<p><i>Campylobacter</i> spp. cause foodborne illness on a global scale. Despite their sensitivity to atmospheric oxygen, <i>Campylobacter</i> spp. often survive O<sub>2</sub> exposure during meat processing. The genetic mechanisms underlying aerotolerance in <i>Campylobacter</i> spp. are not well understood. In this study, <i>C. jejuni</i> strain S2-20 and <i>C. coli</i> strain WA333 were subjected to atmospheric O<sub>2,</sub> and transcriptomes were analyzed at multiple timepoints, using RNA-Seq technology. In both species, a large number of genes involved in ribosomal formation and oxidative phosphorylation were downregulated at most timepoints. Upregulation of genes associated with iron acquisition was noted in <i>C. coli</i> but not <i>C. jejuni</i>. Several genes involved in molybdate and tungstate uptake were upregulated in <i>C. jejuni</i>. Molybdate is important for enzymes that allow the use of alternate electron acceptors instead of O<sub>2</sub>. This finding, along with the downregulation of genes involved in oxidative phosphorylation, suggests a shift in <i>C. jejuni</i> from aerobic to anaerobic respiration during aerobic conditions, possibly reducing oxidative stress. Our results also suggest that <i>C. jejuni</i> and <i>C. coli</i> utilize different strategies to survive aerobic conditions. To our knowledge, this is the first study to use RNA-Seq to investigate <i>C. coli</i> aerotolerance on a genome-wide scale.</p>

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Unraveling aerotolerancy of campylobacter jejuni and campylobacter coli using a transcriptomic approach

  • Elise Delaporte,
  • Anand B. Karki,
  • Mohamed K. Fakhr

摘要

Campylobacter spp. cause foodborne illness on a global scale. Despite their sensitivity to atmospheric oxygen, Campylobacter spp. often survive O2 exposure during meat processing. The genetic mechanisms underlying aerotolerance in Campylobacter spp. are not well understood. In this study, C. jejuni strain S2-20 and C. coli strain WA333 were subjected to atmospheric O2, and transcriptomes were analyzed at multiple timepoints, using RNA-Seq technology. In both species, a large number of genes involved in ribosomal formation and oxidative phosphorylation were downregulated at most timepoints. Upregulation of genes associated with iron acquisition was noted in C. coli but not C. jejuni. Several genes involved in molybdate and tungstate uptake were upregulated in C. jejuni. Molybdate is important for enzymes that allow the use of alternate electron acceptors instead of O2. This finding, along with the downregulation of genes involved in oxidative phosphorylation, suggests a shift in C. jejuni from aerobic to anaerobic respiration during aerobic conditions, possibly reducing oxidative stress. Our results also suggest that C. jejuni and C. coli utilize different strategies to survive aerobic conditions. To our knowledge, this is the first study to use RNA-Seq to investigate C. coli aerotolerance on a genome-wide scale.