Kuesap Jiraporn, Suphakhonchuwong Nutnicha, Eksonthi Benyapa, Huaihongthong Saranchana
Faculty of Allied Health Sciences, Thammasat University, 99 Moo 18 Khlong Nueng, Khlong Luang, Pathumthani, 12120, Thailand.
Faculty of Medical Technology, Rangsit University, Pathumthani, Thailand.
Malar J. 2025 Feb 27;24(1):63. doi: 10.1186/s12936-025-05305-w.
The genetic diversity of malaria parasites varies between regions in the world. The genetic polymorphisms of the genes Pvs48/45 and Pvs47 which encode gametocyte/gamete proteins of Plasmodium vivax, were studied because of their potential as transmission-blocking vaccine (TBV) targets. The aim of the present study was to investigate the genetic diversity of Pvs48/45 and Pvs47 in clinical isolates from endemic areas of Thailand.
Plasmodium vivax samples collected from four provinces neighbouring either Myanmar or Malaysia were analysed using polymerase chain reaction and nucleotide sequencing. RESULTS: Fifteen and 18 amino acid substitutions were observed in 36 Pvs48/45 and 62 Pvs47 deduced amino acid sequences, respectively. Eleven haplotypes were identified in Pvs48/45 and 26 in Pvs47. Overall, low nucleotide diversities were observed for Pvs48/45 (π = 0.00104) and Pvs47 (π = 0.00321). Tajima's D, and Fu and Li's D* and F* values were negative for both genes, Pvs48/45 and Pvs47 while a significant difference was found in Pvs48/45 (P < 0.05).
The limited polymorphism of the two investigated TBV candidate antigens observed in this study is consistent with findings in worldwide isolates. The collected genetic diversity data could be helpful for developing effective TBVs in malaria-endemic areas.
疟原虫的遗传多样性在世界不同地区存在差异。由于间日疟原虫配子体/配子蛋白编码基因Pvs48/45和Pvs47具有作为传播阻断疫苗(TBV)靶点的潜力,因此对其基因多态性进行了研究。本研究的目的是调查泰国流行地区临床分离株中Pvs48/45和Pvs47的遗传多样性。
对从与缅甸或马来西亚接壤的四个省份收集的间日疟原虫样本进行聚合酶链反应和核苷酸测序分析。
在36个Pvs48/45推导氨基酸序列和62个Pvs47推导氨基酸序列中分别观察到15个和18个氨基酸替换。在Pvs48/45中鉴定出11种单倍型,在Pvs47中鉴定出26种单倍型。总体而言,Pvs48/45(π = 0.00104)和Pvs47(π = 0.00321)的核苷酸多样性较低。Pvs48/45和Pvs47这两个基因的Tajima's D以及Fu和Li's D和F值均为阴性,而Pvs48/45存在显著差异(P < 0.05)。
本研究中观察到的两种被研究的TBV候选抗原的有限多态性与全球分离株的研究结果一致。所收集的遗传多样性数据可能有助于在疟疾流行地区开发有效的TBV。