Genetic variation in the 3′ non-coding region of dengue viruses

被引:93
作者
Shurtleff, AC
Beasley, DWC
Chen, JJY
Ni, HL
Suderman, MT
Wang, HM
Xu, RL
Wang, E
Weaver, SC
Watts, DM
Russell, KL
Barrett, ADT [1 ]
机构
[1] Univ Texas, Med Branch, Ctr Trop Dis, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77555 USA
[3] Naval Med Res Ctr Detachment, Lima, Peru
关键词
dengue virus; 3 ' non-coding region; flaviviruses; reverse transcription-polymerase chain reaction;
D O I
10.1006/viro.2000.0748
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The 3' non-coding region (3'NCR) of strains of dengue 1 (DEN 1), DEN 2, DEN 3, and DEN 4 viruses, isolated in different geographical regions, was sequenced and compared to published sequences of the four dengue viruses. A total of 50 DEN 2 strains was compared: 7 West African strains, 3 Indonesian mosquito strains, 1 Indonesian macaque isolate, and 39 human isolates from Southeast Asia, the South Pacific, and the Caribbean and Americas. Nucleotide sequence alignment revealed few deletions and no repeat sequences in the 3' NCR of DEN 2 viruses and showed that much of the 3' NCR was well conserved. The strains could be divided into two groups, sylvatic and human/mosquito/macaque, based on nucleotide sequence homology. A hypervariable region was identified immediately following the NS5 stop codon, which involved a 2-10 nucleotide deletion in human, mosquito, and macaque isolates compared with the sylvatic strains. The DEN 2 3'NCR was also compared with 3'NCR sequences from strains of DEN 1, DEN 3, and DEN 4 viruses. DEN 1 was found to have four copies of an eight nucleotide imperfect repeat following the NS5 stop codon, while DEN 4 virus had a deletion of 75 nucleotides in the 3'NCR. We propose that the variation in nucleotide sequence in the 3'NCR may have evolved as a function of DEN virus transmission and replication in different mosquito and non-human primate/human host cycles. The results from this study are consistent with the hypothesis that DEN viruses arose from sylvatic progenitors and evolved into human epidemic strains. However, the data do not support the hypothesis that variation in the 3'NCR correlates with DEN virus pathogenesis. (C) 2001 Academic Press.
引用
收藏
页码:75 / 87
页数:13
相关论文
共 44 条
[1]   BHK CELL-PROTEINS THAT BIND TO THE 3' STEM-LOOP STRUCTURE OF THE WEST NILE VIRUS GENOME RNA [J].
BLACKWELL, JL ;
BRINTON, MA .
JOURNAL OF VIROLOGY, 1995, 69 (09) :5650-5658
[2]   NUCLEOTIDE-SEQUENCE AND DEDUCED AMINO-ACID SEQUENCE OF THE NONSTRUCTURAL PROTEINS OF DENGUE TYPE-2 VIRUS, JAMAICA GENOTYPE - COMPARATIVE-ANALYSIS OF THE FULL-LENGTH GENOME [J].
DEUBEL, V ;
KINNEY, RM ;
TRENT, DW .
VIROLOGY, 1988, 165 (01) :234-244
[3]  
FELSENSTEIN J, 1985, EVOLUTION, V39, P783, DOI 10.1111/j.1558-5646.1985.tb00420.x
[4]   FULL-LENGTH CDNA SEQUENCE OF DENGUE TYPE-1 VIRUS (SINGAPORE STRAIN S275/90) [J].
FU, JL ;
TAN, BH ;
YAP, EH ;
CHAN, YC ;
TAN, YH .
VIROLOGY, 1992, 188 (02) :953-958
[5]   Complete sequence of two tick-borne flaviviruses isolated from Siberia and the UK: Analysis and significance of the 5' and 3'-UTRs [J].
Gritsun, TS ;
Venugopal, K ;
Zanotto, PMD ;
Mikhailov, MV ;
Sall, AA ;
Holmes, EC ;
Polkinghorne, I ;
Frolova, TV ;
Pogodina, VV ;
Lashkevich, VA ;
Gould, EA .
VIRUS RESEARCH, 1997, 49 (01) :27-39
[6]  
Gubler DJ, 1997, FACTORS IN THE EMERGENCE OF ARBOVIRUS DISEASES, P83
[7]   CONSERVED ELEMENTS IN THE 3' UNTRANSLATED REGION OF FLAVIVIRUS RNAS AND POTENTIAL CYCLIZATION SEQUENCES [J].
HAHN, CS ;
HAHN, YS ;
RICE, CM ;
LEE, E ;
DALGARNO, L ;
STRAUSS, EG ;
STRAUSS, JH .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 198 (01) :33-41
[8]   NUCLEOTIDE-SEQUENCE OF DENGUE-2 RNA AND COMPARISON OF THE ENCODED PROTEINS WITH THOSE OF OTHER FLAVIVIRUSES [J].
HAHN, YS ;
GALLER, R ;
HUNKAPILLER, T ;
DALRYMPLE, JM ;
STRAUSS, JH ;
STRAUSS, EG .
VIROLOGY, 1988, 162 (01) :167-180
[9]   The causes and consequences of genetic variation in dengue virus [J].
Holmes, EC ;
Burch, SS .
TRENDS IN MICROBIOLOGY, 2000, 8 (02) :74-77
[10]   SEQUENCE-ANALYSIS OF CLONED DENGUE VIRUS TYPE-2 GENOME (NEW-GUINEA-C STRAIN) [J].
IRIE, K ;
MOHAN, PM ;
SASAGURI, Y ;
PUTNAK, R ;
PADMANABHAN, R .
GENE, 1989, 75 (02) :197-211