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印度裂殖子表面蛋白1/2遗传多样性的地理和时间动态

Geographical and temporal dynamics of genetic diversity of merozoite surface proteins 1/2 in India.

作者信息

Kojom Foko Loick Pradel, Jakhan Jahnvi, Narang Geetika, Singh Vineeta

机构信息

Parasite and Host Biology Group, ICMR-National Institute of Malaria Research, Dwarka, Sector 8, New-Delhi, 110077 India.

Academy of Scientific and Innovative Research, Ghaziabad, India.

出版信息

J Parasit Dis. 2024 Sep;48(3):610-623. doi: 10.1007/s12639-024-01698-8. Epub 2024 Jun 28.

Abstract

UNLABELLED

The high genetic diversity of () is a big obstacle to successful vaccine development programs. Here, the geographical and temporal dynamics of the genetic diversity of Indian isolates from patients living in Ranchi, Raipur, Mewat, and Rourkela were analyzed. Typing and frequency of merozoite surface protein 1 and 2 genes (), their genotypes, clonality, heterozygosity, multiplicity of infection, and neutral evolution metrics were computed. A phylogenetic analysis was also performed for these two genes. The dominant allelic types were K1 (55%) and MAD20 (55%) for , and FC27 (64.7%) for . Infections were mainly monoclonal in Ranchi and Mewat while polyclonal in Raipur and Rourkela. Polyclonal infections dropped from 57.1 to 71.3% in 2013 to 33.3-33.4% in 2016 in Raipur. K1 and MAD20 sequences were highly diverse due to the organization of the amino acid units SGG, SVA, SVT, and SGN. The IC/3D7-related G,S,A-rich region showed a large variation of four to eight amino acid repeats, including mostly GAVASA (81.8%), GSGA (54.5%), and GASGSA (45.5%). The 32-amino acid sequence of the FC27 type was present in all isolates with several mutations. The sequences were not under neutral evolution, except the K1 family, which is under balancing selection. The sequences are phylogenetically closer to previous Indian sequences than those from Africa, Asia, the Americas, and Oceania. This study outlines a high genetic diversity of infections with complex structure, and evolutionary signature changed with time.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s12639-024-01698-8.

摘要

未标注

()的高遗传多样性是成功疫苗开发计划的一大障碍。在此,分析了来自兰契、赖布尔、默瓦特和鲁尔基拉患者的印度疟原虫分离株遗传多样性的地理和时间动态。计算了裂殖子表面蛋白1和2基因()的分型和频率、它们的基因型、克隆性、杂合性、感染复数以及中性进化指标。还对这两个基因进行了系统发育分析。对于,主要等位基因类型为K1(55%)和MAD20(55%),对于,为FC27(64.7%)。兰契和默瓦特的感染主要为单克隆,而赖布尔和鲁尔基拉的感染为多克隆。赖布尔的多克隆感染从2013年的57.1%至71.3%降至2016年的33.3%至33.4%。由于氨基酸单元SGG、SVA、SVT和SGN的组织,K1和MAD20序列高度多样。IC/3D7相关的富含G、S、A区域显示出四到八个氨基酸重复的大变异,主要包括GAVASA(81.8%)、GSGA(54.5%)和GASGSA(45.5%)。FC27型的32个氨基酸序列存在于所有分离株中,有多个突变。除了处于平衡选择的K1家族外,序列不处于中性进化。与非洲、亚洲、美洲和大洋洲的序列相比,序列在系统发育上更接近先前的印度序列。本研究概述了疟原虫感染的高遗传多样性,其结构复杂,进化特征随时间变化。

补充信息

在线版本包含可在10.1007/s12639-024-01698-8获取的补充材料。

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