The multiplex-crRNA CRISPR/Cas12a detection method saves hands-on time, reduces the risk of aerosol pollution, and can be directly applied to detecting silkworms infected with Nosema bombycis. This study provides a new approach for the inspection and quarantine of silkworm pébrine disease in sericulture and provides a new method for the detection of other pathogens.
Keywords: CRISPR/Cas12a; Nosema bombycis; amplification-free DNA diagnostic; multiplex crRNA; pathogen detection.