- Short report
Leishmania major infection in a dog with cutaneous manifestations
Parasites & Vectorsvolume 9, Article number: 246 (2016)
Leishmania major is a main cause of cutaneous leishmaniasis in humans in an area that stretches from India through Central Asia, the Middle East, to North and West Africa. In Israel, it is a common infection of humans with rodents as the reservoir hosts and Phlebotomus papatasi as its sand fly vector.
A 6 months old spayed female mixed breed dog was referred to the Hebrew University Veterinary Teaching Hospital with a large ulcerative dermal lesion on the muzzle, and lesions in the foot pads and left hind leg. Histopathology of a skin biopsy found chronic lymphohistiocytic dermatitis with the presence of Leishmania spp. amastigotes in the muzzle. Physical examination indicated that the dog was overall in a good clinical condition and the main findings were the skin lesions and enlarged prescapular lymph nodes. Complete blood count and serum biochemistry profile were within reference ranges. Serology by ELISA was positive for Leishmania spp. and PCR of the prescapular lymph node was positive by an ITS1 region PCR-high resolution melt analysis. However, the melt curve and subsequent DNA sequencing indicated that infection was caused by L. major and not L. infantum, which is the main causative agent of canine leishmaniosis in the Mediterranean region. DNA was extracted from the paraffin embedded muzzle biopsy and PCR with sequencing also indicated L. major. The dog’s young age and the absence of hyperglobulinemia and anemia were not typical of L. infantum infection. The dog was treated with allopurinol and the skin lesions improved and later disappeared when the dog was re-evaluated.
This is the first molecularly-confirmed case of L. major infection in a dog. Two previous reports of L. major in dogs originated from Saudi-Arabia and Egypt in 1985 and 1987 were confirmed by enzymatic biochemical techniques. Serology for L. infantum was positive probably due to the well documented serological cross-reactivity between Leishmania spp. Although dogs and wild carnivores are not considered main reservoirs for L. major, the possibility of clinical canine disease and their potential as secondary hosts should be investigated in areas endemic for human L. major infection.
Leishmania major causes human cutaneous leishmaniasis in Asia and Africa. In the Middle East and Israel, it is a common cause of human infection with rodents as reservoir hosts and Phlebotomus papatasi as its sand fly vector.
A 6-month-old mixed-breed female dog from Hadera, on the coastal plain of Israel, was presented in February 2015 to a local veterinary clinic with skin wounds over the muzzle and foot pads and an ulcerative dermal lesion over the left tarsal joint. The dog was adopted at the age of four months from an animal shelter in Tel Aviv and its birthplace was unknown. The lesion on the muzzle was 3 × 4 centimeters in size and composed of a deep skin ulcer with bloody discharge surrounded by an elevated granulating rim (Fig. 1). A full thickness punch biopsy of the muzzle skin lesion was taken under general anesthesia when the dog was neutered and submitted for histological evaluation. Microscopically, the skin showed chronic lymphohistiocytic and granulomatous dermatitis. There was a severe multifocal and coalescing interstitial and perifollicular histiocytic and lymphocytic dermal infiltration with plasma cells and a small number of neutrophils. Macrophages had an expanded vacuolated cytoplasm and in some, there were groups of round to oval organisms, approximately 1 to 2 μm in size, with small basophilic nuclei interpreted as Leishmania spp. amastigotes (Fig. 2). Following the presumptive diagnosis of leishmaniosis, serology for Leishmania infantum was submitted to the Hebrew University School of Veterinary Medicine (HUSVM) and performed by ELISA as previously described . ELISA serology with L. infantum antigen was low positive with an optical density (O.D.) of 0.79 (cut-off 0.6 O.D.). The dog was then referred to the HUSVM for further diagnosis.
On physical examination, the dog had a normal body temperature and good general body condition. The left prescapular lymph node was moderately enlarged and ulcerative skin lesions were found on the muzzle (Figs. 1, 3a) and over the left tarsus, and the right front and hind footpads. A complete blood count (CBC), serum biochemistry panel and urinalysis were taken, as well as blood and lymph-node aspirate for PCR using the ITS1-PCR-high resolution melt (HRM) analysis .
