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2017 年至 2018 年在刚果民主共和国招募的患者中恶性疟原虫 pfhrp2 和 pfhrp3 基因缺失。

Plasmodium falciparum pfhrp2 and pfhrp3 gene deletions among patients in the DRC enrolled from 2017 to 2018.

机构信息

Malaria Branch, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, 30329, USA.

School of Public Health, University of Lubumbashi, Lubumbashi, Democratic Republic of the Congo.

出版信息

Sci Rep. 2021 Nov 26;11(1):22979. doi: 10.1038/s41598-021-02452-3.

Abstract

Rapid diagnostic tests (RDTs) detecting histidine-rich protein 2 (HRP2) and HRP3 are widely used throughout sub-Saharan Africa (SSA) to diagnose Plasmodium falciparum malaria. However, multiple SSA countries have reported pfhrp2 and pfhrp3 (pfhrp2/3) gene deletions. Blood samples (n = 1109) collected from patients with P. falciparum infection from six health facilities throughout the Democratic Republic of the Congo (DRC) from March 2017 to January 2018 were evaluated for pfhrp2/3 deletions. Samples were assayed for HRP2, pan-Plasmodium LDH (pLDH) and aldolase (pAldolase) antigens by bead-based multiplex antigen assay. Samples with low HRP2 concentration compared to pLDH and pAldolase antigens were selected for further pfhrp2/3 genotyping PCRs. The majority of blood samples (93.3%, 1035/1109) had high concentrations of the HRP2 antigen. Single deletions of pfhrp2 were identified in 0.27% (3/1109) of screened samples, with one sample from each of the Kapolowe, Mikalayi, and Rutshuru study sites. A pfhrp3 single deletion (0.09%, 1/1109) was found in the Kapolowe site. Dual pfhrp2 and pfhrp3 deletions were not observed. Due to, the low numbers of pfhrp2 deletions and the sporadic locations of these deletions, the use of HRP2-based RDTs appears to still be appropriate for these locations in DRC.

摘要

快速诊断检测(RDT)检测组氨酸丰富蛋白 2(HRP2)和 HRP3 在撒哈拉以南非洲(SSA)广泛用于诊断恶性疟原虫疟疾。然而,多个 SSA 国家报告了 pfhrp2 和 pfhrp3(pfhrp2/3)基因缺失。从 2017 年 3 月至 2018 年 1 月,从刚果民主共和国(DRC)六个卫生机构的疟原虫感染患者中采集了 1109 份血液样本,用于评估 pfhrp2/3 缺失情况。通过基于珠的多重抗原检测法,对 HRP2、泛疟原虫乳酸脱氢酶(pLDH)和醛缩酶(pAldolase)抗原进行了检测。与 pLDH 和 pAldolase 抗原相比,HRP2 浓度较低的样本被选择进行进一步的 pfhrp2/3 基因分型 PCR。大多数血液样本(93.3%,1035/1109)具有高浓度的 HRP2 抗原。在筛查样本中,有 0.27%(3/1109)的样本检测到 pfhrp2 单缺失,来自 Kapolowe、Mikalayi 和 Rutshuru 研究地点的各有一个样本。在 Kapolowe 地点发现了 pfhrp3 单缺失(0.09%,1/1109)。未观察到双缺失。由于 pfhrp2 缺失数量较少且这些缺失位置分散,因此基于 HRP2 的 RDT 似乎仍然适用于 DRC 中的这些地区。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11b0/8626453/429bb1e0b43b/41598_2021_2452_Fig1_HTML.jpg

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