Abstract

BackgroundThe severity of canine leishmaniosis (CanL) due to Leishmania infantum might be affected by other vector-borne organisms that mimic its clinical signs and clinicopathological abnormalities. The aim of this study was to determine co-infections with other vector-borne pathogens based on serological and molecular techniques in dogs with clinical leishmaniosis living in Spain and to associate them with clinical signs and clinicopathological abnormalities as well as disease severity.MethodsSixty-one dogs with clinical leishmaniosis and 16 apparently healthy dogs were tested for Rickettsia conorii, Ehrlichia canis, Anaplasma phagocytophilum and Bartonella henselae antigens by the immunofluorescence antibody test (IFAT) and for E. canis, Anaplasma spp., Hepatozoon spp., Babesia spp. and filarioid DNA by polymerase chain reaction (PCR).ResultsAmong the dogs examined by IFAT, the seroprevalences were: 69% for R. conorii, 57% for E. canis, 44% for A. phagocytophilum and 37% for B. henselae; while the prevalences found by PCR were: 8% for Ehrlichia/Anaplasma, 3% for Anaplasma platys and 1% for H. canis. No other pathogen DNA was detected. Statistical association was found between dogs with clinical leishmaniosis and seroreactivity to R. conorii antigen (Fisher’s exact test: P = 0.025, OR = 4.1, 95% CI = 1–17) and A. phagocytophilum antigen (Fisher’s exact test: P = 0.002, OR = 14.3, 95% CI = 2–626) and being positive to more than one serological or molecular tests (co-infections) (Mann-Whitney test: U = 243, Z = -2.6, n1 = 14, n2 = 61, P = 0.01) when compared with healthy dogs. Interestingly, a statistical association was found between the presence of R. conorii, E. canis, A. phagocytophilum and B. henselae antibodies in sick dogs and some clinicopathological abnormalities such as albumin and albumin/globulin ratio decrease and increase in serum globulins. Furthermore, seroreactivity with A. phagocytophilum antigens was statistically associated with CanL clinical stages III and IV.ConclusionsThis study demonstrates that dogs with clinical leishmaniosis from Catalonia (Spain) have a higher rate of co-infections with other vector-borne pathogens when compared with healthy controls. Furthermore, positivity to some vector-borne pathogens was associated with more marked clinicopathological abnormalities as well as disease severity with CanL.

Highlights

  • The severity of canine leishmaniosis (CanL) due to Leishmania infantum might be affected by other vector-borne organisms that mimic its clinical signs and clinicopathological abnormalities

  • Tabar et al [43] examined dogs with leishmaniosis and filariosis to detect filarial spp., Wolbachia spp. and Leishmania co-infection, and an increase of disease severity and clinical signs was observed with Leishmania-filarial co-infection, it was suggested that Wolbachia could have a protective role against Leishmania infection

  • In the present study, we report for the first time that certain clinicopathological abnormalities are more marked in dogs with co-infections based on positive serology for R. conorii, A. phagocytophilum, E. canis and B. henselae

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Summary

Introduction

The severity of canine leishmaniosis (CanL) due to Leishmania infantum might be affected by other vector-borne organisms that mimic its clinical signs and clinicopathological abnormalities. The aim of this study was to determine co-infections with other vector-borne pathogens based on serological and molecular techniques in dogs with clinical leishmaniosis living in Spain and to associate them with clinical signs and clinicopathological abnormalities as well as disease severity. Canine leishmaniosis (CanL) is a zoonotic protozoan disease caused by Leishmania infantum endemic in the Mediterranean basin. Prevalence of canine L. infantum infection can be as high as 67% in selected populations [3], but the prevalence of clinical disease is usually lower than 10% [4]. The most useful diagnostic methods of CanL include quantitative serological techniques and PCR, the direct observation of amastigote forms of Leishmania spp. is helpful in the clinical setting [4–6]. The most common clinical signs are skin lesions, generalized lymphadenomegaly, progressive weight loss, decreased appetite, lethargy, muscular atrophy, exercise intolerance, splenomegaly, polyuria and polydipsia, ocular lesions, epistaxis, lameness, vomiting and diarrhea [2, 4, 6]

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