Blood count, serum biochemistry and urinalysis results were within normal limits with no hyperglobulinemia or hypoalbuminemia typical of canine L. infantum infection . Blood was negative by PCR; however, the prescapular lymph node was positive and yielded a DNA sequence that was 100 % identical to Leishmania major (GenBank KM052753) as found by BLAST analysis (http://www.ncbi.nlm.nih.gov/BLAST). Following this, the muzzle biopsy taken earlier by the referring veterinarian was received from the pathology service, sample was deparaffinized and DNA was extracted from the tissue using the QIAamp DNA FFPE tissue kit (QIAgen, Valencia, CA, USA) according to the manufacturer’s instructions. PCR from the muzzle biopsy performed by the ITS1-HRM-PCR was also positive for L. major and confirmed by DNA sequencing as 100 % identical to the same GenBank accession as the dog’s lymph node sequence (KM052753). The dog was diagnosed as having L. major infection and long-term treatment with allopurinol at 10 mg/kg every 12 h was initiated as recommended for dogs infected with L. infantum . The owners were also advised to fit a topical insecticide sand fly repelling collar on the dog.
On a follow-up visit twenty one days after the initiation of treatment, the dog’s skin lesions had improved and the muzzle lesion had shrunk and showed progressive healing (Fig. 3b), but the left prescapular lymph node was still mildly enlarged. The CBC showed a mild leukocytosis (17.0 × 109 leukocytes/l; reference 5.2–13.9) with neutrophilia (12.0 × 109 neutrophils/l; reference 3.9–8.0) and serum biochemistry indicated a mild hypoalbuminemia (28 g/l; reference 30–44) with normal globulin levels (30 g/l; reference 23–53). ITS1-HRM-PCR of tissue aspirates from the two prescapular lymph nodes was positive and compatible with L. major after sequencing, and the blood was PCR-negative again as well as PCR of conjunctival swabs which were negative. Repeat serology was positive (1.3 O.D.). Parasite culture from a pre-scapular lymph node aspirate seeded in NNN slants overlaid with Schneider’s Drosophila medium as previously described was positive . Cultures grew Leishmaia promastigotes which were characterized by ITS1-HRM-PCR and DNA sequencing as L. major. Unfortunately parasites in these cultures did not continue to propagate and eventually growth was halted and parasites could not be maintained longer.
The dog was brought for a third follow-up 59 days after treatment initiation at which the muzzle skin lesion had almost disappeared, there were residual scars on the foot pads and the prescapular lymph nodes were mildly enlarged. ELISA serology at this time was considered negative for L. infantum-infected dogs (0.29 O.D.) and PCR from the pre-scapular lymph node was positive for L. major, while blood PCR was again negative. A fourth and final follow-up visit took place 19 weeks after treatment initiation while the dog continued to receive the allopurinol treatment. The muzzle (Fig. 3c) and footpad skin lesions were not evident any longer and the pre-scapular lymph nodes were small and not readily available for sampling by needle aspiration. The owners reported that the dog was active and in good health. ELISA serology was negative with an even lower O.D. (0.12) than found in the previous visit and blood PCR was negative. The dog continued to be treated with allopurinol at the same dose for one year and follow-up visits to the attending veterinarian were recommended every 6 months.
Additional 400 bp ITS1 fragments were amplified from the parasite promastigote culture and from the muzzle skin biopsy using primers ITS1F and ITS2R4  as previously described  in order to further characterize the L. major strain infecting the dog. The DNA sequences of these amplified ITS1 loci from the two sampled tissues were found identical and submitted to GenBank (KU949581; KU949582). A phylogram of these amplified L. major ITS1 sequences was constructed to compare them to other L. major strains and additional Leishmania spp. present in GenBank. Sequences were analyzed using the MEGA version 6.0 software  (http://www.megasoftware.net) and a phylogram was constructed by the Maximum likelihood algorithm with the Tamura-3-parameter model . Bootstrap replicates were performed to estimate the node reliability, and values were obtained from 1000 randomly selected samples of the aligned sequence data (Fig. 4). The phylogram indicated that the dog’s L. major sequences clustered together with other L. major strains from humans in Israel and other countries, separately from L. infantum and L. tropica strains from dogs and humans, and also away from L. aethiopica, L. amazonensis and L. braziliensis.
Leishmania major is a main cause of cutaneous leishmaniasis in humans in an area that stretches from India through Central Asia, the Middle East, to North and West Africa. In Israel, it is a common infection of humans with different species of rodents as the reservoir hosts and Phlebotomus papatasi as its sand fly vector . A resurgence of human cutaneous leishmaniasis has been reported in Israel during 2001–2012, with increased infection of both L. major and L. tropica with an annual incidence of 4.4 cases per 100,000 inhabitants in 2012 . A sevenfold increase in the laboratory-confirmed cutaneous leishmaniasis cases was observed from 2007 to 2013 in southern Israel where L. major is the main cause of this disease .
