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

2004 ◽  
Vol 186 (17) ◽  
pp. 5808-5818 ◽  
Author(s):  
Anders Johansson ◽  
Jason Farlow ◽  
Pär Larsson ◽  
Meghan Dukerich ◽  
Elias Chambers ◽  
...  

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.

2014 ◽  
Vol 29 (1) ◽  
pp. 8-15 ◽  
Author(s):  
V. S. Timofeev ◽  
T. Yu. Kudryavtseva ◽  
A. N. Mokrievich ◽  
V. M. Pavlov ◽  
I. A. Dyatlov

2000 ◽  
Vol 182 (10) ◽  
pp. 2928-2936 ◽  
Author(s):  
P. Keim ◽  
L. B. Price ◽  
A. M. Klevytska ◽  
K. L. Smith ◽  
J. M. Schupp ◽  
...  

ABSTRACT Bacillus anthracis is one of the most genetically homogeneous pathogens described, making strain discrimination particularly difficult. In this paper, we present a novel molecular typing system based on rapidly evolving variable-number tandem repeat (VNTR) loci. Multiple-locus VNTR analysis (MLVA) uses the combined power of multiple alleles at several marker loci. In our system, fluorescently labeled PCR primers are used to produce PCR amplification products from eight VNTR regions in the B. anthracisgenome. These are detected and their sizes are determined using an ABI377 automated DNA sequencer. Five of these eight loci were discovered by sequence characterization of molecular markers (vrrC 1, vrrC 2,vrrB 1, vrrB 2, and CG3), two were discovered by searching complete plasmid nucleotide sequences (pXO1-aat and pXO2-at), and one was known previously (vrrA). MLVA characterization of 426 B. anthracis isolates identified 89 distinct genotypes. VNTR markers frequently identified multiple alleles (from two to nine), with Nei's diversity values between 0.3 and 0.8. Unweighted pair-group method arithmetic average cluster analysis identified six genetically distinct groups that appear to be derived from clones. Some of these clones show worldwide distribution, while others are restricted to particular geographic regions. Human commerce doubtlessly has contributed to the dispersal of particular clones in ancient and modern times.


2013 ◽  
Vol 66 (6) ◽  
pp. 543-545 ◽  
Author(s):  
Osamu Fujita ◽  
Akitoyo Hotta ◽  
Akihiko Uda ◽  
Yoshie Yamamoto ◽  
Hiromi Fujita ◽  
...  

2000 ◽  
Vol 182 (23) ◽  
pp. 6862-6862 ◽  
Author(s):  
P. Keim ◽  
L. B. Price ◽  
A. M. Klevytska ◽  
K. L. Smith ◽  
J. M. Schupp ◽  
...  

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