Use of Subtractive Hybridization To Identify a Diagnostic Probe for a Cystic Fibrosis Epidemic Strain of Pseudomonas aeruginosa
Open Access
- 1 December 2002
- journal article
- Published by American Society for Microbiology in Journal of Clinical Microbiology
- Vol. 40 (12) , 4607-4611
- https://doi.org/10.1128/jcm.40.12.4607-4611.2002
Abstract
A multiresistant strain of Pseudomonas aeruginosa is widespread among cystic fibrosis (CF) patients attending clinics in Liverpool, United Kingdom. Suppression subtractive hybridization was used to identify sequences present in the Liverpool CF epidemic strain but absent from strain PAO1. Using dot blot and PCR amplification assays, the prevalence of such sequences among a panel of CF isolates was determined. Several sequences were found only in the Liverpool epidemic strain. Some sequences were present in the Liverpool epidemic strain and in a minority of other isolates, including sequences with homology to genes implicated in O6 serotype and siderophore production. The Liverpool epidemic strain and 81% of nonepidemic isolates contained a sequence identified as part of the PAGI-1 genomic island. Other strains implicated in epidemic spread, which were from Manchester, United Kingdom, and Melbourne, Australia, were also screened. None of the sequences identified was present in the Manchester strain. However, one of two Melbourne strains contained some of the sequences found in the Liverpool epidemic strain. All isolates implicated in epidemic spread and 76% of sporadic isolates contained the exoS gene. A sequence present in all isolates of the Liverpool epidemic strain was used to develop a diagnostic PCR test for identification of the strain from colonies or directly from sputum samples.Keywords
This publication has 28 references indexed in Scilit:
- Spread of an epidemic Pseudomonas aeruginosa strain from a patient with cystic fibrosis (CF) to non-CF relativesThorax, 2002
- Epidemic Population Structure of Pseudomonas aeruginosa : Evidence for a Clone That Is Pathogenic to the Eye and That Has a Distinct Combination of Virulence FactorsInfection and Immunity, 2001
- Detection of Bacterial Virulence Genes by Subtractive Hybridization: Identification of Capsular Polysaccharide of Burkholderia pseudomallei as a Major Virulence DeterminantInfection and Immunity, 2001
- High Frequency of Hypermutable Pseudomonas aeruginosa in Cystic Fibrosis Lung InfectionScience, 2000
- Functional analysis of genes responsible for the synthesis of the B-band O antigen of Pseudomonas aeruginosa serotype O6 lipopolysaccharide The GenBank accession number for the sequence reported in this paper is AF035937.Microbiology, 1999
- Differential genome analysis of bacteria by genomic subtractive hybridization and pulsed field gel electrophoresisElectrophoresis, 1998
- Use of Siderophores to Type Pseudomonads: The Three Pseudomonas Aeruginosa Pyoverdine SystemsMicrobiology, 1997
- Spread of β-lactam-resistant Pseudomonas aeruginosa in a cystic fibrosis clinicThe Lancet, 1996
- Detection ofPseudomonas (Burkholderia) cepacia using PCRPediatric Pulmonology, 1995
- Universal chemical assay for the detection and determination of siderophoresAnalytical Biochemistry, 1987