Genomic analysis of diverse rubella virus genotypes

被引:27
作者
Zhou, Yumei
Ushijima, Hiroshi
Frey, Teryl K.
机构
[1] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
[2] Univ Tokyo, Grad Sch Med, Dept Dev Med Sci, Inst Int Hlth, Tokyo, Japan
关键词
D O I
10.1099/vir.0.82495-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Based on the sequence of the El glycoprotein gene, two clades and ten genotypes of Rubella virus have been distinguished; however, genomic sequences have been determined for viruses in only two of these genotypes. In this report, genomic sequences for viruses in an additional six genotypes were determined. The genome was found to be well conserved. The viruses in all eight of these genotypes had the same number of nucleotides in each of the two open reading frames (ORFs) and the untranslated regions (UTRs) at the 5' and 3' ends of the genome. Only the UTR between the ORFs (the junction region) exhibited differences in length. Of the nucleotides in the genome, 78 % were invariant. The greatest observed distance between viruses in different genotypes was 8.74 % and the maximum calculated genetic distance was 14.78 substitutions in 100 sites. This degree of variability was similar among regions of the genome with two exceptions, both within the P150 non-structural protein gene: the N-terminal region that encodes the methyl/guanylyltransferase, domain was less variable, whereas the hypervariable domain in the middle of the gene was more divergent. Comparative phylogenetic analysis of different regions of the genome was done, using sequences from 43 viruses of the non-structural protease (near the 5' end of the genome), the junction region (the middle) and the El gene (the 3' end). Phylogenetic segregation of sequences from these three genomic regions was similar with the exception of genotype 1 B viruses, among which a recombinational event near the junction region was identified.
引用
收藏
页码:932 / 941
页数:10
相关论文
共 45 条
[1]  
[Anonymous], 2005, WKLY EPIDEMIOL REC
[2]   Phylogenetic analysis of hepatitis E virus isolates from India (1976-1993) [J].
Arankalle, VA ;
Paranjape, S ;
Emerson, SU ;
Purcell, RH ;
Walimbe, AM .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :1691-1700
[3]   Nucleotide sequence analysis of a major antigenic domain of the E1 glycoprotein of 22 rubella virus isolates [J].
Bosma, TJ ;
Best, JM ;
Corbett, KM ;
Banatvala, JE ;
Starkey, WG .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :2523-2530
[4]  
CHANTLER J, 2001, FIELDS VIROLOGY, P963
[5]   NUCLEOTIDE-SEQUENCE AND INVITRO EXPRESSION OF RUBELLA-VIRUS 24S SUBGENOMIC MESSENGER-RNA ENCODING THE STRUCTURAL PROTEIN-E1, PROTEIN-E2 AND PROTEIN-C [J].
CLARKE, DM ;
LOO, TW ;
HUI, I ;
CHONG, P ;
GILLAM, S .
NUCLEIC ACIDS RESEARCH, 1987, 15 (07) :3041-3057
[6]   SEQUENCE OF THE GENOME RNA OF RUBELLA-VIRUS - EVIDENCE FOR GENETIC REARRANGEMENT DURING TOGAVIRUS EVOLUTION [J].
DOMINGUEZ, G ;
WANG, CY ;
FREY, TK .
VIROLOGY, 1990, 177 (01) :225-238
[7]   The genomic analysis of rubella virus detected from outbreak and sporadic cases in Rio de Janeiro state, Brazil [J].
Donadio, FF ;
Siqueira, MM ;
Vyse, A ;
Jin, L ;
Oliveira, SA .
JOURNAL OF CLINICAL VIROLOGY, 2003, 27 (02) :205-209
[8]   MOLECULAR-BIOLOGY OF RUBELLA-VIRUS [J].
FREY, TK .
ADVANCES IN VIRUS RESEARCH, VOL 44, 1994, 44 :69-160
[9]   Molecular analysis of rubella virus epidemiology across three continents, North America, Europe, and Asia, 1961-1997 [J].
Frey, TK ;
Abernaty, ES ;
Bosma, TJ ;
Starkey, WG ;
Corbett, KM ;
Best, JM ;
Katow, S ;
Weaver, SC .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (03) :642-650
[10]   Hepatitis E virus: complete genome sequence and phylogenetic analysis of a Nepali isolate [J].
Gouvea, V ;
Snellings, N ;
Popek, MJ ;
Longer, CF ;
Innis, BL .
VIRUS RESEARCH, 1998, 57 (01) :21-26