Leishmania spp. in equids and their potential vectors in endemic areas of canine leishmaniasis
Language English Country United States Media electronic-ecollection
Document type Journal Article
PubMed
39024365
PubMed Central
PMC11257397
DOI
10.1371/journal.pntd.0012290
PII: PNTD-D-24-00441
Knihovny.cz E-resources
- MeSH
- Ceratopogonidae parasitology MeSH
- Endemic Diseases veterinary MeSH
- Equidae * parasitology MeSH
- Insect Vectors * parasitology MeSH
- Horses parasitology MeSH
- Leishmania infantum isolation & purification genetics MeSH
- Leishmania * isolation & purification genetics classification MeSH
- Leishmaniasis * veterinary epidemiology parasitology transmission MeSH
- Horse Diseases parasitology epidemiology MeSH
- Dog Diseases * parasitology epidemiology transmission MeSH
- Dogs MeSH
- Psychodidae parasitology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Dogs MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Italy epidemiology MeSH
Equids may be infected by zoonotic Leishmania spp., including Leishmania infantum, in regions where canine leishmaniasis (CanL) is endemic, and Leishmania martiniquensis, which has been reported in horses from Central Europe. This study was designed to evaluate the occurrence of both Leishmania spp. among equids living in CanL endemic areas of Italy, as well as to identify dipteran vectors from the same habitats. From March to October 2023, blood, serum and tissue samples from skin lesions were collected from equids (n = 98; n = 56 donkeys and n = 42 horses) living in Italy, as well as sand flies and biting midges. Blood samples (n = 98) and skin lesions (n = 56) were tested for Leishmania spp. by conventional and real time PCRs and sera were tested by immunofluorescence antibody tests (IFAT) for both L. infantum and L. martiniquensis. Insects were morphologically identified, and female specimens (n = 268 sand flies, n = 7 biting midges) analyzed for Leishmania DNA, as well as engorged sand flies (n = 16) for blood-meal detection. Two animals with skin lesions (i.e., one donkey and one horse) scored positive for Leishmania spp. DNA, and 19 animals (i.e., 19.4%; n = 13 donkeys and n = 6 horses) were seropositive for L. infantum, with five of them also for L. martiniquensis. Most seropositive animals had no dermatological lesions (i.e., 68.4%) while both animals molecularly positive for Leishmania spp. scored seronegative. Of the 356 sand flies collected, 12 females (i.e., n = 8 Sergentomyia minuta; n = 3 Phlebotomus perniciosus, n = 1 Phlebotomus perfiliewi) were positive for Leishmania spp. DNA, and one out of seven biting midges collected was DNA-positive for L. infantum. Moreover, engorged sand flies scored positive for human and equine DNA. Data suggest that equids living in CanL endemic areas are exposed to Leishmania spp., but their role in the circulation of the parasite needs further investigations.
Department of Parasitology Faculty of Science Charles University Prague Czech Republic
Department of Veterinary Clinical Sciences City University of Hong Kong Hong Kong SAR China
Department of Veterinary Medicine University of Bari Valenzano Italy
Interdisciplinary Department of Medicine University of Bari Bari Italy
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