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印度北部昌迪加尔恶性疟原虫裂殖子表面蛋白-1(第2区)、富含谷氨酸蛋白及有性期抗原Pfs25的遗传多样性

Genetic diversity of Plasmodium falciparum merozoite surface protein-1 (block 2), glutamate-rich protein and sexual stage antigen Pfs25 from Chandigarh, North India.

作者信息

Kaur Hargobinder, Sehgal Rakesh, Goyal Kapil, Makkar Nikita, Yadav Richa, Bharti Praveen K, Singh Neeru, Sarmah Nilanju P, Mohapatra Pradyumna K, Mahanta Jagadish, Bansal Devendra, Sultan Ali A, Kanwar Jagat R

机构信息

Department of Medical Parasitology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

National Institute for Research in Tribal Health, Indian Council of Medical Research, Jabalpur, India.

出版信息

Trop Med Int Health. 2017 Dec;22(12):1590-1598. doi: 10.1111/tmi.12990. Epub 2017 Nov 9.

Abstract

OBJECTIVE

To elucidate the genetic diversity of Plasmodium falciparum in residual transmission foci of northern India.

METHODS

Clinically suspected patients with malaria were screened for malaria infection by microscopy. 48 P. falciparum-infected patients were enrolled from tertiary care hospital in Chandigarh, India. Blood samples were collected from enrolled patients, genomic DNA extraction and nested PCR was performed for further species confirmation. Sanger sequencing was carried out using block 2 region of msp1, R2 region of glurp and pfs25-specific primers.

RESULTS

Extensive diversity was found in msp1 alleles with predominantly RO33 alleles. Overall allelic prevalence was 55.8% for RO33, 39.5% for MAD20 and 4.7% for K1. Six variants were observed in MAD20, whereas no variant was found in RO33 and K1 alleles. A phylogenetic analysis of RO33 alleles indicated more similarity to South African isolates, whereas MAD20 alleles showed similarity with South-East Asian isolates. In glurp, extensive variation was observed with eleven different alleles based on the AAU repeats. However, pfs25 showed less diversity and was the most stable among the targeted genes.

CONCLUSION

Our findings document the genetic diversity among circulating strains of P. falciparum in an area of India with low malaria transmission and could have implications for control strategies to reach the national goal of malaria elimination.

摘要

目的

阐明印度北部残余疟疾传播疫源地中恶性疟原虫的遗传多样性。

方法

对临床疑似疟疾患者进行显微镜检查以筛查疟疾感染情况。从印度昌迪加尔的三级护理医院招募了48名恶性疟原虫感染患者。采集入组患者的血样,进行基因组DNA提取和巢式PCR以进一步确认虫种。使用msp1的第2区、glurp的R2区和pfs25特异性引物进行桑格测序。

结果

在msp1等位基因中发现了广泛的多样性,主要为RO33等位基因。RO33的总体等位基因流行率为55.8%,MAD20为39.5%,K1为4.7%。在MAD20中观察到6个变体,而在RO33和K1等位基因中未发现变体。对RO33等位基因的系统发育分析表明,其与南非分离株更相似,而MAD20等位基因与东南亚分离株相似。在glurp中,基于AAU重复观察到11种不同等位基因的广泛变异。然而,pfs25的多样性较低,是目标基因中最稳定的。

结论

我们的研究结果记录了印度疟疾传播率低的地区恶性疟原虫流行株之间的遗传多样性,可能对实现消除疟疾国家目标的控制策略产生影响。

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