Dash Paban Kumar, Parida Man Mohan, Saxena Parag, Abhyankar Ajay, Singh C P, Tewari K N, Jana Asha Mukul, Sekhar K, Rao P V Lakshmana
Division of Virology, Defence R&D Establishment, Jhansi Road, Gwalior- 474002, MP, India.
Virol J. 2006 Jul 6;3:55. doi: 10.1186/1743-422X-3-55.
Dengue virus infection has recently taken endemic proportion in India implicating all the four known dengue serotypes. There was a major dengue outbreak in northern India including Delhi in October- December, 2003 and again in 2004. We have carried out a detailed investigation of the 2004 outbreak by Serosurveillance, RT-PCR, nested PCR, virus isolation and genotyping. We also report the molecular epidemiological investigation of these outbreaks.
The serological investigation of 162 suspected serum samples using an in-house dengue dipstick ELISA revealed 11%-IgM, 51%-IgG and 38%-both IgM and IgG antibody positivity. The RT-PCR analysis revealed presence of dengue RNA in 17 samples. Further subtyping and genotyping by nested PCR and nucleotide sequencing of C-prM gene junction revealed the association of subtype III of dengue virus type 3 in the outbreak.
The sudden shifting and dominance of the dengue virus serotype-3 (subtype III) replacing the earlier circulating serotype-2 (subtype IV) is a point of major concern and may be attributed to increased incidence of DHF and DSS in India.
登革病毒感染最近在印度呈地方流行态势,涉及所有四种已知的登革热血清型。2003年10月至12月以及2004年,印度北部包括德里在内发生了大规模登革热疫情。我们通过血清学监测、逆转录聚合酶链反应(RT-PCR)、巢式PCR、病毒分离和基因分型对2004年的疫情进行了详细调查。我们还报告了这些疫情的分子流行病学调查情况。
使用自制的登革热试纸条酶联免疫吸附测定法(ELISA)对162份疑似血清样本进行血清学调查,结果显示11%样本IgM呈阳性,51%样本IgG呈阳性,38%样本IgM和IgG抗体均呈阳性。RT-PCR分析显示17份样本中存在登革热RNA。通过巢式PCR和C-prM基因连接处的核苷酸测序进行进一步的亚型分析和基因分型,结果显示此次疫情与登革热病毒3型的III亚型有关。
登革热病毒血清型3(III亚型)突然取代早期流行的血清型2(IV亚型)并占据主导地位,这是一个主要的关注点,可能是印度登革出血热(DHF)和登革休克综合征(DSS)发病率增加的原因。