IAI FigSearch
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
IAI.00440-07v1
75/8/3696    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Simmons, W. L.
Right arrow Articles by Dybvig, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Simmons, W. L.
Right arrow Articles by Dybvig, K.

 Previous Article  |  Next Article 

Infection and Immunity, August 2007, p. 3696-3699, Vol. 75, No. 8
0019-9567/07/$08.00+0     doi:10.1128/IAI.00440-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Biofilms Protect Mycoplasma pulmonis Cells from Lytic Effects of Complement and Gramicidin{triangledown}

Warren L. Simmons* and Kevin Dybvig

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama 35294

Received 26 March 2007/ Returned for modification 7 May 2007/ Accepted 13 May 2007

The length of the tandem repeat region of the Vsa protein of Mycoplasma pulmonis has previously been shown to modulate the susceptibility of mycoplasmas to killing by complement: cells that produce a short form of the Vsa protein are highly sensitive, and cells producing the long Vsa protein are resistant. In contrast to their differing susceptibilities to complement, the mycoplasmas were highly sensitive to gramicidin irrespective of the length of the Vsa protein produced. We show here that when encased within a biofilm, cells of M. pulmonis producing a short form of the Vsa protein were more resistant to complement and gramicidin than mycoplasmas that were dispersed. The resistance appeared to be localized to those mycoplasmas within tower structures of the biofilms. Biofilm formation may be a mechanism that protects mycoplasmas from host immunity.


* Corresponding author. Mailing address: Department of Genetics, University of Alabama at Birmingham, KAUL 720, Birmingham, AL 35294-0004. Phone: (205) 934-2794. Fax: (205) 975-4418. E-mail: wsimmons{at}uab.edu

{triangledown} Published ahead of print on 21 May 2007.

Editor: A. Camilli


Infection and Immunity, August 2007, p. 3696-3699, Vol. 75, No. 8
0019-9567/07/$08.00+0     doi:10.1128/IAI.00440-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2007 by the American Society for Microbiology. All rights reserved.