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Series GSE198718 Query DataSets for GSE198718
Status Public on Mar 18, 2022
Title Genetic and transcriptomic characteristics of RhlR-dependent quorum sensing in cystic fibrosis isolates of Pseudomonas aeruginosa: isolate E131
Organism Pseudomonas aeruginosa
Experiment type Expression profiling by high throughput sequencing
Summary In people with the genetic disease cystic fibrosis (CF), bacterial infections involving the opportunistic pathogen Pseudomonas aeruginosa are a significant cause of morbidity and mortality. P. aeruginosa uses a cell-cell signaling mechanism called quorum sensing (QS) to regulate many virulence functions. One type of QS consists of acyl-homoserine lactone (AHL) signals produced by LuxI-type signal synthases, which bind a cognate LuxR-type transcription factor. In laboratory strains and conditions, P. aeruginosa employs two AHL synthase/receptor pairs arranged in a hierarchy, with the LasI/R system controlling the RhlI/R system and many downstream virulence factors. However, P. aeruginosa isolates with inactivating mutations in lasR are frequently isolated from chronic CF infections. We and others have shown that these isolates frequently use RhlR as the primary QS regulator. RhlR is rarely mutated in CF and environmental settings. We were interested if there were reproducible genetic characteristics of these isolates and if there was a central group of genes regulated by RhlR in all isolates. We examined five isolates and found signatures of adaptation common to CF isolates. Here, we analyzed CF clinial isolate E131. In this strain, RhlR positively regulates 105 genes, including those coding for known virulence factors. These results suggest a key group of QS-regulated factors important for pathogenesis of chronic infection, and position RhlR as a target for anti-QS therapeutics. Our work underscores the need to sample a diversity of isolates to understanding QS beyond what has been described in laboratory strains.
 
Overall design Examination of a rhlR-deletion mutant of a cystic fibrosis isolate of Pseudomonas aeruginosa vs. the isogenic parent strain
 
Contributor(s) Asfahl KL, Smalley NE, Chang AP, Dandekar AA
Citation(s) 35471121
Submission date Mar 15, 2022
Last update date May 05, 2022
Contact name Kyle Lowe Asfahl
E-mail(s) kyleloweasfahl@gmail.com
Organization name University of Washington
Department Microbiology
Street address 1705 NE Pacific St
City Seattle
State/province Washington
ZIP/Postal code 98195
Country USA
 
Platforms (1)
GPL24583 Illumina HiSeq 4000 (Pseudomonas aeruginosa)
Samples (6)
GSM5955723 E131 WT rep1
GSM5955724 E131 WT rep2
GSM5955725 E131 WT rep3
Relations
BioProject PRJNA816521

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Supplementary file Size Download File type/resource
GSE198718_E131completeRAST20201113.faa.gz 1.2 Mb (ftp)(http) FAA
GSE198718_E131completeRAST20201113.fna.gz 1.7 Mb (ftp)(http) FNA
GSE198718_E131completeRAST20201113.gbk.txt.gz 4.1 Mb (ftp)(http) TXT
GSE198718_E131completeRAST20201113.gff.gz 160.3 Kb (ftp)(http) GFF
GSE198718_E131completeRAST20201113.gtf.gz 160.3 Kb (ftp)(http) GTF
GSE198718_E131completeRAST20201113.xls.gz 3.7 Mb (ftp)(http) XLS
GSE198718_E131countMatrix20201114.txt.gz 94.9 Kb (ftp)(http) TXT
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