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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
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Abstrakt

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.
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Organisationer och upphovspersoner

Helsingfors universitet

Balistreri Giuseppe

De Zanetti Lisa

Vapalahti Olli

Ojha Ravi

Quirin Tania

Jyväskylä universitet

Vihinen-Ranta Maija Orcid -palvelun logo

Tammerfors universitet

Mäntylä Elina Orcid -palvelun logo

Helsingforsregionens universitetscentralsjukhus specialupptagningsområde

Balistreri Giuseppe

De Zanetti Lisa

Vapalahti Olli

Ojha Ravi

Quirin Tania

Publikationstyp

Publikationsform

Artikel

Moderpublikationens typ

Tidning

Artikelstyp

En originalartikel

Målgrupp

Vetenskaplig

Kollegialt utvärderad

Kollegialt utvärderad

UKM:s publikationstyp

A1 Originalartikel i en vetenskaplig tidskrift

Publikationskanalens uppgifter

Moderpublikationens namn

PLoS Pathogens

Volym

20

Nummer

11

Artikelnummer

e1012690

Publikationsforum

65164

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

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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