Distribution of Toxocara cati larvae in experimentally infected BALB/c mice.

The experimental infection of mice with Toxocara cati provides one of the best models for pathological and immunological study of the visceral larva migrans syndrome. To broaden our knowledge of T. cati larval migration, BALB/c mice were inoculated with 500 embryonated eggs of T. cati for a period of two months. In the present study, T. cati eggs, obtained from faeces of naturally infected cats, were used for infection. After oral infection of 500 embryonated eggs of T. cati, mice were euthanised at 1, 2, 3, 7, 14, 21, 28, 35, and 70 days post-infection (dpi) in groups of three per day. Systemic cytokine patterns of Th2 cytokines were evaluated 1 and 2 months after the experimental challenge using sandwich ELISA. The mean number of larval recovery from all infected mice was 16.53 % during infection. The highest number of larvae was obtained from the liver at 1 and 2 dpi; from lungs at 2 dpi and from the brain at 28 dpi. In muscles, the highest recovery rates of T. cati were obtained at 28 dpi. Our data showed that experimental infection with T. cati induced Th2 responses during the infection. In addition, IL-4, IL-5, and IL-10 levels increased significantly in the sera of the infected mice compared to the control group. Larval persistence of T. cati in the muscle of BALB/c mice and its migration behaviour highlights the important role of mouse as a paratenic host in the parasite life cycle and the host-parasite relationships, especially in human toxocariasis.

Prevalence and genotyping of Toxoplasma gondii in stray cats in Mashhad area, Iran.

BACKGROUND: Cats as a definitive host have an important role in the epidemiology of toxoplasmosis in humans and animals. The aim of the study was to determine the frequency of Toxoplasma gondii infection and isolate and identify the genotypes of T. gondii in stray cats in the Mashhad suburb. METHODS: From April 2016 to August 2017, 175 fecal samples from stray cats and 31 brain samples from cats killed in driving accidents were collected. The fecal samples were examined by fecal flotation technique and T. gondii-specific PCR. The brain samples were investigated by T. gondii-specific PCR and consequently examined by mice bioassay. The DNA of T. gondii isolated was genotyped using SAG1, SAG2, SAG3, BTUB and GRA6 as PCR-restriction fragment length polymorphism (PCR-RFLP) markers. RESULTS: In the present study, Toxoplasma-like oocysts were microscopically observed in 2.2% (4/175) fecal samples. The presence of Toxoplasma oocysts was confirmed in one microscopy-positive sample by PCR. In addition, T. gondii DNA was detected in 4% (7/175) microscopy-negative samples using PCR. T. gondii was isolated from one brain PCR-positive sample by mice bioassay. The isolate was avirulent and many T. gondii cysts were observed in mice brain. The isolate was successfully genotyped by PCR-RLFP analysis. The isolated genotyped was type II. Besides, eight Toxoplasma-positive fecal samples contained insufficient DNA and only amplified at SAG-3 locus in PCR. These samples were also showed type II pattern at this locus. CONCLUSIONS: Parasitological and molecular results showed low frequency of Toxoplasma infection in the stray cats, and identified the genotype of T. gondii isolate as type II, for the first time in Mashhad area, Khorasan Razavi Province.

A serological and parasitological study of Toxoplasma gondii infection in stray cats of Mashhad, Khorasan Razavi province, Iran.

The aim of the present study was to determine seroprevalence of Toxoplasma gondii infection in stray cats and correlation with oocyst shedding and IFN-γ concentration. From April to August 2016, one hundred fifty-nine stray cats were captured from various localities in Mashhad area. The blood and fecal samples were collected from each cat. The serum samples were examined to detect antibodies against T. gondii infection by ELISA assay and the fecal samples were microscopically examined for T. gondii oocyst detection. The concentration changes of IFN-γ in serum samples of seropositive and seronegative cats were measured using ELISA kit. The results showed that 59.12% (94/159) of cats had antibodies against T. gondii infection. The seroprevalence of T. gondii infection in the adult cats above three years olds was higher than other groups. Regarding gender, month and region factors, the difference of seroprevalence of T. gondii infection was not significant. In this study, the Toxoplasma/Hammondia like oocyst (THLO) were detected in 2.56% (4/156) in fecal samples of one seropositive and three seronegative cats. Results also showed that the mean value for IFN-γ concentration in the seropositive cats was significantly higher than that of the seronegative cats. Based on the results, the high percentages of stray cats were infected with T. gondii in this area. The IFN-γ concentration of seropositive cats was higher than that of the seronegative cats.