Feline leishmaniosis (FeL) is a parasitic disease caused by protozoa of the genus Leishmania and is transmitted through the bite of a female sand fly. Although leishmaniosis primarily affects dogs; an increasing number of cases have been reported in cats. Consequently, feline leishmaniosis is now considered an emerging disease, particularly in regions where canine leishmaniosis (CanL) is endemic.
Transmission
Etiological agent: Leishmania spp. Leishmaniosis is a disease caused by protozoa of the genus Leishmania. It has been reported that cats have been infected by at least eight Leishmania species worldwide, including L. infantum, L. major, L. tropica, L. mexicana, L. braziliensis, L. amazonensis, L. panamensis and L. guyanensis. This article focuses on L. infantum, the primary species responsible for severe disease in both dogs and cats across Europe, Asia, Africa, and the Americas.
Vector The vector is a sandfly belonging to the genus Phlebotomus in the Old World and the genus Lutzomyia in the New World. The average size of sand flies is 3 mm. Cases of canine and feline leishmaniosis caused by L. infantum are widespread in areas where sand flies coexist.
Cycle of transmission and other ways of transmission non vector related Leishmania species are parasites that require two hosts to complete their lifecycle: the phlebotomine sand fly and a vertebrate. This lifecycle consists of two phases: an amastigote stage—a small, round, non-flagellated intracellular form that resides within the macrophages of vertebrate hosts—, and a promastigote stage—a flagellated form that develops in the gut of sand fly vectors.
The cycle proceeds as follows: the sand fly carries extracellular promastigotes, which it transmits to a vertebrate host while feeding on its blood. Once inside the host, the promastigotes are quickly phagocytosed by macrophages and transform into amastigotes. Within these immune cells, they replicate inside intracellular vacuoles, evading the host's immune response. When a female sand fly bites an infected vertebrate, it ingests macrophages containing amastigotes. Inside the gut of the fly, the amastigotes transform back into promastigotes, developing their characteristic flagellum, which enables movement. The promastigotes then multiply and migrate to the fly's proboscis, ready to infect a new vertebrate host during the next blood meal.
Non-vectorial transmission of L. infantum, such as through blood transfusion, vertical transmission, mating, or aggressive interactions, has been documented in dogs, but it has not yet been observed in cats.
Epidemiology
Endemic areas Leishmaniosis, caused by L. infantum, is endemic in the Mediterranean Basin, including Spain, Portugal, southern France, Italy, Greece, Turkey, and Cyprus, as well as in the Middle East. The importation of infected animals can also introduce the disease into non-endemic regions, such as Northern Europe. In Central and South America and the Middle East, L. infantum coexists with other Leishmania species.
Prevalence Since 1977, natural cases of feline leishmaniosis have been documented worldwide, primarily in Mediterranean countries, but also in the southern USA, Brazil, Central and South America, and Iran.
Feline leishmaniosis is an emerging disease that has been increasingly reported over the past two decades, especially in endemic regions. This rise in feline cases may be linked to the use of sand fly repellents in dogs, which forces the sand fly to seek alternative mammalian hosts. Additionally, the availability of more sensitive and specific diagnostic tests, advancements in feline medicine, and greater awareness among veterinarians may have contributed to the increasing number of reported FeL cases.
Over the past 25 years, approximately 100 clinical cases of FeL have been reported in Europe (including Italy, Spain, France, and Portugal), along with a few cases in Switzerland involving cats imported from endemic regions. The prevalence of Leishmania infection in cats in endemic areas varies significantly, ranging from 0% to 68.5%. PCR test positivity rates for Leishmania in blood samples range from 0.43% to 61%, while antibody prevalence varies from 3% to 59%. Despite this, the prevalence of FeL remains lower in cats than in dogs in the same areas.
Geographical distribution of Leishmania spp.
Risk factors Cats that are most susceptible to Leishmania infections are typically short-haired, between 7 and 9 years of age, male, and have access to the outdoors (either as free-roaming or shelter cats). They are more commonly found in urban areas and cohabit with dogs. Unneutered cats are also at higher risk, as are those with concurrent diseases or immunosuppressive conditions, such as a feline immunodeficiency virus (FIV) infection, which is the most common comorbidity.
Public health considerations The L. infantum strains found in cats share the same genetic characteristics as those from humans, dogs, and sand flies. Leishmaniosis is a zoonotic disease that can affect humans, causing cutaneous, mucocutaneous and visceral leishmaniosis. Visceral leishmaniosis in humans is a life-threatening condition. Domestic dogs are typically considered the main reservoir of human L. infantum infection, with transmission occurring mainly through the bites of female sand flies. However, in recent years, cats have garnered increasing attention due to their potential role in transmission and are now considered secondary reservoir hosts. Infected cats may therefore represent an additional source of L. infantum transmission, posing a risk to humans, dogs, and other susceptible animals, including cats themselves.
Clinical signs Most infected cats remain subclinical, and the incubation period can extend for years, as seen in cats relocated from endemic to non-endemic areas, with clinical signs appearing long after they move. These signs can range from isolated dermatological lesions to ocular, renal and systemic manifestations. The disease generally follows a chronic, progressive course, with more systemic clinical signs emerging when the cats' immune system becomes compromised.
