Emerg Infect Dis. 2022 Oct;28(10):2043-2050. doi: 10.3201/eid2810.220695.
Deletions of pfhrp2 and paralogue pfhrp3 (pfhrp2/3) genes threaten Plasmodium falciparum diagnosis by rapid diagnostic test. We examined 1,002 samples from suspected malaria patients in Djibouti City, Djibouti, to investigate pfhrp2/3 deletions. We performed assays for Plasmodium antigen carriage, pfhrp2/3 genotyping, and sequencing for 7 neutral microsatellites to assess relatedness. By PCR assay, 311 (31.0%) samples tested positive for P. falciparum infection, and 296 (95.2%) were successfully genotyped; 37 (12.5%) samples were pfhrp2+/pfhrp3+, 51 (17.2%) were pfhrp2+/pfhrp3-, 5 (1.7%) were pfhrp2-/pfhrp3+, and 203 (68.6%) were pfhrp2-/pfhrp3-. Histidine-rich protein 2/3 antigen concentrations were reduced with corresponding gene deletions. Djibouti P. falciparum is closely related to Ethiopia and Eritrea parasites (pairwise G 0.68 [Ethiopia] and 0.77 [Eritrea]). P. falciparum with deletions in pfhrp2/3 genes were highly prevalent in Djibouti City in 2019-2020; they appear to have arisen de novo within the Horn of Africa and have not been imported.
pfhrp2 和旁系 pfhrp3(pfhrp2/3)基因缺失威胁快速诊断检测对恶性疟原虫的诊断。我们在吉布提市对 1002 份疑似疟疾患者样本进行了研究,以调查 pfhrp2/3 缺失情况。我们进行了疟原虫抗原携带检测、pfhrp2/3 基因分型和 7 个中性微卫星的测序分析,以评估相关性。通过 PCR 检测,311(31.0%)个样本检测到恶性疟原虫感染阳性,296(95.2%)个样本成功进行了基因分型;37(12.5%)个样本为 pfhrp2+/pfhrp3+,51(17.2%)个样本为 pfhrp2+/pfhrp3-,5(1.7%)个样本为 pfhrp2-/pfhrp3+,203(68.6%)个样本为 pfhrp2-/pfhrp3-。相应基因缺失时,富含组氨酸蛋白 2/3 抗原浓度降低。吉布提恶性疟原虫与埃塞俄比亚和厄立特里亚寄生虫密切相关(成对 G 0.68[埃塞俄比亚]和 0.77[厄立特里亚])。2019-2020 年,吉布提市 pfhrp2/3 基因缺失的恶性疟原虫非常普遍;它们似乎是在非洲之角内部产生的,而不是进口的。