Role of N glycosylation of hepatitis B virus envelope proteins in morphogenesis and infectivity of hepatitis delta virus

被引:48
作者
Sureau, C
Fournier-Wirth, C
Maurel, P
机构
[1] INSERM, U76, Inst Natl Transfus Sanguine, Med Virol Lab, F-75739 Paris, France
[2] INSERM, U128, Montpellier, France
[3] Etab Francais Sang, Montpellier, France
[4] SW Fdn Biomed Res, Dept Virol & Immunol, San Antonio, TX 78228 USA
关键词
D O I
10.1128/JVI.77.9.5519-5523.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis delta virus (HDV) particles are coated with the large (L), middle (M), and small (S) hepatitis B virus envelope proteins. In the present study, we constructed glycosylation-defective envelope protein mutants and evaluated their capacity to assist in the maturation of infectious HDV in vitro. We observed that the removal of N-linked carbohydrates on the S, M, and L proteins was tolerated for the assembly of subviral hepatitis B virus (HBV) particles but was partially inhibitory for the formation of HDV virions. However, when assayed on primary cultures of human hepatocytes, virions coated with S, M, and L proteins lacking N-linked glycans were infectious. Furthermore, in the absence of M, HDV particles coated with nonglycosylated S and L proteins retained infectivity. These results indicate that carbohydrates on the HBV envelope proteins are not essential for the in vitro infectivity of HDV.
引用
收藏
页码:5519 / 5523
页数:5
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