Abstract

BackgroundInfection and clinical disease associated with Leishmania major and Leishmania tropica, two common agents of human cutaneous leishmaniosis, have rarely been reported in dogs. This study describes dogs infected with these Leishmania spp. prevalent in the Middle East and North Africa, and compares the serological response of dogs infected with Leishmania infantum, L. major or L. tropica to whole promastigote antigen enzyme-linked immunosorbent assay (ELISA) of each species and to rK39 dipstick.ResultsLeishmania major infection in a 5-month-old male dog was associated with alopecic and ulcerative periocular and limb skin lesions which responded to allopurinol treatment. Infection was detected by skin and blood polymerase chain reaction (PCR) and confirmed by DNA sequencing but the dog was seronegative. Leishmania tropica infection was detected in a 3-month-old female dog co-infected with Babesia vogeli and Anaplasma platys and with no skin lesions. PCR and DNA sequencing of the blood and parasite culture were positive for L. tropica. Sera from 11 dogs infected with L. infantum, L. major or L. tropica were reactive with all three Leishmania spp. antigens except for sera from a dog with L. major infection. No significant differences were found between reactivity of dog sera to the antigen of the infecting species, or to the other Leishmania spp. antigens. Sera from dogs infected with L. infantum and L. tropica were positive with the rK39 antigen kit, while dogs with L. major infection were seronegative.ConclusionsSkin lesions in L. major infected dogs from this study and previous reports (n = 2) were ulcerative and located on the muzzle, feet and foot pads and not associated with generalized lymphadenomegaly and splenomegaly. In previous L. tropica infections, skin lesions were proliferative mucocutaneous in young dogs (n = 2), or associated with widespread dermatitis, lymphadenomegaly and splenomegaly in older dogs with similarity to L. infantum infection (n = 2). This study suggests that ELISA serology with whole promastigote antigen is not distinctive between L. infantum, L. major and L. tropica canine infections and that some L. major infections are not seropositive. PCR with DNA sequencing should be used to discriminate between canine infections with these three species.

Highlights

  • Infection and clinical disease associated with Leishmania major and Leishmania tropica, two common agents of human cutaneous leishmaniosis, have rarely been reported in dogs

  • A complete blood count (CBC) indicated mild normocytic normochromic anemia with a packed cell volume (PCV) of 31% and serum biochemistry panel was within normal limits

  • enzyme-linked immunosorbent assay (ELISA) serology for L. infantum submitted to the Hebrew University School of Veterinary Medicine (HUSVM) was negative, a skin biopsy taken from the eye lesion and submitted for polymerase chain reaction (PCR) for Leishmania spp. at the HUSVM and was positive for Leishmania by high resolution melt (HRM)-PCR with a melt curve pattern compatible with L. major which was confirmed by sequencing of a 240 bp DNA PCR product that had 100% identity to L. major (GenBank: KP773413.1) and was deposited in GenBank (KY524299)

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Summary

Introduction

Infection and clinical disease associated with Leishmania major and Leishmania tropica, two common agents of human cutaneous leishmaniosis, have rarely been reported in dogs. This study describes dogs infected with these Leishmania spp. prevalent in the Middle East and North Africa, and compares the serological response of dogs infected with Leishmania infantum, L. major or L. tropica to whole promastigote antigen enzyme-linked immunosorbent assay (ELISA) of each species and to rK39 dipstick. In the Middle East and Israel, these two Leishmania spp. are common causes of human infection with wildlife mammal reservoirs, with Phlebotomus papatasi as the sand fly vector for L. major, and Phlebotomus. The aim of this study was to describe additional clinical canine cases of L. major and L. tropica infections, compare them to previous ones [6, 7] and study the serological response to infection using antigens of three different Leishmania spp

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