Campylobacter jejunitranscriptome changes during loss of culturability in water
AbstractBackgroundThe natural environment serves as a potential reservoir forCampylobacter,the leading cause of bacterial gastroenteritis in humans. However, little is understood about the mechanisms underlying variations in survival characteristics between different strains ofC. jejuniin natural environments, including water.ResultsWe identified threeCampylobacter jejunistrains that exhibited variability in their ability to retain culturability after suspension in water at two different temperatures (4°C and 25°C). Of the three, strainsC. jejuniM1 exhibited the most rapid loss of culturability whilst retaining viability. Using RNAseq transcriptomics, we characterised C.jejuniM1 gene expression in response to suspension in water by analyzing bacterial suspensions recovered immediately after introduction into water (Time 0), and from two sampling time/temperature combinations where considerable loss of culturability was evident, namely (i) after 24 h at 25°C, and (ii) after 72 h at 4°C. Transcript data were compared with a culture-grown control. Some gene expression characteristics were shared amongst the three populations recovered from water, with more genes being up-regulated than down. Many of the up-regulated genes were identified in the Time 0 sample, whereas the majority of down-regulated genes occurred in the 25°C (24 h) sample.ConclusionsVariations in expression were found amongst genes associated with oxygen tolerance, starvation and osmotic stress. However, we also found upregulation of flagellar assembly genes, accompanied by down-regulation of genes involved in chemotaxis. Our data also suggested a switch from secretion via thesecsystem to via thetatsystem, and that the quorum sensing geneluxSmay be implicated in the survival of strain M1 in water. Variations in gene expression also occurred in accessory genome regions. Our data suggest that despite the loss of culturability,C. jejuniM1 remains viable and adapts via specific changes in gene expression.