Modulation of ADAM17 Levels by Pestiviruses Is Species-Specific.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
02 Oct 2024
Historique:
received: 28 08 2024
revised: 25 09 2024
accepted: 28 09 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 26 10 2024
Statut: epublish

Résumé

Upon host cell infection, viruses modulate their host cells to better suit their needs, including the downregulation of virus entry receptors. ADAM17, a cell surface sheddase, is an essential factor for infection of bovine cells with several pestiviruses. To assess the effect of pestivirus infection on ADAM17, the amounts of cellular ADAM17 and its presence at the cell surface were determined. Mature ADAM17 levels were reduced upon infection with a cytopathic pestivirus bovis (bovine viral diarrhea virus, cpBVDV), pestivirus suis (classical swine fever virus, CSFV) or pestivirus giraffae (strain giraffe), but not negatively affected by pestivirus L (Linda virus, LindaV). A comparable reduction of ADAM17 surface levels, which represents the bioactive form, could be observed in the presence of E2 of BVDV and CSFV, but not LindaV or atypical porcine pestivirus (pestivirus scrofae) E2. Superinfection exclusion in BVDV infection is caused by at least two proteins, glycoprotein E2 and protease/helicase NS3. To evaluate whether the lowered ADAM17 levels could be involved in superinfection exclusion, persistently CSFV- or LindaV-infected cells were challenged with different pestiviruses. Persistently LindaV-infected cells were significantly more susceptible to cpBVDV infection than persistently CSFV-infected cells, whilst the other pestiviruses tested were not or only hardly able to infect the persistently infected cells. These results provide evidence of a pestivirus species-specific effect on ADAM17 levels and hints at the possibility of its involvement in superinfection exclusion.

Identifiants

pubmed: 39459898
pii: v16101564
doi: 10.3390/v16101564
pii:
doi:

Substances chimiques

ADAM17 Protein EC 3.4.24.86
Viral Envelope Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : FWF Austrian Science Fund
ID : P35674

Auteurs

Hann-Wei Chen (HW)

Institute of Virology, Department of Pathobiology, University of Veterinary Medicine, 1210 Vienna, Austria.

Marianne Zaruba (M)

Institute of Virology, Department of Pathobiology, University of Veterinary Medicine, 1210 Vienna, Austria.

Aroosa Dawood (A)

Institute of Virology, Department of Pathobiology, University of Veterinary Medicine, 1210 Vienna, Austria.

Stefan Düsterhöft (S)

Institute for Molecular Pharmacology, RWTH Aachen University, 52062 Aachen, Germany.

Benjamin Lamp (B)

Institute of Virology, Faculty of Veterinary Medicine, Justus-Liebig-University Giessen, Schubertstrasse 81, 35392 Giessen, Germany.

Till Ruemenapf (T)

Institute of Virology, Department of Pathobiology, University of Veterinary Medicine, 1210 Vienna, Austria.

Christiane Riedel (C)

CIRI-Centre International de Recherche en Infectiologie, University Lyon, Université Claude Bernard Lyon 1, Inserm, U1111, CNRS, UMR5308, ENS Lyon, 46 Allée d'Italie, 69007 Lyon, France.

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Classifications MeSH