Hepatitis C virus envelope protein E2 binds to CD81 of tamarins

被引:39
作者
Allander, T
Forns, X
Emerson, SU
Purcell, RH
Bukh, J
机构
[1] NIAID, Hepatitis Viruses Sect, Infect Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Mol Hepatitis Sect, Infect Dis Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1006/viro.2000.0617
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Since recombinant envelope glycoprotein E2 of hepatitis C virus (HCV) binds to CD81 on human and chimpanzee cells, it has been suggested that CD81 may be a receptor for HCV. Humans and chimpanzees are the only species known to be susceptible to HCV infection. E2 has been reported not to bind to CD81 of the African green monkey, mouse, or rat, suggesting that binding of HCV to CD81 is species specific and may determine susceptibility to infection with HCV. We investigated the interaction between E2 of HCV and CD81 of tamarins, a group of small New World monkeys frequently used for the study of human viruses. Tamarins are not susceptible to HCV infection. Nonetheless, we found that three different forms of HCV 52 (intracellular, secreted, and cell surface-displayed) bound more efficiently to recombinant tamarin CD81 than to human CD81, as determined by ELISA and immunofluorescence. The affinity of the interaction was approximately 10-fold higher for tamarin than for human CD81. Binding of E2 to CD81 on cultured or primary tamarin cells was demonstrated by flow cytometry. In contrast to previous reports, there was also a low-affinity interaction between 52 and African green monkey CD81. Thus, the HCV 52 interaction with CD81 is not limited to humans and chimpanzees and does not predict susceptibility to HCV infection.
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页码:358 / 367
页数:10
相关论文
共 24 条
[1]   Hepatitis C virus and other Flaviviridae viruses enter cells via low density lipoprotein receptor [J].
Agnello, V ;
Abel, G ;
Elfahal, M ;
Knight, GB ;
Zhang, QX .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12766-12771
[2]   Toward a surrogate model for hepatitis C virus: An infectious molecular clone of the GB virus-B hepatitis agent [J].
Bukh, J ;
Apgar, CL ;
Yanagi, M .
VIROLOGY, 1999, 262 (02) :470-478
[3]   Five new or recently discovered (GBV-A) virus species are indigenous to New World monkeys and may constitute a separate genus of the Flaviviridae [J].
Bukh, J ;
Apgar, CL .
VIROLOGY, 1997, 229 (02) :429-436
[4]   A retention signal necessary and sufficient for endoplasmic reticulum localization maps to the transmembrane domain of hepatitis C virus glycoprotein E2 [J].
Cocquerel, L ;
Meunier, JC ;
Pillez, A ;
Wychowski, C ;
Dubuisson, J .
JOURNAL OF VIROLOGY, 1998, 72 (03) :2183-2191
[5]  
Deinhardt F, 1978, Primates Med, V10, P277
[6]  
Dubuisson J, 2000, CURR TOP MICROBIOL, V242, P135
[7]   Functional characterization of intracellular and secreted forms of a truncated hepatitis C virus E2 glycoprotein [J].
Flint, M ;
Dubuisson, J ;
Maidens, C ;
Harrop, R ;
Guile, GR ;
Borrow, P ;
McKeating, JA .
JOURNAL OF VIROLOGY, 2000, 74 (02) :702-709
[8]   Characterization of hepatitis C virus E2 glycoprotein interaction with a putative cellular receptor, CD81 [J].
Flint, M ;
Maidens, C ;
Loomis-Price, LD ;
Shotton, C ;
Dubuisson, J ;
Monk, P ;
Higginbottom, A ;
Levy, S ;
McKeating, JA .
JOURNAL OF VIROLOGY, 1999, 73 (08) :6235-6244
[9]   Characterization of modified hepatitis C virus E2 proteins expressed on the cell surface [J].
Forns, X ;
Allander, T ;
Rohwer-Nutter, P ;
Bukh, J .
VIROLOGY, 2000, 274 (01) :75-85
[10]   DNA immunization of mice and macaques with plasmids encoding hepatitis C virus envelope E2 protein expressed intracellularly and on the cell surface [J].
Forns, X ;
Emerson, SU ;
Tobin, GJ ;
Mushahwar, IK ;
Purcell, RH ;
Bukh, J .
VACCINE, 1999, 17 (15-16) :1992-2002