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Role of endocytosis and cathepsin-mediated activation in Nipah virus entry

The recent discovery that the Nipah virus (NiV) fusion protein (F) is activated by endosomal cathepsin L raised the question if NiV utilize pH- and protease-dependent mechanisms of entry. We show here that the NiV receptor ephrin B2, virus-like particles and infectious NiV are internalized from the...

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Detalles Bibliográficos
Autores principales: Diederich, Sandra, Thiel, Lena, Maisner, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103400/
https://www.ncbi.nlm.nih.gov/pubmed/18342904
http://dx.doi.org/10.1016/j.virol.2008.02.019
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author Diederich, Sandra
Thiel, Lena
Maisner, Andrea
author_facet Diederich, Sandra
Thiel, Lena
Maisner, Andrea
author_sort Diederich, Sandra
collection PubMed
description The recent discovery that the Nipah virus (NiV) fusion protein (F) is activated by endosomal cathepsin L raised the question if NiV utilize pH- and protease-dependent mechanisms of entry. We show here that the NiV receptor ephrin B2, virus-like particles and infectious NiV are internalized from the cell surface. However, endocytosis, acidic pH and cathepsin-mediated cleavage are not necessary for the initiation of infection of new host cells. Our data clearly demonstrate that proteolytic activation of the NiV F protein is required before incorporation into budding virions but not after virus entry.
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spelling pubmed-71034002020-03-31 Role of endocytosis and cathepsin-mediated activation in Nipah virus entry Diederich, Sandra Thiel, Lena Maisner, Andrea Virology Article The recent discovery that the Nipah virus (NiV) fusion protein (F) is activated by endosomal cathepsin L raised the question if NiV utilize pH- and protease-dependent mechanisms of entry. We show here that the NiV receptor ephrin B2, virus-like particles and infectious NiV are internalized from the cell surface. However, endocytosis, acidic pH and cathepsin-mediated cleavage are not necessary for the initiation of infection of new host cells. Our data clearly demonstrate that proteolytic activation of the NiV F protein is required before incorporation into budding virions but not after virus entry. Elsevier Inc. 2008-06-05 2008-03-14 /pmc/articles/PMC7103400/ /pubmed/18342904 http://dx.doi.org/10.1016/j.virol.2008.02.019 Text en Copyright © 2008 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Diederich, Sandra
Thiel, Lena
Maisner, Andrea
Role of endocytosis and cathepsin-mediated activation in Nipah virus entry
title Role of endocytosis and cathepsin-mediated activation in Nipah virus entry
title_full Role of endocytosis and cathepsin-mediated activation in Nipah virus entry
title_fullStr Role of endocytosis and cathepsin-mediated activation in Nipah virus entry
title_full_unstemmed Role of endocytosis and cathepsin-mediated activation in Nipah virus entry
title_short Role of endocytosis and cathepsin-mediated activation in Nipah virus entry
title_sort role of endocytosis and cathepsin-mediated activation in nipah virus entry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103400/
https://www.ncbi.nlm.nih.gov/pubmed/18342904
http://dx.doi.org/10.1016/j.virol.2008.02.019
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