MDA-5 recognition of a murine norovirus.

Noroviruses are important human pathogens responsible for most cases of viral epidemic gastroenteritis worldwide. Murine norovirus-1 (MNV-1) is one of several murine noroviruses isolated from research mouse facilities and has been used as a model of human norovirus infection. MNV-1 infection has bee...

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Main Authors: Stephen A McCartney, Larissa B Thackray, Leonid Gitlin, Susan Gilfillan, Herbert W Virgin, Marco Colonna
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-07-01
Series:PLoS Pathogens
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18636103/pdf/?tool=EBI
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spelling doaj-bb03f94d78a9418b89401e29e4d4c8d52021-06-19T04:33:12ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742008-07-0147e100010810.1371/journal.ppat.1000108MDA-5 recognition of a murine norovirus.Stephen A McCartneyLarissa B ThackrayLeonid GitlinSusan GilfillanHerbert W VirginMarco ColonnaNoroviruses are important human pathogens responsible for most cases of viral epidemic gastroenteritis worldwide. Murine norovirus-1 (MNV-1) is one of several murine noroviruses isolated from research mouse facilities and has been used as a model of human norovirus infection. MNV-1 infection has been shown to require components of innate and adaptive immunity for clearance; however, the initial host protein that recognizes MNV-1 infection is unknown. Because noroviruses are RNA viruses, we investigated whether MDA5 and TLR3, cellular sensors that recognize dsRNA, are important for the host response to MNV-1. We demonstrate that MDA5-/- dendritic cells(DC) have a defect in cytokine response to MNV-1. In addition, MNV-1 replicates to higher levels in MDA5-/- DCs as well as in MDA5-/- mice in vivo. Interestingly, TLR3-/- DCs do not have a defect in vitro, but TLR3-/- mice have a slight increase in viral titers. This is the first demonstration of an innate immune sensor for norovirus and shows that MDA5 is required for the control of MNV-1 infection. Knowledge of the host response to MNV-1 may provide keys for prevention and treatment of the human disease.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18636103/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Stephen A McCartney
Larissa B Thackray
Leonid Gitlin
Susan Gilfillan
Herbert W Virgin
Marco Colonna
spellingShingle Stephen A McCartney
Larissa B Thackray
Leonid Gitlin
Susan Gilfillan
Herbert W Virgin
Marco Colonna
MDA-5 recognition of a murine norovirus.
PLoS Pathogens
author_facet Stephen A McCartney
Larissa B Thackray
Leonid Gitlin
Susan Gilfillan
Herbert W Virgin
Marco Colonna
author_sort Stephen A McCartney
title MDA-5 recognition of a murine norovirus.
title_short MDA-5 recognition of a murine norovirus.
title_full MDA-5 recognition of a murine norovirus.
title_fullStr MDA-5 recognition of a murine norovirus.
title_full_unstemmed MDA-5 recognition of a murine norovirus.
title_sort mda-5 recognition of a murine norovirus.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2008-07-01
description Noroviruses are important human pathogens responsible for most cases of viral epidemic gastroenteritis worldwide. Murine norovirus-1 (MNV-1) is one of several murine noroviruses isolated from research mouse facilities and has been used as a model of human norovirus infection. MNV-1 infection has been shown to require components of innate and adaptive immunity for clearance; however, the initial host protein that recognizes MNV-1 infection is unknown. Because noroviruses are RNA viruses, we investigated whether MDA5 and TLR3, cellular sensors that recognize dsRNA, are important for the host response to MNV-1. We demonstrate that MDA5-/- dendritic cells(DC) have a defect in cytokine response to MNV-1. In addition, MNV-1 replicates to higher levels in MDA5-/- DCs as well as in MDA5-/- mice in vivo. Interestingly, TLR3-/- DCs do not have a defect in vitro, but TLR3-/- mice have a slight increase in viral titers. This is the first demonstration of an innate immune sensor for norovirus and shows that MDA5 is required for the control of MNV-1 infection. Knowledge of the host response to MNV-1 may provide keys for prevention and treatment of the human disease.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18636103/pdf/?tool=EBI
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