In Central Europe the wild boar population is permanently growing and consequently Cf foodborne infections. In this study serological and molecular detection of Toxoplasma gondii and Neospora caninum in wild boars was evaluated. Moreover, same samples were screened for the presence and genetic variability of tick-borne bacterium Anaplasma phagocytophilum. Blood samples collected from 113 wild boars from Southern Slovakia were examined for antibodies to T. gondii by indirect and to N. caninum by competitive ELISA. The presence of parasitic DNA in blood samples was determined by standard or real time PCR techniques. Antibodies against T. gondii and N. caninum were detected in 45 (39.8%) and 38 (33.6%) animals, respectively. Females were more frequently infected for both pathogens than males. The high seropositivity against both coccidia indicates a permanent occurrence of these pathogens in the studied locality. T. gondii DNA was confirmed in five seropositive boars (4.4%) and N. caninum in 23 blood samples (20.4%). Three out of 23 N. caninum PCR positive animals did not show seropositivity. Three out of 113 blood samples of wild boars were positive for A. phagocytophilum (2.7%). The obtained A. phagocytophilum sequences were 100% identical with GenBankTM isolates from Slovak dog (KC985242); German horse (JF893938) or wild boar (EF143810) and red deer (EF143808) from Poland. Coinfections of T. gondii with N. caninum and N. caninum with A. phagocytophilum were detected in single cases. Results suggest a potential zoonotic risk of toxoplasmosis transmission to humans and the spread of neosporosis to farm animals.
Parasitic diseases of livestock together with poor welfare conditions can negatively affect the health status and production of small ruminants. Protozoan parasites and tick-borne infectious agents are common threat of livestock including small ruminants mostly during the pasture season. Therefore the priority of the study was to analyse the circulation and presence of two protozoan parasites Toxoplasma gondii and Neospora caninum as well as tick-transmitted bacterium Anaplasma phagocytophilum in one selected goat farm in Eastern Slovakia. Throughout a three-year study period we have repeatedly screened the sera and blood of goats and dogs from monitored farm. In total, 343 blood serum samples from 116 goats were examined by ELISA. The mean seropositivity for T. gondii was 56.9% (66/116, CI (95%) = 48-66.0) and 15.5% (18/116, CI (95%) = 9.3-22.7) for N. caninum. The permanent occurrence of anti-Toxoplasma and anti-Neospora antibodies was detected in repeatedly examined goats during the whole monitored period. The presence of both parasites in the flock was analysed by PCR. DNA of T. gondii was confirmed in 12 out of 25 Toxoplasma-seropositive goats and N. caninum in 14 samples out of 18 Neospora-seropositive animals; four goats were co-infected with both pathogens. The risk of endogenous transmission of both parasites was pursued by examination of 41 kid's sera, where seropositivity for toxoplasmosis was 31.7% and for neosporosis 14.6%. In dogs 61.1% seropositivity for T. gondii and 38.9% for N. caninum was found, however, their faeces were negative for coccidian oocysts. Eight out of 108 tested animals were infected with A. phagocytophilum, the causative agent of tick-borne fever. Seven of them were simultaneously infected with T. gondii and A. phagocytophilum, out of which four goats were concurrently infected with all three pathogens.
Sera or meat juices of 177 red foxes (Vulpes vulpes) originated from the localities of a human-influenced landscape (Group 1) and 126 foxes from the protected mountain region (Group 2) of Slovakia, collected during 2010-2014 were tested for the presence of antibodies against Toxoplasma gondii using indirect ELISA and Neospora caninum by competitive ELISA. The tissue and uncoagulated blood samples were examined for the presence of the parasite's DNA. The total seropositivity to T. gondii was 62.7% (190/303) and to N. caninum 26.4% (80/303). In the Group 1 antibodies to T. gondii were detected in 74.0% (131/177) and to N. caninum in 38.9% (69/177). In the Group 2 significantly lower seropositivity of 46.8% (59/126) to T. gondii antigens (P = 0.0218) and 8.7% (11/126) to N. caninum (P = 0.0001) was detected, respectively. However, by using molecular method, the presence of both parasites, was recorded less frequently. While in Group 1 T. gondii DNA was detected in 10.0% and N. caninum DNA in 18.3% of examined samples, in Group 2 T. gondii DNA was not detected at all and N. caninum was detected in 9.1% samples only. Results indicate that examined infections are highly common in the red foxes in Slovakia and are widespread in the locations of Eastern Slovakia bordering Poland, Ukraine and Hungary. The high infection rate in foxes representing reservoir hosts, presumably originates from their infected prey, ungulate carcasses, or from residual infected tissues in the hunting grounds after evisceration of shot animals during a hunting season.
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