ASSEMBLY OF VACCINIA VIRUS - INCORPORATION OF P14 AND P-32 INTO THE MEMBRANE OF THE INTRACELLULAR MATURE VIRUS

被引:47
作者
SODEIK, B
CUDMORE, S
ERICSSON, M
ESTEBAN, M
NILES, EG
GRIFFITHS, G
机构
[1] EUROPEAN MOLEC BIOL LAB,CELL BIOL PROGRAM,D-69012 HEIDELBERG,GERMANY
[2] CSIC,CTR NACL BIOTECNOL,E-28049 MADRID,SPAIN
[3] SUNY BUFFALO,SCH MED,DEPT BIOCHEM,BUFFALO,NY 14214
关键词
D O I
10.1128/JVI.69.6.3560-3574.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The cytoplasmic assembly of vaccinia virus begins with the transformation of a two-membraned cisterna derived from the intermediate compartment between the endoplasmic reticulum and the Golgi complex. This cisterna develops into a viral crescent which eventually forms a spherical immature virus (IV) that matures into the intracellular mature virus (IMV). Using immunoelectron microscopy, we determined the subcellular localization of p32 and p14, two membrane-associated proteins of vaccinia virus, p32 was associated with vaccinia virus membranes at all stages of virion assembly, starting with the viral crescents, as well as with the membranes which accumulated during the inhibition of assembly by rifampin. There was also low but significant labelling of membranes of some cellular compartments, especially those in the vicinity of the Golgi complex. In contrast, anti-p14 labelled neither the crescents nor the IV but gave strong labelling of an intermediate form between IV and IMV and was then associated with all later viral forms. This protein was also not significantly detected on identifiable cellular membranes. Both p32 and p14 were abundantly expressed on the surface of intact IMV. Our data are consistent with a model whereby p32 would become inserted into cellular membranes before being incorporated into the crescents whereas p14 would be posttranslationally associated with the viral outer membrane at a specific later stage of the viral life cycle.
引用
收藏
页码:3560 / 3574
页数:15
相关论文
共 51 条
[31]   PROTEIN CLEAVAGE AND POXVIRUS MORPHOGENESIS - TRYPTIC PEPTIDE ANALYSIS OF CORE PRECURSORS ACCUMULATED BY BLOCKING ASSEMBLY WITH RIFAMPICIN [J].
MOSS, B ;
ROSENBLUM, EN .
JOURNAL OF MOLECULAR BIOLOGY, 1973, 81 (02) :267-+
[32]  
NAGAYAMA A, 1970, VIROLOGY, V4, P1039
[33]   VACCINIA VIRUS GENE-D8 ENCODES A VIRION TRANSMEMBRANE PROTEIN [J].
NILES, EG ;
SETO, J .
JOURNAL OF VIROLOGY, 1988, 62 (10) :3772-3778
[34]  
NILES EG, UNPUB
[35]   MODIFICATION OF VACCINIA VIRUS PENETRATION PROTEINS ANALYZED BY MONOCLONAL-ANTIBODIES [J].
OIE, M ;
ICHIHASHI, Y .
VIROLOGY, 1987, 157 (02) :449-459
[36]   CHARACTERIZATION OF VACCINIA POLYPEPTIDES [J].
OIE, M ;
ICHIHASHI, Y .
VIROLOGY, 1981, 113 (01) :263-276
[37]   VIRUS ATTENUATION AND IDENTIFICATION OF STRUCTURAL PROTEINS OF VACCINIA VIRUS THAT ARE SELECTIVELY MODIFIED DURING VIRUS PERSISTENCE [J].
PAEZ, E ;
DALLO, S ;
ESTEBAN, M .
JOURNAL OF VIROLOGY, 1987, 61 (08) :2642-2647
[38]   MECHANISM OF VACCINIA VIRUS RELEASE AND ITS SPECIFIC-INHIBITION BY N1-ISONICOTINOYL-N2-3-METHYL-4-CHLOROBENZOYLHYDRAZINE [J].
PAYNE, LG ;
KRISTENSON, K .
JOURNAL OF VIROLOGY, 1979, 32 (02) :614-622
[39]   THE VACCINIA VIRUS 14-KILODALTON FUSION PROTEIN FORMS A STABLE COMPLEX WITH THE PROCESSED PROTEIN ENCODED BY THE VACCINIA VIRUS A17L GENE [J].
RODRIGUEZ, D ;
RODRIGUEZ, JR ;
ESTEBAN, M .
JOURNAL OF VIROLOGY, 1993, 67 (06) :3435-3440
[40]   ISOLATION AND CHARACTERIZATION OF NEUTRALIZING MONOCLONAL-ANTIBODIES TO VACCINIA VIRUS [J].
RODRIGUEZ, JF ;
JANECZKO, R ;
ESTEBAN, M .
JOURNAL OF VIROLOGY, 1985, 56 (02) :482-488