Segment-specific terminal sequences of Bunyamwera bunyavirus regulate genome replication

被引:66
作者
Barr, JN
Elliott, RM
Dunn, EF
Wertz, GW
机构
[1] Univ Alabama Birmingham, Sch Med, Dept Microbiol, Birmingham, AL 35294 USA
[2] Univ Glasgow, Div Virol, Inst Biomed & Life Sci, Glasgow G11 5JR, Lanark, Scotland
基金
英国惠康基金;
关键词
Bunyamwera virus; Bunyaviridae; genome replication; mRNA transcription; unique segment terminal sequences;
D O I
10.1016/S0042-6822(03)00130-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bunyamwera virus (BUNV) is the prototype of both the Orthobunyavirus genus and the Bunyaviridae family of segmented negative sense RNA viruses. The tripartite BUNV genome consists of small (S), medium (M), and large (L) segments that are transcribed to give a single mRNA and replicated to generate an antigenome that is the template for synthesis of further genomic RNA strands. We modified an existing cDNA-derived RNA synthesis system to allow identification of BUNV RNA replication and transcription products by direct metabolic labeling. Direct RNA analysis allowed us to distinguish between template activities that affected either RNA replication or mRNA transcription, an ability that was not possible using previous reporter gene expression assays. We generated genome analogs containing the entire nontranslated terminal sequences of the S, M, and L BUNV segments surrounding a common sequence. Analysis of RNAs synthesized from these templates revealed that the relative abilities of BUNV segments to perform RNA replication was M > L > S. Exchange of segment-specific terminal nucleotides identified a 12-nt region located within both the 3' and 5' termini of the M segment that correlated with its high replication ability. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:326 / 338
页数:13
相关论文
共 59 条
[1]   Activity of Toscana and Rift Valley fever virus transcription complexes on heterologous templates [J].
Accardi, L ;
Prehaud, C ;
Di Bonito, P ;
Mochi, S ;
Bouloy, M ;
Giorgi, C .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :781-785
[2]   Structural features of an influenza virus promoter and their implications for viral RNA synthesis [J].
Bae, SH ;
Cheong, HK ;
Lee, JH ;
Cheong, C ;
Kainosho, M ;
Choi, BS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10602-10607
[3]   Role of the intergenic dinucleotide in vesicular stomatitis virus RNA transcription [J].
Barr, JN ;
Whelan, SPJ ;
Wertz, GW .
JOURNAL OF VIROLOGY, 1997, 71 (03) :1794-1801
[4]  
BEATY BJ, 1991, CURR TOP MICROBIOL, V169, P27
[5]   CHARACTERIZATION OF THE 5' AND 3' ENDS OF VIRAL MESSENGER-RNAS ISOLATED FROM BHK-21-CELLS INFECTED WITH GERMISTON VIRUS (BUNYAVIRUS) [J].
BOULOY, M ;
PARDIGON, N ;
VIALAT, P ;
GERBAUD, S ;
GIRARD, M .
VIROLOGY, 1990, 175 (01) :50-58
[6]   GLOBIN MESSENGER-RNAS ARE PRIMERS FOR TRANSCRIPTION OF INFLUENZA VIRAL-RNA INVITRO [J].
BOULOY, M ;
PLOTCH, SJ ;
KRUG, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (10) :4886-4890
[7]   A reassortant Bunyavirus isolated from acute hemorrhagic fever cases in Kenya and Somalia [J].
Bowen, MD ;
Trappier, SG ;
Sanchez, AJ ;
Meyer, RF ;
Goldsmith, CS ;
Zaki, SR ;
Dunster, LM ;
Peters, CJ ;
Ksiazek, TG ;
Nichol, ST .
VIROLOGY, 2001, 291 (02) :185-190
[8]   Rescue of a segmented negative-strand RNA virus entirely from cloned complementary DNAs [J].
Bridgen, A ;
Elliott, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (26) :15400-15404
[9]   Bunyamwera bunyavirus nonstructural protein NSs is a nonessential gene product that contributes to viral pathogenesis [J].
Bridgen, A ;
Weber, F ;
Fazakerley, JK ;
Elliott, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :664-669
[10]   MESSENGER-RNA OF THE M-SEGMENT RNA OF RIFT-VALLEY FEVER VIRUS [J].
COLLETT, MS .
VIROLOGY, 1986, 151 (01) :151-156