Characterization of ross river virus tropism and virus-induced inflammation in a mouse model of viral arthritis and myositis

被引:167
作者
Morrison, TE
Whitmore, AC
Shabman, RS
Lidbury, BA
Mahalingam, S
Heise, MT
机构
[1] Univ N Carolina, Carolina Vaccine Inst, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Genet, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[4] Univ Canberra, Viral Arthritis Asthma Res Grp, Sch Hlth Sci, Canberra, ACT 2601, Australia
关键词
D O I
10.1128/JVI.80.2.737-749.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mosquito-borne alphaviruses are a significant cause of both encephalitic and arthritic disease in humans worldwide. in contrast to the encephalitic alphaviruses, the pathogenesis of alphavirus-induced arthritic disease is not well understood. Utilizing a mouse model of Ross River virus (RRV) disease, we found that the primary targets of RRV infection are bone, joint, and skeletal muscle tissues of the hind limbs in both outbred CD-1 mice and adult C57BL/6J mice. Moreover, histological analyses demonstrated that RRV infection resulted in severe inflammation of these tissues. Characterization of the inflammatory infiltrate within the skeletal muscle tissue identified inflammatory macrophages, NK. cells, and CD4(+) and CD8(+) T lymphocytes. To determine the contribution of the adaptive immune system, the outcome of RRV-induced disease was examined in C57BL/6J RAG-1(-/-) mice, which lack functional T and B lymphocytes. RAG-1(-/-) and wild-type mice developed similar disease signs, infiltration of inflammatory macrophages and NK cells, and muscle pathology, suggesting that the adaptive immune response does not play a critical role in the development of disease. These results establish the mouse model of RRV disease as a useful system for the identification of viral and host factors that contribute to alphavirus-induced arthritis and myositis.
引用
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页码:737 / 749
页数:13
相关论文
共 43 条
[1]   The V proteins of paramyxoviruses bind the IFN-inducible RNA helicase, mda-5, and inhibit its activation of the IFN-β promoter [J].
Andrejeva, J ;
Childs, KS ;
Young, DF ;
Carlos, TS ;
Stock, N ;
Goodbourn, S ;
Randall, RE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (49) :17264-17269
[2]   Cellular and molecular regulation of muscle regeneration [J].
Chargé, SBP ;
Rudnicki, MA .
PHYSIOLOGICAL REVIEWS, 2004, 84 (01) :209-238
[3]   ROSS RIVER VIRUS 26-S RNA - COMPLETE NUCLEOTIDE-SEQUENCE AND DEDUCED SEQUENCE OF THE ENCODED STRUCTURAL PROTEINS [J].
DALGARNO, L ;
RICE, CM ;
STRAUSS, JH .
VIROLOGY, 1983, 129 (01) :170-187
[4]   Viral infection switches non-plasmacytoid dendritic cells into high interferon producers [J].
Diebold, SS ;
Montoya, M ;
Unger, H ;
Alexopoulou, L ;
Roy, P ;
Haswell, LE ;
Al-Shamkhani, A ;
Flavell, R ;
Borrow, P ;
Sousa, CRE .
NATURE, 2003, 424 (6946) :324-328
[5]  
DOHERTY R. L., 1963, AUSTRALIAN J SCI, V26, P183
[6]   CYTOLOGY OF SYNOVIAL EFFUSIONS IN EPIDEMIC POLYARTHRITIS [J].
FRASER, JRE ;
CUNNINGHAM, AL ;
CLARRIS, BJ ;
AASKOV, JG ;
LEACH, R .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1981, 11 (02) :168-173
[7]   THE EXANTHEM OF ROSS RIVER VIRUS-INFECTION - HISTOLOGY, LOCATION OF VIRUS-ANTIGEN AND NATURE OF INFLAMMATORY INFILTRATE [J].
FRASER, JRE ;
RATNAMOHAN, VM ;
DOWLING, JPG ;
BECKER, GJ ;
VARIGOS, GA .
JOURNAL OF CLINICAL PATHOLOGY, 1983, 36 (11) :1256-1263
[8]   Blood monocytes consist of two principal subsets with distinct migratory properties [J].
Geissmann, F ;
Jung, S ;
Littman, DR .
IMMUNITY, 2003, 19 (01) :71-82
[9]  
Gomez RM, 1996, J VIROL, V70, P8926
[10]  
GRIFFIN DE, 1977, J IMMUNOL, V118, P1070