Protozoa III - Leishmania Flashcards
Describe the epidemiology of leishmaniasis.
Major global zoonosis.
- distributed in tropics and subtropics
- in Europe
- endemic Mediterranean areas
- non-endemic areas
- imported and travelling dogs are relevant
Trend towards geographical extension.
Several species in the genus Leishmania
- Leishmania infantum most important
(= L. chagas)
Three forms of human leishmaniasis:
a) visceral = kala-azar
b) cutaneous
c) mucocutaneous
Dogs are main reservoir for human visceral leishmaniasis.
Non-clinically infected dogs are the main reservoirs of the parasites.
One main form of leishmaniosis in dogs:
- Visceral = viscerocutaneous
= kala-azar, black fever, Dumdum fever
Non-clinically infected dogs are the main reservoirs of the parasites.
Describe leishmaniasis infection in general e.g. hosts, risk factors, IP.
Infection in dogs can be subclinical to fatal.
Cats, horses and other mammals can be hosts.
Risk factors:
- breed (Boxer, Cocker Spaniel, German Shepherd, Rottweiler)
- age (bimodal)
- genetic background
Incubation time: 3 months to 7 years!
Leishmania parasites are transmitted by
sand flies
Sandfly - a name for any species or genus of flying, biting and blood-sucking dipteran in sandy areas.
Transmission of visceral leishmaniosis.
Vector-borne - female sandflies
Transplacental (vertical)
Blood-transfusion
(Direct contact from dog to dog)
Life cycle of Leishmania spp.
Indirect with sandflies.
Sandfly ingests amastigotes from infected host.
Amastigotes transform into promastigotes in fly hindgut, migrate to fly proboscis
and are then transmitted to new host through fly saliva.
In new host, promastigote transforms into amastigote
- hand out intracellular in macrophages
- amastigotes multiply in various other tissues as well.
Pathogenenesis of visceral leishmaniosis
Tissue damage caused by the sandfly bite recruits macrophages to the bite.
The leishmania that has been deposited into the bite, is phagocytosed by the macrophages.
Cell-mediated immune response with cytokines leads to killing and clearance of the parasites in mild cases.
In more severe cases, no or only poor cell-mediated immune response is present which allows leishmania present in macrophages to spread around the body.
Note that severe cases will have high serological titers toward leishmania in an attempt to compensate the poor cell-mediated response with a strong humoral response ?
Clinical findings and symptoms of visceral leishmaniosis.
Chronic and multisystemic disease.
Incubation period from months to years!!
50-60% are asymptomatic – problem bigger as seems!
Cutaneous signs/ skin lesions – without itching
- chancre - sweating ulcerative lesion
- ears, around the eyes, on the back, legs and tail
- non-itchy diffused alopecia
- hyperkeratosis - head, nose, footpads
- claw hypertrophy
Lymphadenopathy - most frequent sign.
Ocular signs
Apathy, anorexia, anemia, fever
Renal insufficiency
Lameness - muscle and joint lesions
define chancre
painless ulcer such as develops in visceral leishmaniasis
(pronounced sh-ahnk) originally french word)
Cutaneous signs/ skin lesions found in visceral leishmaniosis are typically distributed where?
- ears, around the eyes, on the back, legs and tail
- chancres / sweating ulcerative lesions
- non-itchy diffused alopecia
- hyperkeratosis - head, nose, footpads
- claw hypertrophy
Some non-cutaneous signs of leishmaniasis in dogs.
epistaxis
uveitis
conjunctivitis, blepharitis
cachexia
Most important spp. of Leishmania?
L.infantum
Lab abnormalities found in dogs with L.infantum infection.
hypoerglobulinemia
hypoalbuminemia
mild to moderate non-regenerative anemia
leukocytosis OR leukopenia
renal azotemia
mild to severe proteinuria
Diagnosis of visceral leishmaniosis
Biochemical profile and urinalysis
Serology while there are clinical symptoms – high antibody titers in 80-100% of dogs.
- anti-Leishmania antibodies with IFAT, ELISA, DAT
- NB cross-reactivity with Trypanosoma cruzi
Molecular methods (PCR) from bone marrow, lymph nodes, spleen are most sensitive. * are required for importation to non-endemic countries
Cytology or biopsy (+ Giemsa-staining) for detection of amastigotes.
- lymph nodes, spleen, bone marrow, skin
- NB sensitivity is low!