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Journal of Bacteriology, December 2006, p. 8213-8221, Vol. 188, No. 23
0021-9193/06/$08.00+0 doi:10.1128/JB.01202-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Analysis of Pseudomonas aeruginosa Conditional Psl Variants Reveals Roles for the Psl Polysaccharide in Adhesion and Maintaining Biofilm Structure Postattachment
Luyan Ma,1
Kara D. Jackson,1
Rebecca M. Landry,2
Matthew R. Parsek,2,
and
Daniel J. Wozniak1*
Wake Forest University School of Medicine, Winston-Salem, NC 27157,1
University of Iowa, Iowa City, Iowa 522422
Received 2 August 2006/
Accepted 6 September 2006
The ability to form biofilms in the airways of people suffering from cystic fibrosis is a critical element of Pseudomonas aeruginosa pathogenesis. The 15-gene psl operon encodes a putative polysaccharide that plays an important role in biofilm initiation in nonmucoid P. aeruginosa strains. Biofilm initiation by a P. aeruginosa PAO1 strain with disruption of pslA and pslB (
pslAB) was severely compromised, indicating that psl has a role in cell-surface interactions. In this study, we investigated the adherence properties of this
pslAB mutant using biotic surfaces (epithelial cells and mucin-coated surfaces) and abiotic surfaces. Our results showed that psl is required for attachment to a variety of surfaces, independent of the carbon source. To study the potential roles of Psl apart from attachment, we generated a psl-inducible P. aeruginosa strain (
psl/pBAD-psl) by replacing the psl promoter region with araC-pBAD, so that expression of psl could be controlled by addition of arabinose. Analysis of biofilms formed by the
psl/pBAD-psl strain indicated that expression of the psl operon is required to maintain the biofilm structure at steps postattachment. Overproduction of the Psl polysaccharide led to enhanced cell-surface and intercellular adhesion of P. aeruginosa. This translated into significant changes in the architecture of the biofilm. We propose that Psl has an important role in P. aeruginosa adhesion, which is critical for initiation and maintenance of the biofilm structure.
* Corresponding author. Mailing address: Department of Microbiology and Immunology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157. Phone: (336) 716-2016. Fax: (336) 716-9928. E-mail:
dwozniak{at}wfubmc.edu.
Published ahead of print on 15 September 2006.
Present address: University of Washington School of Medicine, Seattle, Wash.
Journal of Bacteriology, December 2006, p. 8213-8221, Vol. 188, No. 23
0021-9193/06/$08.00+0 doi:10.1128/JB.01202-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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