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The Single-Nucleotide Resolution Transcriptome of Pseudomonas aeruginosa Grown in Body Temperature
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نویسنده
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wurtzel o. ,yoder-himes d.r. ,han k. ,dandekar a.a. ,edelheit s. ,greenberg e.p. ,sorek r. ,lory s.
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منبع
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plos pathogens - 2012 - دوره : 8 - شماره : 9
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چکیده
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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. © 2012 wurtzel et al.
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آدرس
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department of molecular genetics,weizmann institute of science,rehovot, Israel, department of microbiology and immunobiology,harvard medical school,boston ma,united states,division of respiratory diseases,boston children's hospital,boston,ma, United States, department of microbiology and immunobiology,harvard medical school,boston ma, United States, department of microbiology,university of washington school of medicine,seattle,wa,united states,division of pulmonary and critical care medicine,university of washington school of medicine,seattle,wa, United States, department of molecular genetics,weizmann institute of science,rehovot, Israel, department of microbiology,university of washington school of medicine,seattle,wa, United States, department of molecular genetics,weizmann institute of science,rehovot, Israel, department of microbiology and immunobiology,harvard medical school,boston ma, United States
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Authors
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