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 Graber, J. R.
Right arrow Articles by Breznak, J. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Graber, J. R.
Right arrow Articles by Breznak, J. A.
Agricola
Right arrow Articles by Graber, J. R.
Right arrow Articles by Breznak, J. A.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, March 2004, p. 1315-1320, Vol. 70, No. 3
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.3.1315-1320.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Description of Treponema azotonutricium sp. nov. and Treponema primitia sp. nov., the First Spirochetes Isolated from Termite Guts

Joseph R. Graber,1 Jared R. Leadbetter,2 and John A. Breznak1*

Department of Microbiology and Molecular Genetics and Center for Microbial Ecology, Michigan State University, East Lansing, Michigan 48824-4320,1 Environmental Science and Engineering, California Institute of Technology, Pasadena, California 91125-78002

Received 12 August 2003/ Accepted 27 November 2003

Long after their original discovery, termite gut spirochetes were recently isolated in pure culture for the first time. They revealed metabolic capabilities hitherto unknown in the Spirochaetes division of the Bacteria, i.e., H2 plus CO2 acetogenesis (J. R. Leadbetter, T. M. Schmidt, J. R. Graber, and J. A. Breznak, Science 283:686-689, 1999) and dinitrogen fixation (T. G. Lilburn, K. S. Kim, N. E. Ostrom, K. R. Byzek, J. R. Leadbetter, and J. A. Breznak, Science 292:2495-2498, 2001). However, application of specific epithets to the strains isolated (Treponema strains ZAS-1, ZAS-2, and ZAS-9) was postponed pending a more complete characterization of their phenotypic properties. Here we describe the major properties of strain ZAS-9, which is readily distinguished from strains ZAS-1 and ZAS-2 by its shorter mean cell wavelength or body pitch (1.1 versus 2.3 µm), by its nonhomoacetogenic fermentation of carbohydrates to acetate, ethanol, H2, and CO2, and by 7 to 8% dissimilarity between its 16S rRNA sequence and those of ZAS-1 and ZAS-2. Strain ZAS-9 is proposed as the type strain of the new species, Treponema azotonutricium. Strains ZAS-1 and ZAS-2, which are H2-consuming, CO2-reducing homoacetogens, are proposed here to be two strains of the new species Treponema primitia. Apart from the salient differences mentioned above, the genomes of all three strains were similar in size (3,461 to 3,901 kb), in G+C content (50.0 to 51.0 mol%), and in possession of 2 copies of the gene encoding 16S rRNA (rrs). For comparison, the genome of the free-living spirochete Spirochaeta aurantia strain J1 was analyzed by the same methods and found to have a size of 3,719 kb, to contain 65.6 mol% G+C, and also to possess 2 copies of the rrs gene.


* Corresponding author. Mailing address: Department of Microbiology and Molecular Genetics, Biomedical and Physical Sciences Building 6190, Michigan State University, East Lansing, MI 48824-4320. Phone: (517) 355-6463, ext. 1607. Fax: (517) 353-8957. E-mail: breznak{at}msu.edu.


Applied and Environmental Microbiology, March 2004, p. 1315-1320, Vol. 70, No. 3
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.3.1315-1320.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Breznak, J. A., Warnecke, F. (2008). Spirochaeta cellobiosiphila sp. nov., a facultatively anaerobic, marine spirochaete. Int. J. Syst. Evol. Microbiol. 58: 2762-2768 [Abstract] [Full Text]  
  • Imachi, H., Sakai, S., Hirayama, H., Nakagawa, S., Nunoura, T., Takai, K., Horikoshi, K. (2008). Exilispira thermophila gen. nov., sp. nov., an anaerobic, thermophilic spirochaete isolated from a deep-sea hydrothermal vent chimney. Int. J. Syst. Evol. Microbiol. 58: 2258-2265 [Abstract] [Full Text]  
  • Droge, S., Rachel, R., Radek, R., Konig, H. (2008). Treponema isoptericolens sp. nov., a novel spirochaete from the hindgut of the termite Incisitermes tabogae. Int. J. Syst. Evol. Microbiol. 58: 1079-1083 [Abstract] [Full Text]  
  • Wertz, J. T., Breznak, J. A. (2007). Physiological Ecology of Stenoxybacter acetivorans, an Obligate Microaerophile in Termite Guts. Appl. Environ. Microbiol. 73: 6829-6841 [Abstract] [Full Text]  
  • Wertz, J. T., Breznak, J. A. (2007). Stenoxybacter acetivorans gen. nov., sp. nov., an Acetate-Oxidizing Obligate Microaerophile among Diverse O2-Consuming Bacteria from Termite Guts. Appl. Environ. Microbiol. 73: 6819-6828 [Abstract] [Full Text]  
  • Safaee, S., Weiser, G. C., Cassirer, E. F., Ramey, R. R., Kelley, S. T. (2006). Microbial diversity in bighorn sheep revealed by culture-independent methods.. J Wildl Dis 42: 545-555 [Abstract] [Full Text]  
  • Horn, M. A., Mertel, R., Gehre, M., Kastner, M., Drake, H. L. (2006). In Vivo Emission of Dinitrogen by Earthworms via Denitrifying Bacteria in the Gut. Appl. Environ. Microbiol. 72: 1013-1018 [Abstract] [Full Text]  
  • Droge, S., Frohlich, J., Radek, R., Konig, H. (2006). Spirochaeta coccoides sp. nov., a Novel Coccoid Spirochete from the Hindgut of the Termite Neotermes castaneus. Appl. Environ. Microbiol. 72: 392-397 [Abstract] [Full Text]  
  • Nordhoff, M., Taras, D., Macha, M., Tedin, K., Busse, H.-J., Wieler, L. H. (2005). Treponema berlinense sp. nov. and Treponema porcinum sp. nov., novel spirochaetes isolated from porcine faeces. Int. J. Syst. Evol. Microbiol. 55: 1675-1680 [Abstract] [Full Text]  
  • Graber, J. R., Breznak, J. A. (2005). Folate Cross-Feeding Supports Symbiotic Homoacetogenic Spirochetes. Appl. Environ. Microbiol. 71: 1883-1889 [Abstract] [Full Text]  
  • (2004). Validation of publication of new names and new combinations previously effectively published outside the IJSEM. Int. J. Syst. Evol. Microbiol. 54: 631-632 [Abstract] [Full Text]  
  • Graber, J. R., Breznak, J. A. (2004). Physiology and Nutrition of Treponema primitia, an H2/ CO2-Acetogenic Spirochete from Termite Hindguts. Appl. Environ. Microbiol. 70: 1307-1314 [Abstract] [Full Text]