Emerg Infect Dis. 2024 Sep;30(9):1770-1778. doi: 10.3201/eid3009.240444. Epub 2024 Jul 10.
Spread of the Anopheles stephensi mosquito, an invasive malaria vector, threatens to put an additional 126 million persons per year in Africa at risk for malaria. To accelerate the early detection and rapid response to this mosquito species, confirming its presence and geographic extent is critical. However, existing molecular species assays require specialized laboratory equipment, interpretation, and sequencing confirmation. We developed and optimized a colorimetric rapid loop-mediated isothermal amplification assay for molecular An. stephensi species identification. The assay requires only a heat source and reagents and can be used with or without DNA extraction, resulting in positive color change in 30-35 minutes. We validated the assay against existing PCR techniques and found 100% specificity and analytical sensitivity down to 0.0003 ng of genomic DNA. The assay can successfully amplify single mosquito legs. Initial testing on samples from Marsabit, Kenya, illustrate its potential as an early vector detection and malaria mitigation tool.
致倦库蚊的传播,一种入侵性疟疾传播媒介,有可能使非洲每年新增 1.26 亿人面临疟疾风险。为了加速对这种蚊子的早期发现和快速反应,确认其存在和地理范围至关重要。然而,现有的分子物种检测方法需要专门的实验室设备、解释和测序确认。我们开发并优化了一种用于分子致倦库蚊种鉴定的比色快速环介导等温扩增检测方法。该检测方法只需要热源和试剂,可以与 DNA 提取一起使用,也可以不提取 DNA,在 30-35 分钟内产生阳性颜色变化。我们用现有的 PCR 技术对该检测方法进行了验证,发现其具有 100%的特异性和分析灵敏度,最低可检测到 0.0003 纳克的基因组 DNA。该检测方法可以成功地扩增单只蚊子的腿。对肯尼亚马萨比特样本的初步测试表明,它有可能成为一种早期的媒介检测和疟疾缓解工具。