Virtually all cells living in multicellular structures such as tissues and organs are encased in an extracellular matrix. One of the most important features of a biofilm is the extracellular polymeric substance that functions as a matrix, holding bacterial cells together. Yet very little is known about how the matrix forms or how matrix components encase bacteria during biofilm development. Pseudomonas aeruginosa forms environmentally and clinically relevant biofilms and is a paradigm organism for the study of biofilms. The extracellular polymeric substance of P. aeruginosa biofilms is an ill defined mix of polysaccharides, nucleic acids, and proteins. Here, we directly visualize the product of the polysaccharide synthesis locus (Psl exopolysaccharide) at different stages of biofilm development. During attachment, Psl is anchored on the cell surface in a helical pattern. This promotes cell-cell interactions and assembly of a matrix, which holds bacteria in the biofilm and on the surface. Chemical dissociation of Psl from the bacterial surface disrupted the Psl matrix as well as the biofilm structure. During biofilm maturation, Psl accumulates on the periphery of 3-D-structured microcolonies, resulting in a Psl matrix-free cavity in the microcolony center. At the dispersion stage, swimming cells appear in this matrix cavity. Dead cells and extracellular DNA (eDNA) are also concentrated in the Psl matrix-free area. Deletion of genes that control cell death and autolysis affects the formation of the matrix cavity and microcolony dispersion. These data provide a mechanism for how P. aeruginosa builds a matrix and subsequently a cavity to free a portion of cells for seeding dispersal. Direct visualization reveals that Psl is a key scaffolding matrix component and opens up avenues for therapeutics of biofilm-related complications.
机构:
Chinese Acad Sci, Inst Microbiol, State Key Lab Microbial Resources, Beijing 100101, Peoples R ChinaChinese Acad Sci, Inst Microbiol, State Key Lab Microbial Resources, Beijing 100101, Peoples R China
Wei, Qing
Ma, Luyan Z.
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Chinese Acad Sci, Inst Microbiol, State Key Lab Microbial Resources, Beijing 100101, Peoples R ChinaChinese Acad Sci, Inst Microbiol, State Key Lab Microbial Resources, Beijing 100101, Peoples R China
机构:
Hosp Sick Children, Peter Gilgan Ctr Res & Learning, Program Mol Med, 686 Bay St, Toronto, ON M5G 0A4, Canada
Univ Toronto, Dept Biochem, Med Sci Bldg,1 Kings Coll Cir, Toronto, ON M5S 1A8, CanadaHosp Sick Children, Peter Gilgan Ctr Res & Learning, Program Mol Med, 686 Bay St, Toronto, ON M5G 0A4, Canada
Gheorghita, Andreea A.
Wozniak, Daniel J.
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Ohio State Univ, Coll Med, Dept Microbial Infect & Immun, 776 Biomed Res Tower,460 W 12th Ave, Columbus, OH 43210 USA
Ohio State Univ Coll, Dept Microbiol, Biol Sci Bldg 105, 484 W 12th Ave, Columbus, OH 43210 USAHosp Sick Children, Peter Gilgan Ctr Res & Learning, Program Mol Med, 686 Bay St, Toronto, ON M5G 0A4, Canada
Wozniak, Daniel J.
Parsek, Matthew R.
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Univ Washington, Dept Microbiol, Hlth Sci Bldg, 1705 NE Pacific St, Seattle, WA 98195 USAHosp Sick Children, Peter Gilgan Ctr Res & Learning, Program Mol Med, 686 Bay St, Toronto, ON M5G 0A4, Canada
Parsek, Matthew R.
Howell, P. Lynne
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Hosp Sick Children, Peter Gilgan Ctr Res & Learning, Program Mol Med, 686 Bay St, Toronto, ON M5G 0A4, Canada
Univ Toronto, Dept Biochem, Med Sci Bldg,1 Kings Coll Cir, Toronto, ON M5S 1A8, CanadaHosp Sick Children, Peter Gilgan Ctr Res & Learning, Program Mol Med, 686 Bay St, Toronto, ON M5G 0A4, Canada