Common manifestations of FeL include cutaneous or mucocutaneous lesions and lymphadenomegaly. Other possible signs are ocular and oral lesions.
Cutaneous and mucocutaneous lesions Dermatological lesions are the most common clinical feature of FeL, accounting for more than half of all cases.
The most frequent manifestations are ulcers and nodules, which typically appear on the head and distal limbs. As a result, ulcerative and nodular dermatitis are the most commonly observed types. These are often followed by exfoliative dermatitis and alopecia.
Ocular lesions Ocular signs usually appear alongside systemic signs.
The most frequent ocular manifestation is anterior uveitis. Less common lesions include panuveitis and corneal melting ulcers (or melting keratitis).
Oral lesions The most common oral lesions are nodules on the tongue and gingiva, often presenting as stomatitis, gingivitis, or feline chronic gingivostomatitis syndrome.
Systemic signs
The most frequent systemic signs are lymphadenomegaly, lethargy, anorexia, and weight loss. Less common signs include pale or icteric mucous membranes, splenomegaly, hepatomegaly, chronic nasal discharge, upper airway obstructive syndrome, cachexia, polyuria, polydipsia, fever, diarrhea, mastitis, subcutaneous panniculitis, abortion, and epistaxis.
Laboratory abnormalities
Most common: polyclonal gammopathy, mild-to-moderate non-regenerative anemia (normocytic, normochromic), and proteinuria. Less common: renal azotemia, hypoalbuminemia, monocytosis, neutrophilia, and pancytopenia.
Comorbidities Comorbidities play a significant role in both susceptibility to L. infantum infection and the onset of clinical signs in cats.
Cats with impaired immune systems are more likely to develop clinical signs of the infection, especially those with pre-existing conditions. Comorbidities affecting the immune system are present in 56% to 73% of cases, with there being a 2.8 times higher risk of developing leishmaniosis when a cat has FIV. Other contributing factors include immunosuppressive conditions caused by prolonged or high-dose glucocorticoid treatment among others, neoplasia (such as epidermoid carcinoma and squamous cell carcinoma), metabolic disorders like diabetes mellitus, co-infections (including Hepatozoon felis, Candidatus mycoplasma, Toxoplasma gondii, feline leukemia virus (FeLV), and feline coronavirus (FCov)), and immune-mediated diseases (such as pemphigus). However, the association between FeL and the majority of these conditions is not well-supported by controlled studies
Diagnostic of Feline Leishmaniosis Source:
The diagnosis of FeL requires a combination of clinical, serological, cytological, and molecular techniques.
Clinical and laboratory findings
Clinical signs compatible with the disease. Clinicopathological abnormalities: abnormalities in serum protein electrophoresis tests such as polyclonal gammopathy.
Serological testing
Qualitative serology (rapid tests) for the detection of anti-L. infantum antibodies are not available for cats, unlike in dogs. Quantitative serology (IFAT, ELISA, DAT) is commonly used for the detection of antibody levels.
Cytological and histopathological evaluations
Cytological analysis of: skin, mucosa, mucocutaneous lesions, lymph nodes, spleen, bone marrow, liver, palpebral conjunctiva or other affected tissues or biological fluids. Possible findings: Lymphoid hyperplasia in lymphoid organs. Neutrophilic and/or macrophagic inflammation. Lymphoplasmacytic inflammation. Visualization of amastigotes (intracellular in macrophages or extracellular). Cytology can also help detect comorbidities.
Histopathology vs. immunohistochemistry (IHC): Amastigotes are rarely visible in histology. IHC is always recommended for confirmation. If IHC is negative, a PCR should be performed.
PCR and tissue sampling
Detection of parasite DNA (PCR) from: bone marrow, lymph nodes, spleen, or affected tissues or biological fluids. In antibody-negative or low-positive cats without tissue lesions, a PCR or cytology may still detect the parasite.
Importance of Comorbidities Since coexisting diseases are common, a thorough investigation is necessary to confirm L. infantumas the cause of clinical signs.
To summarize, a cat is diagnosed with leishmaniosis if the following criteria are met:
There are clinical signs and clinicopathological abnormalities that are compatible with the disease. Confirmation through: Observation of amastigotes via cytology or histology Positive IHC or PCR for Leishmania DNA. Elevated anti-Leishmania antibody titers.
Treatment in cats with clinical leishmaniosis There is no specific treatment approved exclusively for cats, and the approach remains empirical, relying on off-label medications that are primarily prescribed for dogs.
The conventional anti-Leishmania treatments in cats are the following:
Allopurinol: this is the most commonly used treatment for cats. It is administered orally, typically as monotherapy for long-term management, or in combination with meglumine antimoniate, either initially or after a course of subcutaneous injections. Allopurinol can help improve clinical signs, even in FIV-positive cats. However, there is a risk of side effects, particularly involving the kidneys, including acute kidney injury, dermatitis, pruritus, elevated liver enzymes, and xanthinuria. Meglumine antimoniate: this drug is administered subcutaneously and can be used alone or in combination with allopurinol. It may be challenging for owners to administer, especially if the cat is difficult to manage or uncooperative. It can cause renal complications, including acute kidney injury.