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