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哥伦比亚基于HRP2的快速诊断试验呈假阴性的恶性疟原虫疟疾患者中pfhrp2/pfhrp3基因缺失的流行情况。

Prevalence of pfhrp2/pfhrp3 gene deletions among patients with Plasmodium falciparum malaria with false-negative in the HRP2-based rapid diagnostic test in Colombia.

作者信息

Olivera Mario Javier, Guerra Angela Patricia, Cortés Liliana Jazmín, Suárez-Jurado Aravy Geohanna, Ade María de la Paz, Cárdenas Iván Mauricio

机构信息

Instituto Nacional de Salud, Grupo de Parasitología, Bogotá DC, Colombia.

Pan-American Health Organization, Department of Communicable Diseases Prevention, Control and Elimination, District of Columbia, Washington, United States.

出版信息

Mem Inst Oswaldo Cruz. 2025 Jun 13;120:e240134. doi: 10.1590/0074-02760240134. eCollection 2025.

Abstract

BACKGROUND

In malaria-endemic regions, rapid diagnostic tests (RDTs) play a crucial role in promptly identifying infections, especially in remote areas with limited microscopy services.

OBJECTIVES

Conduct a cross-sectional, multi-site study to determine whether the local prevalence of mutations in the Plasmodium falciparum hrp2/3 genes in false-negative RDTs has reached a threshold that might require a local or national change in diagnostic strategy in accordance with the WHO guidelines (2018).

METHODS

Individuals were screened for P. falciparum with microscopy and HRP2-based RDT at health facilities. Discordant results between these two tests triggered diagnostic confirmation by polymerase chain reaction (PCR) and detection of the pfhrp2/pfhrp3 genes.

FINDINGS

Among the 347 patients included, false negatives constituted 4.61% (16/347). Molecular analysis revealed all 16 false negatives were P. falciparum positive with hrp2 gene present, displaying high polymorphism. However, hrp3 gene deletion was observed in 93.8% (15/16) of these cases.

MAIN CONCLUSIONS

The prevalence of false-negative RDTs is low, and these results were not linked to deletions in the hrp2 gene. This suggests that there is no immediate need to modify the RDTs used along the Colombian Pacific Coast. However, molecular surveillance for hrp2 deletions remains crucial to detect any potential increase in prevalence.

摘要

背景

在疟疾流行地区,快速诊断检测(RDTs)在及时识别感染方面发挥着关键作用,尤其是在显微镜检查服务有限的偏远地区。

目的

开展一项横断面、多地点研究,以确定在假阴性RDTs中恶性疟原虫hrp2/3基因突变的当地流行率是否已达到一个阈值,该阈值可能需要根据世界卫生组织指南(2018年)在当地或全国范围内改变诊断策略。

方法

在医疗机构对个体进行恶性疟原虫的显微镜检查和基于HRP2的RDT筛查。这两种检测结果不一致时,通过聚合酶链反应(PCR)进行诊断确认并检测pfhrp2/pfhrp3基因。

结果

在纳入的347例患者中,假阴性占4.61%(16/347)。分子分析显示,所有16例假阴性患者的恶性疟原虫均为hrp2基因阳性,表现出高度多态性。然而,在这些病例中有93.8%(15/16)观察到hrp3基因缺失。

主要结论

RDTs假阴性的流行率较低,且这些结果与hrp2基因缺失无关。这表明哥伦比亚太平洋沿岸目前无需修改所使用的RDTs。然而,对hrp2缺失进行分子监测对于检测流行率的任何潜在增加仍然至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/12165712/a9f111c25624/1678-8060-mioc-120-e240134-gf1.jpg

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