Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression.

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Standard

Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression. / Heydorn, Arne; Ersbøll, Bjarne; Kato, Junichi; Hentzer, Morten; Parsek, Matthew R; Tolker-Nielsen, Tim; Givskov, Michael; Molin, Søren.

In: Applied and Environmental Microbiology, Vol. 68, No. 4, 2002, p. 2008-17.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Heydorn, A, Ersbøll, B, Kato, J, Hentzer, M, Parsek, MR, Tolker-Nielsen, T, Givskov, M & Molin, S 2002, 'Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression.', Applied and Environmental Microbiology, vol. 68, no. 4, pp. 2008-17.

APA

Heydorn, A., Ersbøll, B., Kato, J., Hentzer, M., Parsek, M. R., Tolker-Nielsen, T., Givskov, M., & Molin, S. (2002). Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression. Applied and Environmental Microbiology, 68(4), 2008-17.

Vancouver

Heydorn A, Ersbøll B, Kato J, Hentzer M, Parsek MR, Tolker-Nielsen T et al. Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression. Applied and Environmental Microbiology. 2002;68(4):2008-17.

Author

Heydorn, Arne ; Ersbøll, Bjarne ; Kato, Junichi ; Hentzer, Morten ; Parsek, Matthew R ; Tolker-Nielsen, Tim ; Givskov, Michael ; Molin, Søren. / Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression. In: Applied and Environmental Microbiology. 2002 ; Vol. 68, No. 4. pp. 2008-17.

Bibtex

@article{e0fce690bd4011dd8e02000ea68e967b,
title = "Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression.",
abstract = "Four strains of Pseudomonas aeruginosa (wild type, Delta(pil)HIJK mutant, lasI mutant, and rpoS mutant) were genetically tagged with the green fluorescent protein, and the development of flow chamber-grown biofilms by each of them was investigated by confocal laser scanning microscopy. The structural developments of the biofilms were quantified by the computer program COMSTAT (A. Heydorn, A. T. Nielsen, M. Hentzer, C. Sternberg, M. Givskov, B. K. Ersb{\o}ll, and S. Molin, Microbiology 146:2395-2407, 2000). Two structural key variables, average thickness and roughness, formed the basis for an analysis of variance model comprising the four P. aeruginosa strains, five time points (55, 98, 146, 242, and 314 h), and three independent rounds of biofilm experiments. The results showed that the wild type, the Delta(pil)HIJK mutant, and the rpoS mutant display conspicuously different types of temporal biofilm development, whereas the lasI mutant was indistinguishable from the wild type at all time points. The wild type and the lasI mutant formed uniform, densely packed biofilms. The rpoS mutant formed densely packed biofilms that were significantly thicker than those of the wild type, whereas the Delta(pil)HIJK mutant formed distinct microcolonies that were regularly spaced and almost uniform in size. The results are discussed in relation to the current model of P. aeruginosa biofilm development.",
author = "Arne Heydorn and Bjarne Ersb{\o}ll and Junichi Kato and Morten Hentzer and Parsek, {Matthew R} and Tim Tolker-Nielsen and Michael Givskov and S{\o}ren Molin",
note = "Keywords: Bacterial Proteins; Biofilms; Culture Media; Fimbriae, Bacterial; Green Fluorescent Proteins; Image Processing, Computer-Assisted; Luminescent Proteins; Microscopy, Confocal; Multigene Family; Mutation; Pseudomonas aeruginosa; Sigma Factor",
year = "2002",
language = "English",
volume = "68",
pages = "2008--17",
journal = "Applied and Environmental Microbiology",
issn = "0099-2240",
publisher = "American Society for Microbiology",
number = "4",

}

RIS

TY - JOUR

T1 - Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression.

AU - Heydorn, Arne

AU - Ersbøll, Bjarne

AU - Kato, Junichi

AU - Hentzer, Morten

AU - Parsek, Matthew R

AU - Tolker-Nielsen, Tim

AU - Givskov, Michael

AU - Molin, Søren

N1 - Keywords: Bacterial Proteins; Biofilms; Culture Media; Fimbriae, Bacterial; Green Fluorescent Proteins; Image Processing, Computer-Assisted; Luminescent Proteins; Microscopy, Confocal; Multigene Family; Mutation; Pseudomonas aeruginosa; Sigma Factor

PY - 2002

Y1 - 2002

N2 - Four strains of Pseudomonas aeruginosa (wild type, Delta(pil)HIJK mutant, lasI mutant, and rpoS mutant) were genetically tagged with the green fluorescent protein, and the development of flow chamber-grown biofilms by each of them was investigated by confocal laser scanning microscopy. The structural developments of the biofilms were quantified by the computer program COMSTAT (A. Heydorn, A. T. Nielsen, M. Hentzer, C. Sternberg, M. Givskov, B. K. Ersbøll, and S. Molin, Microbiology 146:2395-2407, 2000). Two structural key variables, average thickness and roughness, formed the basis for an analysis of variance model comprising the four P. aeruginosa strains, five time points (55, 98, 146, 242, and 314 h), and three independent rounds of biofilm experiments. The results showed that the wild type, the Delta(pil)HIJK mutant, and the rpoS mutant display conspicuously different types of temporal biofilm development, whereas the lasI mutant was indistinguishable from the wild type at all time points. The wild type and the lasI mutant formed uniform, densely packed biofilms. The rpoS mutant formed densely packed biofilms that were significantly thicker than those of the wild type, whereas the Delta(pil)HIJK mutant formed distinct microcolonies that were regularly spaced and almost uniform in size. The results are discussed in relation to the current model of P. aeruginosa biofilm development.

AB - Four strains of Pseudomonas aeruginosa (wild type, Delta(pil)HIJK mutant, lasI mutant, and rpoS mutant) were genetically tagged with the green fluorescent protein, and the development of flow chamber-grown biofilms by each of them was investigated by confocal laser scanning microscopy. The structural developments of the biofilms were quantified by the computer program COMSTAT (A. Heydorn, A. T. Nielsen, M. Hentzer, C. Sternberg, M. Givskov, B. K. Ersbøll, and S. Molin, Microbiology 146:2395-2407, 2000). Two structural key variables, average thickness and roughness, formed the basis for an analysis of variance model comprising the four P. aeruginosa strains, five time points (55, 98, 146, 242, and 314 h), and three independent rounds of biofilm experiments. The results showed that the wild type, the Delta(pil)HIJK mutant, and the rpoS mutant display conspicuously different types of temporal biofilm development, whereas the lasI mutant was indistinguishable from the wild type at all time points. The wild type and the lasI mutant formed uniform, densely packed biofilms. The rpoS mutant formed densely packed biofilms that were significantly thicker than those of the wild type, whereas the Delta(pil)HIJK mutant formed distinct microcolonies that were regularly spaced and almost uniform in size. The results are discussed in relation to the current model of P. aeruginosa biofilm development.

M3 - Journal article

C2 - 11916724

VL - 68

SP - 2008

EP - 2017

JO - Applied and Environmental Microbiology

JF - Applied and Environmental Microbiology

SN - 0099-2240

IS - 4

ER -

ID: 8780321