Literature DB >> 22947467

Filter-based pathogen enrichment technology for detection of multiple viable foodborne pathogens in 1 day.

Taku Murakami1.   

Abstract

Conventional foodborne pathogen assays currently used in the food industry often require long culture enrichments to increase pathogen levels so they can be detected. Even using sensitive real-time PCR assays, culture enrichment at least overnight is necessary especially for detection of pathogens with slow growth rates such as Listeria monocytogenes. To eliminate this cumbersome enrichment step and detect minute amounts of pathogens within 1 day, filter-based pathogen enrichment technology was developed utilizing a unique combination of glass fiber depth filter and porous filter aid materials to efficiently separate pathogens from food homogenates and avoid filter clogging by food particles. After pathogen immobilization in depth filters, only viable pathogens were selectively collected in a small volume of growth medium via microbial multiplication and migration; nonviable pathogens remained inside the filters. By assaying viable pathogens using real-time PCRs, multiple species of foodborne pathogens were detected, including L. monocytogenes, Salmonella enterica, and Escherichia coli O157:H7, at around 1 CFU/ml or 1 CFU/g in various food samples. This filter-based pathogen enrichment technology is a unique bacterial enrichment alternative to the conventional culture enrichment step and can significantly shorten the time necessary to obtain assay results.

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Year:  2012        PMID: 22947467     DOI: 10.4315/0362-028X.JFP-12-039

Source DB:  PubMed          Journal:  J Food Prot        ISSN: 0362-028X            Impact factor:   2.077


  4 in total

1.  Rapid sample processing for detection of food-borne pathogens via cross-flow microfiltration.

Authors:  Xuan Li; Eduardo Ximenes; Mary Anne Roshni Amalaradjou; Hunter B Vibbert; Kirk Foster; Jim Jones; Xingya Liu; Arun K Bhunia; Michael R Ladisch
Journal:  Appl Environ Microbiol       Date:  2013-09-06       Impact factor: 4.792

2.  Detection of viable but non-culturable Escherichia coli O157:H7 by PCR in combination with propidium monoazide.

Authors:  Junliang Zhong; Xihong Zhao
Journal:  3 Biotech       Date:  2017-12-22       Impact factor: 2.406

3.  Rapid detection of E. coli O157:H7 by a novel access with combination of improved sample preparation and real-time PCR.

Authors:  Jin-Hee Kim; Se-Wook Oh
Journal:  Food Sci Biotechnol       Date:  2020-05-03       Impact factor: 2.391

4.  Genomic analysis of high copy-number sequences for the targeted detection of Listeria species using a flow-through surveillance system.

Authors:  Beatriz Quiñones; Jaszemyn C Yambao; Veronica S De Guzman; Bertram G Lee; David L Medin
Journal:  Arch Microbiol       Date:  2021-06-02       Impact factor: 2.552

  4 in total

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