Infection with canine vector-borne pathogens was evaluated in dogs from four different regions of Costa Rica by PCR. Demographic data, clinical signs, packed cell volume values, and the presence of tick infestation were recorded for each dog. Forty seven percent (69/146) of the dogs were infected with at least one pathogen and 12% were co-infected with two pathogens. Ehrlichia canis was detected in 34%, Anaplasma platys in 10%, Babesia vogeli in 8%, and Hepatozoon canis in 7.5% of the blood samples. No infection was detected with Leishmania spp. in blood, skin scrapings or conjunctival swabs. Thirty percent of the dogs presented at least one clinical sign compatible with vector-borne disease, and of those, 66% were infected with a pathogen. Subclinical infections were determined in 58% of the infected dogs including 82% (9/11), 58% (29/50), 42% (5/12) and 36% (5/14) of the dogs with H. canis, E. canis, B. vogeli and A. platys infections, respectively. A distinct relationship was found between infection and anemia. The mean PCV values were 34.4% in dogs with no infection, 31.5% in those who had a single infection and 23% in those with co-infection. Co-infected dogs had significantly lower PCV values compared to non-infected and single-infected dogs (p<0.0001). Thirty five percent (51/146) of the dogs were infested with ticks, 82% of them were infested with Rhipicephalus sanguineus sensu lato and 18% with Amblyomma ovale. Dogs infected with A. platys, B. vogeli, or E. canis were significantly associated with R. sanguineus s.l. infestation (p<0.029). This is the first description of infections with B. vogeli and H. canis in Costa Rica as well as in Central America. The results of this study indicate that multiple vector-borne pathogens responsible for severe diseases infect dogs in Costa Rica and therefore, increased owner and veterinarian awareness are needed. Moreover, prevention of tick infestation is recommended to decrease the threat of these diseases to the canine population.

BackgroundCanine filarioids are important nematodes transmitted to dogs by arthropods. Diagnosis of canine filariosis is accomplished by the microscopic identification of microfilariae, serology or PCR for filarial-DNA. The aim of this study was to evaluate a molecular assay for the detection of canine filariae in dog blood, to compare its performance to other diagnostic techniques, and to determine the relationship between microfilarial concentration and infection with other vector-borne pathogens.MethodsBlood samples from 146 dogs from Costa Rica were subjected to the detection of canine filarioids by four different methods: the microhematocrit tube test (MCT), Knott’s modified test, serology and a high resolution melt and quantitative real-time PCR (HRM-qPCR). Co-infection with other vector-borne pathogens was also evaluated.ResultsFifteen percent of the dogs were positive to Dirofilaria immitis by at least one of the methods. The HRM-qPCR produced distinctive melting plots for the different filarial worms and revealed that 11.6% of dogs were infected with Acanthocheilonema reconditum. The latter assay had a limit of detection of 2.4x10−4 mf/μl and detected infections with lower microfilarial concentrations in comparison to the microscopic techniques and the serological assay. The MCT and Knott’s test only detected dogs with D. immitis microfilaremias above 0.7 mf/μl. Nevertheless, there was a strong correlation between the microfilarial concentration obtained by the Knott’s modified test and the HRM-qPCR (r = 0.906, p < 0.0001). Interestingly, one dog was found infected with Cercopithifilaria bainae infection. Moreover, no association was found between microfilaremia and co-infection and there was no significant difference in microfilarial concentration between dogs infected only with D. immitis and dogs co-infected with Ehrlichia canis, Anaplasma platys or Babesia vogeli.ConclusionsThis is the first report of A. reconditum and C. bainae in Costa Rica and Central America. Among the evaluated diagnostic techniques, the HRM-qPCR showed the most sensitive and reliable performance in the detection of blood filaroids in comparison to the Knott’s modified test, the MCT test and a serological assay.Electronic supplementary materialThe online version of this article (doi:10.1186/s13071-015-0783-8) contains supplementary material, which is available to authorized users.

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Para estimar la prevalencia anual y mensual de Fasciola hepatica y las pérdidas económicas anuales asociadas al decomiso de hígados por presencia del parásito, se analizaron los registros del Ministerio de Agricultura y Ganadería de Costa Rica, Dirección de Inocuidad de Productos de Origen Animal (DIPOA), para el 2014, provenientes de 3 mataderos clase A localizados en el área metropolitana de Costa Rica; en estos mataderos se sacrificaron 249 108 reses, de las cuales 4547 hígados fueron decomisados por presencia de F. hepatica en el órgano. Las mayores prevalencias, entre 2,33 y 2,55%, se presentaron en enero, febrero y marzo, y las menores, entre 1,32 y 1,56%, durante agosto, setiembre y octubre. La prevalencia anual según estos registros fue 1,83% (IC 95%: 1,77-1,88). Las pérdidas económicas asociadas al decomiso de hígados fueron de 36.379.000 CRC, equivalentes a 67.438 USD. Se resalta el perjuicio económico de este parásito a nivel nacional y la utilidad del decomiso y registro de vísceras afectadas en los establecimientos de sacrificio de bovinos, como herramienta diagnóstica para la vigilancia epidemiológica, disponible para conocer sobre el estado de esta parasitosis. Como alternativas de control y prevención de la enfermedad, se plantea considerar las condiciones específicas de las regiones afectadas y así controlar esta parasitosis con un manejo integral, que involucre la fuente de alimento, desparasitación regular del ganado, con registro y monitoreo farmacológico de las drogas utilizadas, y saneamiento ambiental en fincas afectadas.