Francisella tularensis

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Francisella tularensis
Francisella tularensis bacteria (blue) infecting a macrophage (yellow)
Scientific classification Edit this classification
Domain: Bacteria
Phylum: Pseudomonadota
Class: Gammaproteobacteria
Order: Thiotrichales
Family: Francisellaceae
Genus: Francisella
Species:
F. tularensis
Binomial name
Francisella tularensis
(McCoy and Chapin 1912)
Dorofe'ev 1947

Francisella tularensis is a

Select Agent by the U.S. government, along with other potential agents of bioterrorism such as Yersinia pestis, Bacillus anthracis, and Ebola virus. When found in nature, Francisella tularensis can survive for several weeks at low temperatures in animal carcasses, soil, and water. In the laboratory, F. tularensis appears as small rods (0.2 by 0.2 µm), and is grown best at 35–37 °C.[4]

History

This species was discovered in ground squirrels in Tulare County, California in 1911. Bacterium tularense was soon isolated by George Walter McCoy (1876–1952) of the US Plague Lab in San Francisco and reported in 1912. In 1922, Edward Francis (1872–1957), a physician and medical researcher from Ohio, discovered that Bacterium tularense was the causative agent of tularemia, after studying several cases with symptoms of the disease. Later, it became known as Francisella tularensis, in honor of the discovery by Francis.[5][6][7]

The disease was also described in the Fukushima region of Japan by Hachiro Ohara in the 1920s, where it was associated with hunting rabbits.[8] In 1938, Soviet bacteriologist Vladimir Dorofeev (1911–1988) and his team recreated the infectious cycle of the pathogen in humans, and his team was the first to create protection measures. In 1947, Dorofeev independently isolated the pathogen that Francis discovered in 1922. Hence it is commonly known as Francisella dorofeev in former Soviet countries.

Classification

Three subspecies (biovars) of F. tularensis are recognised (as of 2020):[8]

  1. F. t. tularensis (or type A), found predominantly in North America, is the most virulent of the four known subspecies, and is associated with lethal pulmonary infections. This includes the primary type A laboratory strain, SCHUS4.
  2. F. t. holarctica (also known as biovar F. t. palearctica or type B) is found predominantly in Europe and Asia, but rarely leads to fatal disease. An attenuated live vaccine strain of subspecies F. t. holarctica has been described, though it is not yet fully licensed by the Food and Drug Administration as a vaccine. This subspecies lacks the citrulline ureidase activity and ability to produce acid from glucose of biovar F. t. palearctica.
  3. F. t. mediasiatica, is found primarily in central Asia; little is currently known about this subspecies or its ability to infect humans.

Additionally,

immunocompromised
individuals.

Pathogenesis

F. tularensis has been reported in

rodents,[8] galliform birds and deer.[citation needed] Infection via fomites (objects) is also important.[8] Human-to-human transmission has been demonstrated via solid organ transplantation.[10]

F. tularensis can survive for weeks outside a mammalian host[

Epidemiological studies have shown a positive correlation between occupations involving the above activities and infection with F. tularensis.[citation needed
]

Human infection with F. tularensis can occur by several routes. Portals of entry are through blood and the respiratory system. The most common occurs via skin contact, yielding an ulceroglandular form of the disease. Inhalation of bacteria,

conjunctival infection due to inoculation at the eye.[8]

Lifecycle

F. tularensis is a facultative intracellular bacterium that is capable of infecting most cell types, but primarily infects

macrophages in the host organism.[citation needed] Entry into the macrophage occurs by phagocytosis and the bacterium is sequestered from the interior of the infected cell by a phagosome.[citation needed] 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 in a single "burst" event[11]
to initiate new rounds of infection.

Virulence factors

A tularemia lesion on the dorsal skin of a 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.[12] A hemolysin activity, named NlyA, with immunological reactivity to Escherichia coli anti-HlyA antibody, was identified in biovar F. t. novicida.[13] 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.

