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Tularemia |
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Causative Agent |
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A
tick-borne, potentially
zoonotic disease, primarily of rodents and
lagomorphs
. Caused by the
bacteria, Francisella tularensis.
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Two different sub-species of F. tularensis:
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Click on a photo to enlarge. |
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Small white dots of necrosis on the liver of this beaver are typical of tularemia. |
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Enlargement of the spleen is typically observed in animals with tularemia. |
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Distribution |
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Geographic:
Seasonality:
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Ticks
are only present on hares from May to September (Alaska data); as a result, the disease essentially disappears from October through April.
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Human cases may also occur throughout the fall and winter following exposure to rabbits during rabbit-hunting season.
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Hosts, Transmission and Life Cycle |
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Hosts:
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F. t. tularensis:
rodents and
lagomorphs.
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F. t. palaearctica:
aquatic rodents.
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In North America, tularemia occurs most commonly in cottontail rabbits, muskrats, ground squirrels, and beavers.
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It is thought that tularemia is often fatal in the above species, but not so for the snowshoe hare.
Transmission:
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F. t. tularensis:
transmission occurs among hosts primarily through
ticks, but also by
mites, mosquitoes, fleas,
lice and biting flies (Tabanidae).
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F. t. palaearctica:
transmission occurs directly through water, which may remain infectious for weeks to months following contamination.
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For both species, transmission may also occur through contact with feces, urine or body parts of infected animals.
Life Cycle:
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Although often fatal, the
bacterium can infect both
lagomorph and rodent hosts without apparent ill-effects. These hosts can then remain infected for extended periods serving as
“reservoirs of infection” for other animals and biting arthropods.
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Ticks
act not only as
vectors of transmission but also as
reservoirs of the
bacterium which can live in certain
tick species for months.
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F. t. palaearctica
may also be transferred among voles (Microtus spp.) through cannibalism of infected individuals.
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The mammal and
arthropod associations differ from location to location.
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Signs and Symptoms |
Animals:
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In the most sensitive species,
clinical signs are not often observed due to the short duration of infection before death occurs. These animals are usually in good body condition at death.
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In less sensitive species, during the latter stages of the disease, animals may become lethargic or depressed and have elevated body temperature.
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Tularemia is most often recognized during examination at a
diagnostic laboratory.
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Tiny, pale spots on the liver, spleen or lung are typical
lesions of tularemia.
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Spleen or liver may become enlarged.
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As in humans, an
ulcer may form where the
bacteria have entered the body.
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Thin, whitish strands of material may be present in the abdominal cavity.
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Above
lesions are not unique to tularemia: see also
plague.
Humans:
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Initially, symptoms are: generalized fever-like illness (e.g., fever with chills, headache, vomiting) beginning 1-10 days after infection.
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Confirmation of the disease is usually accomplished using blood tests.
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The course of the disease depends on the route of infection:
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arthropod
bite: an
ulcer forms at the bite wound followed by enlargement of the
lymph nodes draining the area of the bite wound.
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inhalation: inhalation of infected material results in
pneumonia.
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ingestion: of infected water or meat leads to
inflammation of the posterior portion of the oral cavity and intestines.
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Disease resulting from F. t. tularensis is more serious than that caused by F. t. palaearctica.
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40-60% of untreated cases of
pneumonia or
inflammation of the inner surface of the intestines and 7% of all forms of untreated infection with F. t. tularensis have resulted in fatalities. In contrast, 1% overall
fatality in untreated infections with F. t. palaearctica have been reported.
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Human to human transmission is rare.
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F. t. palaearctica
is common in trappers.
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Meat Edible? |
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Normal cooking temperatures destroy
bacteria in the meat – it is therefore safe to eat when thoroughly cooked.
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Human exposure typically results from preparing carcasses.
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Human Health Concerns and Risk Reduction |
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Human infection in North America prior to 1950 has been closely associated with exposure to cottontail rabbits infected with the F. t. tularensis strain.
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After 1950, the major risk factor to humans has switched to muskrats infected with the F. t. palaearctica strain.
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Taking precautions such as: basic hygiene, use of insect repellents and protective clothing to avoid
arthropod bites, inspection and removal of
ticks, use of gloves when handling and dissecting wild animals, particularly rodents and
lagomorphs, should help to reduce the chance of exposure to the tularemia
bacteria.
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Vaccination against tularemia may be warranted in high-risk areas.
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Dogs and cats can die from tularemia. Since infected animals are easier to catch, pets may become infected after eating the internal organs of the diseased animal. Keeping pets from roaming free should help to reduce the spread of tularemia.
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Tularemia is readily treated with antibiotics if treatment is started early in the course of the disease.
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Thus, symptoms of general malaise and fever should not be ignored and medical attention sought. Medical personnel should be advised that you may have been exposed to wildlife and so may be at risk with respect to various wildlife diseases
including tularemia.
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Samples for Diagnosis |
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Submission of entire carcass or just the spleen or liver.
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Similar Diseases |
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Lesions in animals infected with
plague, yersiniosis and other
bacterial infections may be similar to that of tularemia.
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Further Reading |
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Canadian Cooperative Wildlife Heath Centre. 1995. Tularemia. Pp. 17-19. Health risks to wildlife personnel: hazards from disease-causing agents. Canadian Cooperative Wildlife Heath Centre, Western College of Veterinary Medicine, University of
Saskatchewan. Saskatoon, SK
Elkin, B, and R. L. Zamke. 2001. Common wildlife diseases and parasites in Alaska. Alaska Department of Fish and Game. Anchorage, AK.
Mörner, T., and E. Addison. 2001. Tularemia. Pp. 303-312 in E. S. Williams and I. K. Barker (eds.), Infectious Diseases of Wild Mammals. 3rd Ed. Iowa State University Press, Ames, IA.
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