Dynamin independent endocytosis is an alternative cell entry mechanism for multiple animal viruses
Publiceringsår
2024
Upphovspersoner
Ojha, Ravi; Jiang, Anmin; Mäntylä, Elina; Quirin, Tania; Modhira, Naphak; Witte, Robert; Gaudin, Arnaud; De Zanetti, Lisa; Gormal, Rachel Sarah; Vihinen-Ranta, Maija; Mercer, Jason; Suomalainen, Maarit; Greber, Urs F.; Yamauchi, Yohei; Lozach, Pierre-Yves; Helenius, Ari; Vapalahti, Olli; Young, Paul; Watterson, Daniel; Meunier, Frédéric A.; Joensuu, Merja; Balistreri, Giuseppe
Visa merAbstrakt
Mammalian receptor-mediated endocytosis (RME) often involves at least one of three isoforms of the large GTPase dynamin (Dyn). Dyn pinches-off vesicles at the plasma membrane and mediates uptake of many viruses, although some viruses directly penetrate the plasma membrane. RME is classically interrogated by genetic and pharmacological interference, but this has been hampered by undesired effects. Here we studied virus entry in conditional genetic knock-out (KO) mouse embryonic fibroblasts lacking expression of all three dynamin isoforms (Dyn-KO-MEFs). The small canine parvovirus known to use a single receptor, transferrin receptor, strictly depended on dynamin. Larger viruses or viruses known to use multiple receptors, including alphaviruses, influenza, vesicular stomatitis, bunya, adeno, vaccinia, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and rhinoviruses infected Dyn-KO-MEFs, albeit at higher dosage than wild-type MEFs. In absence of the transmembrane protease serine subtype 2 (TMPRSS2), which normally activates the SARS-CoV-2 spike protein for plasma membrane fusion, SARS-CoV-2 infected angiotensin-converting enzyme 2 (ACE2)-expressing MEFs predominantly through dynamin- and actin-dependent endocytosis. In presence of TMPRSS2 the ancestral Wuhan-strain bypassed both dynamin-dependent and -independent endocytosis, and was less sensitive to endosome maturation inhibitors than the Omicron B1 and XBB variants, supporting the notion that the Omicron variants do not efficiently use TMPRSS2. Collectively, our study suggests that dynamin function at endocytic pits can be essential for infection with single-receptor viruses, while it is not essential but increases uptake and infection efficiency of multi-receptor viruses that otherwise rely on a functional actin network for infection.
Visa merOrganisationer och upphovspersoner
Helsingforsregionens universitetscentralsjukhus specialupptagningsområde
Balistreri Giuseppe
De Zanetti Lisa
Vapalahti Olli
Ojha Ravi
Quirin Tania
Publikationstyp
Publikationsform
Artikel
Moderpublikationens typ
Tidning
Artikelstyp
En originalartikel
Målgrupp
VetenskapligKollegialt utvärderad
Kollegialt utvärderadUKM:s publikationstyp
A1 Originalartikel i en vetenskaplig tidskriftPublikationskanalens uppgifter
Journal
Moderpublikationens namn
Volym
20
Nummer
11
Artikelnummer
e1012690
ISSN
Publikationsforum
Publikationsforumsnivå
3
Öppen tillgång
Öppen tillgänglighet i förläggarens tjänst
Ja
Öppen tillgång till publikationskanalen
Helt öppen publikationskanal
Parallellsparad
Ja
Parallellagringens licens
CC BY
Övriga uppgifter
Vetenskapsområden
Biokemi, cell- och molekylärbiologi; Växtbiologi, mikrobiologi, virologi; Biomedicinska vetenskaper; Folkhälsovetenskap, miljö och arbetshälsa
Nyckelord
[object Object],[object Object],[object Object],[object Object],[object Object]
Publiceringsland
Förenta staterna (USA)
Förlagets internationalitet
Internationell
Språk
engelska
Internationell sampublikation
Ja
Sampublikation med ett företag
Nej
DOI
10.1371/journal.ppat.1012690
Publikationen ingår i undervisnings- och kulturministeriets datainsamling
Ja