Complete Genome Characterisation of a Novel 26th Bluetongue Virus Serotype from Kuwait

被引:140
作者
Maan, Sushila [1 ]
Maan, Narender S. [1 ]
Nomikou, Kyriaki [1 ]
Veronesi, Eva [1 ]
Bachanek-Bankowska, Katarzyna [1 ]
Belaganahalli, Manjunatha N. [1 ]
Attoui, Houssam [1 ]
Mertens, Peter P. C. [1 ]
机构
[1] Inst Anim Hlth, Vector Borne Dis Programme, Woking, Surrey, England
来源
PLOS ONE | 2011年 / 6卷 / 10期
基金
英国生物技术与生命科学研究理事会;
关键词
COMPLETE NUCLEOTIDE-SEQUENCE; AFRICAN HORSE SICKNESS; RT-PCR ASSAY; PHYLOGENETIC ANALYSIS; PURIFYING SELECTION; POSITIVE SELECTION; MULTIPLE ALIGNMENT; FAMILY REOVIRIDAE; ANALYSIS TOOLS; ORBIVIRUS;
D O I
10.1371/journal.pone.0026147
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bluetongue virus is the "type'' species of the genus Orbivirus, family Reoviridae. Twenty four distinct bluetongue virus (BTV) serotypes have been recognized for decades, any of which is thought to be capable of causing "bluetongue'' (BT), an insect-borne disease of ruminants. However, two further BTV serotypes, BTV-25 (Toggenburg orbivirus, from Switzerland) and BTV-26 (from Kuwait) have recently been identified in goats and sheep, respectively. The BTV genome is composed of ten segments of linear dsRNA, encoding 7 virus-structural proteins (VP1 to VP7) and four distinct non-structural (NS) proteins (NS1 to NS4). We report the entire BTV-26 genome sequence (isolate KUW2010/02) and comparisons to other orbiviruses. Highest identity levels were consistently detected with other BTV strains, identifying KUW2010/02 as BTV. The outer-core protein and major BTV serogroup-specific antigen "VP7'' showed 98% aa sequence identity with BTV-25, indicating a common ancestry. However, higher level of variation in the nucleotide sequence of Seg-7 (81.2% identity) suggests strong conservation pressures on the protein of these two strains, and that they diverged a long time ago. Comparisons of Seg-2, encoding major outer-capsid component and cell-attachment protein "VP2'' identified KUW2010/02 as 26th BTV, within a 12th Seg-2 nucleotype [nucleotype L]. Comparisons of Seg-6, encoding the smaller outer capsid protein VP5, also showed levels of nt/aa variation consistent with identification of KUW2010/02 as BTV-26 (within a 9th Seg-6 nucleotype - nucleotype I). Sequence data for Seg-2 of KUW2010/02 were used to design four sets of oligonucleotide primers for use in BTV-26, type-specific RT-PCR assays. Analyses of other more conserved genome segments placed KUW2010/02 and BTV-25/SWI2008/01 closer to each other than to other "eastern'' or "western'' BTV strains, but as representatives of two novel and distinct geographic groups (topotypes). Our analyses indicate that all of the BTV genome segments have evolved under strong purifying selection.
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