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ESCRT Requirements for Murine Leukemia Virus Release

The Murine Leukemia Virus (MLV) is a gammaretrovirus that hijack host components of the endosomal sorting complex required for transport (ESCRT) for budding. To determine the minimal requirements for ESCRT factors in MLV viral and viral-like particles (VLP) release, an siRNA knockdown screen of ESCR...

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Autores principales: Bartusch, Christina, Prange, Reinhild
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848597/
https://www.ncbi.nlm.nih.gov/pubmed/27096867
http://dx.doi.org/10.3390/v8040103
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author Bartusch, Christina
Prange, Reinhild
author_facet Bartusch, Christina
Prange, Reinhild
author_sort Bartusch, Christina
collection PubMed
description The Murine Leukemia Virus (MLV) is a gammaretrovirus that hijack host components of the endosomal sorting complex required for transport (ESCRT) for budding. To determine the minimal requirements for ESCRT factors in MLV viral and viral-like particles (VLP) release, an siRNA knockdown screen of ESCRT(-associated) proteins was performed in MLV-producing human cells. We found that MLV VLPs and virions primarily engage the ESCRT-I factor Tsg101 and marginally the ESCRT-associated adaptors Nedd4-1 and Alix to enter the ESCRT pathway. Conversely, the inactivation of ESCRT-II had no impact on VLP and virion egress. By analyzing the effects of individual ESCRT-III knockdowns, VLP and virion release was profoundly inhibited in CHMP2A- and CHMP4B-knockdown cells. In contrast, neither the CHMP2B and CHMP4A isoforms nor CHMP3, CHMP5, and CHMP6 were found to be essential. In case of CHMP1, we unexpectedly observed that the CHMP1A isoform was specifically required for virus budding, but dispensable for VLP release. Hence, MLV utilizes only a subset of ESCRT factors, and viral and viral-like particles differ in ESCRT-III factor requirements.
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spelling pubmed-48485972016-05-04 ESCRT Requirements for Murine Leukemia Virus Release Bartusch, Christina Prange, Reinhild Viruses Article The Murine Leukemia Virus (MLV) is a gammaretrovirus that hijack host components of the endosomal sorting complex required for transport (ESCRT) for budding. To determine the minimal requirements for ESCRT factors in MLV viral and viral-like particles (VLP) release, an siRNA knockdown screen of ESCRT(-associated) proteins was performed in MLV-producing human cells. We found that MLV VLPs and virions primarily engage the ESCRT-I factor Tsg101 and marginally the ESCRT-associated adaptors Nedd4-1 and Alix to enter the ESCRT pathway. Conversely, the inactivation of ESCRT-II had no impact on VLP and virion egress. By analyzing the effects of individual ESCRT-III knockdowns, VLP and virion release was profoundly inhibited in CHMP2A- and CHMP4B-knockdown cells. In contrast, neither the CHMP2B and CHMP4A isoforms nor CHMP3, CHMP5, and CHMP6 were found to be essential. In case of CHMP1, we unexpectedly observed that the CHMP1A isoform was specifically required for virus budding, but dispensable for VLP release. Hence, MLV utilizes only a subset of ESCRT factors, and viral and viral-like particles differ in ESCRT-III factor requirements. MDPI 2016-04-18 /pmc/articles/PMC4848597/ /pubmed/27096867 http://dx.doi.org/10.3390/v8040103 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bartusch, Christina
Prange, Reinhild
ESCRT Requirements for Murine Leukemia Virus Release
title ESCRT Requirements for Murine Leukemia Virus Release
title_full ESCRT Requirements for Murine Leukemia Virus Release
title_fullStr ESCRT Requirements for Murine Leukemia Virus Release
title_full_unstemmed ESCRT Requirements for Murine Leukemia Virus Release
title_short ESCRT Requirements for Murine Leukemia Virus Release
title_sort escrt requirements for murine leukemia virus release
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848597/
https://www.ncbi.nlm.nih.gov/pubmed/27096867
http://dx.doi.org/10.3390/v8040103
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