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J. Bacteriol. doi:10.1128/JB.01512-06
Copyright (c) 2006, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

A Stochastic Mechanism for Biofilm Formation by Mycoplasma pulmonis

Department of Genetics and Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA

^* To whom correspondence should be addressed. Email: wsimmons{at}uab.edu,

	Abstract

Bacterial biofilms are communities of bacteria that are enclosed in an extracellular matrix. Within a biofilm the bacteria are protected from antimicrobials, environmental stresses, and immune responses from the host. Biofilms are often believed to have a highly-developed organization that is derived from differential regulation of the genes that direct the synthesis of the extracellular matrix and the attachment to surfaces. The mycoplasmas have the smallest of the prokaryotic genomes and apparently lack complex gene-regulatory systems. We examined biofilm formation by Mycoplasma pulmonis and found it to be dependent on the length of the tandem repeat region of the Vsa (variable surface antigen) protein. Mycoplasmas that produced a short Vsa protein with few tandem repeats formed biofilms that attached to polystyrene and glass. Mycoplasmas that produced a long Vsa protein with many tandem repeats formed microcolonies that floated freely in the medium. The biofilms and the microcolonies contained an extracellular matrix which contained Vsa protein, lipid, DNA and saccharide. As variation in the number of Vsa tandem repeats occurs by slipped-strand mispairing, the ability of the mycoplasmas to form a biofilm switches stochastically.

This article has been cited by other articles:

• Simmons, W. L., Dybvig, K. (2007). Biofilms Protect Mycoplasma pulmonis Cells from Lytic Effects of Complement and Gramicidin. Infect. Immun. 75: 3696-3699 [Abstract] [Full Text]