Acute hepatic failure in IFN-γ-deficient BALB/c mice after murine coronavirus infection

被引:15
作者
Kyuwa, S
Shibata, S
Tagawa, Y
Iwakura, Y
Machii, K
Urano, T
机构
[1] Univ Tokyo, Grad Sch Agr & Life, Dept Vet Pathol, Bunkyo Ku, Tokyo 1138657, Japan
[2] Univ Tokyo, Inst Med Sci, Ctr Expt Med, Tokyo 1088639, Japan
[3] Inst Publ Hlth, Dept Vet Publ Hlth, Tokyo 1080071, Japan
[4] Kumamoto Univ, Ctr Anim Resources & Dev, Div Microbiol & Genet, Kumamoto 8600811, Japan
基金
日本学术振兴会;
关键词
acute hepatic failure; genetic background; interferon-gamma-deficient mice; mouse hepatitis virus;
D O I
10.1016/S0168-1702(01)00432-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We previously showed that an intraperitoneal infection with mouse hepatitis virus (MHV) persists in interferon-gamma (IFN-gamma)-deficient C57BL/6 (B6-GKO) mice and results in subacute fatal peritonitis, which bears a resemblance to feline infectious peritonitis. To examine the role of other host factors in MHV infection in mice, IFN-gamma-deficient mice with a BALB/c background (BALB-GKO) were infected intraperitoneally with MHV and compared with B6-GKO mice. In contrast to B6-GKO mice, BALB-GKO mice died within I week due to acute hepatic failure. The viral titer of the liver in BALB-GKO mice was significantly higher than that in B6-GKO mice. All hepatocytes in BALB-GKO mice were necrotic at 5 days post-infection, which was clearly distinct from large but limited lesion in the liver from infected B6-GKO mice, The serum alanine aminotransferase activity of infected BALB-GKO mice were higher than that of B6-GKO mice and was paralleled with the severity of the pathological changes and viral titers in infected mice. Administration of exogenous IFN-gamma to BALB-GKO partially inhibited the acute death. These results indicate that BALB-GKO and B6-GKO mice clearly show different diseases following MHV infection, although wild type counterparts of both mice apparently showed the same clinical course after MHV infection. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:169 / 177
页数:9
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