Literature DB >> 18159282

How novel methods can help discover more information about foodborne pathogens.

M W Griffiths1.   

Abstract

Considerable emphasis is being placed on quantitative risk assessment modelling as a basis for regulation of trade in food products. However, for models to be accurate, information about the behaviour of potential pathogens in foods needs to be available. The question is how to obtain this knowledge in a simple and cost effective way. One technique that has great potential is the use of reporter bacteria which have been genetically modified to express a phenotype that can be easily monitored, such as light production in luminescent organisms. Bacteria carrying these (lux) genes can easily be detected using simple luminometers or more sophisticated low light imaging equipment.By monitoring light output from these bacteria over time, it can easily be determined if the organism is growing (resulting in an increase in light emission), is dead (causing a decrease in light production) or is injured (light output remains constant). The use of imaging systems allows the response of bioluminescent bacteria to be studied directly on the food, making the technique even more useful. Applications of bioluminescence are discussed below and include use as reporters of gene expression; biocide efficacy and antibiotic susceptibility; sub-lethal injury; adhesion and biofilm formation; the microbial ecology of foods; pathogenesis; and as biosensors.

Keywords:  Bioluminescence; Ecology; Foodborne pathogens; Gene expression

Year:  2000        PMID: 18159282      PMCID: PMC2094761          DOI: 10.1155/2000/364050

Source DB:  PubMed          Journal:  Can J Infect Dis        ISSN: 1180-2332


  109 in total

1.  Near on-line detection of enteric bacteria using lux recombinant bacteriophage.

Authors:  C P Kodikara; H H Crew; G S Stewart
Journal:  FEMS Microbiol Lett       Date:  1991-10-15       Impact factor: 2.742

2.  Susceptibility of suspended and surface-attached Salmonella enteritidis to biocides and elevated temperatures.

Authors:  V K Dhir; C E Dodd
Journal:  Appl Environ Microbiol       Date:  1995-05       Impact factor: 4.792

3.  In vivo bioluminescence to detect the attachment of L-forms of Listeria monocytogenes to food and clinical contact surfaces.

Authors:  A M Hibma; S A Jassim; M W Griffiths
Journal:  Int J Food Microbiol       Date:  1996-12       Impact factor: 5.277

4.  Hypochlorous acid activates the heat shock and soxRS systems of Escherichia coli.

Authors:  S Dukan; S Dadon; D R Smulski; S Belkin
Journal:  Appl Environ Microbiol       Date:  1996-11       Impact factor: 4.792

5.  Modelling the thermal inactivation of Salmonella typhimurium using bioluminescence data.

Authors:  A Ellison; W Anderson; M B Cole; G S Stewart
Journal:  Int J Food Microbiol       Date:  1994-11       Impact factor: 5.277

6.  Identification and quantification of toxic chemicals by use of Escherichia coli carrying lux genes fused to stress promoters.

Authors:  O Ben-Israel; H Ben-Israel; S Ulitzur
Journal:  Appl Environ Microbiol       Date:  1998-11       Impact factor: 4.792

7.  Expression of bacterial luciferase genes from Vibrio harveyi in Bacillus subtilis and in Escherichia coli.

Authors:  M Karp
Journal:  Biochim Biophys Acta       Date:  1989-01-23

8.  Cloning and sequence analysis of cDNA for the Ca(2+)-activated photoprotein, clytin.

Authors:  S Inouye; F I Tsuji
Journal:  FEBS Lett       Date:  1993-01-11       Impact factor: 4.124

9.  The antibacterial activity of Virkon measured by colony growth and bioluminescence of lux recombinant Listeria monocytogenes.

Authors:  A J Walker; J T Holah; S P Denyer; G S Stewart
Journal:  Lett Appl Microbiol       Date:  1992-08       Impact factor: 2.858

Review 10.  Luminescence-based systems for detection of bacteria in the environment.

Authors:  J I Prosser; K Killham; L A Glover; E A Rattray
Journal:  Crit Rev Biotechnol       Date:  1996       Impact factor: 8.429

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