环介导等温扩增
人乳头瘤病毒
核酸
检出限
基因组DNA
宫颈癌
生物
DNA
分子生物学
化学
色谱法
遗传学
医学
癌症
内科学
作者
Maria Barra,Megan M. Chang,Mila Pontremoli Salcedo,Kathleen M. Schmeler,Michael E. Scheurer,Mauricio Maza,Leticia Rodríguez López,Karla Alfaro,Rebecca Richards‐Kortum
标识
DOI:10.1016/j.ab.2024.115480
摘要
Isothermal nucleic acid amplification methods have many advantages for use at the point of care. However, there is a lack of multiplexed isothermal amplification tests to detect multiple targets in a single reaction, which would be valuable for many diseases, such as infection with high-risk human papillomavirus (hrHPV). In this study, we developed a multiplexed loop-mediated isothermal amplification (LAMP) reaction to detect the three most common hrHPV types that cause cervical cancer (HPV16, HPV18, and HPV45) and a cellular control for sample adequacy. First, we characterized the assay limit of detection (LOD) in a real-time reaction with fluorescence readout; after 30 min of amplification the LOD was 100, 10, and 10 copies/reaction of HPV16, HPV18, and HPV45, respectively, and 0.1 ng/reaction of human genomic DNA (gDNA). Next, we implemented the assay on lateral flow strips, and the LOD was maintained for HPV16 and HPV18, but increased to 100 copies/reaction for HPV45 and to 1 ng/reaction for gDNA. Lastly, we used the LAMP test to evaluate total nucleic acid extracted from 38 clinical samples; compared to qPCR, the LAMP test had 89% sensitivity and 95% specificity. When integrated with sample preparation, this multiplexed LAMP assay could be useful for point-of-care testing.
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