The Effect of Atmospheric Cold Plasma on Bacterial Stress Responses and Virulence Using Knockout Mutants.

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2019
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Abstract
is an opportunistic intracellular pathogen commonly associated with serious infections and multiple food-borne outbreaks. In this study, we investigated the influence of atmospheric cold plasma (80 kV, 50 Hz) on (EGD-e) and its knockout mutants of , , , , and genes at different treatment time intervals. Further, to ascertain if sub-lethal environmental stress conditions could influence survival and growth responses, atmospheric cold plasma (ACP) resistance was evaluated for the cultures exposed to cold (4°C) or acid (pH 4) stress for 1 h. The results demonstrate that both wild-type and knockout mutants were similarly affected after 1 min exposure to ACP ( > 0.05), with a difference in response noted only after 3 min of treatment. While all strains exposed to acid/cold stress were hypersensitive to ACP treatment and were significantly reduced or inactivated within 1 min of treatment ( < 0.05). The results indicate and are important for general stress resistance and biofilm, respectively, loss of these two genes significantly reduced bacterial resistance to ACP treatment. In addition, exposure to sub-lethal 1min ACP increased the gene expression of stress associated genes. showed the highest gene expression, increasing by 15.60 fold, followed by (7.19) and (8.6) after 1 min exposure. Overall, an increase in gene expression was seen in all stress associated genes analyzed both at 1 min treatment; while long treatment time reduced the gene expression and some cases down-regulated and gene expression. By comparing the response of mutants under ACP exposure to key processing parameters, the experimental results presented here provide a baseline for understanding the bacterial genetic response and resistance to cold plasma stress and offers promising insights for optimizing ACP applications.
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Authors Patange, Apurva;O'Byrne, Conor;Boehm, Daniela;Cullen, P J;Keener, Kevin;Bourke, Paula;
Journal Frontiers in microbiology
Year 2019
DOI 10.3389/fmicb.2019.02841
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