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Tetraspanins 10 and 15 support Venezuelan equine encephalitis virus replication in astrocytoma cells
Institute for Biochemistry and Research Center for Emerging Infections and Zoonoses (RIZ), University of Veterinary Medicine Hannover, Hannover, Germany.
Institute for Biochemistry and Research Center for Emerging Infections and Zoonoses (RIZ), University of Veterinary Medicine Hannover, Hannover, Germany.
School of Biosciences, College of Life and Environmental Sciences, University of Birmingham, United Kingdom; Centre of Membrane Proteins and Receptors (COMPARE), Universities of Birmingham and Nottingham, The Midlands, United Kingdom.
Institute for Biochemistry and Research Center for Emerging Infections and Zoonoses (RIZ), University of Veterinary Medicine Hannover, Hannover, Germany.
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2025 (English)In: Molecular Biology of the Cell, ISSN 1059-1524, E-ISSN 1939-4586, Vol. 36, no 3, article id 35Article in journal (Refereed) Published
Abstract [en]

Tetraspanins (Tspans) are transmembrane proteins that coordinate life cycle steps of viruses from distinct families. Here, we identify the human Tspan10 and Tspan15, both members of the TspanC8 subfamily, as replication factors for alphavirus Venezuelan equine encephalitis virus (VEEV) in astrocytoma cells. Pharmacological inhibition and small interfering RNA (siRNA)-mediated silencing of TspanC8 interactor a disintegrin and metalloproteinase 10 (ADAM10) reduced VEEV infection. Silencing of Tspan10, Tspan15, and ADAM10 did not affect VEEV entry but diminished viral genome replication. We report that Tspan10 is important for VEEV infection of several cell lines, while silencing of Tspan15 diminishes infection with several alphaviruses, but not flaviviruses, in astrocytoma cells. Conversely, we demonstrate that siRNA-mediated silencing of Tspan14, another member of the TspanC8 family, enhances infection with lentiviral pseudoparticles harbouring the envelope proteins of VEEV, identifying it as a restriction factor for VEEV entry. Silencing of ADAM10/Tspan15 substrate neuronal (N)-cadherin reduced VEEV infectivity, suggesting potential roles of ADAM10 substrates in VEEV infection. In sum, our study identifies three TspanC8s and ADAM10 as important modulators of VEEV infectivity.

Place, publisher, year, edition, pages
American Society for Cell Biology , 2025. Vol. 36, no 3, article id 35
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Cell and Molecular Biology
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URN: urn:nbn:se:umu:diva-236208DOI: 10.1091/mbc.E24-12-0574PubMedID: 39878649Scopus ID: 2-s2.0-85218495095OAI: oai:DiVA.org:umu-236208DiVA, id: diva2:1943865
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Knut and Alice Wallenberg FoundationAvailable from: 2025-03-12 Created: 2025-03-12 Last updated: 2025-03-12Bibliographically approved

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Gerold, Gisa

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Wallenberg Centre for Molecular Medicine at Umeå University (WCMM)Department of Clinical Microbiology
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