Affiliation:
1. ARC Special Research Centre for Functional and Applied Genomics, Institute for Molecular Bioscience
2. Department of Biochemistry, University of Queensland, Brisbane, Queensland 4072, Australia
Abstract
ABSTRACT
It has been reported that mutations in the quorum-sensing genes
lasI
and
rhlI
in
Pseudomonas aeruginosa
result in, among many other things, loss of twitching motility (A. Glessner, R. S. Smith, B. H. Iglewski, and J. B. Robinson, J. Bacteriol. 181:1623-1629, 1999). We constructed knockouts of
lasI
and
rhlI
and the corresponding regulatory genes
lasR
and
rhlR
and found no effect on twitching motility. However, twitching-defective variants accumulated during culturing of
lasI
and
rhlI
mutants. Further analysis showed that the stable twitching-defective variants of
lasI
and
rhlI
mutants had arisen as a consequence of secondary mutations in
vfr
and
algR
, respectively, both of which encode key regulators affecting a variety of phenotypes, including twitching motility. In addition, when grown in shaking broth culture,
lasI
and
rhlI
mutants, but not the wild-type parent, also accumulated unstable variants that lacked both twitching motility and swimming motility and appeared to be identical in phenotype to the S1 and S2 variants that were recently reported to occur at high frequencies in
P. aeruginosa
strains grown as a biofilm or in static broth culture (E. Deziel, Y. Comeau, and R. Villemur, J. Bacteriol. 183:1195-1204, 2001). These results indicate that mutations in one regulatory system may create distortions that select during subsequent culturing for compensatory mutations in other regulatory genes within the cellular network. This problem may have compromised some past studies of regulatory hierarchies controlled by quorum sensing and of bacterial regulatory systems in general.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
105 articles.
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