MDA-5 recognition of a murine norovirus

被引:178
作者
McCartney, Stephen A. [1 ]
Thackray, Larissa B. [1 ]
Gitlin, Leonid [1 ]
Gilfillan, Susan [1 ]
Virgin, Herbert W. [1 ]
Colonna, Marco [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63130 USA
关键词
D O I
10.1371/journal.ppat.1000108
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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共 52 条
[1]   Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3 [J].
Alexopoulou, L ;
Holt, AC ;
Medzhitov, R ;
Flavell, RA .
NATURE, 2001, 413 (6857) :732-738
[2]   Dendritic cells respond to influenza virus through TLR7- and PKR-independent pathways [J].
Barchet, W ;
Krug, A ;
Cella, M ;
Newby, C ;
Fischer, JAA ;
Dzionek, A ;
Pekosz, A ;
Colonna, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (01) :236-242
[3]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[4]   Structural requirements for the assembly of Norwalk virus-like particles [J].
Bertolotti-Ciarlet, A ;
White, LJ ;
Chen, R ;
Prasad, BVV ;
Estes, MK .
JOURNAL OF VIROLOGY, 2002, 76 (08) :4044-4055
[5]   Processing of Norwalk virus nonstructural proteins by a 3C-like cysteine proteinase [J].
Blakeney, SJ ;
Cahill, A ;
Reilly, PA .
VIROLOGY, 2003, 308 (02) :216-224
[6]   Organization and expression of calicivirus genes [J].
Clarke, IN ;
Lambden, PR .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 :S309-S316
[7]   Innate antiviral responses by means of TLR7-mediated recognition of single-stranded RNA [J].
Diebold, SS ;
Kaisho, T ;
Hemmi, H ;
Akira, S ;
Sousa, CRE .
SCIENCE, 2004, 303 (5663) :1529-1531
[8]  
Dolin R, 2004, J INFECT DIS, V189, P2142
[9]   Does Toll-like receptor 3 play a biological role in virus infections? [J].
Edelmann, KH ;
Richardson-Burns, S ;
Alexopoulou, L ;
Tyler, KL ;
Flavell, RA ;
Oldstone, MBA .
VIROLOGY, 2004, 322 (02) :231-238
[10]   Noroviruses everywhere: has something changed? [J].
Estes, Mary K. ;
Prasad, B. V. Verkataram ;
Atmar, Robert L. .
CURRENT OPINION IN INFECTIOUS DISEASES, 2006, 19 (05) :467-474