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Published on: March 8, 2012
PCR-LbCas12a Assay for Genotyping of HPV 16 and 18
ChonIl Paek1,2, Jin Zhou3, HuiYon Sin4
1Faculty of Life Science, KIM IL SUNG University, Pyongyang, Democratic People's Republic of Korea. ci.paek0112@ryongnamsan.edu.kp.
Abstract:
CRISPR/Cas12a systems have been widely used in nucleic acid detection, because of their high specificity and trans-cleavage activity. We combined the specificity of CRISPR/Cas12a system with the sensitivity of PCR, to develop a new HPV detection assay with high specificity and sensitivity, called PCR-LbCas12a assay. Here, we pre-amplified almost all high-risk HPV genotypes with consensus primer (MY09/11) and added to new tubes containing HPV 16 or 18 CRISPR/Cas12a system for HPV genotyping. The LOD of PCR-LbCas12a for HPV16 or HPV18 DNA was 100 copies and 10 copies per reaction, respectively. In mixed samples of HPV 16 and HPV 18 DNA, PCR-LbCas12a assay could detect HPV16 DNA from samples containing 102 copies of HPV16 and 104 copies of HPV18. On the other hand, HPV18 DNA was detected from samples containing 103 copies of HPV16 and HPV18, respectively. Following validation with HPV-positive and HPV-negative cell lines (SiHa, HeLa, and C-33A), the PCR-LbCas12a assay was evaluated using 39 clinical samples previously characterized by type-specific qPCR. The assay demonstrated a sensitivity of 91.3 (95 CI 71.9-98.9) and a specificity of 100. The PCR-LbCas12a assay can discriminate the HPV 16 and HPV 18 genotypes, and holds great potential in simultaneous detection of most high-risk HPV genotypes including HPV 16 and HPV18.