Nyari N, Maan H S, Sharma S, Pandey S N, Dhole T N
Department of Microbiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Rai Barelly Road, Lucknow 226014, Uttar Pradesh, India.
Department of Botany, Lucknow University Uttar Pradesh, India.
Acta Trop. 2016 Jun;158:117-124. doi: 10.1016/j.actatropica.2016.02.019. Epub 2016 Mar 2.
Chikungunya fever is an emerging mosquito-borne disease caused by the infection with chikungunya virus (CHIKV). The CHIKV has been rarely detected in mosquito vectors from Northern India, since vector surveillance is an effective strategy in controlling and preventing CHIKV transmission. Thus, virological investigation for CHIKV among mosquitoes of Aedes (A.) species was carried out in the Lucknow district during March 2010 to October 2011. We collected adult mosquitoes from areas with CHIKV positive patients. The adult Aedes mosquito samples were pooled, homogenized, clarified and tested for CHIKV by nonstructural protein 1 (nsP1) gene based polymerase chain reaction (PCR). A total 91 mosquito pools comprising of adult A. aegypti and A. albopictus were tested for CHIKV. The partial envelope protein (E1) gene sequences of mosquito-borne CHIKV strains were analyzed for genotyping. Of 91 pools, 6 pools of A. aegypti; and 2 pools of A. albopictus mosquitoes were identified positive for CHIKV by PCR. The phylogenetic analysis revealed clustering of CHIKV strains in two sub-lineages within the monophyletic East-Central South African (ECSA) genotype. Novel amino acid changes at the positions 294 (P294L) and 295 (S295F) were observed during analysis of amino acid sequence of the partial E1 gene. This study demonstrates the genetic diversity of circulating CHIKV strains and reports the first detection of CHIKV strains in Aedes vector species from the state of Uttar Pradesh. These findings have implication for vector control strategies to mitigate vector population to prevent the likelihood of CHIKV epidemic in the near future.
基孔肯雅热是一种由感染基孔肯雅病毒(CHIKV)引起的新发蚊媒疾病。由于媒介监测是控制和预防CHIKV传播的有效策略,在印度北部的蚊媒中很少检测到CHIKV。因此,于2010年3月至2011年10月在勒克瑙地区对伊蚊属蚊子进行了CHIKV的病毒学调查。我们从有CHIKV阳性患者的地区收集成年蚊子。将成年伊蚊样本汇集、匀浆、澄清,并通过基于非结构蛋白1(nsP1)基因的聚合酶链反应(PCR)检测CHIKV。总共对91个包含埃及伊蚊和白纹伊蚊成虫的蚊群进行了CHIKV检测。对蚊媒传播的CHIKV毒株的部分包膜蛋白(E1)基因序列进行分析以进行基因分型。在91个蚊群中,有6个埃及伊蚊蚊群和2个白纹伊蚊蚊群经PCR鉴定为CHIKV阳性。系统发育分析显示,CHIKV毒株在单系东中非南非(ECSA)基因型内的两个亚谱系中聚类。在分析部分E1基因的氨基酸序列时,在第294位(P294L)和第295位(S295F)观察到新的氨基酸变化。本研究证明了流行的CHIKV毒株的遗传多样性,并报告了在北方邦首次从伊蚊媒介物种中检测到CHIKV毒株。这些发现对媒介控制策略具有启示意义,以减少媒介种群数量,防止在不久的将来发生CHIKV流行。