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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
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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
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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.
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Contributor(s) |
Son MS, Matthews WJ, Kang Y, Nguyen DT, Hoang TT |
Citation(s) |
17724070 |
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Submission date |
May 03, 2007 |
Last update date |
Jul 06, 2016 |
Contact name |
Tung Hoang |
E-mail(s) |
[email protected]
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Phone |
808-956-5035
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Organization name |
University of Hawaii at Manoa
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Department |
Microbiology
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Lab |
LSB 318
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Street address |
1800 East-West Road
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City |
Honolulu |
State/province |
HI |
ZIP/Postal code |
96822 |
Country |
USA |
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Platforms (1) |
GPL84 |
[Pae_G1a] Affymetrix Pseudomonas aeruginosa Array |
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Samples (14)
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GSM187265 |
PAO1 minimal media citrate replicate1 |
GSM187266 |
PAO1 minimal media citrate replicate2 |
GSM187267 |
PAO1 minimal media citrate replicate3 |
GSM187270 |
CF Sputum pool isolate minimal media citrate replicate1 |
GSM187281 |
CF Sputum pool isolate minimal media citrate replicate2 |
GSM187282 |
CF Sputum pool isolate minimal media citrate replicate3 |
GSM187283 |
CF Sputum in vivo replicate1 |
GSM187284 |
CF Sputum in vivo replicate2 |
GSM198186 |
PAO1 minimal media palmitate replicate 1 |
GSM198187 |
PAO1 minimal media palmitate replicate 2 |
GSM198188 |
PAO1 minimal media palmitate replicate 3 |
GSM198189 |
PAO1 minimal media phosphatidylcholine replicate 1 |
GSM198190 |
PAO1 minimal media phosphatidylcholine replicate 2 |
GSM198191 |
PAO1 minimal media phosphatidylcholine replicate 3 |
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Relations |
BioProject |
PRJNA99427 |
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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