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    Transcriptome analysis of Listeria monocytogenes exposed to biocide stress reveals a multi-system response involving cell wall synthesis, sugar uptake, and motility

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    Author
    Casey, A.
    Fox, Edward M.
    Schmitz-Esser, Stephan
    Coffey, Aidan
    McAuliffe, Olivia
    Jordan, Kieran cc
    Keyword
    Listeria monocytogenes
    RNA-seq
    Benzethonium chloride
    Transcriptome
    Gene expression
    Biocide stress
    Date
    28/02/2014
    
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    URI
    http://hdl.handle.net/11019/802
    Citation
    Casey A, Fox EM, Schmitz-Esser S, Coffey A, McAuliffe O and Jordan K (2014) Transcriptome analysis of Listeria monocytogenes exposed to biocide stress reveals a multi-system response involving cell wall synthesis, sugar uptake, and motility. Front. Microbiol. 5:68. doi: 10.3389/fmicb.2014.00068
    Abstract
    Listeria monocytogenes is a virulent food-borne pathogen most often associated with the consumption of “ready-to-eat” foods. The organism is a common contaminant of food processing plants where it may persist for extended periods of time. A commonly used approach for the control of Listeria monocytogenes in the processing environment is the application of biocides such as quaternary ammonium compounds. In this study, the transcriptomic response of a persistent strain of L. monocytogenes (strain 6179) on exposure to a sub-lethal concentration of the quaternary ammonium compound benzethonium chloride (BZT) was assessed. Using RNA-Seq, gene expression levels were quantified by sequencing the transcriptome of L. monocytogenes 6179 in the presence (4 ppm) and absence of BZT, and mapping each data set to the sequenced genome of strain 6179. Hundreds of differentially expressed genes were identified, and subsequent analysis suggested that many biological processes such as peptidoglycan biosynthesis, bacterial chemotaxis and motility, and carbohydrate uptake, were involved in the response of L. monocyotogenes to the presence of BZT. The information generated in this study further contributes to our understanding of the response of bacteria to environmental stress. In addition, this study demonstrates the importance of using the bacterium's own genome as a reference when analysing RNA-Seq data.
    Funder
    European Union; Teagasc Walsh Fellowship Programme
    Grant Number
    265877; 266061
    ae974a485f413a2113503eed53cd6c53
    http://dx.doi.org/10.3389/fmicb.2014.00068
    Scopus Count
    Collections
    Food Safety
    Food Biosciences
    Food Biosciences
    Food Biosciences
    Food Biosciences

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