A method for Neisseria gonorrhoeae (NG)/Chlamydia trachomatis (CT) detection is developed using multiplex-recombinase polymerase amplification and Cas12a/Cas13a. This method can detect NG and CT simultaneously with high sensitivity and specificity. This method has great potential to be further developed into larger-scale screening and point-of-care testing (POCT).
Keywords: CRISPR‒Cas12a; CRISPR‒Cas13a; Chlamydia trachomatis; Neisseria gonorrhoeae; coinfection; dual-target detection.