Biofilm differentiation and dispersal in mucoid pseudomonas aeruginosa isolates from patients with cystic fibrosis
Biofilm differentiation and dispersal in mucoid pseudomonas aeruginosa isolates from patients with cystic fibrosis
Intractable biofilm infections with Pseudomonas aeruginosa are the major cause of premature death associated with cystic fibrosis (CF). Few studies have explored the biofilm developmental cycle of P. aeruginosa isolates from chronically infected individuals. This study shows that such clinical isolates exhibit biofilm differentiation and dispersal processes similar to those of the better-studied laboratory P. aeruginosa strain PAO1 in the glass flow-cell (continuous-culture) biofilm model, albeit they are initially less adherent and their microcolonies are slower to develop and show heterogeneous, strain-specific variations in architecture. Confocal scanning laser microscopy combined with LIVE/DEAD viability staining revealed that in all CF biofilms bacterial cell death occurred in maturing biofilms, extending from the substratum to the central regions of mature microcolonies to varying degrees, depending on the strain. Bacteriophage activity was detected in the maturing biofilms of all CF strains examined and the amount of phage produced paralleled the degree of cell death seen in the biofilm. Some CF strains exhibited 'seeding dispersal' associated with the above phenomena, producing 'hollowing' as motile cells evacuated from the microcolony interiors as has been described for strain PAO1. Moreover, morphotypic cell variants were seen in the biofilm effluents of all CF strains. For those CF strains where marked cell death and seeding dispersal occurred in the microcolonies, variants were more diverse (up to five morphotypes) compared to those of strain PAO1 (two morphotypes). Given that variants of strain PAO1 have enhanced colonization traits, it seems likely that the similar biofilm dispersal events described here for CF strains contribute to the variability seen in clinical isolates and the overall persistence of the P. aeruginosa in the CF airway
3264-3274
Kirov, Sylvia M.
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Webb, Jeremy S.
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O'May, Che Y.
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Reid, David W.
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Woo, Jerry K. K.
d83ef1a2-a8d2-4abb-aabd-84668b75e631
Rice, Scott A.
360e3518-ad14-43a5-80e3-3f33e2d13e87
Kjelleberg, Staffan
043b66b5-130c-42f2-99b3-ec3eecf3248e
October 2007
Kirov, Sylvia M.
bd1930ba-d565-44b0-a8d5-2bd3b6e53d9a
Webb, Jeremy S.
ec0a5c4e-86cc-4ae9-b390-7298f5d65f8d
O'May, Che Y.
32896834-3e33-4623-aa7d-632073b153a9
Reid, David W.
b760e6b5-ca9f-4dc1-b0a0-b7465711858f
Woo, Jerry K. K.
d83ef1a2-a8d2-4abb-aabd-84668b75e631
Rice, Scott A.
360e3518-ad14-43a5-80e3-3f33e2d13e87
Kjelleberg, Staffan
043b66b5-130c-42f2-99b3-ec3eecf3248e
Kirov, Sylvia M., Webb, Jeremy S., O'May, Che Y., Reid, David W., Woo, Jerry K. K., Rice, Scott A. and Kjelleberg, Staffan
(2007)
Biofilm differentiation and dispersal in mucoid pseudomonas aeruginosa isolates from patients with cystic fibrosis.
Microbiology, 153 (10), .
(doi:10.1099/mic.0.2007/009092-0).
(PMID:17906126)
Abstract
Intractable biofilm infections with Pseudomonas aeruginosa are the major cause of premature death associated with cystic fibrosis (CF). Few studies have explored the biofilm developmental cycle of P. aeruginosa isolates from chronically infected individuals. This study shows that such clinical isolates exhibit biofilm differentiation and dispersal processes similar to those of the better-studied laboratory P. aeruginosa strain PAO1 in the glass flow-cell (continuous-culture) biofilm model, albeit they are initially less adherent and their microcolonies are slower to develop and show heterogeneous, strain-specific variations in architecture. Confocal scanning laser microscopy combined with LIVE/DEAD viability staining revealed that in all CF biofilms bacterial cell death occurred in maturing biofilms, extending from the substratum to the central regions of mature microcolonies to varying degrees, depending on the strain. Bacteriophage activity was detected in the maturing biofilms of all CF strains examined and the amount of phage produced paralleled the degree of cell death seen in the biofilm. Some CF strains exhibited 'seeding dispersal' associated with the above phenomena, producing 'hollowing' as motile cells evacuated from the microcolony interiors as has been described for strain PAO1. Moreover, morphotypic cell variants were seen in the biofilm effluents of all CF strains. For those CF strains where marked cell death and seeding dispersal occurred in the microcolonies, variants were more diverse (up to five morphotypes) compared to those of strain PAO1 (two morphotypes). Given that variants of strain PAO1 have enhanced colonization traits, it seems likely that the similar biofilm dispersal events described here for CF strains contribute to the variability seen in clinical isolates and the overall persistence of the P. aeruginosa in the CF airway
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Published date: October 2007
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Local EPrints ID: 186809
URI: http://eprints.soton.ac.uk/id/eprint/186809
ISSN: 1350-0872
PURE UUID: 0bc9f409-e2b4-4363-b508-ae472c2b43a9
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Date deposited: 18 May 2011 10:15
Last modified: 15 Mar 2024 03:26
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Author:
Sylvia M. Kirov
Author:
Che Y. O'May
Author:
David W. Reid
Author:
Jerry K. K. Woo
Author:
Scott A. Rice
Author:
Staffan Kjelleberg
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