Different Leishmania spp. have been reported to infect dogs in a variety of regions in the world , however, to our best knowledge, only two previous reports of natural canine L. major infection have been published. These descriptions which originated from Saudi-Arabia and Egypt in 1985 and 1987, respectively, were confirmed for infection with L. major by enzymatic biochemical techniques [12–15]. While L. major was apparently isolated from the scrotum and an ear ulcer of Saudi-Arabian dogs [12, 14], isolation was made from the spleen of an emaciated dog with diarrhea and from the blood of a lethargic dog with mild alopecia, both in Egypt . No additional clinical information is available on these dogs, no serology was carried out and confirmation by molecular biology techniques was not done as it was unavailable at that time. Furthermore, no treatment of these dogs has been reported. Our report is thus the first description of clinical L. major infection in a dog which was confirmed by molecular methods and the first to follow the treatment of disease and report its progression.
The affected dog described here was young, had only cutaneous manifestations of disease and did not develop the common CBC and serum biochemistry abnormalities of dogs with L. infantum infection such as anemia and hyperglobulinemia . Although both skin lesions and superficial lymph nodes were positive for L. major by PCR and culture, and the dog was seropositive for Leishmania spp. by ELISA, PCR of the blood was consistently negative and no systemic manifestations attributable to Leishmania infection were recorded. It also responded well to long-term allopurinol treatment with gradual disappearance of its dermal abnormalities and a considerable decrease in antibody levels over time, reaching a level that would be considered below the cut-off for dogs with L. infantum infection.
The mild neutrophilia found on the dog’s second follow-up at the HUSVM could be attributed to an inflammatory response to the dermatitis or to possible secondary bacterial infection of the skin. The mild hypoalbuminemia may also be explained by an inflammatory response as albumin is a negative acute phase protein which may decrease during inflammation . The seropositivity to L. infantum antigen was not surprising as there is a strong serological cross-reactivity between different Leishmania species and it was also reported in cases of canine L. tropica infection [5, 17, 18]. The presence of L. major in regional lymph node, as found in this dog has also been demonstrated in human patients with this disease and indicates that the parasite may reach the lymph nodes draining the local cutaneous sites of infection . The excellent response to allopurinol treatment and the healing of the dog’s lesions suggest that allopurinol used as the major drug against canine L. infantum infection , is also effective against canine L. major infection.
Very few studies have evaluated the involvement of companion animals in the epidemiology of L. major infection. A study from the Kerman province in southeast Iran, a focus of human L. major cutaneous leishmaniasis, has evaluated dogs and rodents as reservoirs for this infection and found no evidence of canine involvement . Nevertheless, another study from Turkey detected widespread sub-clinical L. major and L. tropica infections in cats from the Aegean region of Turkey . Further studies should be conducted in L. major foci to evaluate the possible involvement of domestic and wildlife carnivores in the epidemiology of this widespread zoonotic human infection.
This is the first molecularly-confirmed report of clinical L. major infection in a dog and its response to anti-leishmanial treatment. Domestic and wild canine infection with L. major may be more prevalent in areas of endemic human L. major cutaneous leishmaniasis than currently recognized, and canines should be evaluated as possible additional reservoirs for human infection.
Animal ethics statement
This study was carried out in accordance with the Hebrew University ethic regulations for experimentation in animals. The study involved exclusive use of samples taken as a part of the animal’s diagnostic procedure by attending veterinarians.
complete blood count
high resolutions melt
Hebrew University School of Veterinary Medicine
internal transcribed spacer
polymerase chain reaction
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This study was supported by the Deutsche Forschungsgemeinschaft (DFG) as part of a German-Israeli-Palestinian cooperative project on the Emergence of Cutaneous Leishmaniasis in the Middle East: ‘An investigation of Leishmania tropica in the Palestinian Authority and Israel’ (SCHO 448/8-1). Publication of this paper has been sponsored by Bayer Animal Health in the framework of the 11th CVBD World Forum Symposium. All authors read and approved the final version of the manuscript.
The authors declare that they have no competing interests.
GB collected the data, sampled the dog and wrote the manuscript; SG is the veterinarian who saw the dog, biopsied it, and continued to monitor its progress; YNB and AR performed serology, PCR and DNA sequencing and performed the phylogenetic analysis; MSS monitored the dog’s clinical progression, and assisted in conceiving the manuscript and writing it, DYS isolated L. major and grew the parasite in culture; and OB performed and interpreted the histopathology of the lesion. All authors read and approved the final version of the manuscript.