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The Single-nucleotide Resolution Transcriptome of Pseudomonas Aeruginosa Grown in Body Temperature

Overview
Journal PLoS Pathog
Specialty Microbiology
Date 2012 Oct 3
PMID 23028334
Citations 151
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Abstract

One of the hallmarks of opportunistic pathogens is their ability to adjust and respond to a wide range of environmental and host-associated conditions. The human pathogen Pseudomonas aeruginosa has an ability to thrive in a variety of hosts and cause a range of acute and chronic infections in individuals with impaired host defenses or cystic fibrosis. Here we report an in-depth transcriptional profiling of this organism when grown at host-related temperatures. Using RNA-seq of samples from P. aeruginosa grown at 28°C and 37°C we detected genes preferentially expressed at the body temperature of mammalian hosts, suggesting that they play a role during infection. These temperature-induced genes included the type III secretion system (T3SS) genes and effectors, as well as the genes responsible for phenazines biosynthesis. Using genome-wide transcription start site (TSS) mapping by RNA-seq we were able to accurately define the promoters and cis-acting RNA elements of many genes, and uncovered new genes and previously unrecognized non-coding RNAs directly controlled by the LasR quorum sensing regulator. Overall we identified 165 small RNAs and over 380 cis-antisense RNAs, some of which predicted to perform regulatory functions, and found that non-coding RNAs are preferentially localized in pathogenicity islands and horizontally transferred regions. Our work identifies regulatory features of P. aeruginosa genes whose products play a role in environmental adaption during infection and provides a reference transcriptional landscape for this pathogen.

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References
1.
Gaille C, Reimmann C, Haas D . Isochorismate synthase (PchA), the first and rate-limiting enzyme in salicylate biosynthesis of Pseudomonas aeruginosa. J Biol Chem. 2003; 278(19):16893-8. DOI: 10.1074/jbc.M212324200. View

2.
Furste J, Pansegrau W, Frank R, Blocker H, Scholz P, Bagdasarian M . Molecular cloning of the plasmid RP4 primase region in a multi-host-range tacP expression vector. Gene. 1986; 48(1):119-31. DOI: 10.1016/0378-1119(86)90358-6. View

3.
Nechooshtan G, Elgrably-Weiss M, Sheaffer A, Westhof E, Altuvia S . A pH-responsive riboregulator. Genes Dev. 2009; 23(22):2650-62. PMC: 2779765. DOI: 10.1101/gad.552209. View

4.
Schuster M, Greenberg E . Early activation of quorum sensing in Pseudomonas aeruginosa reveals the architecture of a complex regulon. BMC Genomics. 2007; 8:287. PMC: 2018727. DOI: 10.1186/1471-2164-8-287. View

5.
Toledo-Arana A, Dussurget O, Nikitas G, Sesto N, Guet-Revillet H, Balestrino D . The Listeria transcriptional landscape from saprophytism to virulence. Nature. 2009; 459(7249):950-6. DOI: 10.1038/nature08080. View