CRISPR-Based Multiplex Detection of Human Papillomaviruses for One-Pot Point-of-Care Diagnostics

被引:12
|
作者
Ghouneimy, Ahmed [1 ]
Ali, Zahir [1 ]
Aman, Rashid [1 ]
Jiang, Wenjun [1 ]
Aouida, Mustapha [2 ]
Mahfouz, Magdy [1 ]
机构
[1] 4700 King Abdullah Univ Sci & Technol, Div Biol Sci, Lab Genome Engn & Synthet Biol, Thuwal 239556900, Saudi Arabia
[2] Hamad Bin Khalifa Univ, Coll Hlth & Life Sci, Div Biol & Biomed Sci, Doha 34110, Qatar
来源
ACS SYNTHETIC BIOLOGY | 2024年 / 13卷 / 03期
关键词
CRISPR-Cas; human papillomavirus; sexuallytransmitted infections; molecular diagnostics; multiplexdetection; point-of-care detection; cervical cancer; NUCLEIC-ACID DETECTION; CERVICAL-CANCER; MOLECULAR-BIOLOGY; INFECTION; LAMP;
D O I
10.1021/acssynbio.3c00655
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The World Health Organization's global initiative toward eliminating high-risk Human Papillomavirus (hrHPV)-related cancers recommends DNA testing over visual inspection in all settings for primary cancer screening and HPV eradication by 2100. However, multiple hrHPV types cause different types of cancers, and there is a pressing need for an easy-to-use, multiplex point-of-care diagnostic platform for detecting different hrHPV types. Recently, CRISPR-Cas systems have been repurposed for point-of-care detection. Here, we established a CRISPR-Cas multiplexed diagnostic assay (CRISPRD) to detect cervical cancer-causing hrHPVs in one reaction (one-pot assay). We harnessed the compatibility of thermostable AapCas12b, TccCas13a, and HheCas13a nucleases with isothermal amplification and successfully detected HPV16 and HPV18, along with an internal control in a single-pot assay with a limit of detection of 10 copies and 100% specificity. This platform offers a rapid and practical solution for the multiplex detection of hrHPVs, which may facilitate large-scale hrHPV point-of-care screening. Furthermore, the CRISPRD platform programmability enables it to be adapted for the multiplex detection of any two nucleic acid biomarkers as well as internal control.
引用
收藏
页码:837 / 850
页数:14
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