Rapid visual detection of <i>Vibrio parahaemolyticus</i> by combining LAMP-CRISPR/Cas12b with heat-labile uracil-DNA glycosylase to eliminate carry-over contamination.

Fang WU; Chen LU; Wenhao HU; Xin Guo; Jiayue Chen; Zhidan Luo

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Rapid visual detection of Vibrio parahaemolyticus by combining LAMP-CRISPR/Cas12b with heat-labile uracil-DNA glycosylase to eliminate carry-over contamination.

Author: Fang WU ¹ ; Chen LU ¹ ; Wenhao HU ¹ ; Xin GUO ² ; Jiayue CHEN ¹ ; Zhidan LUO ³
Author Information

1. Jiangsu Key Laboratory of Marine Biological Resources and Environment, Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening, Jiangsu Ocean University, Lianyungang 222005, China.
2. BestEnzymes Biotech Co., Ltd., Lianyungang 222005, China.
3. Jiangsu Key Laboratory of Marine Biological Resources and Environment, Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening, Jiangsu Ocean University, Lianyungang 222005, China. lzd@jou.edu.cn.
Publication Type:Journal Article
Keywords: CRISPR/Cas12b; LAMP; One-pot detection; UDG; Vibrio parahaemolyticus
MeSH: Vibrio parahaemolyticus/genetics*; Uracil-DNA Glycosidase/genetics*; Hot Temperature; CRISPR-Cas Systems; Food Safety
From: Journal of Zhejiang University. Science. B 2023;24(8):749-754
CountryChina
Language:English
Abstract: Vibrio parahaemolyticus is a major pathogen frequently found in seafood. Rapid and accurate detection of this pathogen is important for the control of bacterial foodborne diseases and to ensure food safety. In this study, we established a one-pot system that combines uracil-DNA glycosylase (UDG), loop-mediated isothermal amplification (LAMP), and clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 12b (Cas12b) for detecting V. parahaemolyticus in seafood. This detection system can effectively perform identification using a single tube and avoid the risk of carry-over contamination.