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Application of real-time PCR using Taqman probe was tested for jaagsiekte sheep retrovirus (JSRV) detection. Sensitivity of real-time PCR and hemi-nested PCR methods was compared using plasmid DNA. The methods, along with RT PCR and real-time RT PCR, were tested for the possibility of JSRV genome (LTR region) detection in biological material from experimentally and naturally infected sheep. The experimental group of eight animals was used, including five lambs infected with JSRV by intratracheal inoculation at the age of 2 weeks. The samples collected from the animals ante-mortem included blood and respiratory tract fluid. Lung tissue, mediastinal lymph nodes, spleen, and liver were collected post-mortem. The field studies included blood samples collected from sheep from Polish flocks and lung samples obtained from slaughterhouse. In addition, DNA samples isolated from blood of sheep from the abroad located flocks with history of ovine pulmonary adenomatosis (OPA) were also included. Lung samples were examined histologically for the presence of pulmonary adenocarcinoma. The sensitivity of PCR, hemi-nested PCR, and real-time PCR using Taqman probe was evaluated as 10³, 10², and 10² viral copies, respectively. Both viral RNA and DNA were detected in the lung fluid taken from JSRV infected sheep showing clinical sings of OPA and in all neoplastic tissues. Proviral DNA was found in mediastinal lymph node of one experimental sheep. Five of the 66 DNA samples from the abroad located farms were positive for the presence of JSRV LTR. All blood and lung samples collected from Polish sheep were negative for the presence of JSRV LTR. The characteristic adenocarcinoma lesions were found in all lung sections of experimentally infected sheep. Implementation of the real-time PCR method is a good alternative to traditional PCR and hnPCR in JSRV detection and, apart from histopathological and immunohistochemical examinations, may be used as a confirmatory test in clinically suspected cases, or as a screening method in control or eradication scheme.
The purpose of the study was to evaluate the efficacy of praziquantel at 3.75 mg/kg b.w. and 5 mg/kg b.w. in treating Moniezia expansa and to observe the appearance of the parasite in the faeces of sheep following the treatment. Thirty-six sheep (24 male + 12 female), naturally infected with Moniezia expansa, were allocated to three groups according to the following dosage regimes: Group 1-3.75 mg/kg b.w., n = 12; Group 2-5 mg/kg b.w., n = 12; Control group, n = 12. The sheep were around 6-7 months old and weighed between 17.7 - 35 kg. Sheep were randomly divided into equal groups based on mean weight and sex. Faeces were collected after 12, 36, 60, 84, 108, 132 and 156 hours and just before slaughter (final 24 hours faeces) into faecal collection bags in the treatment groups. The collected faeces were then examined macroscopically for any parasite segments and microscopically for parasite eggs. After treatment the sheep excreted parasite segments as either normal parasite forms or deformed forms (melted and capsule or rosary forms). Equal numbers of animals (3 from each group) were slaughtered 10, 11, 12 and 13 days following treatment and their intestinal contents examined for the presence of parasites. None of the treated animals either in group1 or group 2 had strobilae or scolices of M. expansa in their intestine contents after the slaughter. In contrast, sheep in the control group had 0.5-61 ml strobilae and 1-8 scolices belonging to M. expansa, Thysaniezia giardi and Stilesia globipunctata. It was concluded that praziquantel at the dose rates used in the study was 100 % effective against Moniezia expansa.
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