Worldwide Genetic Relationships among Francisella tularensis Isolates Determined by Multiple-Locus Variable-Number Tandem Repeat Analysis

Author:

Johansson Anders12,Farlow Jason3,Larsson Pär2,Dukerich Meghan3,Chambers Elias3,Byström Mona2,Fox James3,Chu May4,Forsman Mats2,Sjöstedt Anders5,Keim Paul3

Affiliation:

1. Divisions of Infectious Diseases

2. Department of NBC Analysis, Swedish Defence Research Agency, Umeå, Sweden

3. Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona

4. Centers for Disease Control and Prevention, Fort Collins, Colorado

5. Clinical Bacteriology, Department of Clinical Microbiology, Umeå University

Abstract

ABSTRACT The intracellular bacterium Francisella tularensis is the causative agent of tularemia and poses a serious threat as an agent of bioterrorism. We have developed a highly effective molecular subtyping system from 25 variable-number tandem repeat (VNTR) loci. In our study, multiple-locus VNTR analysis (MLVA) was used to analyze genetic relationships and potential population structure within a global collection of 192 F. tularensis isolates, including representatives from each of the four subspecies. The VNTR loci displayed between 2 and 31 alleles with Nei's diversity values between 0.05 and 0.95. Neighbor-joining cluster analysis of VNTR data revealed 120 genotypes among the 192 F. tularensis isolates, including accurate subspecies identification. F. tularensis subsp. tularensis (type A) isolates showed great diversity at VNTR loci, while F. tularensis subsp. holarctica (type B) isolates showed much lower levels despite a much broader geographical prevalence. The resolution of two distinct clades within F. tularensis subsp. tularensis (designated A.I and A.II) revealed a previously unrecognized genetic division within this highly virulent subspecies. F. tularensis subsp. holarctica appears to have recently spread globally across continents from a single origin, while F. tularensis subsp. tularensis has a long and complex evolutionary history almost exclusively in North America. The sole non-North American type A isolates (Slovakian) were closely related to the SCHU S4 strain. Significant linkage disequilibrium was detected among VNTR loci of F. tularensis consistent with a clonal population structure. Overall, this work greatly augments the study of tularemia ecology and epidemiology, while providing a framework for future forensic analysis of F. tularensis isolates.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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