ICMR-Regional Medical Research Centre, Dibrugarh, India.
Weill Cornell Medicine-Qatar, Cornell University, Doha, Qatar.
Indian J Med Res. 2017 Sep;146(3):375-380. doi: 10.4103/ijmr.IJMR_291_16.
BACKGROUND & OBJECTIVES: Northeast (NE) India is one of the high endemic regions for malaria with a preponderance of Plasmodium falciparum, resulting in high morbidity and mortality. The P. falciparum parasite of this region showed high polymorphism in drug-resistant molecular biomarkers. However, there is a paucity of information related to merozoite surface protein 1 (msp-1) and glutamate-rich protein (glurp) which have been extensively studied in various parts of the world. The present study was, therefore, aimed at investigating the genetic diversity of P. falciparum based on msp-1 and glurp in Arunachal Pradesh, a State in NE India.
Two hundred and forty nine patients with fever were screened for malaria, of whom 75 were positive for P. falciparum. Blood samples were collected from each microscopically confirmed patient. The DNA was extracted; nested polymerase chain reaction and sequencing were performed to study the genetic diversity of msp-1 (block 2) and glurp.
The block 2 of msp-1 gene was found to be highly polymorphic, and overall allelic distribution showed that RO33 was the dominant allele (63%), followed by MAD20 (29%) and K1 (8%) alleles. However, an extensive diversity (9 alleles and 4 genotypes) and 6-10 repeat regions exclusively of R2 type were observed in glurp.
INTERPRETATION & CONCLUSIONS: The P. falciparum population of NE India was diverse which might be responsible for higher plasticity leading to the survival of the parasite and in turn to the higher endemicity of falciparum malaria of this region.
印度东北部(NE)是疟疾高发地区之一,以恶性疟原虫(Plasmodium falciparum)为主,导致发病率和死亡率较高。该地区的恶性疟原虫寄生虫在耐药性分子生物标志物方面表现出高度多态性。然而,有关裂殖子表面蛋白 1(msp-1)和谷氨酸丰富蛋白(glurp)的信息很少,这些蛋白在世界其他地区已经得到了广泛研究。因此,本研究旨在调查印度东北部的阿鲁纳恰尔邦(Arunachal Pradesh)基于 msp-1 和 glurp 的恶性疟原虫的遗传多样性。
对 249 例发热患者进行疟疾筛查,其中 75 例为恶性疟原虫阳性。从每个经显微镜确认的患者采集血液样本。提取 DNA;进行巢式聚合酶链反应和测序,以研究 msp-1(第 2 块)和 glurp 的遗传多样性。
msp-1 基因的第 2 块表现出高度多态性,总体等位基因分布表明 RO33 是主要等位基因(63%),其次是 MAD20(29%)和 K1(8%)等位基因。然而,在 glurp 中观察到广泛的多样性(9 个等位基因和 4 种基因型)和 6-10 个重复区仅为 R2 型。
印度东北部的恶性疟原虫种群多样,这可能是导致寄生虫更高可塑性的原因,从而导致该地区恶性疟的更高流行率。