferrin receptor 1 (TfR1) as a candidate entry protein. Genetic gain-of-function and loss-of-function experiments, as well as in vitro and in vivo chemical inhibition, confirmed the functional involvement of TfR1 in IAV entry. Recycling deficient mutants of TfR1 do not support entry, indicating that TfR1 recycling is essential for this function. The binding of virions to TfR1 via sialic acids confirmed its role as a directly acting entry factor, but unexpectedly even headless TfR1 promoted IAV particle uptake in trans . TIRF microscopy localized the entering virus-like particles in the vicinity of TfR1. Our data identify TfR1 recycling as a revolving door mechanism exploited by IAV to enter host cells.

  • Antiviral
  • Endocytosis
  • Influenza A virus
  • Recycling
  • Transferrin receptor 1
Citation (ISO format)
MAZEL-SANCHEZ, Beryl et al. Influenza A virus exploits transferrin receptor recycling to enter host cells. In: Proceedings of the National Academy of Sciences of the United States of America, 2023, vol. 120, n° 21, p. e2214936120. doi: 10.1073/pnas.2214936120
Main files (1)
Article (Published version)
Secondary files (8)
ISSN of the journal0027-8424

Technical informations

Creation05/17/2023 7:36:41 AM
First validation05/23/2023 2:21:26 PM
Update time05/23/2023 2:21:26 PM
Status update05/23/2023 2:21:26 PM
Last indexation05/06/2024 3:57:33 PM
All rights reserved by Archive ouverte UNIGE and the University of GenevaunigeBlack