This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rickard, A. H.
Right arrow Articles by Gilbert, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rickard, A. H.
Right arrow Articles by Gilbert, P.
Agricola
Right arrow Articles by Rickard, A. H.
Right arrow Articles by Gilbert, P.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, December 2004, p. 7426-7435, Vol. 70, No. 12
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.12.7426-7435.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Shear Rate Moderates Community Diversity in Freshwater Biofilms

Alexander H. Rickard,* Andrew J. McBain, Amy T. Stead, and Peter Gilbert

School of Pharmacy and Pharmaceutical Sciences, University of Manchester, Manchester, United Kingdom

Received 3 March 2004/ Accepted 20 July 2004

The development of freshwater multispecies biofilms at solid-liquid interfaces occurs both in quiescent waters and under conditions of high shear rates. However, the influence of hydrodynamic shear rates on bacterial biofilm diversity is poorly understood. We hypothesized that different shear rates would significantly influence biofilm diversity and alter the relative proportions of coaggregating and autoaggregating community isolates. In order to study this hypothesis, freshwater biofilms were developed at five shear rates (<0.1 to 305 S–1) in a rotating concentric cylinder reactor fed with untreated potable water. Eubacterial diversity was assessed by denaturing gradient gel electrophoresis (DGGE) and culturing on R2A agar. Fifty morphologically distinct biofilm strains and 16 planktonic strains were isolated by culturing and identified by partial 16S rRNA gene sequencing, and their relatedness was determined by the construction of a neighbor-joining phylogenetic tree. Phylogenetic and DGGE analyses showed an inverse relationship between shear rate and bacterial diversity. An in vitro aggregation assay was used to assess the relative proportions of coaggregating and autoaggregating species from each biofilm. The highest proportion of autoaggregating bacteria was present at high shear rates (198 to 305 S–1). The intermediate shear rate (122 S–1) selected for the highest proportion of coaggregating bacteria (47%, or 17 of a possible 36 coaggregation interactions). Under static conditions (<0.1 S–1), 41 (33%) of a possible 125 coaggregation interactions were positive. Few coaggregation (3.3%) or autoaggregation (25%) interactions occurred between the 16 planktonic strains. In conclusion, these data show that shear rates affect biofilm diversity as well as the relative proportions of aggregating bacteria.


* Corresponding author. Present address: NIDCR, Building 30, Room 310, National Institutes of Health, 30 Convent Dr., MSC 4350, Bethesda, MD 20892-4350. Phone: (301) 451-9447. Fax: (301) 402-0396. E-mail: arickard{at}mail.nih.gov.


Applied and Environmental Microbiology, December 2004, p. 7426-7435, Vol. 70, No. 12
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.12.7426-7435.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Min, K. R., Rickard, A. H. (2009). Coaggregation by the Freshwater Bacterium Sphingomonas natatoria Alters Dual-Species Biofilm Formation. Appl. Environ. Microbiol. 75: 3987-3997 [Abstract] [Full Text]  
  • Simoes, L. C., Simoes, M., Vieira, M. J. (2007). Biofilm Interactions between Distinct Bacterial Genera Isolated from Drinking Water. Appl. Environ. Microbiol. 73: 6192-6200 [Abstract] [Full Text]  
  • Besemer, K., Singer, G., Limberger, R., Chlup, A.-K., Hochedlinger, G., Hodl, I., Baranyi, C., Battin, T. J. (2007). Biophysical Controls on Community Succession in Stream Biofilms. Appl. Environ. Microbiol. 73: 4966-4974 [Abstract] [Full Text]  
  • Elliott, D. R., Wilson, M., Buckley, C. M. F., Spratt, D. A. (2006). Aggregative Behavior of Bacteria Isolated from Canine Dental Plaque. Appl. Environ. Microbiol. 72: 5211-5217 [Abstract] [Full Text]  
  • Busscher, H. J., van der Mei, H. C. (2006). Microbial Adhesion in Flow Displacement Systems. Clin. Microbiol. Rev. 19: 127-141 [Abstract] [Full Text]  
  • Rickard, A. H., Stead, A. T., O'May, G. A., Lindsay, S., Banner, M., Handley, P. S., Gilbert, P. (2005). Adhaeribacter aquaticus gen. nov., sp. nov., a Gram-negative isolate from a potable water biofilm. Int. J. Syst. Evol. Microbiol. 55: 821-829 [Abstract] [Full Text]