Previous Article | Next Article ![]()
Applied and Environmental Microbiology, January 2007, p. 605-614, Vol. 73, No. 2
0099-2240/07/$08.00+0 doi:10.1128/AEM.01893-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
Department of Oral Biology, University of Medicine and Dentistry of New Jersey, Newark, New Jersey 07103,1 Department of Microbiology and Immunology, Dartmouth Medical School, Hanover, New Hampshire 037552
Received 8 August 2006/ Accepted 1 November 2006
The host specificity of the gram-negative exoparasitic predatory bacterium Micavibrio aeruginosavorus was examined. M. aeruginosavorus preyed on Pseudomonas aeruginosa, as previously reported, as well as Burkholderia cepacia, Klebsiella pneumoniae, and numerous clinical isolates of these species. In a static assay, a reduction in biofilm biomass was observed as early as 3 hours after exposure to M. aeruginosavorus, and an
100-fold reduction in biofilm cell viability was detected following a 24-h exposure to the predator. We observed that an initial titer of Micavibrio as low as 10 PFU/well or a time of exposure to the predator as short as 30 min was sufficient to reduce a P. aeruginosa biofilm. The ability of Micavibrio to reduce an existing biofilm was confirmed by scanning electron microscopy. In static and flow cell experiments, M. aeruginosavorus was able to modify the overall P. aeruginosa biofilm structure and markedly decreased the viability of P. aeruginosa. The altered biofilm structure was likely caused by an increase in cell-cell interactions brought about by the presence of the predator or active predation. We also conducted a screen to identify genes important for P. aeruginosa-Micavibrio interaction, but no candidates were isolated among the
10,000 mutants tested.
Published ahead of print on 10 November 2006.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»