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Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane

Formation of cytoplasmic inclusion bodies (IBs) is a hallmark of infections with non-segmented negative-strand RNA viruses (order Mononegavirales). We show here that Nipah virus (NiV), a bat-derived highly pathogenic member of the Paramyxoviridae family, differs from mononegaviruses of the Rhabdo-,...

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Autores principales: Ringel, Marc, Heiner, Anja, Behner, Laura, Halwe, Sandro, Sauerhering, Lucie, Becker, Nico, Dietzel, Erik, Sawatsky, Bevan, Kolesnikova, Larissa, Maisner, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488097/
https://www.ncbi.nlm.nih.gov/pubmed/31034506
http://dx.doi.org/10.1371/journal.ppat.1007733
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author Ringel, Marc
Heiner, Anja
Behner, Laura
Halwe, Sandro
Sauerhering, Lucie
Becker, Nico
Dietzel, Erik
Sawatsky, Bevan
Kolesnikova, Larissa
Maisner, Andrea
author_facet Ringel, Marc
Heiner, Anja
Behner, Laura
Halwe, Sandro
Sauerhering, Lucie
Becker, Nico
Dietzel, Erik
Sawatsky, Bevan
Kolesnikova, Larissa
Maisner, Andrea
author_sort Ringel, Marc
collection PubMed
description Formation of cytoplasmic inclusion bodies (IBs) is a hallmark of infections with non-segmented negative-strand RNA viruses (order Mononegavirales). We show here that Nipah virus (NiV), a bat-derived highly pathogenic member of the Paramyxoviridae family, differs from mononegaviruses of the Rhabdo-, Filo- and Pneumoviridae families by forming two types of IBs with distinct localizations, formation kinetics, and protein compositions. IBs in the perinuclear region form rapidly upon expression of the nucleocapsid proteins. These IB(peri) are highly mobile and associate with the aggresome marker y-tubulin. IB(peri) can recruit unrelated overexpressed cytosolic proteins but do not contain the viral matrix (M) protein. Additionally, NiV forms an as yet undescribed IB population at the plasma membrane (IB(PM)) that is y-tubulin-negative but contains the M protein. Infection studies with recombinant NiV revealed that IB(PM) require the M protein for their formation, and most likely represent sites of NiV assembly and budding. The identification of this novel type of plasma membrane-associated IBs not only provides new insights into NiV biology and may open new avenues to develop novel antiviral approaches to treat these highly pathogenic viruses, it also provides a basis for a more detailed characterization of IBs and their role in virus assembly and replication in infections with other Mononegavirales.
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spelling pubmed-64880972019-05-17 Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane Ringel, Marc Heiner, Anja Behner, Laura Halwe, Sandro Sauerhering, Lucie Becker, Nico Dietzel, Erik Sawatsky, Bevan Kolesnikova, Larissa Maisner, Andrea PLoS Pathog Research Article Formation of cytoplasmic inclusion bodies (IBs) is a hallmark of infections with non-segmented negative-strand RNA viruses (order Mononegavirales). We show here that Nipah virus (NiV), a bat-derived highly pathogenic member of the Paramyxoviridae family, differs from mononegaviruses of the Rhabdo-, Filo- and Pneumoviridae families by forming two types of IBs with distinct localizations, formation kinetics, and protein compositions. IBs in the perinuclear region form rapidly upon expression of the nucleocapsid proteins. These IB(peri) are highly mobile and associate with the aggresome marker y-tubulin. IB(peri) can recruit unrelated overexpressed cytosolic proteins but do not contain the viral matrix (M) protein. Additionally, NiV forms an as yet undescribed IB population at the plasma membrane (IB(PM)) that is y-tubulin-negative but contains the M protein. Infection studies with recombinant NiV revealed that IB(PM) require the M protein for their formation, and most likely represent sites of NiV assembly and budding. The identification of this novel type of plasma membrane-associated IBs not only provides new insights into NiV biology and may open new avenues to develop novel antiviral approaches to treat these highly pathogenic viruses, it also provides a basis for a more detailed characterization of IBs and their role in virus assembly and replication in infections with other Mononegavirales. Public Library of Science 2019-04-29 /pmc/articles/PMC6488097/ /pubmed/31034506 http://dx.doi.org/10.1371/journal.ppat.1007733 Text en © 2019 Ringel et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ringel, Marc
Heiner, Anja
Behner, Laura
Halwe, Sandro
Sauerhering, Lucie
Becker, Nico
Dietzel, Erik
Sawatsky, Bevan
Kolesnikova, Larissa
Maisner, Andrea
Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane
title Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane
title_full Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane
title_fullStr Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane
title_full_unstemmed Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane
title_short Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane
title_sort nipah virus induces two inclusion body populations: identification of novel inclusions at the plasma membrane
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488097/
https://www.ncbi.nlm.nih.gov/pubmed/31034506
http://dx.doi.org/10.1371/journal.ppat.1007733
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