基于 ParaHIT® HRP2 的快速诊断检测的性能和多哥恶性疟原虫组氨酸富集蛋白 2/3 基因缺失的比例。

Diwaba Carmel Teou,Ameyo Monique Dorkenoo,Essoham Ataba,Kossi Yakpa,Efoe Sossou,Laurence Ma,Emmanuelle Caspar,Manani Hemou,Agueregna Abdou-Kerim,Didier Menard
{"title":"基于 ParaHIT® HRP2 的快速诊断检测的性能和多哥恶性疟原虫组氨酸富集蛋白 2/3 基因缺失的比例。","authors":"Diwaba Carmel Teou,Ameyo Monique Dorkenoo,Essoham Ataba,Kossi Yakpa,Efoe Sossou,Laurence Ma,Emmanuelle Caspar,Manani Hemou,Agueregna Abdou-Kerim,Didier Menard","doi":"10.4269/ajtmh.24-0197","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":520106,"journal":{"name":"The American Journal of Tropical Medicine and Hygiene","volume":"18 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Performance of ParaHIT® HRP2-Based Rapid Diagnostic Test and Proportions of Plasmodium falciparum Histidine-Rich Protein 2/3 Gene Deletions in Togo.\",\"authors\":\"Diwaba Carmel Teou,Ameyo Monique Dorkenoo,Essoham Ataba,Kossi Yakpa,Efoe Sossou,Laurence Ma,Emmanuelle Caspar,Manani Hemou,Agueregna Abdou-Kerim,Didier Menard\",\"doi\":\"10.4269/ajtmh.24-0197\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":520106,\"journal\":{\"name\":\"The American Journal of Tropical Medicine and Hygiene\",\"volume\":\"18 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The American Journal of Tropical Medicine and Hygiene\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4269/ajtmh.24-0197\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The American Journal of Tropical Medicine and Hygiene","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4269/ajtmh.24-0197","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

在疟疾流行和显微镜缺乏的地区,快速诊断检测(RDT)是早期诊断和及时有效治疗的重要工具。然而,由于恶性疟原虫寄生虫不携带 pfhrp2 或 pfhrp3 基因,导致假阴性结果的出现,基于 HRP2 的快速诊断检测受到威胁。因此,本研究旨在评估 ParaHIT RDT 的性能以及多哥 pfhrp2/3 基因缺失的恶性疟原虫寄生虫的比例。2021 年 9 月至 2022 年 1 月,在两个哨点对 6-59 个月大的儿童进行了横断面研究,通过刺破手指采集毛细血管血,测定了 RDT 与显微镜和聚合酶链反应(PCR)的性能比较。采集的血样用于分子分析。目标区域(hrp2 和 hrp3 基因的外显子 2)的扩增子通过多重嵌套 PCR 生成,并使用 Illumina 的 MiSeq 协议进行测序。共对 278 份样本进行了 ParaHIT RDT 评估分析。与显微镜检测相比,RDT 检测的灵敏度和特异性分别为 96.4% 和 85.7%,与 PCR 检测相比,灵敏度和特异性分别提高到 97.9% 和 90.7%。在显微镜和 PCR 阳性的恶性疟原虫样本中,138 份样本进行了测序,以检测 pfhrp2/3 缺失。没有一个寄生虫出现单个 pfhrp2 缺失或单个 pfhrp3 缺失。在这项评估中,ParaHIT RDT 的性能达到了可接受的水平,证实了在多哥没有显微镜的地区,可以使用基于 HRP2 的 RDT 检测恶性疟原虫感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Performance of ParaHIT® HRP2-Based Rapid Diagnostic Test and Proportions of Plasmodium falciparum Histidine-Rich Protein 2/3 Gene Deletions in Togo.
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.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信