Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary movies
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Purevdorj-Gage, B.
Right arrow Articles by Stoodley, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Purevdorj-Gage, B.
Right arrow Articles by Stoodley, P.
Agricola
Right arrow Articles by Purevdorj-Gage, B.
Right arrow Articles by Stoodley, P.
Microbiology 151 (2005), 1569-1576; DOI  10.1099/mic.0.27536-0
© 2005 Society for General Microbiology

Phenotypic differentiation and seeding dispersal in non-mucoid and mucoid Pseudomonas aeruginosa biofilms

B. Purevdorj-Gage1, W. J. Costerton1 and P. Stoodley1,2

1 Center for Biofilm Engineering, 366 EPS Building – PO Box 173980, Montana State University-Bozeman, MT 59717, USA
2 Center for Genomic Sciences, Allegheny-Singer Research Institute, Pittsburgh, USA

Correspondence
B. Purevdorj-Gage
laura_p{at}erc.montana.edu

There is growing evidence that Pseudomonas aeruginosa biofilms exhibit a multicellular developmental life cycle analogous to that of the myxobacteria. In non-mucoid PAO1 biofilms cultured in glass flow cells the phenotypic differentiation of microcolonies into a motile phenotype in the interior of the microcolony and a non-motile surrounding ‘wall phenotype’ are described. After differentiation the interior cells coordinately evacuated the microcolony from local break out points and spread over the wall of the flow cell, suggesting that the specialized microcolonies were analogous to crude fruiting bodies. A microcolony diameter of approximately 80 µm was required for differentiation, suggesting that regulation was related to cell density and mass transfer conditions. This phenomenon was termed ‘seeding dispersal’ to differentiate it from ‘erosion’ which is the passive removal of single cells by fluid shear. Using the flow cell culturing method, in which reproducible seeding phenotype in PAO1 wild-type was demonstrated, the effects of quorum sensing (QS) and rhamnolipid production (factors previously identified as important in determining biofilm structure) on seeding dispersal using knockout mutants isogenic with PAO1 was investigated. Rhamnolipid (rhlA) was not required for seeding dispersal but las/rhl QS (PAO1-JP2) was, in our system. To assess the clinical relevance of these data, mucoid P. aeruginosa cystic fibrosis isolate FRD1 was also investigated and was seeding-dispersal-negative.


Abbreviations: CF, cystic fibrosis; QS, quorum sensing




This article has been cited by other articles:


Home page
MicrobiologyHome page
S. M. Kirov, J. S. Webb, C. Y. O'May, D. W. Reid, J. K. K. Woo, S. A. Rice, and S. Kjelleberg
Biofilm differentiation and dispersal in mucoid Pseudomonas aeruginosa isolates from patients with cystic fibrosis
Microbiology, October 1, 2007; 153(10): 3264 - 3274.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
P. Ymele-Leki and J. M. Ross
Erosion from Staphylococcus aureus Biofilms Grown under Physiologically Relevant Fluid Shear Forces Yields Bacterial Cells with Reduced Avidity to Collagen
Appl. Envir. Microbiol., March 15, 2007; 73(6): 1834 - 1841.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
J. A. J. Haagensen, M. Klausen, R. K. Ernst, S. I. Miller, A. Folkesson, T. Tolker-Nielsen, and S. Molin
Differentiation and Distribution of Colistin- and Sodium Dodecyl Sulfate-Tolerant Cells in Pseudomonas aeruginosa Biofilms
J. Bacteriol., January 1, 2007; 189(1): 28 - 37.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
N. Barraud, D. J. Hassett, S.-H. Hwang, S. A. Rice, S. Kjelleberg, and J. S. Webb
Involvement of Nitric Oxide in Biofilm Dispersal of Pseudomonas aeruginosa.
J. Bacteriol., November 1, 2006; 188(21): 7344 - 7353.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
T. Romeo
When the Party Is Over: a Signal for Dispersal of Pseudomonas aeruginosa Biofilms
J. Bacteriol., November 1, 2006; 188(21): 7325 - 7327.
[Full Text] [PDF]


Home page
Infect. Immun.Home page
K. Shen, S. Sayeed, P. Antalis, J. Gladitz, A. Ahmed, B. Dice, B. Janto, R. Dopico, R. Keefe, J. Hayes, et al.
Extensive Genomic Plasticity in Pseudomonas aeruginosa Revealed by Identification and Distribution Studies of Novel Genes among Clinical Isolates
Infect. Immun., September 1, 2006; 74(9): 5272 - 5283.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2005 Society for General Microbiology.