Phenotypic characterization of an international Pseudomonas aeruginosa reference panel: strains of cystic fibrosis (CF) origin show less in vivo virulence than non-CF strains
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
Grantová podpora
MR/L011263/1
Medical Research Council - United Kingdom
PubMed
26253522
DOI
10.1099/mic.0.000155
Knihovny.cz E-zdroje
- MeSH
- analýza přežití MeSH
- cystická fibróza komplikace MeSH
- fenotyp * MeSH
- LD50 MeSH
- Lepidoptera mikrobiologie MeSH
- lidé MeSH
- lokomoce MeSH
- mikrobiologie životního prostředí * MeSH
- modely nemocí na zvířatech MeSH
- pseudomonádové infekce mikrobiologie MeSH
- Pseudomonas aeruginosa klasifikace izolace a purifikace patogenita fyziologie MeSH
- virulence MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
Pseudomonas aeruginosa causes chronic lung infections in people with cystic fibrosis (CF) and acute opportunistic infections in people without CF. Forty-two P. aeruginosa strains from a range of clinical and environmental sources were collated into a single reference strain panel to harmonise research on this diverse opportunistic pathogen. To facilitate further harmonized and comparable research on P. aeruginosa, we characterized the panel strains for growth rates, motility, virulence in the Galleria mellonella infection model, pyocyanin and alginate production, mucoid phenotype, LPS pattern, biofilm formation, urease activity, and antimicrobial and phage susceptibilities. Phenotypic diversity across the P. aeruginosa panel was apparent for all phenotypes examined, agreeing with the marked variability seen in this species. However, except for growth rate, the phenotypic diversity among strains from CF versus non-CF sources was comparable. CF strains were less virulent in the G. mellonella model than non-CF strains (P = 0.037). Transmissible CF strains generally lacked O-antigen, produced less pyocyanin and had low virulence in G. mellonella. Furthermore, in the three sets of sequential CF strains, virulence, O-antigen expression and pyocyanin production were higher in the earlier isolate compared to the isolate obtained later in infection. Overall, this full phenotypic characterization of the defined panel of P. aeruginosa strains increases our understanding of the virulence and pathogenesis of P. aeruginosa and may provide a valuable resource for the testing of novel therapies against this problematic pathogen.
Cardiff School of Biosciences Cardiff University Cardiff UK
Centre of Microbial Host Interactions Institute of Technology Tallaght Tallaght Dublin 24 Ireland
Department of Clinical Microbiology Freeman Hospital Newcastle Newcastle upon Tyne UK
Department of Microbiology Jan Kochanowski University in Kielce Kielce Poland
Institute for Infection and Global Health University of Liverpool Liverpool UK
Institute of Genetics and Microbiology University of Wroclaw Wroclaw Poland
Institute of Microbiology Bulgarian Academy of Sciences Acad G Bonchev Str Bl 26 Sofia 1113 Bulgaria
Laboratory of Gene Technology KU Leuven Leuven Belgium
Laboratory of Pharmaceutical Microbiology Ghent University Ghent Belgium
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