Faculté des Sciences, Université de Lomé, Lomé, Togo.
Faculté des Sciences de la Santé, Université de Lomé, Lomé, Togo.
Am J Trop Med Hyg. 2024 Sep 17;111(5):977-983. doi: 10.4269/ajtmh.24-0197. Print 2024 Nov 6.
In areas where malaria is endemic and microscopes are unavailable, rapid diagnostic tests (RDTs) are essential tools for early diagnosis and prompt and effective treatment. However, HRP2-based RDTs are threatened by the emergence of Plasmodium falciparum parasites that do not carry the pfhrp2 or pfhrp3 gene, leading to false-negative results. Therefore, the aim of this study was to evaluate the performance of the ParaHIT RDT together with the proportion of pfhrp2/3 gene-deleted P. falciparum parasites in Togo. The performance of RDTs compared with microscopy and polymerase chain reaction (PCR) was determined using capillary blood collected by finger prick during a cross-sectional study conducted from September 2021 to January 2022 in children aged 6-59 months at two sentinel sites. Blood spots were collected for molecular analysis. Amplicons from the target regions (exon 2 of hrp2 and hrp3 genes) were generated by multiplex nested PCR and sequenced using Illumina's MiSeq protocol. A total of 278 samples were analyzed for ParaHIT RDT evaluation. The sensitivity and specificity of the RDT test compared with microscopy were 96.4% and 85.7%, respectively, which increased to 97.9% and 90.7%, respectively, when compared with PCR. Of the microscopically and PCR-positive P. falciparum samples, 138 were sequenced to detect pfhrp2/3 deletions. None of the parasites had a single pfhrp2 deletion or a single pfhrp3 deletion. The ParaHIT RDT demonstrated an acceptable level of performance in this evaluation, confirming the use of HRP2-based RDTs for the detection of P. falciparum infection in areas where microscopy is not available in Togo.
在疟疾流行地区,如果没有显微镜,快速诊断检测(RDT)是进行早期诊断以及及时、有效治疗的重要工具。然而,基于 HRP2 的 RDT 受到了威胁,因为有些恶性疟原虫寄生虫不携带 pfhrp2 或 pfhrp3 基因,导致检测结果呈假阴性。因此,本研究旨在评估 ParaHIT RDT 在多哥的性能,以及 pfhrp2/3 基因缺失的恶性疟原虫寄生虫的比例。在 2021 年 9 月至 2022 年 1 月期间,在两个哨点进行了一项横断面研究,通过手指刺取毛细血管血,收集了年龄在 6-59 个月的儿童的血液样本,用于评估 RDT 的性能。采集血斑进行分子分析。采用多重巢式 PCR 生成靶区(hrp2 和 hrp3 基因外显子 2)的扩增子,并使用 Illumina 的 MiSeq 方案进行测序。共分析了 278 个样本用于评估 ParaHIT RDT。与显微镜相比,RDT 检测的灵敏度和特异性分别为 96.4%和 85.7%,与 PCR 相比,分别增加到 97.9%和 90.7%。在显微镜和 PCR 阳性的恶性疟原虫样本中,有 138 个样本进行了测序,以检测 pfhrp2/3 缺失。没有一个寄生虫只有单个 pfhrp2 缺失或单个 pfhrp3 缺失。在这项评估中,ParaHIT RDT 表现出可接受的性能水平,证实了在多哥没有显微镜的地区,基于 HRP2 的 RDT 可用于检测恶性疟原虫感染。