A point-of-care rapid HIV-1 test using an isothermal recombinase-aided amplification and CRISPR Cas12a-mediated detection

重组酶聚合酶扩增 生物 病毒学 环介导等温扩增 清脆的 检测点注意事项 逆转录酶 人类免疫缺陷病毒(HIV) 分子生物学 聚合酶链反应 DNA 基因 遗传学 免疫学
作者
Jianhui Zhao,Cailing Ao,Zhengwei Wan,Emmanuel Enoch Dzakah,Yuanhao Liang,Hongqing Lin,Haiying Wang,Shixing Tang
出处
期刊:Virus Research [Elsevier BV]
卷期号:303: 198505-198505 被引量:35
标识
DOI:10.1016/j.virusres.2021.198505
摘要

Human immunodeficiency virus type one (HIV-1) infection is one of the major public health problems worldwide. Effective control of HIV-1 epidemic relies on early diagnosis of HIV-1 infection by using simple, rapid point-of-care test (POCT). An integrated assay was developed and evaluated in this study to combine a real-time isothermal reverse-transcription recombinase-aided amplification (rRT-RAA) and CRISPR Cas12a-mediated detection for HIV-1. The testing results could be directly observed with naked eye using a blue light imager, making it a suitable on-site testing assay. Our preliminary data indicated that the assay was capable of detecting 20 copies of purified HIV-1 DNA or RNA per reaction or as low as 123 copies/ml of HIV-1 viral load in clinical samples. When screening 155 clinical samples with or without HIV-1 infection, the sensitivity and specificity of the rRT-RAA assay were 98.95% (94/95) and 100% (60/60), respectively. The coefficient value was 0.986 when compared with the Chinese FDA approved HIV-1 RT-qPCR assay. Furthermore, the newly developed HIV-1 rRT-RAA assay could detect the major HIV-1 genotypes CRF01_AE, CRF07_BC, CRF08_BC, CRF08_BC and subtype B in China. Our preliminary results indicated that the rRT-RAA assay or its combination with CRISPR Cas12a-mediated detection could serve as a rapid, convenient, and robust assay for HIV-1 detection.
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