| Literature DB >> 33321741 |
Jinghua Wu1, Omar Mukama2,3,4, Wei Wu5, Zhiyuan Li2, Jean De Dieu Habimana2, Yinghui Zhang1, Rong Zeng1, Chengrong Nie1, Lingwen Zeng1,6.
Abstract
Cross-border pathogens such as the African swine fever virus (ASFV) still pose a socio-economic threat. Cheaper, faster, and accurate diagnostics are imperative for healthcare and food safety applications. Currently, the discovery of the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) has paved the way for the diagnostics based on Cas13 and Cas12/14 that exhibit collateral cleavage of target and single-stranded DNA (ssDNA) reporter. The reporter is fluorescently labeled to report the presence of a target. These methods are powerful; however, fluorescence-based approaches require expensive apparatuses, complicate results readout, and exhibit high-fluorescence background. Here, we present a new CRISPR-Cas-based approach that combines polymerase chain reaction (PCR) amplification, Cas12a, and a probe-based lateral flow biosensor (LFB) for the simultaneous detection of seven types of ASFV. In the presence of ASFVs, the LFB responded to reporter trans-cleavage by naked eyes and achieved a sensitivity of 2.5 × 10-15 M within 2 h, and unambiguously identified ASFV from swine blood. This system uses less time for PCR pre-amplification and requires cheaper devices; thus, it can be applied to virus monitoring and food samples detection.Entities:
Keywords: African swine fever virus; CRISPR–Cas12a; detection; lateral flow biosensor; target pre-amplification
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Year: 2020 PMID: 33321741 PMCID: PMC7763806 DOI: 10.3390/bios10120203
Source DB: PubMed Journal: Biosensors (Basel) ISSN: 2079-6374