Combinations of two capsid regions controlling canine host range determine canine transferrin receptor binding by canine and feline parvoviruses

被引:83
作者
Hueffer, K
Govindasamy, L
Agbandje-McKenna, M
Parrish, CR
机构
[1] Cornell Univ, Coll Vet Med, James A Baker Inst, Dept Microbiol & Immunol, Ithaca, NY 14853 USA
[2] Univ Florida, Coll Med, Inst Brain, Ctr Struct Biol,Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
关键词
D O I
10.1128/JVI.77.18.10099-10105.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Feline panleukopenia virus (FPV) and its host range variant, canine parvovirus (CPV), can bind the feline transferrin receptor (TfR), while only CPV binds to the canine TfR. Introducing two CPV-specific changes into FPV (at VP2 residues 93 and 323) endowed that virus with the canine TfR binding property and allowed canine cell infection, although neither change alone altered either property. In CPV the reciprocal changes of VP2 residue 93 or 323 to the FPV sequences individually resulted in modest reductions in infectivity for canine cells. Changing both residues in CPV to the FPV amino acids blocked the canine cell infection, but that virus was still able to bind the canine TfR at low levels. This shows that both CPV-specific changes control canine TfR binding but that binding is not always sufficient to mediate infection.
引用
收藏
页码:10099 / 10105
页数:7
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