ANALYSIS OF THE COMPLETE GENOME OF SMALLPOX VARIOLA MAJOR VIRUS-STRAIN BANGLADESH-1975

被引:216
作者
MASSUNG, RF
LIU, LI
QI, J
KNIGHT, JC
YURAN, TE
KERLAVAGE, AR
PARSONS, JM
VENTER, JC
ESPOSITO, JJ
机构
[1] CTR DIS CONTROL, NATL CTR INFECT DIS, DIV VIRAL & RICKETTSIAL DIS, ATLANTA, GA 30333 USA
[2] NINCDS, BETHESDA, MD 20892 USA
[3] INST GENOM RES, GAITHERSBURG, MD 20878 USA
关键词
D O I
10.1006/viro.1994.1288
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We analyzed the 186,102 base pairs (bp) that constitute the entire DNA genome of a highly virulent variola virus isolated from Bangladesh in 1975. The linear, double-stranded molecule has relatively small (725 bp) inverted terminal repeat (ITR) sequences containing three 69-bp direct repeat elements, a 54-bp partial repeat element, and a 105-base telomeric end-loop that can be maximally base-paired to contain 17 mismatches. Proximal to the right-end ITR sequences are another seven 69-bp elements and a 53- and a 27-bp partial element. Sequence analysis showed 187 closely spaced open reading frames specifying putative major proteins containing greater than or equal to 65 amino acids. Most of the virus proteins correspond to proteins in current databases, including 150 proteins that have > 90% identity to major gene products encoded by vaccinia virus, the smallpox vaccine. Variola virus has a group of proteins that are truncated compared with vaccinia virus counterparts and a smaller group of proteins that are elongated. The terminal regions encode several novel proteins and variants of other poxvirus proteins that potentially augment variola virus transmissibility and virulence for its only natural host, humans. (C) 1994 Academic Press, Inc.
引用
收藏
页码:215 / 240
页数:26
相关论文
共 229 条
[1]   NUCLEOTIDE-SEQUENCE OF 21.8 KBP OF VARIOLA MAJOR VIRUS-STRAIN HARVEY AND COMPARISON WITH VACCINIA VIRUS [J].
AGUADO, B ;
SELMES, IP ;
SMITH, GL .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :2887-2902
[2]   MOLECULAR-CLONING AND EXPRESSION OF THE HUMAN INTERFERON-GAMMA RECEPTOR [J].
AGUET, M ;
DEMBIC, Z ;
MERLIN, G .
CELL, 1988, 55 (02) :273-280
[3]   RNA POLYMERASE-ASSOCIATED TRANSCRIPTION SPECIFICITY FACTOR ENCODED BY VACCINIA VIRUS [J].
AHN, BY ;
MOSS, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (08) :3536-3540
[4]   IDENTIFICATION OF THE VACCINIA VIRUS GENE ENCODING AN 18-KILODALTON SUBUNIT OF RNA-POLYMERASE AND DEMONSTRATION OF A 5' POLY(A) LEADER ON ITS EARLY TRANSCRIPT [J].
AHN, BY ;
JONES, EV ;
MOSS, B .
JOURNAL OF VIROLOGY, 1990, 64 (06) :3019-3024
[5]   IDENTIFICATION OF RPO30, A VACCINIA VIRUS-RNA POLYMERASE GENE WITH STRUCTURAL SIMILARITY TO A EUKARYOTIC TRANSCRIPTION ELONGATION-FACTOR [J].
AHN, BY ;
GERSHON, PD ;
JONES, EV ;
MOSS, B .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5433-5441
[6]   IDENTIFICATION AND EXPRESSION OF RPO19, A VACCINIA VIRUS GENE ENCODING A 19-KILODALTON DNA-DEPENDENT RNA-POLYMERASE SUBUNIT [J].
AHN, BY ;
ROSEL, J ;
COLE, NB ;
MOSS, B .
JOURNAL OF VIROLOGY, 1992, 66 (02) :971-982
[7]   VAR1 GENE ON THE MITOCHONDRIAL GENOME OF TORULOPSIS-GLABRATA [J].
AINLEY, WM ;
MACREADIE, IG ;
BUTOW, RA .
JOURNAL OF MOLECULAR BIOLOGY, 1985, 184 (04) :565-576
[8]  
ALANI E, 1989, GENETICS, V122, P47
[9]   NEW MEMBER OF THE MULTIGENE FAMILY OF COMPLEMENT CONTROL PROTEINS IN HERPESVIRUS SAIMIRI [J].
ALBRECHT, JC ;
FLECKENSTEIN, B .
JOURNAL OF VIROLOGY, 1992, 66 (06) :3937-3940
[10]   PRIMARY STRUCTURE OF THE HERPESVIRUS SAIMIRI GENOME [J].
ALBRECHT, JC ;
NICHOLAS, J ;
BILLER, D ;
CAMERON, KR ;
BIESINGER, B ;
NEWMAN, C ;
WITTMANN, S ;
CRAXTON, MA ;
COLEMAN, H ;
FLECKENSTEIN, B ;
HONESS, RW .
JOURNAL OF VIROLOGY, 1992, 66 (08) :5047-5058