Biomedicine and biotechnology Department, University of Alcalá, Ctra.Madrid-Barcelona Km.33,600, 28871, Alcalá de Henares, Spain.
National Centre of Tropical Medicine, Carlos III Institute of Health, C/ Sinesio Delgado 10, 28029, Madrid, Spain.
Malar J. 2024 Jul 18;23(1):215. doi: 10.1186/s12936-024-05036-4.
Pfhrp2 and pfhrp3 deletions are threatening Plasmodium falciparum malaria diagnosis by rapid diagnostic tests (RDT) due to false negatives. This study assesses the changes in the frequencies of pfhrp2 and pfhrp3 deletions (pfhrp2 and pfhrp3, respectively) and the genes in their flaking regions, before and after RDT introduction in Equatorial Guinea.
A total of 566 P. falciparum samples were genotyped to assess the presence of pfhrp2 and pfhrp3 deletions and their flanking genes. The specimens were collected 18 years apart from two provinces of Equatorial Guinea, North Bioko (Insular Region) and Litoral Province (Continental Region). Orthologs of pfhrp2 and pfhrp3 genes from other closely related species were used to compare sequencing data to assess pfhrp2 and pfhrp3 evolution. Additionally, population structure was studied using seven neutral microsatellites.
This study found that pfhrp2Del and pfhrp3Del were present before the introduction of RDT; however, they increased in frequency after their use, reaching more than 15%. Haplotype networks suggested that pfhrp2Del and pfhrp3Del emerged multiple times. Exon 2 of pfhrp2 and pfhrp3 genes had high variability, but there were no significant changes in amino acid sequences.
Baseline sampling before deploying interventions provides a valuable context to interpret changes in genetic markers linked to their efficacy, such as the dynamic of deletions affecting RDT efficacy.
Pfhrp2 和 pfhrp3 缺失会导致快速诊断检测(RDT)出现假阴性,从而威胁到恶性疟原虫疟疾的诊断。本研究评估了在赤道几内亚引入 RDT 前后 Pfhrp2 和 Pfhrp3 缺失(分别为 pfhrp2 和 pfhrp3)及其侧翼基因的频率变化。
共对 566 个恶性疟原虫样本进行基因分型,以评估 pfhrp2 和 pfhrp3 缺失及其侧翼基因的存在情况。这些样本分别采集自赤道几内亚的两个省,北比奥科岛(岛屿地区)和滨海省(大陆地区),相隔 18 年。使用来自其他密切相关物种的 pfhrp2 和 pfhrp3 基因的直系同源物来比较测序数据,以评估 pfhrp2 和 pfhrp3 的进化情况。此外,还使用了七个中性微卫星来研究种群结构。
本研究发现,pfhrp2Del 和 pfhrp3Del 在引入 RDT 之前就已经存在,但在使用后其频率增加,超过 15%。单倍型网络表明,pfhrp2Del 和 pfhrp3Del 多次出现。pfhrp2 和 pfhrp3 基因的外显子 2 具有高度的变异性,但氨基酸序列没有显著变化。
在部署干预措施之前进行基线采样,可以为解释与干预措施疗效相关的遗传标记的变化提供有价值的背景信息,例如影响 RDT 疗效的缺失动态。