The structure of a highly virulent Theiler's murine encephalomyelitis virus (GDVII) and implications for determinants of viral persistence

被引:27
作者
Luo, M
Toth, KS
Zhou, L
Pritchard, A
Lipton, HL
机构
[1] UNIV ALABAMA,DEPT MICROBIOL,BIRMINGHAM,AL 35294
[2] EVANSTON HOSP CORP,DIV NEUROL,EVANSTON,IL 60201
[3] NORTHWESTERN UNIV,DEPT BIOCHEM MOL BIOL & CELL BIOL,EVANSTON,IL 60208
[4] UNIV COLORADO,HLTH SCI CTR,DEPT BIOCHEM,DENVER,CO 80262
关键词
D O I
10.1006/viro.1996.0309
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
GDVII is a highly virulent Theiler's murine encephalomyelitis virus (TMEV) which causes acute encephalitis in mice, while the BeAn and DA strains are the less virulent TMEV which cause chronic demyelinating disease in the central nervous system as a result of persistent infection. Purified GDVII virus isolated from infected BHK-21 cells was crystallized and its structure was determined to 3.5-Angstrom resolution by X-ray crystallography, In contrast to other TMEV structures, the VPI C-terminus of GDVII virus has an ordered conformation that forms a hook over the VP3 knob near the threefold axis. Comparisons with the atomic structures of the less virulent BeAn and DA viruses revealed significant structural variations in a major site (cluster B) on the protruding surface loop puff B of VP2. Puff B is located near the VP3 GH loop region which is structurally analogous to the host receptor attachment site of the major serogroup of human rhinoviruses. Mutations at residue 1101 in VP1 and residue 2141 in VP2, which are also near the VP3 GH loop and adjacent to cluster B, were previously shown to influence persistence or DA virus. These observations indicate that the characteristic interaction with the host receptor through these sites may potentially alter TMEV persistence. (C) 1996 Academic Press, Inc.
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页码:246 / 250
页数:5
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