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Nipah virus induces two inclusion body populations: Identification of novel inclusions at the plasma membrane
Author(s) -
Marc Ringel,
Anja Heiner,
Laura Behner,
Sandro Halwe,
Lucie Sauerhering,
Nico Becker,
Erik Dietzel,
Bevan Sawatsky,
Larissa Kolesnikova,
Andrea Maisner
Publication year - 2019
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1007733
Subject(s) - biology , viral matrix protein , mononegavirales , virology , virus , paramyxoviridae , vesicular stomatitis virus , inclusion bodies , population , viral replication , rna virus , recombinant dna , microbiology and biotechnology , rna , genetics , gene , viral disease , demography , sociology
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 Mononegavirale s.

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