LOCALIZATION OF VIRAL PROTEIN-X IN SIMIAN IMMUNODEFICIENCY VIRUS MACAQUE STRAIN AND ANALYSIS OF ITS PACKAGING REQUIREMENTS

被引:16
作者
LISKA, V
SPEHNER, D
MEHTALI, M
SCHMITT, D
KIRN, A
AUBERTIN, AM
机构
[1] UNIV STRASBOURG 1,INSERM,U74,F-67000 STRASBOURG,FRANCE
[2] UNIV STRASBOURG 1,FAC MED,INST VIROL,F-67000 STRASBOURG,FRANCE
[3] TRANSGENE SA,F-67082 STRASBOURG,FRANCE
关键词
D O I
10.1099/0022-1317-75-11-2955
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Simian immunodeficiency virus (SIV) and human immunodeficiency virus type 2 (HIV-2) encode the accessory viral protein X (Vpx) known to be incorporated into virions in amounts comparable to those of the Gag proteins. The localization of Vpx within SIVmac-infected HUT-78 cells and SIVmac virions was studied by immunoelectron microscopy. Vpx appeared to be associated with extracellular virions as well as budding viral particles at the surface of infected cells. Immunolabelling of purified viral cores suggested that Vpx was a component of the amorphous material surrounding the core structure. Furthermore, a detergent insoluble fraction containing SIV core proteins was devoid of Vpx. To investigate the protein requirement for packaging of Vpx, BHK-21 cells were co-infected with vaccinia virus recombinants encoding Vpx and other SIV proteins able to assemble into virus-like particles. Analysis by immunoprecipitation of the extracellular particulate material as well as immunoelectron microscopy demonstrated that co-expression of Vpx with the Pr56(gag) polyprotein was sufficient for the formation of pseudo-virions containing Vpx. Virus-like particles that appeared upon expression of p16(gag) did not contain Vpx. The results suggest that Vpx is packaged into viral particles through its binding to the Gag polyprotein. The precise positioning of Vpx within the space separating the viral envelope from the core structure is postulated to result from the reorganization of viral proteins that occurs upon Gag polyprotein cleavage and budding.
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页码:2955 / 2962
页数:8
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