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Title: Complete Genome Sequence of Francisella tularensis Subspecies holarctica FTNF002-00

Journal Article · · PLoS ONE
 [1];  [1];  [1];  [2];  [2];  [3];  [3];  [4];  [4];  [4];  [5];  [6];  [3]
  1. Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Bioscience Division; USDOE Joint Genome Institute (JGI), Walnut Creek, CA (United States)
  2. Univ. of Nebraska Medical Center, Omaha, NE (United States). Dept. of Pathology and Microbiology
  3. Armed Forces Inst. of Pathology, Washington, DC (United States). Division of Microbiology
  4. Southern Methodist Univ., Dallas, TX (United States). Dept. of Pathology. BioHealthBase
  5. Northrop Grumman Information Technology, Rockville, MD (United States). BioHealthBase
  6. Centre Hospitalier et Universitaire, Nancy (France). Lab. de Bacteriologie

Francisella tularensis subspecies holarctica FTNF002-00 strain was originally obtained from the first known clinical case of bacteremic F. tularensis pneumonia in Southern Europe isolated from an immunocompetent individual. The FTNF002-00 complete genome contains the RD23 deletion and represents a type strain for a clonal population from the first epidemic tularemia outbreak in Spain between 1997–1998. Here, we present the complete sequence analysis of the FTNF002-00 genome. The complete genome sequence of FTNF002-00 revealed several large as well as small genomic differences with respect to two other published complete genome sequences of F. tularensis subsp. holarctica strains, LVS and OSU18. The FTNF002-00 genome shares .99.9% sequence similarity with LVS and OSU18, and is also ,5 MB smaller by comparison. The overall organization of the FTNF002-00 genome is remarkably identical to those of LVS and OSU18, except for a single 3.9 kb inversion in FTNF002-00. Twelve regions of difference ranging from 0.1–1.5 kb and forty-two small insertions and deletions were identified in a comparative analysis of FTNF002-00, LVS, and OSU18 genomes. Two small deletions appear to inactivate two genes in FTNF002-00 causing them to become pseudogenes; the intact genes encode a protein of unknown function and a drug:H+ antiporter. In addition, we identified ninety-nine proteins in FTNF002-00 containing amino acid mutations compared to LVS and OSU18. Several non-conserved amino acid replacements were identified, one of which occurs in the virulence-associated intracellular growth locus subunit D protein. Many of these changes in FTNF002-00 are likely the consequence of direct selection that increases the fitness of this subsp. holarctica clone within its endemic population. Our complete genome sequence analyses lay the foundation for experimental testing of these possibilities.

Research Organization:
Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Biological and Environmental Research (BER). Biological Systems Science Division
Grant/Contract Number:
AC52-06NA25396
OSTI ID:
1627385
Journal Information:
PLoS ONE, Vol. 4, Issue 9; ISSN 1932-6203
Publisher:
Public Library of ScienceCopyright Statement
Country of Publication:
United States
Language:
English

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Comparison of virulence of Francisella tularensis ssp. holarctica genotypes B.12 and B.FTNF002-00 journal December 2016
Phylogeographical pattern of Francisella tularensis in a nationwide outbreak of tularaemia in Norway, 2011 journal May 2015
Comparative review of Francisella tularensis and Francisella novicida journal March 2014
Revisiting Francisella tularensis subsp. holarctica, Causative Agent of Tularemia in Germany With Bioinformatics: New Insights in Genome Structure, DNA Methylation and Comparative Phylogenetic Analysis journal March 2018
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