Intraclonal diversity of the Pseudomonas aeruginosa cystic fibrosis airway isolates TBCF10839 and TBCF121838: distinct signatures of transcriptome, proteome, metabolome, adherence and pathogenicity despite an almost identical genome sequence. (8th August 2012)
- Record Type:
- Journal Article
- Title:
- Intraclonal diversity of the Pseudomonas aeruginosa cystic fibrosis airway isolates TBCF10839 and TBCF121838: distinct signatures of transcriptome, proteome, metabolome, adherence and pathogenicity despite an almost identical genome sequence. (8th August 2012)
- Main Title:
- Intraclonal diversity of the Pseudomonas aeruginosa cystic fibrosis airway isolates TBCF10839 and TBCF121838: distinct signatures of transcriptome, proteome, metabolome, adherence and pathogenicity despite an almost identical genome sequence
- Authors:
- Klockgether, Jens
Miethke, Norbert
Kubesch, Peter
Bohn, Yu‐Sing
Brockhausen, Inka
Cramer, Nina
Eberl, Leo
Greipel, Joachim
Herrmann, Christian
Herrmann, Susanne
Horatzek, Sonja
Lingner, Meike
Luciano, Liliana
Salunkhe, Prabhakar
Schomburg, Dietmar
Wehsling, Maria
Wiehlmann, Lutz
Davenport, Colin F.
Tümmler, Burkhard - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Summary</title> <p>Microevolution of closely related <italic>Pseudomonas aeruginosa</italic> was compared in the clone TB strains TBCF10839 and TBCF121838 which had been isolated from two unrelated individuals with cystic fibrosis who had acquired clone TB during a local outbreak. Compared with the strain PAO1 reference sequence the two clone TB genomes shared 23 155 nucleotide exchanges, 32 out‐of‐frame indels in the coding region and another repertoire of replacement and genomic islands such as PAGI‐1, PAGI‐2, PAGI‐5, LESGI‐1 and LES‐prophage 4. Only TBCF121838 carried a genomic island known from <italic>Ralstonia pickettii</italic>. Six of the seven strain‐specific sequence variations in the core genome were detected in genes affecting motility, biofilm formation or virulence, i.e. non‐synonymous nucleotide substitutions in <italic>mexS, </italic> PA3729, PA5017, <italic>mifR, </italic> a frameshift mutation in <italic>pilF</italic> (TBCF121838) and an intragenic deletion in <italic>pilQ</italic> (TBCF10839). Despite their almost identical genome sequence the two strains differed strongly from each other in transcriptome and metabolome profiles, mucin adherence and phagocytosis assays. TBCF121838 was susceptible to killing by neutrophils, but TBCF10839 could grow in leucocytes. Microevolution in <italic>P. aeruginosa</italic> apparently can generate novel complex traits by few or even single mutations provided that<abstract abstract-type="main" xml:lang="en"> <title>Summary</title> <p>Microevolution of closely related <italic>Pseudomonas aeruginosa</italic> was compared in the clone TB strains TBCF10839 and TBCF121838 which had been isolated from two unrelated individuals with cystic fibrosis who had acquired clone TB during a local outbreak. Compared with the strain PAO1 reference sequence the two clone TB genomes shared 23 155 nucleotide exchanges, 32 out‐of‐frame indels in the coding region and another repertoire of replacement and genomic islands such as PAGI‐1, PAGI‐2, PAGI‐5, LESGI‐1 and LES‐prophage 4. Only TBCF121838 carried a genomic island known from <italic>Ralstonia pickettii</italic>. Six of the seven strain‐specific sequence variations in the core genome were detected in genes affecting motility, biofilm formation or virulence, i.e. non‐synonymous nucleotide substitutions in <italic>mexS, </italic> PA3729, PA5017, <italic>mifR, </italic> a frameshift mutation in <italic>pilF</italic> (TBCF121838) and an intragenic deletion in <italic>pilQ</italic> (TBCF10839). Despite their almost identical genome sequence the two strains differed strongly from each other in transcriptome and metabolome profiles, mucin adherence and phagocytosis assays. TBCF121838 was susceptible to killing by neutrophils, but TBCF10839 could grow in leucocytes. Microevolution in <italic>P. aeruginosa</italic> apparently can generate novel complex traits by few or even single mutations provided that predisposing mutational events had occurred before in the clonal lineage.</p> </abstract> … (more)
- Is Part Of:
- Environmental microbiology. Volume 15:Number 1(2013:Jan.)
- Journal:
- Environmental microbiology
- Issue:
- Volume 15:Number 1(2013:Jan.)
- Issue Display:
- Volume 15, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 15
- Issue:
- 1
- Issue Sort Value:
- 2013-0015-0001-0000
- Page Start:
- 191
- Page End:
- 210
- Publication Date:
- 2012-08-08
- Subjects:
- Microbial ecology -- Periodicals
Environmental Microbiology -- Periodicals
579.17 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1462-2912;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1462-2920/issues ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=emi ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/j.1462-2920.2012.02842.x ↗
- Languages:
- English
- ISSNs:
- 1462-2912
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- Legaldeposit
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