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colspan=2 style="text-align: center
lightgrey" | Francisella tularensis
Francisella tularensis 01
F. tularensis colonies on an agar plate.
colspan=2 style="text-align: center
lightgrey" | Scientific classification
Kingdom: Bacteria
Phylum: Proteobacteria
Class: Gamma Proteobacteria
Order: Thiotrichales
Family: Francisellaceae
Genus: Francisella
Species: F. tularensis
colspan=2 style="text-align: center
lightgrey" | Binomial name
Francisella tularensis
(McCoy and Chapin 1912)
Dorofe'ev 1947

Francisella tularensis is a pathogenic species of gram-negative bacteria and the causative agent of tularemia or rabbit fever. It is a facultative intracellular bacterium. [1] Due to its ease of spread by aerosol and its high virulence, F. tularensis is classified as a Class A agent by the U.S. government.[2]


This species was discovered in ground squirrels in Tulare County, California in 1911; Bacterium tularense was soon isolated by George Walter McCoy of the US Plague Lab in San Francisco and reported in 1912.[3][4][5] Four subspecies (biovars) of F. tularensis have been classified. The biovar tularensis (or type A) is found predominantly in North America and is the most virulent of the four known subspecies and is associated with lethal pulmonary infections. Biovar palearctica (also known as biovar holarctica or type B) is found predominantly in Europe and Asia but rarely leads to fatal disease. An attenuated live vaccine strain of subspecies palearctica has been described, though it is not yet fully licensed by the FDA as a vaccine. Subspecies novicida (previously classified as F. novicida [6]) was characterized as a relatively nonvirulent strain; only two tularemia cases in North America have been attributed to novicida and these were only in severely immunocompromised individuals. The fourth, biovar mediasiatica, is found primarily in central Asia; little is currently known about this subspecies or its ability to infect humans.


F. tularensis is capable of infecting a number of small mammals such as voles, rabbits, and muskrats, as well as humans. Despite this, no case of tularemia has been shown to be initiated by human-to-human transmission. Rather, tularemia is caused by contact with infected animals or vectors such as ticks, mosquitos, and deer flies.

Infection with F. tularensis can occur via several routes. The most common occurs via skin contact, yielding an ulceroglandular form of the disease. Inhalation of bacteria - particularly biovar tularensis, leads to the potentially lethal tularemia. While the pulmonary and ulceroglandular forms of tularemia are more common, other routes of inoculation have been described and include oropharyngeal infection due to consumption of contaminated food and conjunctival infection due to inoculation at the eye.

F. tularensis is capable of surviving outside of a mammalian host for weeks at a time and has been found in water, grassland, and haystacks. Aerosols containing the bacteria may be generated by disturbing carcasses due to brushcutting or lawn mowing; as a result, tularemia has been referred to as lawnmower disease. Recent epidemiological studies have shown a positive correlation between occupations involving the above activities and infection with F. tularensis.

Life cycleEdit

F. tularensis is a facultative intracellular bacterium that is capable of infecting most cell types but primarily infects macrophages in the host organism. F. tularensis entry into the macrophage occurs via phagocytosis and the bacterium is sequestered from the interior of the infected cell by a phagosome. F. tularensis then breaks out of this phagosome into the cytosol and rapidly proliferates. Eventually the infected cell undergoes apoptosis, and the progeny bacteria are released to initiate new rounds of infection.

Virulence factorsEdit

Tularemia lesion

A Tularemia lesion on the dorsal skin of right hand.

The virulence mechanisms for F. tularensis have not been well characterized. Like other intracellular bacteria that break out of phagosomal compartments to replicate in the cytosol, F. tularensis strains produce different hemolytic agents, which may facilitate degradation of the phagosome.[7] A hemolysin activity, named NlyA, with immunological reactivity to Escherichia coli anti-HlyA antibody was identified in biovar novicida.[8] Acid phosphatase AcpA has been found in other bacteria to act as a hemolysin, whereas in Francisella its role as a virulence factor is under vigorous debate.

