Suppr超能文献

利用新型快速等温扩增侧向流检测试剂盒检测间日疟原虫。

Detection of P. malariae using a new rapid isothermal amplification lateral flow assay.

机构信息

Ethiopian Public Health Institute, Addis Ababa, Ethiopia.

Institute of Global Health and Infectious Diseases, University of North Carolina School of Medicine, Chapel Hill, NC, USA.

出版信息

Malar J. 2024 Apr 12;23(1):104. doi: 10.1186/s12936-024-04928-9.

Abstract

BACKGROUND

While Plasmodium falciparum and Plasmodium vivax cause the majority of malaria cases and deaths, infection by Plasmodium malariae and other Plasmodium species also causes morbidity and mortality. Current understanding of these infections is limited in part by existing point-of-care diagnostics that fail to differentiate them and have poor sensitivity for low-density infections. Accurate diagnosis currently requires molecular assays performed in well-resourced laboratories. This report describes the development of a P. malariae diagnostic assay that uses rapid, isothermal recombinase polymerase amplification (RPA) and lateral-flow-strip detection.

METHODS

Multiple combinations of custom RPA primers and probes were designed using publicly available P. malariae genomic sequences, and by modifying published primer sets. Based on manufacturer RPA reaction conditions (TwistDx nfo kit), an isothermal assay was optimized targeting the multicopy P. malariae 18S rRNA gene with 39 °C incubation and 30-min run time. RPA product was visualized using lateral strips (FAM-labeled, biotinylated amplicon detected by a sandwich immunoassay, visualized using gold nanoparticles). Analytical sensitivity was evaluated using 18S rRNA plasmid DNA, and clinical sensitivity determined using qPCR-confirmed samples collected from Tanzania, Ethiopia, and the Democratic Republic of the Congo.

RESULTS

Using 18S rRNA plasmid DNA, the assay demonstrates a detection limit of 10 copies/µL (~ 1.7 genome equivalents) and 100% analytical specificity. Testing in field samples showed 95% clinical sensitivity and 88% specificity compared to qPCR. Total assay time was less than 40 min.

CONCLUSION

Combined with simplified DNA extraction methods, the assay has potential for future field-deployable, point-of-care use to detect P. malariae infection, which remains largely undiagnosed but a neglected cause of chronic malaria. The assay provides a rapid, simple readout on a lateral flow strip without the need for expensive laboratory equipment.

摘要

背景

虽然恶性疟原虫和间日疟原虫引起了大多数疟疾病例和死亡,但疟原虫属和其他疟原虫的感染也会导致发病和死亡。目前对这些感染的认识有限,部分原因是现有的即时检测诊断方法无法区分它们,而且对低密度感染的敏感性较差。准确的诊断目前需要在资源充足的实验室中进行分子检测。本报告介绍了一种利用快速等温重组酶聚合酶扩增(RPA)和侧流条带检测的疟原虫属诊断检测方法的开发。

方法

使用公开的疟原虫属基因组序列和修改的已发表引物组,设计了多个定制 RPA 引物和探针组合。根据制造商的 RPA 反应条件(TwistDx nfo 试剂盒),针对多拷贝疟原虫属 18S rRNA 基因进行了优化,在 39°C 孵育和 30 分钟运行时间的等温条件下进行反应。使用侧流条带(FAM 标记,生物素标记的扩增子通过夹心免疫测定检测,使用金纳米颗粒可视化)可视化 RPA 产物。使用 18S rRNA 质粒 DNA 评估分析灵敏度,使用来自坦桑尼亚、埃塞俄比亚和刚果民主共和国的 qPCR 确认样本评估临床灵敏度。

结果

使用 18S rRNA 质粒 DNA,该检测方法的检测限为 10 拷贝/µL(~1.7 个基因组当量),分析特异性为 100%。与 qPCR 相比,在现场样本中检测到的检测率为 95%,特异性为 88%。总检测时间不到 40 分钟。

结论

与简化的 DNA 提取方法相结合,该检测方法具有未来在现场部署、即时使用的潜力,可用于检测疟原虫属感染,而这种感染在很大程度上未被诊断,但却是慢性疟疾的一个被忽视的原因。该检测方法在不需要昂贵的实验室设备的情况下,在侧流条带上提供了快速、简单的读取结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/11015614/1ecdaa31f0e0/12936_2024_4928_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验