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恶性疟原虫缺乏富含组氨酸蛋白 2对疟疾控制规划的主要威胁,厄立特里亚。

Major Threat to Malaria Control Programs by Plasmodium falciparum Lacking Histidine-Rich Protein 2, Eritrea.

出版信息

Emerg Infect Dis. 2018 Mar;24(3):462-470. doi: 10.3201/eid2403.171723.

DOI:10.3201/eid2403.171723
PMID:29460730
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5823352/
Abstract

False-negative results for Plasmodium falciparum histidine-rich protein (HRP) 2-based rapid diagnostic tests (RDTs) are increasing in Eritrea. We investigated HRP gene 2/3 (pfhrp2/pfhrp3) status in 50 infected patients at 2 hospitals. We showed that 80.8% (21/26) of patients at Ghindae Hospital and 41.7% (10/24) at Massawa Hospital were infected with pfhrp2-negative parasites and 92.3% (24/26) of patients at Ghindae Hospital and 70.8% (17/24) at Massawa Hospital were infected with pfhrp3-negative parasites. Parasite densities between pfhrp2-positive and pfhrp2-negative patients were comparable. All pfhrp2-negative samples had no detectable HRP2/3 antigen and showed negative results for HRP2-based RDTs. pfhrp2-negative parasites were genetically less diverse and formed 2 clusters with no close relationships to parasites from Peru. These parasites probably emerged independently by selection in Eritrea. High prevalence of pfhrp2-negative parasites caused a high rate of false-negative results for RDTs. Determining prevalence of pfhrp2-negative parasites is urgently needed in neighboring countries to assist case management policies.

摘要

在厄立特里亚,恶性疟原虫 HRP2 快速诊断检测(RDT)的假阴性结果正在增加。我们在两家医院的 50 名感染患者中调查了 HRP 基因 2/3(pfhrp2/pfhrp3)的情况。我们表明,在 Ghindae 医院的 80.8%(21/26)的患者和 Massawa 医院的 41.7%(10/24)的患者感染了 pfhrp2 阴性寄生虫,在 Ghindae 医院的 92.3%(24/26)的患者和 Massawa 医院的 70.8%(17/24)的患者感染了 pfhrp3 阴性寄生虫。pfhrp2 阳性和 pfhrp2 阴性患者之间的寄生虫密度相当。所有 pfhrp2 阴性样本均未检测到 HRP2/3 抗原,并且 HRP2 基于 RDT 的检测结果呈阴性。pfhrp2 阴性寄生虫的遗传多样性较低,形成了 2 个簇,与来自秘鲁的寄生虫没有密切关系。这些寄生虫可能是在厄立特里亚通过选择独立出现的。pfhrp2 阴性寄生虫的高流行率导致 RDT 的假阴性率很高。迫切需要在邻国确定 pfhrp2 阴性寄生虫的流行率,以协助病例管理政策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/216b809a2f4c/17-1723-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/6a07b068a02f/17-1723-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/b67f5e08edd5/17-1723-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/a99809695c66/17-1723-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/3c0862ef3716/17-1723-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/216b809a2f4c/17-1723-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/6a07b068a02f/17-1723-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/b67f5e08edd5/17-1723-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/a99809695c66/17-1723-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/3c0862ef3716/17-1723-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/5823352/216b809a2f4c/17-1723-F5.jpg

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