Cited by 138Bacterial biofilms and quorum sensingCystic Fibrosis Research AdvancesPlant Pathogenic Bacteria Studies

Pseudomonas aeruginosa lasR Transcription Correlates with the Transcription of lasA , lasB , and toxA in Chronic Lung Infections Associated with Cystic Fibrosis

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Storey, Douglas G., Ujack, Eva E., Rabin, Harvey R., Mitchell, Ian·1998·Infection and Immunity

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 expression 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 RNAs 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 determine if there was an association between the population transcript accumulations for the three genes. The correlations between the transcript accumulation 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 , lasB , toxA , and algD probes. Statistical analysis indicated that lasR transcript accumulation correlated to lasA , lasB , toxA , and algD transcript accumulations. These results indicated that lasR may at least partially regulate or be coordinately regulated with lasA , lasB , toxA , and algD during the lung infections associated with CF. These results also 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.

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Crossref · 10.1128/iai.66.6.2521-2528.1998

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  1. [40]40. Ryan, B. F., and B. L. Joiner. 1994. Minitab handbook. Duxbury Press, Belmont, Calif.
  2. [50]50. Zar, J. H. 1974. Rank correlation, p. 243-245. In W. D. McElroy and C. P. Swanson (ed.), Biostatistical analysis. Prentice-Hall, Inc., Englewood Cliffs, N.J.

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Authors
Storey, D. G., Ujack, E. E., Rabin, H. R., & Mitchell, I.
Affiliations
  • <!--label omitted: 1-->Departments of Biological Sciences,1
  • Foothills Medical Centre (CA)
  • University of Calgary (CA)
Venue
Infection and Immunity
Published
1998-06
Volume
66
Issue
6
Pages
2521-2528
ISSN
  • 0019-9567 (ISSN-L)
  • 1098-5522
OpenAlex
W2113890225
Cited by
138
References
50
Citations by year
2026: 2 · 2025: 3 · 2024: 2 · 2023: 4 · 2022: 3 · 2021: 2 · 2020: 5 · 2019: 5 · 2018: 2 · 2017: 4 · 2016: 6 · 2015: 4 · 2014: 6 · 2013: 7 · 2012: 5
FWCI
1.40
Type
journal article
Language
en
Open access
Locations
  • Infection and Immunity (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Pathogenic Bacteria Studies
Keywords
Pseudomonas aeruginosa, LASA, lasB, ToxA, algD, virulence factors, cystic fibrosis lung infection, transcriptional regulation
MeSH terms
Pseudomonas aeruginosa Exotoxin A, Adolescent, Bacterial Proteins, Bacterial Toxins, Chronic Disease, Cystic Fibrosis, DNA-Binding Proteins, Exotoxins, Female, Half-Life, Humans, Lung Diseases, Male, Metalloendopeptidases, Nucleic Acid Hybridization, Pseudomonas Infections, Respiratory Tract Infections, RNA, Bacterial, RNA, Messenger, Sensitivity and Specificity, Transcription, Genetic, Trans-Activators, ADP Ribose Transferases, Virulence Factors

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