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Volume 11, Number 12—December 2005
Synopsis

Francisella tularensis in the United States

Jason Farlow*, David M. Wagner*, Meghan Dukerich*, Miles Stanley*, May Chu†, Kristy Kubota†, Jeannine Petersen†, and Paul Keim*Comments to Author 
Author affiliations: *Northern Arizona University, Flagstaff, Arizona, USA; †Centers for Disease Control and Prevention, Fort Collins, Colorado, USA

Main Article

Figure 1

Genetic relationships among 48 North American Francisella tularensis subsp. tularensis A.I. subpopulation isolates based upon allelic differences at 24 variable number tandem repeat (VNTR) markers. County, state, and year of isolation are specified to the right of each branch or clade. G indicates number of distinct VNTR marker genotypes, dots indicate host-linked isolates, boxed designation indicates prominent F. tularensis subsp. tularensis laboratory strain SCHU S4, and asterisks indicate iso

Figure 1. Genetic relationships among 48 North American Francisella tularensis subsp. tularensis A.I. subpopulation isolates based upon allelic differences at 24 variable number tandem repeat (VNTR) markers. County, state, and year of isolation are specified to the right of each branch or clade. G indicates number of distinct VNTR marker genotypes, dots indicate host-linked isolates, boxed designation indicates prominent F. tularensis subsp. tularensis laboratory strain SCHU S4, and asterisks indicate isolates with an unknown year of isolation.

Main Article

Page created: February 02, 2012
Page updated: February 02, 2012
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The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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