Enhancing detection of Listeria monocytogenes in food products using an enzyme

被引:2
作者
Felton, Samantha [1 ]
Armstrong, Cheryl [2 ]
Chen, Chin-Yi [2 ]
He, Yiping [2 ]
Lee, Joe [2 ]
Reed, Sue [2 ]
Akula, Nikki [1 ]
Walker, Sharon [3 ]
Berger, Bryan W. [4 ]
Capobianco, Joseph [2 ]
机构
[1] Univ Virginia, Dept Biomed Engn, Charlottesville, VA USA
[2] United States Dept Agr USDA, Eastern Reg Res Ctr ERRC, Agr Res Serv ARS, Wyndmoor, PA 19038 USA
[3] Drexel Univ, Dept Civil Architectural & Environm Engn, Philadelphia, PA USA
[4] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22901 USA
关键词
Food safety; Biofilm; Enzyme; Glycosyl hydrolase; Sample preparation; Pathogen detection; Listeria; BIOFILM FORMATION;
D O I
10.1016/j.foodcont.2022.109445
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
There is a need to identify the presence of microorganisms, in particular human pathogens, in food processing facilities and products. Adhesion of pathogens to surfaces poses a detection challenge with biofilms greatly hindering detection by precluding the transfer of specific material to downstream sensors. Enzymes that disrupt biofilms can therefore enhance detection of foodborne pathogens through facilitating their release from abiotic and biotic surfaces. In this study, a recombinant enzyme, CAase, was applied to improve detection of biofilm-embedded Listeria monocytogenes on food and food contact surfaces. Microbiological and molecular detection methods demonstrated that biofilms treated with enzyme for longer than 4 h resulted in a significant increase in the number of cells released into the media compared to untreated controls. This work demonstrates the benefits of inclusion of enzymes and biosurfactants within sample processing and detection protocols because of their ability to contribute to a more rapid, accurate, reliable, and repeatable microbial detection assay when biofilm embedded pathogens are present.
引用
收藏
页数:9
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