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Series GSE63622 Query DataSets for GSE63622
Status Public on Nov 26, 2014
Title Transcriptomic change of Legionella pneumophila in water.
Organism Legionella pneumophila subsp. pneumophila str. Philadelphia 1
Experiment type Expression profiling by array
Summary Legionella pneumophila (Lp) is an opportunistic pathogen and its survival in water is critical for human infection. Therefore, identifying the genes of Lp that are required for survival in water may help devise strategies to prevent Legionella outbreaks. In this study, we exposed Lp in rich medium and in an artificial freshwater medium (Fraquil) for 2, 6 and 24 hours to uncover the global transcriptomic changes of Lp in water. The repression of major metabolic pathways, such as division, transcription and translation, suggests that Lp enters a dormant state in water. The induction of the flagellar associated genes (flg, fli and mot), enhance entry genes (enh) and some Icm/Dot effectors suggests that Lp may be waiting to establish intracellular replication in suitable host.
Moreover, many genes involved in resistance to antibiotic and oxidative stress were induced, suggesting that Lp may be more tolerant to environmental stresses in water. Indeed, Lp exposed to water is more resistant to erythromycin, gentamycin and kanamycin than those cultured in rich medium. Apart from this, the gene bdhA involved in the degradation of the intracellular energy storage compound poly-hydroxybutyrate is highly expressed in water. Further characterization shows that bdhA is positively regulated by RpoS during short-term exposure to water. The deletion mutant of bdhA had a survival defect in water at 37°C, demonstrating that this gene is important for maintaining the long-term survivorship of Lp in water. Other identified genes highly induced upon exposure to water could also be necessary for Lp to survive in water.
 
Overall design Legionella pneumophila Philadelphia-1 strain JR32 was grown in AYE broth at 25°C shaking to OD600 of 1 in triplicate. Samples were taken for analysis; this is the control. Then the cultures were washed three times in Fraquil and resuspended in Fraquil to an OD600 of 1 and transfered to vessels of bioreactior (Biostat Q-plus). Samples were taken after 2h, 6h and 24h.
 
Contributor(s) Li L, Mendis N, Trigui H, Faucher SP
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Submission date Nov 25, 2014
Last update date Nov 26, 2014
Contact name Sebastien Faucher
E-mail(s) sebastien.faucher@gmail.com
Phone 514-398-7886
Organization name McGill University
Department Natural Resource Sciences
Lab Faucher
Street address 21,111 Lakeshore
City St-Anne-de-Bellevue
State/province QC
ZIP/Postal code H9X 3V9
Country Canada
 
Platforms (1)
GPL19458 Legionella pneumophila Philadelphia-1 3x15K array
Samples (12)
GSM1553881 Legionella pneumophila grown in AYE to OD600 of 1, biological replicate 1
GSM1553882 Legionella pneumophila grown in AYE to OD600 of 1, biological replicate 2
GSM1553883 Legionella pneumophila grown in AYE to OD600 of 1, biological replicate 3
Relations
BioProject PRJNA268489

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE63622_RAW.tar 23.1 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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