Saha Pabitra, Ganguly Swagata, Maji Ardhendu K
Calcutta School of Tropical Medicine, 108, C. R. Avenue, Kolkata 700 073, India; Department of Zoology, A. P. C. Roy Govt. College, Himachal Bihar, Matigara, Siliguri, 734010, West Bengal, India.
Calcutta School of Tropical Medicine, 108, C. R. Avenue, Kolkata 700 073, India; Department of Microbiology, N. R. S. Medical College & Hospital, Kolkata, West Bengal, India.
Infect Genet Evol. 2016 Sep;43:239-44. doi: 10.1016/j.meegid.2016.05.038. Epub 2016 May 31.
The study of genetic diversity of Plasmodium falciparum is necessary to understand the distribution and dynamics of parasite populations. The genetic diversity of P. falciparum merozoite surface protein-1 and 2 has been extensively studied from different parts of world. However, limited data are available from India. This study was aimed to determine the genetic diversity and multiplicity of infection (MOI) of P. falciparum population in Kolkata, West Bengal, India. A total of 80day-zero blood samples from Kolkata were collected during a therapeutic efficacy study in 2008-2009. DNA was extracted; allelic frequency and diversity were investigated by PCR-genotyping method for msp1 and msp2 gene and fragment sizing was done by Bio-Rad Gel-Doc system using Image Lab (version 4.1) software. P. falciparum msp1 and msp2 markers were highly polymorphic with low allele frequencies. In Kolkata, 27 msp1 different genotypes (including 11of K1, 6 of MAD20 and 10 of Ro33 allelic families) and 30 different msp2 genotypes (of which 17 and 13 belonged to the FC27 and 3D7 allelic families, respectively) were recorded. The majority of these genotypes occurred at a frequency below 10%. The mean MOI for msp1 and msp2 gene were 2.05 and 3.72, respectively. The P. falciparum population of Kolkata was genetically diverse. As the frequencies of most of the msp1 and msp2 alleles were low, the probability of new infection with genotype identical to that in pretreatment infection was very rare. This information will serve as baseline data for evaluation of malaria control interventions as well as for monitoring the parasite population structure.
研究恶性疟原虫的遗传多样性对于理解寄生虫种群的分布和动态十分必要。世界各地已对恶性疟原虫裂殖子表面蛋白-1和-2的遗传多样性展开了广泛研究。然而,印度的相关数据有限。本研究旨在确定印度西孟加拉邦加尔各答市恶性疟原虫种群的遗传多样性和感染复数(MOI)。2008年至2009年在一项治疗效果研究期间,共采集了加尔各答市80份零日血样。提取DNA;采用PCR基因分型方法对msp1和msp2基因进行等位基因频率和多样性研究,并使用Bio-Rad凝胶成像系统及Image Lab(4.1版)软件进行片段大小测定。恶性疟原虫msp1和msp2标记具有高度多态性,等位基因频率较低。在加尔各答,记录到27种不同的msp1基因型(包括11种K1、6种MAD20和10种Ro33等位基因家族)以及30种不同的msp2基因型(其中17种和13种分别属于FC27和3D7等位基因家族)。这些基因型中的大多数出现频率低于10%。msp1和msp2基因的平均MOI分别为2.05和3.72。加尔各答的恶性疟原虫种群具有遗传多样性。由于大多数msp1和msp2等位基因的频率较低,新感染与治疗前感染基因型相同的可能性非常小。这些信息将作为评估疟疾控制干预措施以及监测寄生虫种群结构的基线数据。