» Articles » PMID: 36524221

Visual and Label-free ASFV and PCV2 Detection by CRISPR-Cas12a Combined with G-quadruplex

Overview
Journal Front Vet Sci
Date 2022 Dec 16
PMID 36524221
Authors
Affiliations
Soon will be listed here.
Abstract

African swine fever (ASF) and postweaning multisystemic wasting syndrome (PMWS) are acute infectious diseases caused by the African swine fever virus (ASFV) and porcine circovirus type 2 (PCV2). At present, there are no effective vaccines for the prevention of ASFV. PMWS, which is harmful to the domestic and even the world pig industry, is difficult to cure and has a high mortality. So, developing simple, inexpensive, and accurate analytical methods to detect and effectively diagnose ASFV and PCV2 can be conducive to avoid ASFV and PCV2 infection. CRISPR has become a potentially rapid diagnostic tool due to recent discoveries of the trans-cleavage properties of CRISPR type V effectors. Herein, we report the visual detection based on CRISPR-Cas12a (cpf1), which is more convenient than fluorescence detection. Through cleavage target DNA activation, Cas12a can trans-cleavage ssDNA G-quadruplex. TMB/HO and Hemin cannot be catalyzed by cleavaged G-DNA to produce green color products. This protocol is useful for the detection of ASFV and PCV2 with high sensitivity. This method can enable the development of visual and label-free ASFV and PCV2 detection and can be carried out in the field without relying on instruments or power. This method can complete nucleic acid detection at 37 °C without using other instruments or energy. Our research has expanded the application of Cas12a and laid the foundation for the field's rapid detection of viral nucleic acid in future.

Citing Articles

Detection of Porcine Circovirus (PCV) Using CRISPR-Cas12a/13a Coupled with Isothermal Amplification.

Wang H, Zhou G, Liu H, Peng R, Sun T, Li S Viruses. 2024; 16(10).

PMID: 39459882 PMC: 11512303. DOI: 10.3390/v16101548.


Strategic nucleic acid detection approaches for diagnosing African swine fever (ASF): navigating disease dynamics.

Zhu Y, Zhang M, Jie Z, Guo S, Zhu Z, Tao S Vet Res. 2024; 55(1):131.

PMID: 39375775 PMC: 11460097. DOI: 10.1186/s13567-024-01386-8.


Bridging the Gap: Can COVID-19 Research Help Combat African Swine Fever?.

Pakotiprapha D, Kuhaudomlarp S, Tinikul R, Chanarat S Viruses. 2023; 15(9).

PMID: 37766331 PMC: 10536364. DOI: 10.3390/v15091925.

References
1.
Ge S, Li J, Fan X, Liu F, Li L, Wang Q . Molecular Characterization of African Swine Fever Virus, China, 2018. Emerg Infect Dis. 2018; 24(11):2131-2133. PMC: 6199985. DOI: 10.3201/eid2411.181274. View

2.
Kosman J, Juskowiak B . Peroxidase-mimicking DNAzymes for biosensing applications: a review. Anal Chim Acta. 2011; 707(1-2):7-17. DOI: 10.1016/j.aca.2011.08.050. View

3.
Xi H, Juhas M, Zhang Y . G-quadruplex based biosensor: A potential tool for SARS-CoV-2 detection. Biosens Bioelectron. 2020; 167:112494. PMC: 7403137. DOI: 10.1016/j.bios.2020.112494. View

4.
Yang L, Wang L, Lv M, Sun Y, Cao J . Clinical Validation of DNA Extraction-Free qPCR, Visual LAMP, and Fluorescent LAMP Assays for the Rapid Detection of African Swine Fever Virus. Life (Basel). 2022; 12(7). PMC: 9320077. DOI: 10.3390/life12071067. View

5.
Zhao K, Shi W, Han F, Xu Y, Zhu L, Zou Y . Specific, simple and rapid detection of porcine circovirus type 2 using the loop-mediated isothermal amplification method. Virol J. 2011; 8:126. PMC: 3315793. DOI: 10.1186/1743-422X-8-126. View