While F. tularensis does not contain virulence secretion systems typical of some better-characterized pathogenic bacteria, it does contain a number of ATP binding cassette (ABC) proteins that may be linked to the secretion of virulence factors.[9] In addition, F. tularensis uses type IV pili to bind to the exterior of a host cell and thus become phagocytosed. Mutant strains lacking pili show severely attenuated pathogenicity.

The expression of a 23-kD protein known as IglC is required for F. tularensis phagosomal breakout and intracellular replication; in its absence mutant F. tularensis die and are degraded by the macrophage. This protein is located in a putative pathogenicity island regulated by the transcription factor MglA.

F. tularensis, in vitro, downregulates the immune response of infected cells, a tactic used by a significant number of pathogenic organisms to ensure that replication is (albeit briefly) unhindered by the host immune system by blocking the warning signals from the infected cells. This downmodulation of the immune response requires the IglC protein, though again it is not clear what the contributions of IglC and other genes are.

Several other putative virulence genes exist but have yet to be characterized for function in F. tularensis pathogenicity.


Like many other bacteria, F. tularensis undergoes asexual replication. Bacteria will divide into two daughter cells, each of which contains identical genetic information. Genetic variation may be introduced via mutation or horizontal gene transfer.

The genome of F. tularensis biovar tularensis strain SCHU4 has been sequenced.[10] The studies resulting from the sequencing suggest that a number of gene coding regions in the F. tularensis genome are disrupted by mutations and thus create blocks in a number of metabolic and synthetic pathways that are required for survival. This indicates that F. tularensis has evolved to depend on the host organism for certain nutrients and other processes ordinarily taken care of by these disrupted genes.

The F. tularensis genome contains unusual transposon-like elements resembling counterparts that normally are found in eukaryotic organisms.

Use as a biological weaponEdit

When the U.S. biological warfare program ended in 1969 F. tularensis was one of seven standardized biological weapons it had developed.[11]



  1. Ryan KJ; Ray CG (editors) (2004). Sherris Medical Microbiology (4th ed.). McGraw Hill. pp. 488–90. ISBN 0-8385-8529-9. 
  2. Oyston P, Sjostedt A, Titball R (2004). "Tularaemia: bioterrorism defence renews interest in Francisella tularensis". pp. 967–78. Digital object identifier:10.1038/nrmicro1045. PMID 15550942. 
  3. A. Tärnvik1 and L. Berglund, Tularaemia. Eur Respir J 2003; 21:361-373.
  4. McCoy GW, Chapin CW. Bacterium tularense, the cause of a plaguelike disease of rodents. Public Health Bull 1912;53:17–23.
  5. Jeanette Barry, Notable Contributions to Medical Research by Public Health Service Scientists. National Institute of Health, Public Health Service Publication No. 752, 1960, p. 36.
  6. Sjöstedt AB. "Genus I. Francisella Dorofe'ev 1947, 176AL.". New York: Springer. pp. 200–210. 
  9. Atkins H, Dassa E, Walker N, Griffin K, Harland D, Taylor R, Duffield M, Titball R (2006). "The identification and evaluation of ATP binding cassette systems in the intracellular bacterium Francisella tularensis". pp. 593–604. Digital object identifier:10.1016/j.resmic.2005.12.004. PMID 16503121. 
  10. Larsson P, Oyston P, Chain P, et al. (2005). "The complete genome sequence of Francisella tularensis, the causative agent of tularemia". pp. 153–9. Digital object identifier:10.1038/ng1499. PMID 15640799. 
  11. Croddy, Eric C. and Hart, C. Perez-Armendariz J., Chemical and Biological Warfare, (Google Books), Springer, 2002, pp. 30-31, (ISBN 0387950761), accessed October 24, 2008.

External linksEdit

Template:Gram-negative bacterial diseases

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