Detection of the SARS-CoV-2 D614G mutation using engineered Cas12a guide RNA.

Meng, Qingzhou; Wang, Xinjie; Wang, Yanqun; Dang, Lu; Liu, Xinyi; Ma, Xiaodong; Chi, Tian; Wang, Xian; Zhao, Qin; Yang, Guang; Liu, Ming; Huang, Xingxu; Ma, Peixiang

Detection of pathogens with single-nucleotide variations is indispensable for the disease tracing, but remains technically challenging. The D614G mutation in the SARS-CoV-2 spike protein is known to markedly enhance viral infectivity but is difficult to detect. Here, we report an effective approach called "synthetic mismatch integrated crRNA guided Cas12a detection" (symRNA-Cas12a) to detect the D614 and G614 variants effectively. Using this method, we systemically screened a pool of crRNAs that contain all the possible nucleotide substitutions covering the -2 to +2 positions around the mutation and identify one crRNA that can efficiently increase the detection specificity by 13-fold over the ancestral crRNA. With this selected crRNA, the symRNA-Cas12a assay can detect as low as 10 copies of synthetic mutant RNA and the results are confirmed to be accurate by Sanger sequencing. Overall, we have developed the symRNA-Cas12a method to specifically, sensitively and rapidly detect the SARS-CoV-2 D614G mutation. This article is protected by copyright. All rights reserved.