Cascade CRISPR/cas Enables More Sensitive Detection of Toxoplasma gondii and Listeria monocytogenes than Single CRISPR/cas
Year: 2025
Type: article
Abstract: Foodborne pathogens represent a class of pathogenic microorganisms capable of causing food poisoning or serving as foodborne vectors, constituting a major source of food safety concerns. With increasing demands for rapid diagnostics, conventional culture-based methods and PCR assays face limitations due to prolonged turnaround times and specialized facility requirements. While CRISPR-based detection has emerged as a promising rapid diagnostic platform, its inherent inability to detect low-abundance targets necessitates coupling with isothermal amplification, thereby increasing operational complexity. In this study, we developed a novel amplification-free Cascade-CRISPR detection system utilizing hairpin DNA amplifier. This method achieves detection sensitivity as low as 10 fM for DNA targets within 30 minutes without requiring pre-amplification, with background signal suppression achieved through optimized NaCl concentration. Validation using artificially contaminated food samples demonstrated the platform's robust performance for both Toxoplasma gondii(T. gondii) and Listeria monocytogenes(L. monocytogenes) detection, confirming broad applicability. In summary, this study establishes an amplification-free Cascade-CRISPR detection platform that achieves high sensitivity and rapid turnaround, demonstrating strong potential for on-site screening of foodborne pathogens.
Source: Microorganisms
Authors: Dawei Chen, Min Sun, Bingbing Li, Jian Ma, Qinjun Zhang, Wanli Yin, Jie Li, Mingyue Wei, Liang Liu, Pengfei Yang, Yujuan Shen
Language: English
Subfield: Biomedical Engineering
Field: Engineering
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $3,258
Awards: G6238395865, G8209457962
OpenAlex ID: W4413378330
