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基于裂殖子表面蛋白 1 的 C 末端 19kDa 结构域的时空单体型模式分析泰国地区恶性疟原虫的多样性和种群结构。

Diversity and population structure of Plasmodium falciparum in Thailand based on the spatial and temporal haplotype patterns of the C-terminal 19-kDa domain of merozoite surface protein-1.

机构信息

Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.

出版信息

Malar J. 2014 Feb 12;13:54. doi: 10.1186/1475-2875-13-54.

DOI:10.1186/1475-2875-13-54
PMID:24521474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3931489/
Abstract

BACKGROUND

The 19-kDa C-terminal region of the merozoite surface protein-1 of the human malaria parasite Plasmodium falciparum (PfMSP-119) constitutes the major component on the surface of merozoites and is considered as one of the leading candidates for asexual blood stage vaccines. Because the protein exhibits a level of sequence variation that may compromise the effectiveness of a vaccine, the global sequence diversity of PfMSP-119 has been subjected to extensive research, especially in malaria endemic areas. In Thailand, PfMSP-119 sequences have been derived from a single parasite population in Tak province, located along the Thailand-Myanmar border, since 1995. However, the extent of sequence variation and the spatiotemporal patterns of the MSP-119 haplotypes along the Thai borders with Laos and Cambodia are unknown.

METHODS

Sixty-three isolates of P. falciparum from five geographically isolated populations along the Thai borders with Myanmar, Laos and Cambodia in three transmission seasons between 2002 and 2008 were collected and culture-adapted. The msp-1 gene block 17 was sequenced and analysed for the allelic diversity, frequency and distribution patterns of PfMSP-119 haplotypes in individual populations. The PfMSP-119 haplotype patterns were then compared between parasite populations to infer the population structure and genetic differentiation of the malaria parasite.

RESULTS

Five conserved polymorphic positions, which accounted for five distinct haplotypes, of PfMSP-119 were identified. Differences in the prevalence of PfMSP-119 haplotypes were detected in different geographical regions, with the highest levels of genetic diversity being found in the Kanchanaburi and Ranong provinces along the Thailand-Myanmar border and Trat province located at the Thailand-Cambodia border. Despite this variability, the distribution patterns of individual PfMSP-119 haplotypes seemed to be very similar across the country and over the three malarial transmission seasons, suggesting that gene flow may operate between parasite populations circulating in Thailand and the three neighboring countries.

CONCLUSION

The major MSP-119 haplotypes of P. falciparum populations in all endemic populations during three transmission seasons in Thailand were identified, providing basic information on the common haplotypes of MSP-119 that is of use for malaria vaccine development and inferring the population structure of P. falciparum populations in Thailand.

摘要

背景

人类疟原虫恶性疟原虫表面蛋白-1 的 19kDa C 端区域(PfMSP-119)构成了裂殖子表面的主要成分,被认为是无性血期疫苗的主要候选者之一。由于该蛋白表现出可能影响疫苗效果的序列变异水平,PfMSP-119 的全球序列多样性已受到广泛研究,尤其是在疟疾流行地区。在泰国,自 1995 年以来,PfMSP-119 序列来自位于泰国-缅甸边境的塔可省的单一寄生虫种群。然而,与老挝和柬埔寨接壤的泰国边境沿线 MSP-119 单倍型的序列变异程度和时空模式尚不清楚。

方法

2002 年至 2008 年三个传播季节期间,从与缅甸、老挝和柬埔寨接壤的泰国边境的五个地理隔离的人群中采集了 63 株恶性疟原虫分离株,并进行了培养适应。对 msp-1 基因块 17 进行测序,并对个体人群中 PfMSP-119 单倍型的等位基因多样性、频率和分布模式进行分析。然后将寄生虫种群之间的 PfMSP-119 单倍型模式进行比较,以推断疟原虫的种群结构和遗传分化。

结果

鉴定了 PfMSP-119 的 5 个保守多态性位置,这些位置构成了 5 个不同的单倍型。在不同的地理区域检测到 PfMSP-119 单倍型的流行率存在差异,在泰国-缅甸边境的坎查纳布利和拉农省以及泰国-柬埔寨边境的特拉特省发现了最高的遗传多样性水平。尽管存在这种变异性,但全国各地和三个疟疾传播季节的单个 PfMSP-119 单倍型的分布模式似乎非常相似,这表明在泰国和三个邻国循环的寄生虫种群之间可能存在基因流。

结论

确定了泰国所有流行人群在三个传播季节中恶性疟原虫种群的主要 MSP-119 单倍型,为 MSP-119 常见单倍型的疫苗开发提供了基本信息,并推断了泰国恶性疟原虫种群的种群结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/f6fa382c6148/1475-2875-13-54-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/fd5c3349e798/1475-2875-13-54-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/41c1116a425e/1475-2875-13-54-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/bfc117a815b6/1475-2875-13-54-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/f6fa382c6148/1475-2875-13-54-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/fd5c3349e798/1475-2875-13-54-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/41c1116a425e/1475-2875-13-54-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/bfc117a815b6/1475-2875-13-54-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1987/3931489/f6fa382c6148/1475-2875-13-54-4.jpg

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