Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Jan;8(1):66-70.
doi: 10.1016/j.jcf.2008.09.006. Epub 2008 Oct 29.

Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression

Affiliations

Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression

Lucas R Hoffman et al. J Cyst Fibros. 2009 Jan.

Abstract

Background: Pseudomonas aeruginosa with mutations in the transcriptional regulator LasR chronically infect the airways of people with cystic fibrosis (CF), yet the prevalence and clinical implications of lasR mutant infection are unknown.

Methods: In an exploratory study, we screened 166 P. aeruginosa isolates from 58 CF patients for LasR inactivation and mucoidy, and compared clinical characteristics among source patients.

Results: lasR mutation prevalence was comparable to that of mucoidy, the best-described CF-adapted phenotype, but affected patients were on average approximately 2 years younger. In a regression analysis, lung function decline with age was worse among patients with lasR mutant infection than in those without, similar to the effect of mucoidy.

Conclusions: Culture positivity for lasR mutant P. aeruginosa may serve as a marker of early CF adaptive change of prognostic significance. Furthermore, as LasR inactivation alters susceptibility to antibiotics, infection with lasR mutant P. aeruginosa may impact response to therapy.

PubMed Disclaimer

Conflict of interest statement

All authors declare no conflict of interest.

Figures

Figure 1
Figure 1. Characteristic colony morphology identifies lasR mutant P. aeruginosa CF isolates
(a) LB agar-grown colonies of two clonally-related clinical isolates of P. aeruginosa from a single CF patient, one with an inactivating lasR mutation and the other with wild-type lasR, as indicated. The lasR mutant isolate displays phenotypes characteristic of lasR mutants, including surface iridescent, metallic sheen, which is particularly evident in this photograph (yellow arrow). (b) Another pair of LB agar-grown, clonally-related clinical P. aeruginosa isolates in which one isolate has an inactivating lasR mutation that demonstrates colony lysis and flattening (blue arrow). (c) An LB agar-grown P. aeruginosa isolate that is mucoid and has wild-type LasR protein function, for comparison with (d–e). (d) A mucoid P. aeruginosa isolate with an inactivating lasR mutation, exhibiting floating, iridescent material (yellow arrow). (e) Another mucoid isolate with inactivating lasR mutation in which colony lysis is particularly evident (blue arrow).

Similar articles

Cited by

References

    1. Smith EE, Buckley DG, Wu Z, Saenphimmachak C, Hoffman LR, D’Argenio DA, et al. Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients. Proc Natl Acad Sci U S A. 2006 May 30;103(22):8487–92. - PMC - PubMed
    1. Govan JR, Deretic V. Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia. Microbiol Rev. 1996;60(3):539–74. - PMC - PubMed
    1. Li Z, Kosorok MR, Farrell PM, Laxova A, West SE, Green CG, et al. Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis. Jama. 2005 Feb 2;293(5):581–8. - PubMed
    1. Fothergill JL, Panagea S, Hart CA, Walshaw MJ, Pitt TL, Winstanley C. Widespread pyocyanin over-production among isolates of a cystic fibrosis epidemic strain. BMC Microbiol. 2007;7:45. - PMC - PubMed
    1. Tingpej P, Smith L, Rose B, Zhu H, Conibear T, Al Nassafi K, et al. Phenotypic characterization of clonal and nonclonal Pseudomonas aeruginosa strains isolated from lungs of adults with cystic fibrosis. J Clin Microbiol. 2007 Jun;45(6):1697–704. - PMC - PubMed

Publication types

Substances