F. tularensis contains type VI secretion system (T6SS), also present in some other pathogenic bacteria.[14] It also contains a number of

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 cells 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 their 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 the contributions of IglC and other genes are unclear. Several other putative virulence genes exist, but have yet to be characterized for function in F. tularensis pathogenicity.

Genetics

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

The

sequenced.[16]
The studies resulting from the sequencing suggest a number of gene-coding regions in the F. tularensis genome are disrupted by mutations, thus create blocks in a number of metabolic and synthetic pathways required for survival. This indicates 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.

Phylogenetics

Much of the known global genetic diversity of F. t. holarctica is present in Sweden.[17] This suggests this subspecies originated in Scandinavia and spread from there to the rest of Eurosiberia.

Use as a biological weapon

See also: Tularemia

When the U.S. biological warfare program ended in 1969, F. tularensis was one of seven standardized biological weapons it had developed as part of German-American cooperation in the 1920s–1930s.[18]

Diagnosis, treatment, and prevention

F. tularensis colonies on an agar plate
Diagnosis

Infection by F. tularensis is diagnosed by clinicians based on symptoms and patient history, imaging, and laboratory studies.

Treatment

Tularemia is treated with antibiotics, such as aminoglycosides, tetracyclines, or fluoroquinolones. About 15 proteins were suggested that could facilitate drug and vaccine design pipeline.[19]

Prevention

Preventive measures include preventing bites from ticks, flies, and mosquitos; ensuring that all game is cooked thoroughly; refraining from drinking untreated water and using insect repellents. If working with cultures of F. tularensis, in the lab, wear a gown, impermeable gloves, mask, and eye protection. When dressing game, wear impermeable gloves. A live attenuated vaccine is available for individuals who are at high risk for exposure such, as laboratory personnel.[20]

Genomics

See also

References

  1. ^ "Francisella tularensis" (PDF). health.ny.gov. Wadsworth Center: New York State Department of Health. Retrieved 12 May 2015.
  2. ^ "Tularemia (Francisella tularensis)" (PDF). michigan.gov. Michigan Department of Community Health. Retrieved 12 May 2015.
  3. ISBN 0-8385-8529-9
    .
  4. ^ "Francisella tularensis". Microbewiki.kenyon.edu.
  5. S2CID 219200617
    . Retrieved 20 March 2022.
  6. ^ McCoy GW, Chapin CW. Bacterium tularense, the cause of a plaguelike disease of rodents. Public Health Bull 1912;53:17–23.
  7. ^ 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.
  8. ^
    doi:10.1146/annurev-ento-011019-025134
  9. ^ Sjöstedt AB. "Genus I. Francisella Dorofe'ev 1947, 176AL". Bergey's Manual of Systematic Bacteriology. Vol. 2 (The Proteobacteria), part B (The Gammaproteobacteria) (2nd ed.). New York: Springer. pp. 200–210.
  10. PMID 30730826.{{cite journal}}: CS1 maint: multiple names: authors list (link
    )
  11. PMID 32479491
    .
  12. PMID 18490464
    .
  13. ^ "Wiley Online Library". Onlinelibrary.wiley.com. Retrieved 20 March 2022.
  14. PMID 28060573
    .
  15. PMID 16503121
    .
  16. PMID 15640799
    .
  17. ^ Karlsson E, Svensson K, Lindgren P, Byström M, Sjödin A, Forsman M, Johansson A (2012) The phylogeographic pattern of Francisella tularensis in Sweden indicates a Scandinavian origin of Eurosiberian tularaemia. Environ Microbiol doi: 10.1111/1462-2920.12052
  18. ISBN 0387950761
    ), accessed October 24, 2008.
  19. ^ Francisella tularensis: In silico Identification of Drug and Vaccine Targets by Metabolic Pathway Analysis J Harati, J Fallah The 6th Conference on Bioinformatics
  20. ^ "Part IV : Acute Communicable Diseases" (PDF). Publichealth.lacounty.gov. Retrieved 20 March 2022.

External links

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