SEQUENCE CONSERVATION IN-FIELD AND EXPERIMENTAL ISOLATES OF BORNA-DISEASE VIRUS

被引:97
作者
SCHNEIDER, PA
BRIESE, T
ZIMMERMANN, W
LUDWIG, H
LIPKIN, WI
机构
[1] UNIV CALIF IRVINE, DEPT NEUROL, IRVINE, CA 92717 USA
[2] UNIV CALIF IRVINE, DEPT ANAT & NEUROBIOL, IRVINE, CA 92717 USA
[3] UNIV CALIF IRVINE, DEPT MICROBIOL & MOLEC GENET, IRVINE, CA 92717 USA
[4] FREE UNIV BERLIN, INST VIROL, D-13353 BERLIN, GERMANY
关键词
D O I
10.1128/JVI.68.1.63-68.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Coding and noncoding sequences were analyzed from field and experimental isolates of Borna disease virus. For a 24-kDa protein, maximum divergence was 1.5% at the predicted amino acid level and 3.1% at the nucleotide level. For a 40-kDa protein, maximum divergence was 1.1% at the predicted amino acid level and 4.1% at the nucleotide level. The highest variability in sequence (10%) was found in a 40-nucleotide stretch of genomic RNA between coding sequences for the 40- and 24-kDa proteins. The degree of sequence conservation in these isolates, passaged in various host species in vivo and in vitro over a period of 64 years, is unusual for negative-strand RNA viruses.
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页码:63 / 68
页数:6
相关论文
共 35 条
[1]  
BODE L, 1988, LANCET, V2, P689
[2]   PRECISE MISSENSE AND SILENT POINT MUTATIONS ARE FIXED IN THE GENOMES OF POLIOVIRUS MUTANTS FROM PERSISTENTLY INFECTED-CELLS [J].
BORZAKIAN, S ;
PELLETIER, I ;
CALVEZ, V ;
COLBEREGARAPIN, F .
JOURNAL OF VIROLOGY, 1993, 67 (05) :2914-2917
[3]   BORNA DISEASE VIRUS, A NEGATIVE-STRAND RNA VIRUS, TRANSCRIBES IN THE NUCLEUS OF INFECTED-CELLS [J].
BRIESE, T ;
DELATORRE, JC ;
LEWIS, A ;
LUDWIG, H ;
LIPKIN, WI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (23) :11486-11489
[4]  
BRIESE T, IN PRESS BORNA DISEA
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   MOLECULAR CHARACTERIZATION OF THE BORNA DISEASE AGENT [J].
DELATORRE, JC ;
CARBONE, KM ;
LIPKIN, WI .
VIROLOGY, 1990, 179 (02) :853-856
[8]   THE ROLE OF A REPETITIVE PALINDROMIC SEQUENCE ELEMENT IN THE HUMAN CYTOMEGALO-VIRUS MAJOR IMMEDIATE EARLY ENHANCER [J].
FICKENSCHER, H ;
STAMMINGER, T ;
RUGER, R ;
FLECKENSTEIN, B .
JOURNAL OF GENERAL VIROLOGY, 1989, 70 :107-123
[9]   TRANSCRIPTION-DEPENDENT COMPETITION FOR A HOST FACTOR - THE FUNCTION AND OPTIMAL SEQUENCE OF THE PHAGE-LAMBDA-BOXA TRANSCRIPTION ANTITERMINATION SIGNAL [J].
FRIEDMAN, DI ;
OLSON, ER ;
JOHNSON, LL ;
ALESSI, D ;
CRAVEN, MG .
GENES & DEVELOPMENT, 1990, 4 (12A) :2210-2222
[10]   DETECTION OF BORNA DISEASE VIRUS-REACTIVE ANTIBODIES FROM PATIENTS WITH AFFECTIVE-DISORDERS BY WESTERN IMMUNOBLOT TECHNIQUE [J].
FU, ZF ;
AMSTERDAM, JD ;
KAO, M ;
SHANKAR, V ;
KOPROWSKI, H ;
DIETZSCHOLD, B .
JOURNAL OF AFFECTIVE DISORDERS, 1993, 27 (01) :61-68