Viral Disease Biology Program, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.
Virol J. 2013 Jan 29;10:37. doi: 10.1186/1743-422X-10-37.
Local epidemiology of Dengue is defined by the genetic diversity of the circulating Dengue virus (DENV) strains. This important information is not available for the virus strains from most parts of the Indian subcontinent. The present study focused on the genetic diversity of the serotype 3 DENV strains (DENV-3) from India.
A total of 22 DENV-3 strains identified by reverse-transcription PCR analysis of serum samples from 709 patients were studied. These samples were collected over a period of 4 years (2008-2011) from dengue fever suspected patients from Kerala, a dengue endemic state in South India. Comparison of a 1740bp nucleotide sequence of the viral Capsid-Pre-membrane-Envelope coding region of our strains and previously reported DENV-3 strains from India, South Asia and South America revealed non-synonymous substitutions that were genotype III-specific as well as sporadic. Evidence of positive selection was detected in the I81 amino acid residue of the envelope protein. Out of the 22 samples, three had I81A and 18 had I81V substitutions. In the phylogenetic analysis by maximum likelihood method the strains from Kerala clustered in two different lineages (lineage III and IV) within genotype III clade of DENV-3 strains. The ten strains that belonged to lineage IV had a signature amino acid substitution T219A in the envelope protein. Interestingly, all these strains were found to be closely related to a Singapore strain GU370053 isolated in 2007.
Our study identifies for the first time the presence of lineage IV strains in the Indian subcontinent. Results indicate the possibility of a recent exotic introduction and also a shift from the existing lineage III strains to lineage IV. Lineage shifts in DENV-3 strains have been attributed to dramatic increase in disease severity in many parts of the world. Hence the present observation could be significant in terms of the clinical severity of future dengue cases in the region.
登革热的局部流行病学由循环登革病毒(DENV)株的遗传多样性定义。对于印度次大陆大部分地区的病毒株,这一重要信息尚不清楚。本研究集中于印度血清型 3 登革热病毒(DENV-3)的遗传多样性。
对来自喀拉拉邦 709 例疑似登革热患者血清样本进行逆转录-PCR 分析,共鉴定出 22 株 DENV-3 株。这些样本是在 4 年(2008-2011 年)期间从印度南部的登革热流行州喀拉拉邦采集的。对我们的菌株和之前报道的来自印度、南亚和南美洲的 DENV-3 菌株的病毒衣壳-前膜-包膜编码区的 1740bp 核苷酸序列进行比较,发现非同义突变是 III 型特有的,也是散在的。在包膜蛋白的 I81 氨基酸残基中检测到正选择的证据。在 22 个样本中,有 3 个样本具有 I81A 和 18 个样本具有 I81V 取代。在最大似然法的系统进化分析中,来自喀拉拉邦的菌株聚类在 DENV-3 株 III 型聚类的两个不同谱系(谱系 III 和 IV)中。属于谱系 IV 的 10 株菌株在包膜蛋白中具有 T219A 特征性氨基酸取代。有趣的是,所有这些菌株都与 2007 年分离的新加坡株 GU370053 密切相关。
本研究首次在印度次大陆发现了谱系 IV 株的存在。结果表明,最近有外来菌株传入的可能性,以及从现有谱系 III 菌株向谱系 IV 的转变。DENV-3 株的谱系转变归因于世界许多地区疾病严重程度的急剧增加。因此,这一观察结果可能对该地区未来登革热病例的临床严重程度具有重要意义。