Precise pathogen quantification by CRISPR-Cas: a sweet but tough nut to crack

被引:2
|
作者
Yao, Zhihao [1 ,2 ]
Li, Wanglu [1 ]
He, Kaiyu [1 ]
Wang, Hongmei [1 ]
Xu, Yan [2 ]
Xu, Xiahong [1 ]
Wu, Qun [2 ]
Wang, Liu [1 ,3 ]
机构
[1] Zhejiang Acad Agr Sci, State Key Lab Managing Biot & Chem Threats Qual &, Inst Agroprod Safety & Nutr, Hangzhou 310021, Peoples R China
[2] Jiangnan Univ, State Key Lab Food Sci & Technol, Lab Brewing Microbiol & Appl Enzymol, Key Lab Ind Biotechnol,Minist Educ,Sch Biotechnol, Wuxi 214122, Jiangsu, Peoples R China
[3] Minist Agr & Rural Affairs, Key Lab Traceabil Agr Genet Modified Organisms, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Pathogen; CRISPR-Cas; biosensor; quantification; isothermal amplification; ISOTHERMAL AMPLIFICATION; DNA; CRISPR-CAS12A; GUIDE; SERS;
D O I
10.1080/1040841X.2024.2404041
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pathogen detection is increasingly applied in medical diagnosis, food processing and safety, and environmental monitoring. Rapid, sensitive, and accurate pathogen quantification is the most critical prerequisite for assessing protocols and preventing risks. Among various methods evolved, those based on clustered regularly interspaced short palindromic repeats (CRISPR)-associated proteins (Cas) have been developed as important pathogen detection strategies due to their distinct advantages of rapid target recognition, programmability, ultra-specificity, and potential for scalability of point-of-care testing (POCT). However, arguments and concerns on the quantitative capability of CRISPR-based strategies are ongoing. Herein, we systematically overview CRISPR-based pathogen quantification strategies according to the principles, properties, and application scenarios. Notably, we review future challenges and perspectives to address the of precise pathogen quantification by CRISPR-Cas. We hope the insights presented in this review will benefit development of CRISPR-based pathogen detection methods.
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收藏
页数:19
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