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Peer-reviewed veterinary case report

Risk of Ehrlichia canis infection in dogs with leishmaniosis

By Attipa, Charalampos et al.·Published in Parasites & vectors·2018·Bristol Veterinary School and Langford Vets, United Kingdom·View original on PubMed

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Original publication title: Association between canine leishmaniosis and Ehrlichia canis co-infection: a prospective case-control study.

Species:
dog

Plain-English summary

A group of dogs with leishmaniosis, a disease caused by the Leishmania parasite, were found to have a higher risk of also being infected with Ehrlichia canis, a bacteria that can cause serious health issues. In a study of 50 dogs with leishmaniosis, nearly 12% tested positive for Ehrlichia canis, compared to only 1% in healthy dogs. This suggests that if your dog is diagnosed with leishmaniosis, it's important to have them tested for Ehrlichia canis as well. Early detection and treatment can help manage both infections effectively.

People also search for: dog leishmaniosis symptoms · Ehrlichia canis treatment for dogs · testing for dog infections

Abstract

BACKGROUND: In the Mediterranean basin, Leishmania infantum is a major cause of disease in dogs, which are frequently co-infected with other vector-borne pathogens (VBP). However, the associations between dogs with clinical leishmaniosis (ClinL) and VBP co-infections have not been studied. We assessed the risk of VBP infections in dogs with ClinL and healthy controls. METHODS: We conducted a prospective case-control study of dogs with ClinL (positive qPCR and ELISA antibody for L. infantum on peripheral blood) and clinically healthy, ideally breed-, sex- and age-matched, control dogs (negative qPCR and ELISA antibody for L. infantum on peripheral blood) from Paphos, Cyprus. We obtained demographic data and all dogs underwent PCR on EDTA-blood extracted DNA for haemoplasma species, Ehrlichia/Anaplasma spp., Babesia spp., and Hepatozoon spp., with DNA sequencing to identify infecting species. We used logistic regression analysis and structural equation modelling (SEM) to evaluate the risk of VBP infections between ClinL cases and controls. RESULTS: From the 50 enrolled dogs with ClinL, DNA was detected in 24 (48%) for Hepatozoon spp., 14 (28%) for Mycoplasma haemocanis, 6 (12%) for Ehrlichia canis and 2 (4%) for Anaplasma platys. In the 92 enrolled control dogs, DNA was detected in 41 (45%) for Hepatozoon spp., 18 (20%) for M. haemocanis, 1 (1%) for E. canis and 3 (3%) for A. platys. No Babesia spp. or "Candidatus Mycoplasma haematoparvum" DNA was detected in any dog. No statistical differences were found between the ClinL and controls regarding age, sex, breed, lifestyle and use of ectoparasitic prevention. A significant association between ClinL and E. canis infection (OR = 12.4, 95% CI: 1.5-106.0, P = 0.022) was found compared to controls by multivariate logistic regression. This association was confirmed using SEM, which further identified that younger dogs were more likely to be infected with each of Hepatozoon spp. and M. haemocanis, and dogs with Hepatozoon spp. were more likely to be co-infected with M. haemocanis. CONCLUSIONS: Dogs with ClinL are at a higher risk of co-infection with E. canis than clinically healthy dogs. We recommend that dogs diagnosed with ClinL should be tested for E. canis co-infection using PCR.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/29554932/