h. r. varshoiee

Peste des Petits Ruminunts (PPR) is an acute and contagious viral disease with rapid infection and transmission in sheep and goats. Vaccination of livestock is the best solution to prevent the spread and control of the disease. The aim of this study was to evaluate the immune response derived from vaccination with six formulations of inactivated PPR vaccine in goats and sheep using a completely randomized design with 2 × 2 factorial arrangement. The attenuated PPR virus was amplified in a highly manipulated suspension lymphoid cell having a high passage potential, and then inactivated using two inactivators (4 mM bromoethylene imine [BEI] or 3% hydrogen peroxide [H2O2]). Thereafter each inactivated virus was formulated using three different helpers (aluminum hydroxide, aluminum phosphate, and a 50% mixture of each of these two adjuvants). Iimmunogenicity and safety of the formulated candidate vaccines were evaluated by respective two doses of 0.1 and 1 (10-fold doses) ml of the vaccines administrated into 38 sheep and 28 goats. Each dose was subcutaneously administrated on 0 and 21 days of the experiment and post vaccination sera antibody titer against PPR virus was measured on days 0, 14, 21, 35, 42 and 60. The results showed that the mean antibody titer against PPR virus was not influenced neither by inactivator nor adjuvant up to 21- and 60-days post vaccination (P> 0.05). Also, no significant interaction was observed between different inactivators and adjuvants (P> 0.05). The appropriate antibody titers observed in different experimental groups indicated a good immunization of the formulated vaccines; however, their efficacy remained to be investigated using challenge test. Also, due to the lack of carcinogenicity, cheapness and environmental compatibility reported for H2O2, it is nominated as an inactivator in production inactivated PPR vaccine.

Lumpy skin disease (LSD) is a highly contagious disease of cattle and buffaloes that cause considerable economic losses to the livestock industry in endemic regions. Although the virus neutralization index (VNI) is the gold standard test for the detection of LSD antibodies, the use of this test in seroepidemiology studies and serosurveillance is laborious and time-consuming. Accordingly, for serodiagnosis of capripox diseases, ELISA assay has been developed, but the lack of information about its performance and efficiency is one of the limiting factors in the use of this test in seroepidemiological studies. In this study, the diagnosis agreement between a recently developed ELISA based on P32 recombinant protein and the VNI method, as a gold standard for serological diagnosis of Capripox virus, was evaluated using 95 sera samples including 25 negative control, 14 positive control, and 56 suspected cattle sera. Result showed that all the negative control sera assessed by VNI and ELISA had no antibody titers against LSD. All the 14 (100%) positive control sera had VNI values ≥1.5 and were considered as the positive sera; however, by ELISA method, 13 samples (93%) were diagnosed as the positive. Among the 56 samples collected from LSD-suspected cattle, 16 samples (29%) were detected as the positive by VNI, whereas 13 samples (23%) were detected as the positive sera by ELISA method. There was no statistically significant difference between the percentages of negative or positive samples assessed by ELISA or VNI method (P>0.05), associated with the Kappa index value of 0.71 showing the substantial agreement. These findings indicating an acceptable agreement and performance of the developed ELISA system based on P32 recombinant protein in comparison to VNI method for diagnosing antibody against LSD virus in cattle.

Lumpy skin disease (LSD) is a viral infectious disease of cattle associated with a drastic economic loss in the livestock industry. The aim of this study was to investigate sequence and phylogenetic analysis of LSD142 gene, a putative virulence gene in Capripoxviruses, in six lumpy skin disease viruses isolated in Iran during 2013 to 2014 and Capripoxvirus in the Genbank. The LSD viruses were isolated from different provinces of Iran, including Kermanshah, West-Azerbaijan, Fars, Qom, Khuzestan, and North Khorasan, and following sequencing the LSD142 gene, its homology was compared with other Capripoxvirus in the Genbank using phylogenetic analysis. The isolated LSD viruses showed a 100% identity in LSDV142 gene sequences with the virulent LSD viruses and with each other. Phylogenetic analysis revealed that not only the candidate gene has the potential to differentiate Capripoxvirus into three groups including LSD, sheep pox virus (SPV) and goat pox virus (GPV), but also the vaccinal and virulent strain of LSD virus could be divided. The GPV group was divided three geographical categories including Southwest and African strains, East Asia strains and Northwest Asia strains. In the SPV group, the African virus was separated from other strains of the SPV. These findings suggest that the LSD142 gene could be used for the genotyping and molecular epidemiology studies of the Capripoxvirus.