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坦桑尼亚不同疟疾流行程度地区环子孢子蛋白基因的遗传多态性及选择特征证据

Genetic polymorphism and evidence of signatures of selection in the circumsporozoite protein gene in Tanzanian regions with different malaria endemicity.

作者信息

Lyimo Beatus M, Bakari Catherine, Popkin-Hall Zachary R, Giesbrecht David J, Seth Misago D, Pereus Dativa, Moshi Ramadhan, Boniface Ruth, Mandara Celine I, Madebe Rashid, Juliano Jonathan J, Bailey Jeffrey A, Ishengoma Deus S

机构信息

National Institute for Medical Research, Dar es Salaam, Tanzania.

Nelson Mandela African Institution of Science and Technology, Arusha, Tanzania.

出版信息

medRxiv. 2024 Jan 23:2024.01.23.24301587. doi: 10.1101/2024.01.23.24301587.

Abstract

BACKGROUND

In 2021 and 2023, the World Health Organization approved RTS, S/AS01 and R21/Matrix M malaria vaccines, respectively, for routine immunization of children in African countries with moderate to high transmission. These vaccines are made of circumsporozoite protein ( but polymorphisms in this gene raises concerns regarding strain-specific responses and the long-term efficacy of these vaccines. This study assessed the genetic diversity, population structure and signatures of selection among parasites from areas of different malaria transmission in mainland Tanzania, to generate baseline data before the introduction of the malaria vaccines in the country.

METHODS

The analysis involved 589 whole genome sequences generated by and as part of the MalariaGEN Community Project. The samples were collected between 2013 and January 2015 from five regions of mainland Tanzania: Morogoro and Tanga (Muheza) (moderate transmission areas), and Kagera (Muleba), Lindi (Nachingwea), and Kigoma (Ujiji) (high transmission areas). Wright's inbreeding coefficient (F), Wright's fixation index (F), principal component analysis, nucleotide diversity, and Tajima's D were used to assess within-host parasite diversity, population structure and natural selection.

RESULTS

Based on F (< 0.95), there was high polyclonality (ranged from 69.23% in Nachingwea to 56.9% in Muheza). No population structure was detected in the gene in the five regions (mean F= 0.0068). The average nucleotide diversity (π), nucleotide differentiation (K) and haplotype diversity (Hd) in the five regions were 4.19, 0.973 and 0.0035, respectively. The C-terminal region of showed high nucleotide diversity at Th2R and Th3R regions. Positive values for the Tajima's D were observed in the Th2R and Th3R regions consistent with balancing selection. The C-terminal sequences had 50 different haplotypes (H_1 to H_50) and only 2% of sequences matched the 3D7 strain haplotype (H_50).

CONCLUSIONS

The findings demonstrate high diversity of the gene with limited population differentiation. The gene showed positive Tajima's D values for parasite populations, consistent with balancing selection for variants within Th2R and Th3R regions. This data is consistent with other studies conducted across Africa and worldwide, which demonstrate low 3D7 haplotypes and little population structure. Therefore, additional research is warranted, incorporating other regions and more recent data to comprehensively assess trends in genetic diversity within this important gene. Such insights will inform the choice of alleles to be included in the future vaccines.

摘要

背景

2021年和2023年,世界卫生组织分别批准了RTS,S/AS01和R21/Matrix M疟疾疫苗用于非洲疟疾传播程度为中度至高的国家的儿童常规免疫。这些疫苗由环子孢子蛋白制成(但该基因的多态性引发了对菌株特异性反应以及这些疫苗长期疗效的担忧)。本研究评估了坦桑尼亚大陆不同疟疾传播地区寄生虫的基因多样性、种群结构和选择特征,以便在该国引入疟疾疫苗之前生成基线数据。

方法

分析涉及由疟疾基因组社区项目生成并作为该项目一部分的589个全基因组序列。样本于2013年至2015年1月期间从坦桑尼亚大陆的五个地区采集:莫罗戈罗和坦噶(穆赫扎)(中度传播地区),以及卡盖拉(穆莱巴)、林迪(纳钦韦亚)和基戈马(乌吉吉)(高度传播地区)。使用赖特近交系数(F)、赖特固定指数(F)、主成分分析、核苷酸多样性和塔吉玛D来评估宿主体内寄生虫的多样性、种群结构和自然选择。

结果

基于F(<0.95),多克隆性较高(范围从纳钦韦亚的69.23%到穆赫扎的56.9%)。在五个地区的该基因中未检测到种群结构(平均F = 0.0068)。五个地区的平均核苷酸多样性(π)、核苷酸分化(K)和单倍型多样性(Hd)分别为4.19、0.973和0.0035。该基因的C末端区域在Th2R和Th3R区域显示出高核苷酸多样性。在Th2R和Th3R区域观察到塔吉玛D的正值,与平衡选择一致。该基因的C末端序列有50种不同的单倍型(H_1至H_50),只有2%的序列与3D7菌株单倍型(H_50)匹配。

结论

研究结果表明该基因具有高度多样性且种群分化有限。该基因显示出寄生虫种群的塔吉玛D正值,与Th2R和Th3R区域内变体的平衡选择一致。这些数据与在非洲和全球范围内进行的其他研究一致,这些研究表明3D7单倍型较低且种群结构较少。因此,有必要进行更多研究,纳入其他地区和更新的数据,以全面评估这个重要基因内的遗传多样性趋势。这些见解将为未来疫苗中包含的等位基因选择提供参考。

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