PSEUDOMONAS-AERUGINOSA LASR TRANSCRIPTION CORRELATES WITH THE TRANSCRIPTION OF LASA, LASB, AND TOXA IN CHRONIC LUNG INFECTIONS ASSOCIATED WITH CYSTIC-FIBROSIS

Citation
Dg. Storey et al., PSEUDOMONAS-AERUGINOSA LASR TRANSCRIPTION CORRELATES WITH THE TRANSCRIPTION OF LASA, LASB, AND TOXA IN CHRONIC LUNG INFECTIONS ASSOCIATED WITH CYSTIC-FIBROSIS, Infection and immunity, 66(6), 1998, pp. 2521-2528
Citations number
52
Categorie Soggetti
Immunology,"Infectious Diseases
Journal title
ISSN journal
00199567
Volume
66
Issue
6
Year of publication
1998
Pages
2521 - 2528
Database
ISI
SICI code
0019-9567(1998)66:6<2521:PLTCWT>2.0.ZU;2-S
Abstract
The role of Pseudomonas aeruginosa quorum-sensing systems in the lung infections associated with cystic fibrosis (CF) has not been examined. The purpose of this study was to determine if genes regulated by the LasR-LasI quorum-sensing system were coordinately regulated by the P. aeruginosa populations during the lung infections associated with CF. We also wanted to ascertain if there was a relationship between the ex pression of lasR, a transcriptional regulator, and some P. aeruginosa virulence factors during these infections. We extracted RNAs from the bacterial populations of 131 sputa taken from 23 CF patients. These RN As were blotted and hybridized with probes to P. aeruginosa lasA, lasB , and toxA. The hybridization signals from each probe were ranked, and the rankings were analyzed by a Spearman rank correlation to determin e if there was an association between the population transcript accumu lations for the three genes. The correlations between the transcript a ccumulation patterns of pairs of the genes suggested that lasA, lasB, and toxA might be coordinately regulated during CF lung infections. To determine if this coordinate regulation might be due to regulation by LasR, we probed RNAs, extracted from 84 sputa, with the lasR, lasA, l asB, toxA, and algD probes. Statistical analysis indicated that lasR t ranscript accumulation correlated to lasA, lasB, toxA, and algD transc ript accumulations. These results indicated that lasR may at least par tially regulate or be coordinately regulated with lasA, lasB, toxA, an d algD during the lung infections associated with CF. These results al so suggested that the LasR-LasI quorum-sensing system may control the expression of at least some virulence factors in the lungs of patients with CF.