Das Biswadeep, Patra Aparna P, Das Mumani, Mahapatra Namita, Tripathy Harekrushna, Kar Santanu K, Hazra Rupenangshu K
Regional Medical Research Centre, Chandrasekharpur, Bhubaneswar 751023, Odisha, India.
Regional Medical Research Centre, Chandrasekharpur, Bhubaneswar 751023, Odisha, India.
Acta Trop. 2014 Sep;137:130-9. doi: 10.1016/j.actatropica.2014.05.002. Epub 2014 May 10.
Anopheles annularis is one of the major vectors of malaria in Odisha, India. The present study was undertaken to determine the vectorial capacity and assess the genetic diversity of An. annularis collected from different endemic regions of Odisha. Mosquitoes were collected from thirteen endemic districts using standard entomological collection methods from 2009 to 2011. Sibling species of An. annularis were identified by PCR-RFLP and sequencing of D3 region of 28S ribosomal DNA (rDNA) region. Plasmodium falciparum (Pf) sporozoite rate and human blood fed percentage (HBF) were estimated by multiplex PCR using Pf and human specific primers. Genetic diversity of An. annularis was estimated by ISSR markers. Out of 1647 An. annularis collected, 1353 (82.15%) were collected by mechanical aspirators and 294 (17.85%) by light trap. 49 (2.97%) were positive for human blood and 18 (1.09%) were positive for Pf sporozoite. PCR-RFLP and sequencing analyses detected only An annularis A in the study areas. Overall genetic differentiation among An. annularis populations was moderate (FST=0.048) and showed significant correlation between genetic distance and geographic distance (r=0.882; P<0.05). Angul population proved to be genetically unique and was highly divergent FST>0.110) from other populations, suggesting low gene flow between them. The study indicated that only An. annularis A was found in Odisha with potential vectorial capacity that can play a major role in malaria transmission. ISSR markers proved to be useful molecular tools to evaluate genetic variability in An. annularis populations.
环纹按蚊是印度奥里萨邦疟疾的主要传播媒介之一。本研究旨在确定环纹按蚊的传病力,并评估从奥里萨邦不同流行地区采集的环纹按蚊的遗传多样性。2009年至2011年期间,采用标准昆虫学采集方法从13个流行区收集蚊子。通过PCR-RFLP和28S核糖体DNA(rDNA)区域D3区测序鉴定环纹按蚊的近缘种。使用恶性疟原虫(Pf)和人类特异性引物通过多重PCR估计恶性疟原虫子孢子率和人血喂养百分比(HBF)。通过ISSR标记估计环纹按蚊的遗传多样性。在收集的1647只环纹按蚊中,1353只(82.15%)通过机械吸气器收集,294只(17.85%)通过诱虫灯收集。49只(2.97%)人血检测呈阳性,18只(1.09%)Pf子孢子检测呈阳性。PCR-RFLP和测序分析在研究区域仅检测到环纹按蚊A。环纹按蚊种群之间的总体遗传分化程度中等(FST=0.048),遗传距离与地理距离之间存在显著相关性(r=0.882;P<0.05)。安古尔种群在遗传上被证明是独特的,并且与其他种群高度分化(FST>0.110),表明它们之间的基因流动较低。该研究表明,在奥里萨邦仅发现了具有潜在传病力的环纹按蚊A,其在疟疾传播中可发挥主要作用。ISSR标记被证明是评估环纹按蚊种群遗传变异性的有用分子工具。