Literature DB >> 20023018

Genome diversity of Pseudomonas aeruginosa PAO1 laboratory strains.

Jens Klockgether1, Antje Munder, Jens Neugebauer, Colin F Davenport, Frauke Stanke, Karen D Larbig, Stephan Heeb, Ulrike Schöck, Thomas M Pohl, Lutz Wiehlmann, Burkhard Tümmler.   

Abstract

Pseudomonas aeruginosa PAO1 is the most commonly used strain for research on this ubiquitous and metabolically versatile opportunistic pathogen. Strain PAO1, a derivative of the original Australian PAO isolate, has been distributed worldwide to laboratories and strain collections. Over decades discordant phenotypes of PAO1 sublines have emerged. Taking the existing PAO1-UW genome sequence (named after the University of Washington, which led the sequencing project) as a blueprint, the genome sequences of reference strains MPAO1 and PAO1-DSM (stored at the German Collection for Microorganisms and Cell Cultures [DSMZ]) were resolved by physical mapping and deep short read sequencing-by-synthesis. MPAO1 has been the source of near-saturation libraries of transposon insertion mutants, and PAO1-DSM is identical in its SpeI-DpnI restriction map with the original isolate. The major genomic differences of MPAO1 and PAO1-DSM in comparison to PAO1-UW are the lack of a large inversion, a duplication of a mobile 12-kb prophage region carrying a distinct integrase and protein phosphatases or kinases, deletions of 3 to 1,006 bp in size, and at least 39 single-nucleotide substitutions, 17 of which affect protein sequences. The PAO1 sublines differed in their ability to cope with nutrient limitation and their virulence in an acute murine airway infection model. Subline PAO1-DSM outnumbered the two other sublines in late stationary growth phase. In conclusion, P. aeruginosa PAO1 shows an ongoing microevolution of genotype and phenotype that jeopardizes the reproducibility of research. High-throughput genome resequencing will resolve more cases and could become a proper quality control for strain collections.

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Year:  2009        PMID: 20023018      PMCID: PMC2812968          DOI: 10.1128/JB.01515-09

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  37 in total

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4.  Comprehensive transposon mutant library of Pseudomonas aeruginosa.

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Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-14       Impact factor: 11.205

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Journal:  J Bacteriol       Date:  2001-09       Impact factor: 3.490

8.  Achilles' heel cleavage: creation of rare restriction sites in lambda phage genomes and evaluation of additional operators, repressors and restriction/modification systems.

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Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-30       Impact factor: 11.205

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Journal:  EMBO J       Date:  1989-12-20       Impact factor: 11.598

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  110 in total

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Journal:  J Bacteriol       Date:  2019-02-11       Impact factor: 3.490

2.  Protein Network of the Pseudomonas aeruginosa Denitrification Apparatus.

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4.  Imaging and analysis of Pseudomonas aeruginosa swarming and rhamnolipid production.

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5.  β-Aminopeptidases: Insight into Enzymes without a Known Natural Substrate.

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6.  Dry powder aerosols to co-deliver antibiotics and nutrient dispersion compounds for enhanced bacterial biofilm eradication.

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Review 7.  Sensory Repertoire of Bacterial Chemoreceptors.

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8.  Developing an international Pseudomonas aeruginosa reference panel.

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Journal:  Microbiologyopen       Date:  2013-11-11       Impact factor: 3.139

9.  Antipseudomonal Bacteriophage Reduces Infective Burden and Inflammatory Response in Murine Lung.

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10.  Host Adaptation Predisposes Pseudomonas aeruginosa to Type VI Secretion System-Mediated Predation by the Burkholderia cepacia Complex.

Authors:  Andrew I Perault; Courtney E Chandler; David A Rasko; Robert K Ernst; Matthew C Wolfgang; Peggy A Cotter
Journal:  Cell Host Microbe       Date:  2020-08-04       Impact factor: 21.023

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