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Journal ArticleDOI

CRISPR-Cas-based detection for food safety problems: Current status, challenges, and opportunities.

Yaru Li, +4 more
- 07 Jul 2022 - 
- Vol. 21, Iss: 4, pp 3770-3798
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TLDR
In this article , a review on CRISPR-Cas-based detection and its current status and huge potential specifically for food safety inspection is presented. But, the current food safety detection methods are still unsatisfactory in some ways such as being timeconsuming, displaying unmet sensitivity and specificity standards, and there is a comparative paucity of multiplexed testing and POCT.
Abstract
Food safety is one of the biggest public issues occurring around the world. Microbiological, chemical, and physical hazards can lead to food safety issues, which may occur at all stages of the supply chain. In order to tackle food safety issues and safeguard consumer health, rapid, accurate, specific, and field-deployable detection methods meeting diverse requirements are one of the imperative measures for food safety assurance. CRISPR-Cas system, a newly emerging technology, has been successfully repurposed in biosensing and has demonstrated huge potential to establish conceptually novel detection methods with high sensitivity and specificity. This review focuses on CRISPR-Cas-based detection and its current status and huge potential specifically for food safety inspection. We firstly illustrate the pending problems in food safety and summarize the popular detection methods. We then describe the potential applications of CRISPR-Cas-based detection in food safety inspection. Finally, the challenges and futuristic opportunities are proposed and discussed. Generally speaking, the current food safety detection methods are still unsatisfactory in some ways such as being time-consuming, displaying unmet sensitivity and specificity standards, and there is a comparative paucity of multiplexed testing and POCT. Recent studies have shown that CRISPR-Cas-based biosensing is an innovative and fast-expanding technology, which could make up for the shortcomings of the existing methods or even replace them. To sum up, the implementation of CRISPR-Cas and the integration of CRISPR-Cas with other techniques is promising and desirable, which is expected to provide "customized" and "smart" detection methods for food safety inspection in the coming future.

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Citations
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Novel non-nucleic acid targets detection strategies based on CRISPR/Cas toolboxes: A review.

TL;DR: A comprehensive review of CRISPR/Cas-based tools for non-nucleic acid target detection can be found in this article , where the authors summarize the strategies and prospects of these tools in this field.
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A ratiometric fluorescent biosensing platform for ultrasensitive detection of Salmonella typhimurium via CRISPR/Cas12a and silver nanoclusters

TL;DR: In this paper , the authors used ratiometric fluorescence in CRISPR/Cas-based detection, which minimizes interference and improves reliability for pathogenic bacteria detection in real food samples.
Journal ArticleDOI

Comparison of CRISPR/Cas and Argonaute for nucleic acid tests.

TL;DR: In this article , a comparison of two nucleases side by side in terms of similarities, differences, and complementarities is proposed for the design of nucleic acid tests (NATs).
Journal ArticleDOI

A ratiometric fluorescent biosensing platform for ultrasensitive detection of Salmonella typhimurium via CRISPR/Cas12a and silver nanoclusters.

TL;DR: In this paper , the authors used ratiometric fluorescence in CRISPR/Cas-based detection, which minimizes interference and improves reliability for pathogenic bacteria detection in real food samples.
Journal ArticleDOI

Recent advances on CRISPR/Cas system-enabled portable detection devices for on-site agri-food safety assay

TL;DR: In this article , a review comprehensively summarized the recent advances on the construction of CRISPR/Cas systems-based on-site detection technologies and their portable detection devices, as well as their promising applications in the field of agri-food safety.
References
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Journal ArticleDOI

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Multiplex Genome Engineering Using CRISPR/Cas Systems

TL;DR: Two different type II CRISPR/Cas systems are engineered and it is demonstrated that Cas9 nucleases can be directed by short RNAs to induce precise cleavage at endogenous genomic loci in human and mouse cells, demonstrating easy programmability and wide applicability of the RNA-guided nuclease technology.
Journal ArticleDOI

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Journal ArticleDOI

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TL;DR: In this paper, the authors characterized Cpf1, a putative class 2 CRISPR effector, which is a single RNA-guided endonuclease lacking tracrRNA and utilizes a T-rich protospacer-adjacent motif.