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The present study was designed to assess the importance of ovine neosporosis in abortion of Iraninan sheep. Seventy aborted foetuses and dams from ovine dairy farms in northwest of Iran were analyzed to investigate the role of Neospora caninum (N. caninum) in ovine abortion. Diagnosis of the infection was determined by serology and polymerase chain reaction (PCR). A total of 70 aborted dairy ovine were blood sampled and used to evaluate serological status for N. caninum infection by enzymelinked immunosorbent assay (ELISA) and extracted DNA from the same aborted foetuses were subjected to PCR. Data were compared using Kruscal-Wallis test. From A total of the 70 sheeps, four (5.7 %) of the dams were seropositive. DNA from aborted foetuses was extracted primarily from placenta and CNS tissues. Extracted DNA from foetuses were analyzed using PCR with primers Np21 ? and Np6 ? . Out of the 70 ovine fetuses 8.5 % were considered to be infected by PCR. This study confirms the importance of N. caninum as an important cause of ovine abortion in northwest of Iran.

Background:Linoleic acid (LA) is a polyunsaturated fatty acid present in high concentrations in follicular fluid, when added to maturation culture media, it affects oocyte competence.Objective:In the present study, we investigated effect of linoleic acid supplementation on in vitro maturation, embryo development and apoptotic related gene expression in ovineMaterials and Methods:The experiments conducted on 450 ovine Cumulus-oocyte complexes (COCs) with homogenous ooplasm and more than two compact layers of cumulus cells. For in vitro maturation COCs were randomly allocated into four treatment groups for 24 hr period. Treatment groups were as follow: control maturation media, 0 µM LA, 50 µM LA, 100 µM LA and 200 µM LA. The cumulus cell expansion and blastocysts rates were recorded. Total RNA was isolated from embryo pools, reverse transcribed into cDNA, and subjected to apoptotic gene expression by real-time PCR.Results: Highest concentration (200 µM/mL) of LA significantly decreased the rate of fully expanded cumulus cells 24 hr after in vitro maturation (IVM) and the percentage of blastocyste rate compared with the control (p<0.05). These inhibitory effects were associated with an increased in relative mRNA expression of Bax (Bcl-2- associated X) gene compared with controls. Conclusion:Data obtained in present study suggest that low concentration of LA used for maturation had no deleterious effect on subsequent embryonic development compared to high concentration of LA. Relative expression of Bcl-2 (B-cell lymphoma 2) and Bax in embryos seems to be associated with LA concentration.

Enzootic bovine leukosis is a chronic lymphoproliferative disorder in cattle caused by the exogenous retrovirus, bovine leukemia virus (BLV). There are numerous molecular protocols for the detection of bovine leukosis provirus in blood and semen. The aim of this study was to investigate the serology status of BLV infection in bulls in Tabriz, Iran and polymerase chain reaction (PCR) detection of viral genome of BLV in seminal cellular fraction and blood samples in sero-positive and sero-negative bulls. In this study, 45 serum samples from bulls from 18 different herds referred to the Artificial Insemination Centre were used to evaluate the serology infection of BLV by enzyme-linked immunosorbent assay. In addition, blood and semen samples of related bulls were used for the detection of BLV DNA. Antibodies against BLV were detected in five of 45 blood samples (4.4%), and PCR demonstrated that semen and blood samples of five seropositive and one sero-negative bull were infected by BLV. Our findings support the power of a PCR test for BLV detection in bovine semen and blood samples and could be easily used for routine diagnosis. This data strongly suggest that semen from sero-positive bulls could result positive by PCR.