Harnessing Multiplex CrRNA Enables an Amplification-free/CRISPR-Cas12a-based Diagnostic Methodology for
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Abstract
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 . 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.
References
1.
Li S, Cheng Q, Wang J, Li X, Zhang Z, Gao S
. CRISPR-Cas12a-assisted nucleic acid detection. Cell Discov. 2018; 4:20.
PMC: 5913299.
DOI: 10.1038/s41421-018-0028-z.
View
2.
Wu J, Mukama O, Wu W, Li Z, Habimana J, Zhang Y
. A CRISPR/Cas12a Based Universal Lateral Flow Biosensor for the Sensitive and Specific Detection of African Swine-Fever Viruses in Whole Blood. Biosensors (Basel). 2020; 10(12).
PMC: 7763806.
DOI: 10.3390/bios10120203.
View
3.
He Z, Ni Q, Song Y, Wang R, Tang Y, Wu Y
. Development of a nucleic acid lateral flow strip for rapid, visual detection of Nosema bombycis in silkworm eggs. J Invertebr Pathol. 2019; 164:59-65.
DOI: 10.1016/j.jip.2019.04.004.
View
4.
Kajiwara H, Murakami R
. Rapid detection of silkworm microsporidia by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. J Invertebr Pathol. 2019; 166:107223.
DOI: 10.1016/j.jip.2019.107223.
View
5.
Keeling P, Fast N
. Microsporidia: biology and evolution of highly reduced intracellular parasites. Annu Rev Microbiol. 2002; 56:93-116.
DOI: 10.1146/annurev.micro.56.012302.160854.
View