CRISPR-Cas-based techniques for pathogen detection: Retrospect, recent advances, and future perspectives

被引:32
|
作者
Huang, Tao
Zhang, Rui [1 ]
Li, Jinming [1 ]
机构
[1] Chinese Acad Med Sci, Inst Geriatr Med, Beijing Hosp, Natl Ctr Clin Labs,Natl Ctr Gerontol, 1 Da HuaRoad, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
CRISPR-Cas; Pathogen detection; Point-of-care testing; Standardized testing; RECOMBINASE POLYMERASE AMPLIFICATION; ISOTHERMAL AMPLIFICATION; DNA; SARS-COV-2; PCR; ENDONUCLEASE; PERFORMANCE; TECHNOLOGY; CHALLENGES; BIOSENSOR;
D O I
10.1016/j.jare.2022.10.011
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Early detection of pathogen-associated diseases are critical for effective treatment. Rapid, specific, sensitive, and cost-effective diagnostic technologies continue to be challenging to develop. The current gold standard for pathogen detection, polymerase chain reaction technology, has limitations such as long operational cycles, high cost, and high technician and instrumentation requirements.Aim of review: This review examines and highlights the technical advancements of CRISPR-Cas in patho-gen detection and provides an outlook for future development, multi-application scenarios, and clinical translation.Key scientific concepts of review: Approaches enabling clinical detection of pathogen nucleic acids that are highly sensitive, specific, cheap, and portable are necessary. CRISPR-Cas9 specificity in targeting nucleic acids and "collateral cleavage" activity of CRISPR-Cas12/Cas13/Cas14 show significant promise in nucleic acid detection technology. These methods have a high specificity, versatility, and rapid detection cycle. In this paper, CRISPR-Cas-based detection methods are discussed in depth. Although CRISPR-Cas-mediated pathogen diagnostic solutions face challenges, their powerful capabilities will pave the way for ideal diagnostic tools.& COPY; 2023 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:69 / 82
页数:14
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