A viral phospholipase A2 is required for parvovirus infectivity

被引:414
作者
Zádori, Z
Szelei, J
Lacoste, MC
Li, Y
Gariépy, S
Raymond, P
Allaire, M
Nabi, IR
Tijssen, P
机构
[1] Univ Quebec, Inst Armand Frappier, INRS, Ctr Microbiol & Biotechnol, Laval, PQ H7V 1B7, Canada
[2] Univ Montreal, Dept Pathol & Biol Cellulaire, Montreal, PQ H3T 1J4, Canada
基金
匈牙利科学研究基金会; 加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/S1534-5807(01)00031-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sequence analysis revealed phospholipase A(2) (PLA(2)) motifs in capsid proteins of parvoviruses. Although PLA2 activity is not known to exist in viruses, putative PLA(2)s from divergent parvoviruses, human B19, porcine parvovirus, and insect GmDNV (densovirus from Galleria mellonella), can emulate catalytic properties of secreted PLA(2-) Mutations of critical amino acids strongly reduce both PLA(2) activity and, proportionally, viral infectivity, but cell surface attachment, entry, and endocytosis by PLA(2)-deficient virions are not affected. PLA(2) activity is critical for efficient transfer of the viral genome from late endosomes/lysosomes to the nucleus to initiate replication. These findings offer the prospect of developing PLA(2) inhibitors as a new class of antiviral drugs against parvovirus infections and associated diseases.
引用
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页码:291 / 302
页数:12
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