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 Bacon, R. M.
Right arrow Articles by Schwan, T. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bacon, R. M.
Right arrow Articles by Schwan, T. G.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, May 2004, p. 2326-2328, Vol. 42, No. 5
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.5.2326-2328.2004

Glycerophosphodiester Phosphodiesterase Gene (glpQ) of Borrelia lonestari Identified as a Target for Differentiating Borrelia Species Associated with Hard Ticks (Acari:Ixodidae)

Rendi Murphree Bacon,1* Mark A. Pilgard,1 Barbara J. B. Johnson,1 Sandra J. Raffel,2 and Tom G. Schwan2

Bacterial Zoonoses Branch, Division of Vector-Borne Infectious Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado 80521,1 Laboratory of Human Bacterial Pathogenesis, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana 598402

Received 23 September 2003/ Returned for modification 7 January 2004/ Accepted 27 January 2004

A glpQ ortholog was identified in DNA from Borrelia lonestari-positive Amblyomma americanum, providing further evidence that B. lonestari is more closely related to the relapsing fever group spirochetes than to borreliae that cause Lyme disease. This finding provides a basis for developing diagnostic assays to differentiate species of borrelia transmitted by hard ticks.


* Corresponding author. Mailing address: Bacterial Zoonoses Branch, CDC/NCID/DVBID, P.O. Box 2087, Fort Collins, CO 80522. Phone: (970) 266-3528. Fax: (970) 221-6476. E-mail: rbacon{at}cdc.gov.


Journal of Clinical Microbiology, May 2004, p. 2326-2328, Vol. 42, No. 5
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.5.2326-2328.2004




This article has been cited by other articles:

  • Porcella, S. F., Raffel, S. J., Anderson, D. E. Jr., Gilk, S. D., Bono, J. L., Schrumpf, M. E., Schwan, T. G. (2005). Variable Tick Protein in Two Genomic Groups of the Relapsing Fever Spirochete Borrelia hermsii in Western North America. Infect. Immun. 73: 6647-6658 [Abstract] [Full Text]  
  • Schwan, T. G., Raffel, S. J., Schrumpf, M. E., Policastro, P. F., Rawlings, J. A., Lane, R. S., Breitschwerdt, E. B., Porcella, S. F. (2005). Phylogenetic Analysis of the Spirochetes Borrelia parkeri and Borrelia turicatae and the Potential for Tick-Borne Relapsing Fever in Florida. J. Clin. Microbiol. 43: 3851-3859 [Abstract] [Full Text]  
  • Revel, A. T., Blevins, J. S., Almazan, C., Neil, L., Kocan, K. M., de la Fuente, J., Hagman, K. E., Norgard, M. V. (2005). bptA (bbe16) is essential for the persistence of the Lyme disease spirochete, Borrelia burgdorferi, in its natural tick vector. Proc. Natl. Acad. Sci. USA 102: 6972-6977 [Abstract] [Full Text]