AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental material
Right arrow Other Versions of this Article:
AEM.01522-07v1
74/1/336    most recent
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 Google Scholar
Google Scholar
Right arrow Articles by Molins-Schneekloth, C. R.
Right arrow Articles by Petersen, J. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Molins-Schneekloth, C. R.
Right arrow Articles by Petersen, J. M.
Agricola
Right arrow Articles by Molins-Schneekloth, C. R.
Right arrow Articles by Petersen, J. M.
Applied and Environmental Microbiology, January 2008, p. 336-341, Vol. 74, No. 1
0099-2240/08/$08.00+0     doi:10.1128/AEM.01522-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Genomic Markers for Differentiation of Francisella tularensis subsp. tularensis A.I and A.II Strains{triangledown} ,{dagger}

Claudia R. Molins-Schneekloth,1,2 John T. Belisle,2 and Jeannine M. Petersen1*

Division of Vector-Borne Infectious Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado,1 Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado2

Received 28 June 2007/ Accepted 30 October 2007

Tularemia is caused by two subspecies of Francisella tularensis, F. tularensis subsp. tularensis (type A) and F. tularensis subsp. holarctica (type B). F. tularensis subsp. tularensis is further subdivided into two genetically distinct populations (A.I and A.II) that differ with respect to geographical location, anatomical source of recovered isolates, and disease outcome. Using two human clinical isolates, suppression subtractive hybridization was performed to identify 13 genomic regions of difference between A.I and A.II strains. Two PCR assays, one to identify A.I and A.II as well as to discriminate between F. tularensis subsp. holarctica and F. novicida and another specific for A.I, were developed. This is the first report to identify and characterize conserved genomic differences between A.I and A.II.


* Corresponding author. Mailing address: Centers for Disease Control and Prevention, Division of Vector-Borne Infectious Diseases, Bacterial Diseases Branch, 3150 Rampart Road, Fort Collins, CO 80521. Phone: (970) 266-3524. Fax: (970) 494-6631. E-mail: JPetersen{at}cdc.gov

{triangledown} Published ahead of print on 16 November 2007.

{dagger} Supplemental material for this article may be found at http://aem.asm.org/.


Applied and Environmental Microbiology, January 2008, p. 336-341, Vol. 74, No. 1
0099-2240/08/$08.00+0     doi:10.1128/AEM.01522-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 2008 by the American Society for Microbiology. All rights reserved.