Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Mar 20;13(1):115.
doi: 10.1186/s13071-020-3989-3.

Leishmania infection in cats and dogs housed together in an animal shelter reveals a higher parasite load in infected dogs despite a greater seroprevalence among cats

Affiliations

Leishmania infection in cats and dogs housed together in an animal shelter reveals a higher parasite load in infected dogs despite a greater seroprevalence among cats

Gad Baneth et al. Parasit Vectors. .

Abstract

Background: An outbreak of leishmaniosis was studied in cats and dogs housed together with no separation in an animal shelter in Israel.

Methods: The study included recording of clinical signs, serology for Leishmania infection by ELISA, PCR of blood for Leishmania DNA by ITS1 HRM and kDNA PCR, parasite quantification, and trapping of sand flies around the shelter.

Results: Thirty-seven % (22/60) of the dogs and 75% (50/67) of the cats were seropositive to L. infantum with a significantly higher seropositivity rate in the cat population (χ2 = 42.160, P < 0.0001). Twenty-five percent (15/60) of the dogs were positive for Leishmania by blood PCR, 12% by the Leishmania ITS1 HRM PCR and 22% by kDNA PCR. Of the cats, 16% (11/67) were positive by kDNA PCR and none by ITS1 HRM PCR. All the PCR-positive animals were infected by L. infantum verified by DNA sequencing and there was no significant difference between the PCR-positivity in the dog and cat populations. Altogether, 43% (26/60) of the dogs and 79% (53/67) of the cats were positive by serology or PCR for L. infantum. The average Leishmania parasite load in the blood of PCR-positive dogs (42,967 parasites/ml) was significantly higher than in PCR-positive cats (1259 parasites/ml) (t(12) = 2.33, P = 0.037). Dogs that were positive by the Leishmania ITS1 HRM PCR and kDNA PCR had significantly higher parasite loads than dogs positive only by the kDNA PCR (t(11) = - 3.186580, P < 0.009). No significant effect was found for FIV seropositivity on Leishmania infection in the cats (χ2 = 0.506, P = 0.777). A higher percentage of Leishmania-positive dogs showed clinical signs compatible with leishmaniosis compared to Leishmania-positive cats (100 vs 52.8%, χ2 =15.242, P < 0.0001). Phlebotomus perfiliewi, a proven vector of L. infantum, comprised 92% of trapped sand flies.

Conclusions: Comparisons of populations of cats and dogs exposed to sand flies and L. infantum under the same conditions indicated that although a high rate of exposure was detected in cats as manifested by a significantly greater degree of seropositivity, dogs had significantly higher blood parasite loads, and were likely to be more infectious to sand flies than cats.

Keywords: Cat; Dog; High resolution melt analysis PCR; ITS1 PCR; Leishmania infantum; Parasite load.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
A dog from the animal shelter that was positive for L. infantum by serology and PCR. The dog has overt alopecia and hyperkeratosis with purulent keratoconjunctivitis typical of canine leishmaniosis
Fig. 2
Fig. 2
Aural alopecia and in a cat from the animal shelter that was seropositive with a high antibody level for L. infantum
Fig. 3
Fig. 3
Ulcerative skin lesions, partial alopecia and scales on the ear of a cat from the animal shelter that was seropositive with a high antibody level for L. infantum
Fig. 4
Fig. 4
Complete alopecia and skin ulceration in the ear of a L. infantum-seropositive cat with a high antibody level

References

    1. Solano-Gallego L, Miró G, Koutinas A, Cardoso L, Pennisi MG, Ferrer L, Bourdeau P, et al. LeishVet guidelines for the practical management of canine leishmaniosis. Parasites Vectors. 2011;4:86. doi: 10.1186/1756-3305-4-86. - DOI - PMC - PubMed
    1. Pennisi MG, Cardoso L, Baneth G, Bourdeau P, Koutinas A, Miró G, et al. LeishVet update and recommendations on feline leishmaniosis. Parasites Vectors. 2015;8:302. doi: 10.1186/s13071-015-0909-z. - DOI - PMC - PubMed
    1. Pennisi MG, Persichetti MF. Feline leishmaniosis: is the cat a small dog? Vet Parasitol. 2018;251:131–137. doi: 10.1016/j.vetpar.2018.01.012. - DOI - PMC - PubMed
    1. Baneth G, Dank G, Keren-Kornblatt E, Sekeles E, Adini I, Eisenberger CL, et al. Emergence of visceral leishmaniasis in central Israel. Am J Trop Med Hyg. 1998;59:722–725. doi: 10.4269/ajtmh.1998.59.722. - DOI - PubMed
    1. Nicolas L, Milon G, Prina E. Rapid differentiation of Old World Leishmania species by LightCycler polymerase chain reaction and melting curve analysis. J Microbiol Methods. 2002;51:295–299. doi: 10.1016/S0167-7012(02)00099-4. - DOI - PubMed