Anoop M, Mathew Ashish J, Jayakumar B, Issac Aneesh, Nair Sajith, Abraham Rachy, Anupriya M G, Sreekumar E
Rajiv Gandhi Centre for Biotechnology, Thycaud PO, Thiruvananthapuram, 695014 Kerala, India.
Virus Genes. 2012 Aug;45(1):1-13. doi: 10.1007/s11262-012-0756-3. Epub 2012 May 22.
In this study, dengue virus (DENV) isolates from a localized, small-scale, non-seasonal dengue outbreak were genetically characterized. The outbreak occurred during the pre-monsoon months (April-May) in a medical college campus in Kerala, South India in 2009 affecting 76 people. Analysis of 39 viral RNA positive serum samples by a serotype specific reverse-transcription polymerase chain reaction identified dengue virus serotype 1 (DENV1) as the causative strain. Formation of a distinct genetic clade was revealed in the initial phylogenetic analysis using nucleotide sequences of a partial (303 bp) Capsid-Pre-membrane protein (C-PrM) coding region of 37 outbreak strains. The sequences of these strains clustered with that of the Genotype III DENV-1 strains from India, and 32 among them formed a single major sub-clade. Whole-genome sequencing (10,693 bp) of two strains (RGCB585/2009 and RGCB592/2009) selected from this major sub-clade, and subsequent phylogenetic analysis using the full-length coding region sequence showed that the sequences grouped with that of the isolates from Thailand (1980), Comoros (1993), Singapore (1993), and Brunei (2005) among the Indo-Pacific isolates. The sequences of the two strains had a nucleotide identity of 97-98 % and an amino acid identity of 98-99 % with these closely related strains. Maximum amino acid similarity was shown with the Singapore 8114/93 isolate (99.6 %). Four mutations-L46M in the capsid, D278N in the NS1, L123I, and L879S in the NS5 protein coding regions-were seen as signature substitutions uniformly in RGCB585/2009 and RGCB592/2009; in another isolate from Kerala (RGCB419/2008) and in the Brunei isolate (DS06-210505). These four isolates also had in common a 21-nucleotide deletion in the hyper-variable region of the 3'-non-translated region. This first report on the complete genome characterization of DENV-1 isolates from India reveals a dengue outbreak caused by a genetically different viral strain. The results point to the possibility of exotic introduction of these circulating viral strains in the region.
在本研究中,对来自局部小规模非季节性登革热疫情的登革热病毒(DENV)分离株进行了基因特征分析。该疫情于2009年印度南部喀拉拉邦一所医学院校园的季风前月份(4月至5月)爆发,影响了76人。通过血清型特异性逆转录聚合酶链反应对39份病毒RNA阳性血清样本进行分析,确定登革热病毒血清型1(DENV1)为致病菌株。在对37株疫情菌株的衣壳-前膜蛋白(C-PrM)编码区部分(303 bp)核苷酸序列进行的初步系统发育分析中,发现形成了一个独特的遗传分支。这些菌株的序列与来自印度的基因型III DENV-1菌株聚类,其中32株形成了一个主要的亚分支。从这个主要亚分支中选择的两株菌株(RGCB585/2009和RGCB592/2009)进行全基因组测序(10,693 bp),随后使用全长编码区序列进行系统发育分析,结果表明这些序列与印度-太平洋分离株中来自泰国(1980年)、科摩罗(1993年)、新加坡(1993年)和文莱(2005年)的分离株聚类。这两株菌株的序列与这些密切相关菌株的核苷酸同一性为97 - 98%,氨基酸同一性为98 - 99%。与新加坡8114/93分离株的氨基酸相似性最高(99.6%)。在RGCB585/2009和RGCB592/2009中均匀地观察到四个突变——衣壳中的L46M、NS1中的D278N、NS5蛋白编码区中的L123I和L879S;在来自喀拉拉邦的另一株分离株(RGCB419/2008)和文莱分离株(DS06 - 210505)中也有这些突变。这四株分离株在3' - 非翻译区的高变区还共同存在一个21核苷酸缺失。这份关于印度DENV-1分离株全基因组特征的首次报告揭示了由基因不同的病毒株引起的登革热疫情。结果表明该地区存在这些传播病毒株外来引入的可能性。