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应用环介导等温扩增结合侧流分析可视化检测疟原虫kelch 13 C580Y 突变用于临床样本中的青蒿素耐药性检测。

Application of loop-mediated isothermal amplification combined with lateral flow assay visualization of Plasmodium falciparum kelch 13 C580Y mutation for artemisinin resistance detection in clinical samples.

机构信息

Division of Biological Science, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.

Haematology Unit, Department of Medical Technology and Pathology, Suratthani Hospital, Surat Thani Province, Thailand.

出版信息

Acta Trop. 2023 Oct;246:106998. doi: 10.1016/j.actatropica.2023.106998. Epub 2023 Aug 5.

Abstract

Resistance to the antimalarial drug artemisinin (ART) has emerged in Greater Mekong Subregion. The molecular marker predominantly used to identify ART resistance is the C580Y mutation in Pfkelch13 of Plasmodium falciparum. Rapid and accurate detection of ART resistance in the field is necessary to guide malaria containment and elimination interventions. Our study evaluates the PfC580Y by using the loop-mediated isothermal amplification and single nucleotide polymorphism analysis visualization using a lateral flow assay (LAMP-SNP-LFA) method for detecting ART resistance in clinical samples collected from Thailand between 2014 and 2019. The optimized incubation condition for the reaction was determined as 45 min at 56 °C, followed by visual detection of positive amplicons using LFA. The assay demonstrated high analytical sensitivity and specificity, with a limit of detection of 16.8 copies of C580Y plasmid/µL of and 100% accuracy for C580Y mutation detection. The PfC580Y LAMP-SNP-LFA method is faster and simpler than conventional polymerase chain reaction/DNA sequencing and has the potential to support antimalarial management policies, malaria control, and global elimination efforts.

摘要

在大湄公河次区域已经出现了对抗疟药物青蒿素(ART)的耐药性。目前,用于鉴定青蒿素耐药性的主要分子标记是恶性疟原虫 Pfkelch13 中的 C580Y 突变。在现场快速准确地检测青蒿素耐药性对于指导疟疾控制和消除干预措施非常必要。我们的研究使用环介导等温扩增和单核苷酸多态性分析可视化(LAMP-SNP-LFA)方法评估 PfC580Y,该方法用于检测 2014 年至 2019 年期间在泰国采集的临床样本中的青蒿素耐药性。确定的最佳反应孵育条件为在 56°C 下孵育 45 分钟,然后使用 LFA 对阳性扩增子进行目视检测。该检测方法具有较高的分析灵敏度和特异性,其检测 C580Y 质粒的检测限为 16.8 拷贝/µL,对 C580Y 突变的检测准确率为 100%。PfC580Y LAMP-SNP-LFA 方法比常规聚合酶链反应/DNA 测序更快、更简单,具有支持抗疟管理政策、疟疾控制和全球消除努力的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1270/10465885/e3ecdca8f95c/gr1.jpg

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