Literature DB >> 9105939

PCR detection of Listeria monocytogenes in 'gravad' rainbow trout.

H Ericsson1, P Stålhandske.   

Abstract

'Gravad' rainbow trout artificially contaminated with Listeria monocytogenes was analyzed by use of a 4 h enrichment period followed by extraction of DNA and PCR amplification. This procedure made it possible to detect 10-100 cfu L. monocytogenes per gram 'gravad' rainbow trout, within 12 h. After a prolonged enrichment period of 24 h, numbers as low as 1-10 cfu L. monocytogenes per gram could be detected. The method described may be a useful tool for screening samples of 'gravad' rainbow trout for the presence of L. monocytogenes, since it is sensitive, rapid and simple.

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Year:  1997        PMID: 9105939     DOI: 10.1016/s0168-1605(97)01246-4

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


  3 in total

Review 1.  Specificity and performance of PCR detection assays for microbial pathogens.

Authors:  Konrad Sachse
Journal:  Mol Biotechnol       Date:  2004-01       Impact factor: 2.695

2.  Quantitative detection of Listeria monocytogenes in biofilms by real-time PCR.

Authors:  Morgan Guilbaud; Pierre de Coppet; Fabrice Bourion; Cinta Rachman; Hervé Prévost; Xavier Dousset
Journal:  Appl Environ Microbiol       Date:  2005-04       Impact factor: 4.792

3.  Development and application of a simple loop-mediated isothermal amplification method on rapid detection of Listeria monocytogenes strains.

Authors:  Li Wang; Yue Li; Jin Chu; Zhenbo Xu; Qingping Zhong
Journal:  Mol Biol Rep       Date:  2011-05-14       Impact factor: 2.316

  3 in total

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