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 Breitbart, M.
Right arrow Articles by Rohwer, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Breitbart, M.
Right arrow Articles by Rohwer, F.
Agricola
Right arrow Articles by Breitbart, M.
Right arrow Articles by Rohwer, F.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, March 2004, p. 1633-1640, Vol. 70, No. 3
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.3.1633-1640.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Phage Community Dynamics in Hot Springs

Mya Breitbart,1 Linda Wegley,1 Steven Leeds,1 Tom Schoenfeld,2 and Forest Rohwer1,3*

Department of Biology,1 Center for Microbial Sciences, San Diego State University, San Diego, California 92182-4614,3 Lucigen Corporation, Middleton, Wisconsin 535622

Received 19 June 2003/ Accepted 18 November 2003

In extreme thermal environments such as hot springs, phages are the only known microbial predators. Here we present the first study of prokaryotic and phage community dynamics in these environments. Phages were abundant in hot springs, reaching concentrations of a million viruses per milliliter. Hot spring phage particles were resistant to shifts to lower temperatures, possibly facilitating DNA transfer out of these extreme environments. The phages were actively produced, with a population turnover time of 1 to 2 days. Phage-mediated microbial mortality was significant, making phage lysis an important component of hot spring microbial food webs. Together, these results show that phages exert an important influence on microbial community structure and energy flow in extreme thermal environments.


* Corresponding author. Mailing address: Department of Biology, LS316, San Diego State University, 5500 Campanile Dr., San Diego, CA 92182-4614. Phone: (619) 594-7829. Fax: (619) 595-5676. E-mail: forest{at}sunstroke.sdsu.edu.


Applied and Environmental Microbiology, March 2004, p. 1633-1640, Vol. 70, No. 3
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.3.1633-1640.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Bettarel, Y., Bouvier, T., Bouvy, M. (2009). Viral persistence in water as evaluated from a tropical/temperate cross-incubation. J PLANKTON RES 31: 909-916 [Abstract] [Full Text]  
  • Schoenfeld, T., Patterson, M., Richardson, P. M., Wommack, K. E., Young, M., Mead, D. (2008). Assembly of Viral Metagenomes from Yellowstone Hot Springs. Appl. Environ. Microbiol. 74: 4164-4174 [Abstract] [Full Text]  
  • Daniel, A., Bonnen, P. E., Fischetti, V. A. (2007). First Complete Genome Sequence of Two Staphylococcus epidermidis Bacteriophages. J. Bacteriol. 189: 2086-2100 [Abstract] [Full Text]  
  • Kwan, T., Liu, J., DuBow, M., Gros, P., Pelletier, J. (2005). The complete genomes and proteomes of 27 Staphylococcus aureus bacteriophages. Proc. Natl. Acad. Sci. USA 102: 5174-5179 [Abstract] [Full Text]  
  • Sano, E., Carlson, S., Wegley, L., Rohwer, F. (2004). Movement of Viruses between Biomes. Appl. Environ. Microbiol. 70: 5842-5846 [Abstract] [Full Text]