Kumar Dinesh, Dhiman Sunil, Rabha Bipul, Goswami Diganta, Deka Manab, Singh Lokendra, Baruah Indra, Veer Vijay
Medical Entomology Division, Defence Research Laboratory, Tezpur, Assam 784001, India.
Malar J. 2014 Nov 21;13:450. doi: 10.1186/1475-2875-13-450.
The R2 repeat region of GLURP has been reported as a good genetic marker for Plasmodium falciparum genotyping. Proper knowledge of the extent and nature of P. falciparum genetic diversity using highly immunogenic R2 repeat region in malaria-endemic areas is a crucial element to understand various aspects related to immunity acquisition and disease pathogenesis.
Population diversity of P. falciparum GLURP and amino acid sequence repeats in GLURP R2 region was studied in malaria-endemic Assam state, northeast India and compared at an interval of five years during 2005 (Group-A) and 2011 (Group-B).
Of the 66 samples, a total of 55 samples showed positive PCR bands for GLURP R2 region and altogether ten types of alleles with size ranging from 501 bp to 1,050 bp (50 bp bin) were observed and coded as genotypes I-X. In Group-A (n = 29), 24 samples were found infected with single, four with double and one with triple P. falciparum genotype, while in Group-B (n = 26), single genotype was found in 23 samples, double in two samples and triple in one sample. Genotype IV showed significant increase (p = 0.002) during 2011 (Group-B). Genotypes I to V were more common in Group-B (62%), however genotypes VI to X were more frequently distributed in Group-A. The expected heterozygosity was found slightly higher in Group-A (HE = 0.87) than Group-B (HE = 0.85), whereas multiplicity of infection (MOI) in Group-A (MOI = 1.21 ± 0.49) and Group-B (MOI = 1.12 ± 0.43) did not display significant variation. The amino acid repeat sequence unit (AAU) DKNEKGQHEIVEVEEILPE (called 'a') was more frequent in the well-conserved part of R2 repeat region.
The present study is the first extensive study in India which has generated substantial data for understanding the type and distribution of naturally evolved genetic polymorphism at amino acid sequence level in GLURP R2 repeat region in P. falciparum. There was decrease in the PCR amplicon size as well as the number of AAU [amino acid repeat unit] in Group-B displaying the bottleneck effect. The present study described a new type of AAU 'd' which varied from the other previous known AAUs.
已报道谷氨酸富蛋白(GLURP)的R2重复区域是恶性疟原虫基因分型的良好遗传标记。利用疟疾流行地区高免疫原性的R2重复区域,充分了解恶性疟原虫遗传多样性的程度和性质,是理解与免疫获得和疾病发病机制相关的各个方面的关键要素。
在印度东北部疟疾流行的阿萨姆邦研究了恶性疟原虫GLURP的群体多样性和GLURP R2区域的氨基酸序列重复,并在2005年(A组)和2011年(B组)期间每隔五年进行比较。
在66个样本中,共有55个样本的GLURP R2区域PCR条带呈阳性,共观察到10种等位基因,大小从501 bp到1050 bp(以50 bp为间隔),并编码为基因型I-X。在A组(n = 29)中,发现24个样本感染单一恶性疟原虫基因型,4个感染双重基因型,1个感染三重基因型;而在B组(n = 26)中,23个样本为单一基因型,2个为双重基因型,1个为三重基因型。2011年(B组)基因型IV显著增加(p = 0.002)。基因型I至V在B组中更常见(62%),然而基因型VI至X在A组中分布更频繁。发现A组的预期杂合度(HE = 0.87)略高于B组(HE = 0.85),而A组(MOI = 1.21±0.49)和B组(MOI = 1.12±0.43)的感染复数未显示出显著差异。氨基酸重复序列单元(AAU)DKNEKGQHEIVEVEEILPE(称为“a”)在R2重复区域的保守部分更频繁出现。
本研究是印度首次进行的广泛研究,已生成大量数据,用于了解恶性疟原虫GLURP R2重复区域氨基酸序列水平上自然进化的遗传多态性的类型和分布。B组中PCR扩增子大小以及AAU(氨基酸重复单元)数量减少,显示出瓶颈效应。本研究描述了一种新型的AAU“d”,它与先前已知的其他AAU不同。