Literature DB >> 8751091

Probes and polymerase chain reaction for detection of food-borne bacterial pathogens.

J E Olsen1, S Aabo, W Hill, S Notermans, K Wernars, P E Granum, T Popovic, H N Rasmussen, O Olsvik.   

Abstract

DNA-hybridization and the polymerase chain reaction (PCR) are techniques commonly used to detect pathogenic bacteria. In this paper, the use of these techniques for detection of Salmonella, E. coli, V. cholerae, non-O1 Vibrio, Yersinia enterocolitica, Campylobacter, Listeria monocytogenes, Staphylococcus aureus, Bacillus cereus, Clostridium perfringens, and C. botulinum is reviewed with emphasis on application in food microbiology. In food control, DNA-techniques have most often been used in a 'culture confirmation' fashion, i.e. bacteria are enriched and sometimes even purified by traditional culture procedures and thereafter identified by the use of DNA-based methods. The most desirable approach is, however, to detect organisms directly in the food, but major problems remain to be solved before this can be routinely performed.

Entities:  

Mesh:

Year:  1995        PMID: 8751091     DOI: 10.1016/0168-1605(94)00159-4

Source DB:  PubMed          Journal:  Int J Food Microbiol        ISSN: 0168-1605            Impact factor:   5.277


  19 in total

1.  Inhibitory effects of collagen on the PCR for detection of Clostridium perfringens.

Authors:  S Kim; R G Labbe; S Ryu
Journal:  Appl Environ Microbiol       Date:  2000-03       Impact factor: 4.792

Review 2.  Methodologies for the characterization of microbes in industrial environments: a review.

Authors:  Johanna Maukonen; Jaana Mättö; Gun Wirtanen; Laura Raaska; Tiina Mattila-Sandholm; Maria Saarela
Journal:  J Ind Microbiol Biotechnol       Date:  2003-05-23       Impact factor: 3.346

3.  Toward an international standard for PCR-based detection of food-borne thermotolerant Campylobacters: validation in a multicenter collaborative trial.

Authors:  P S Lübeck; N Cook; M Wagner; P Fach; J Hoorfar
Journal:  Appl Environ Microbiol       Date:  2003-09       Impact factor: 4.792

4.  Identification and detection of Bacillus sporothermodurans spores in 1, 10, and 100 milliliters of raw milk by PCR.

Authors:  L M Herman; M J Vaerewijck; R J Moermans; G M Waes
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

5.  Development of a cell culture method to isolate and enrich Salmonella enterica serotype enteritidis from shell eggs for subsequent detection by real-time PCR.

Authors:  J B Day; U Basavanna; S K Sharma
Journal:  Appl Environ Microbiol       Date:  2009-06-26       Impact factor: 4.792

6.  A gyrB-targeted PCR for rapid identification of Salmonella.

Authors:  Xuhong Ye; Yiming Wang; Xiangui Lin
Journal:  Curr Microbiol       Date:  2011-09-03       Impact factor: 2.188

7.  Detection of mRNA by reverse transcription-PCR as an indicator of viability in Escherichia coli cells.

Authors:  G E Sheridan; C I Masters; J A Shallcross; B M MacKey
Journal:  Appl Environ Microbiol       Date:  1998-04       Impact factor: 4.792

8.  Automated 5' nuclease PCR assay for identification of Salmonella enterica.

Authors:  J Hoorfar; P Ahrens; P Rådström
Journal:  J Clin Microbiol       Date:  2000-09       Impact factor: 5.948

9.  TaqMan PCR for detection of Vibrio cholerae O1, O139, non-O1, and non-O139 in pure cultures, raw oysters, and synthetic seawater.

Authors:  W J Lyon
Journal:  Appl Environ Microbiol       Date:  2001-10       Impact factor: 4.792

10.  An automated fluorescent PCR method for detection of shiga toxin-producing Escherichia coli in foods.

Authors:  S Chen; R Xu; A Yee; K Y Wu; C N Wang; S Read; S A De Grandis
Journal:  Appl Environ Microbiol       Date:  1998-11       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.