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用于测定裂殖子表面蛋白1基因第2区遗传多样性的巢式PCR-异源双链迁移率分析方法的建立

Development of Nested PCR-Heteroduplex Mobility Assay for Determination of Genetic Diversity in the Block 2 Region of the Merozoite Surface Protein 1 Gene.

作者信息

Kritsiriwuthinan Kanyanan, Ngrenngarmlert Warunee, Sunantaraporn Sakone, Jehmah Anna

机构信息

Faculty of Medical Technology, Rangsit University, Pathumthani, Thailand 12000.

Faculty of Medical Technology, Mahidol University, Nakhon Pathom, Thailand 73170.

出版信息

J Parasitol Res. 2020 Apr 8;2020:9520326. doi: 10.1155/2020/9520326. eCollection 2020.

Abstract

Genetic diversity of parasite has significantly related to malaria control and vaccine development. The merozoite surface protein 1 () gene is a commonly used molecular marker to differentiate genetic diversity. This study is aimed at developing a nested PCR-Heteroduplex Mobility Assay (nPCR-HMA) for determination of the block 2 of the gene. The MAD20 family allele of was used as a control for optimization of the annealing and polyacrylamide gel electrophoresis conditions. In order to evaluate the developed nPCR-HMA, 8 clinical isolates were examined for allelic variants. The results revealed 9 allelic variants. Our study indicated that the successful nPCR-HMA with good precision and accuracy offers a more rapid, efficient, and cheap method for large-scale molecular epidemiological studies as compared to nucleotide sequencing.

摘要

疟原虫的遗传多样性与疟疾控制及疫苗研发密切相关。裂殖子表面蛋白1(MSP1)基因是用于区分遗传多样性的常用分子标记。本研究旨在开发一种巢式聚合酶链反应-异源双链迁移率分析(nPCR-HMA)方法,用于测定MSP1基因的第2区。以MSP1的MAD20家族等位基因作为对照,优化退火和聚丙烯酰胺凝胶电泳条件。为评估所开发的nPCR-HMA,对8株临床分离株进行了等位基因变异检测。结果显示有9种等位基因变异。我们的研究表明,成功开发的nPCR-HMA具有良好的精密度和准确性,与核苷酸测序相比,为大规模分子流行病学研究提供了一种更快速、高效且廉价的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/116b/7168720/4454afcf95ee/JPR2020-9520326.001.jpg

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