Vaccinia virus WR gene A5L is required for morphogenesis of mature virions

被引:32
作者
Williams, O
Wolffe, EJ
Weisberg, AS
Merchlinsky, M
机构
[1] US FDA, Ctr Biol Evaluat & Res, Viral Dis Lab, Rockville, MD 20852 USA
[2] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1128/JVI.73.6.4590-4599.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The vaccinia virus WR A5L open reading frame (corresponding to open reading frame A4L in vaccinia virus Copenhagen) encodes an immunodominant late protein found in the core of the vaccinia virion. To investigate the role of this protein in vaccinia virus replication,,ve have constructed a recombinant virus, vA5Li, in which the endogenous gene has been deleted and an inducible copy of the A5 gene dependent on isopropyl-beta-D-thiogalactopyranoside (IPTG) for expression has been inserted into the genome. In the absence of inducer, the yield of infectious virus was dramatically reduced. However, DNA synthesis and processing, viral protein expression (except for A5), and early stages in virion formation were indistinguishable from the analogous steps in a normal infection. Electron microscopy revealed that the major vaccinia virus structural form present in cells infected with vA5Li in the absence of inducer was immature virions. Viral particles were purified from vA5Li-infected cells in the presence and absence of inducer. Both particles contained viral DNA and the full complement of viral proteins, except for A5, which was missing from particles prepared in the absence of inducer. The particles prepared in the presence of IPTG were more infectious than those prepared in its absence. The A5 protein appears to be required for the immature virion to form the brick-shaped intracellular mature virion.
引用
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页码:4590 / 4599
页数:10
相关论文
共 57 条
[1]   REGULATED EXPRESSION OF FOREIGN GENES IN VACCINIA VIRUS UNDER THE CONTROL OF BACTERIOPHAGE-T7 RNA-POLYMERASE AND THE ESCHERICHIA-COLI LAC REPRESSOR [J].
ALEXANDER, WA ;
MOSS, B ;
FUERST, TR .
JOURNAL OF VIROLOGY, 1992, 66 (05) :2934-2942
[2]   The complete genomic sequence of the modified vaccinia Ankara strain: Comparison with other orthopoxviruses [J].
Antoine, G ;
Scheiflinger, F ;
Dorner, F ;
Falkner, FG .
VIROLOGY, 1998, 244 (02) :365-396
[3]   EXTRACELLULAR VACCINIA VIRUS FORMATION AND CELL-TO-CELL VIRUS TRANSMISSION ARE PREVENTED BY DELETION OF THE GENE ENCODING THE 37,000-DALTON OUTER ENVELOPE PROTEIN [J].
BLASCO, R ;
MOSS, B .
JOURNAL OF VIROLOGY, 1991, 65 (11) :5910-5920
[4]   THE INITIATION OF VACCINIA INFECTION [J].
CAIRNS, J .
VIROLOGY, 1960, 11 (03) :603-623
[5]   DNA packaging mutant: Repression of the vaccinia virus A32 gene results in noninfectious, DNA-deficient, spherical, enveloped particles [J].
Cassetti, MC ;
Merchlinsky, M ;
Wolffe, EJ ;
Weisberg, AS ;
Moss, B .
JOURNAL OF VIROLOGY, 1998, 72 (07) :5769-5780
[6]   A vaccinia virus core protein, p39, is membrane associated [J].
Cudmore, S ;
Blasco, R ;
Vincentelli, R ;
Esteban, M ;
Sodeik, B ;
Griffiths, G ;
Locker, JK .
JOURNAL OF VIROLOGY, 1996, 70 (10) :6909-6921
[7]   DEVELOPMENT OF VACCINIA VIRUS IN EARLES L STRAIN CELLS AS EXAMINED BY ELECTRON MICROSCOPY [J].
DALES, S ;
SIMINOVITCH, L .
JOURNAL OF BIOPHYSICAL AND BIOCHEMICAL CYTOLOGY, 1961, 10 (04) :475-&
[8]   IDENTIFICATION AND CHARACTERIZATION OF VACCINIA VIRUS GENES ENCODING PROTEINS THAT ARE HIGHLY ANTIGENIC IN ANIMALS AND ARE IMMUNODOMINANT IN VACCINATED HUMANS [J].
DEMKOWICZ, WE ;
MAA, JS ;
ESTEBAN, M .
JOURNAL OF VIROLOGY, 1992, 66 (01) :386-398
[9]   IDENTIFICATION AND CHARACTERIZATION OF AN EXTRACELLULAR ENVELOPE GLYCOPROTEIN AFFECTING VACCINIA VIRUS EGRESS [J].
DUNCAN, SA ;
SMITH, GL .
JOURNAL OF VIROLOGY, 1992, 66 (03) :1610-1621
[10]  
EARL PL, 1991, CURRENT PROTOCOLS MO, V2