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Series GSE7704 Query DataSets for GSE7704
Status Public on Aug 15, 2007
Title In vivo evidence of Pseudomonas aeruignosa nutrient acquisition and pathogenesis in the cystic fibrosis lung
Organism Pseudomonas aeruginosa
Experiment type Expression profiling by array
Summary One of the hallmarks of Pseudomonas aeruginosa cystic fibrosis (CF) infection is very high-cell-density (HCD) replication in the lung, allowing this bacterium to induce virulence controlled by HCD quorum-sensing systems. However, the nutrient sources sustaining HCD replication in this chronic infection is largely unknown. Hence, understanding the nutrient factors contributing to HCD in the CF lung will yield new insights into the 'metabolic pathogenicity' and potential treatment of CF infections caused by P. aeruginosa. Herein, we performed microarray studies of P. aeruginosa directly isolated from the CF lung to demonstrate its metabolic capability and virulence in vivo. Our in vivo microarray data, confirmed by real-time reverse-transcription-PCR, indicated P. aeruginosa expressed several genes for virulence, drug-resistance, and utilization of multiple nutrient sources (lung surfactant lipids and amino acids) contributing to HCD replication. The data also indicates deregulation of several pathways, suggesting in vivo evolution by deregulation of a large portion of the transcriptome during chronic CF infection. To our knowledge, this is the first in vivo transcriptome of P. aeruginosa in a natural CF infection, and it indicates several important aspects of pathogenesis, drug-resistance, and nutrient-utilization never before observed in vivo.
Keywords: in vivo gene induction
 
Overall design The purpose of the experiment was to observe which genes are upregulated in P. aeruginosa during chronic CF lung infection as compared to PAO1. All in vitro studies were grown in 1x M9 minimal media supplemented with 20 mM citrate and grown to mid-log phase prior to RNA isolation. The in vivo RNA was isolated directly from CF sputum samples after TRIzol treatment. Each in vitro sample (both for PAO1 and the CF sputum pool isolate) were processed individually and in triplicate. Two in vivo isolations from sputum were conducted from the same patient but two different sputum samples. After isolation of total RNA, samples were processed for microarrays (i.e. cDNA synthesis, fragmentation, labeling, etc) as recommended by Affymetrix, and processed on the GeneChip as recommended by Affymetrix.
 
Contributor(s) Son MS, Matthews WJ, Kang Y, Nguyen DT, Hoang TT
Citation(s) 17724070
Submission date May 03, 2007
Last update date Jul 06, 2016
Contact name Tung Hoang
E-mail(s) [email protected]
Phone 808-956-5035
Organization name University of Hawaii at Manoa
Department Microbiology
Lab LSB 318
Street address 1800 East-West Road
City Honolulu
State/province HI
ZIP/Postal code 96822
Country USA
 
Platforms (1)
GPL84 [Pae_G1a] Affymetrix Pseudomonas aeruginosa Array
Samples (14)
GSM187265 PAO1 minimal media citrate replicate1
GSM187266 PAO1 minimal media citrate replicate2
GSM187267 PAO1 minimal media citrate replicate3
Relations
BioProject PRJNA99427

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
GSE7704_RAW.tar 14.5 Mb (http)(custom) TAR (of CEL, CHP)
Processed data provided as supplementary file

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