Affiliation:
1. Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry
2. Department of Environmental Medicine and Center for Functional Genomics, University of Rochester Medical Center, Rochester, New York 14642
Abstract
ABSTRACT
Bacterial communication via quorum sensing (QS) has been reported to be important in the production of virulence factors, antibiotic sensitivity, and biofilm development. Two QS systems, known as the
las
and
rhl
systems, have been identified previously in the opportunistic pathogen
Pseudomonas aeruginosa
. High-density oligonucleotide microarrays for the
P. aeruginosa
PAO1 genome were used to investigate global gene expression patterns modulated by QS regulons. In the initial experiments we focused on identifying
las
and/or
rhl
QS-regulated genes using a QS signal generation-deficient mutant (PAO-JP2) that was cultured with and without added exogenous autoinducers [
N
-(3-oxododecanoyl) homoserine lactone and
N
-butyryl homoserine lactone]. Conservatively, 616 genes showed statistically significant differential expression (
P
≤ 0.05) in response to the exogenous autoinducers and were classified as QS regulated. A total of 244 genes were identified as being QS regulated at the mid-logarithmic phase, and 450 genes were identified as being QS regulated at the early stationary phase. Most of the previously reported QS-promoted genes were confirmed, and a large number of additional QS-promoted genes were identified. Importantly, 222 genes were identified as being QS repressed. Environmental factors, such as medium composition and oxygen availability, eliminated detection of transcripts of many genes that were identified as being QS regulated.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
772 articles.
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