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2007年小反刍兽疫(PPR)在我国西藏首次暴发,在西藏和新疆部分地区使用PPR Nigeria 75/1疫苗株制造的疫苗进行免疫接种。为明确疫苗的安全性,中国兽医药品监察所国家牛瘟参考实验室对其安全性能进行了系统评价。健康易感山羊、绵羊及怀孕山羊、怀孕绵羊按不同剂量接种疫苗后,均未观察到异常临床反应;怀孕母羊所产羔羊数量与对照组无明显差异。疫苗对小白鼠、豚鼠的非特异性安全试验表明,所有接种动物均健活。结果表明该疫苗安全性良好,可在田间大规模使用。 相似文献
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小反刍兽疫活疫苗临床试验研究 总被引:2,自引:0,他引:2
通过观察免疫接种后动物的临床症状,采用中和试验法检测小反刍兽疫活疫苗(75/1株)免疫后3个月、15个月和26个月时免疫动物血清的抗体水平,评价和测定小反刍兽疫活疫苗在新疆和西藏地区临床应用的安全状况、免疫效果和免疫持续时间。结果显示,免疫动物未发现任何免疫接种引起的不良反应,表明疫苗对山羊和绵羊具有良好的安全性;免疫后3个月、15个月和26个月时,血清中和抗体阳性率分别为89.8%、93.6%和83.95%,表明该疫苗的免疫效力良好,免疫期至少可达26个月。 相似文献
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小反刍兽疫病毒(PPRV)是副黏病毒科(Paramyxoviridae)麻疹病毒属(Morbolivirus)的成员,主要感染山羊、绵羊等小反刍动物,引起一种高度接触性病毒性传染病。小反刍兽疫为一种重大的外来性疾病,2007年在中国西藏自治区日土县首次发生。自2013年末以来中国新疆、青海、甘肃、宁夏、内蒙、湖南、辽宁等地频繁暴发小反兽疫疫情,给中国的畜牧业带来了巨大的损失,引起极大的重视。为更好的分析小反刍兽疫的病原特性及采取有效的防控措施,文章对小反刍兽疫的病原学及疫苗研究进展进行论述。 相似文献
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为研究已免疫小反刍兽疫(PPR)活疫苗的羊群经二次免疫后PPR抗体水平的变化趋势,对初免21 d羊群进行了第二次免疫,同时监测初免21 d及二免后3 d、7 d、14 d、21 d的血清中和抗体。结果显示,一次免疫羊21 d PPR中和抗体滴度平均可达5.18±2.87,阳性率为84%;二次免疫后3 d、7 d、14 d、21 d,PPR抗体呈上升趋势,平均滴度分别为5.65±2.56、6.95±1.82、7.28±1.18、8.12±1.31,阳性率分别为90%、100%、100%、100%。一免试验组21 d~323 d PPR抗体阳性率为83%,二免试验组在二次免疫7 d PPR抗体阳性率达到100%,并且维持到21 d。试验表明,活疫苗二次免疫增强了免疫效果,对已经有PPR抗体的羊进行二次免疫,可明显提升免疫抗体阳性率。 相似文献
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试验旨在探索小反刍兽疫疫苗和羊痘疫苗相互之间免疫效果的影响,选择90只参试羊采用单独免疫小反刍兽疫疫苗和羊痘疫苗以及两种疫苗联合免疫方式,并于免疫前及免疫后第7、14、21、28、90、210 d采集血液样本,通过阻断ELISA和间接ELISA检测其抗体水平。结果显示,两种疫苗单独免疫的抗体合格率到免疫后210 d时均在75%以上,达到国家规定标准(70%)。两种疫苗联合分点免疫情况下,小反刍兽疫疫苗免疫效果比单独免疫效果好,其抗体阳性率在免疫后第7、14 d时极显著高于单独免疫(P<0.01),21 d时显著高于单独免疫(P<0.05);羊痘疫苗免疫效果比单独免疫效果较差,其抗体阳性率在免疫后第7、14、21 d时极显著低于单独免疫(P<0.01),28 d时显著低于单独免疫(P<0.05),到免疫后210 d时抗体合格率仅为63.3%,未达到国家标准。研究表明,羊痘疫苗与小反刍兽疫疫苗联合免疫时,羊痘疫苗可以促进小反刍兽疫疫苗的免疫效果,而小反刍兽疫疫苗却抑制了羊痘疫苗的免疫效果。 相似文献
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概述了小反刍兽疫的易感动物、临床症状及病原的理化特征和基因组结构,重点阐述了病毒6种结构蛋白的大小和组成、小反刍兽疫病毒的分离培养、血清学及分子生物学诊断技术,并对其传统疫苗以及新型基因工程疫苗的研制进行了详细论述,以为该病的流行病学研究、诊断和免疫防制提供参考。 相似文献
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Comparative nucleotide sequence analysis of the phosphoprotein gene of peste des petits ruminants vaccine virus of Indian origin 总被引:2,自引:0,他引:2
Muthuchelvan D Sanyal A Sarkar J Sreenivasa BP Bandyopadhyay SK 《Research in veterinary science》2006,81(1):158-164
The nucleotide sequences of the phosphoprotein (P) gene of peste des petits ruminants (PPRV) vaccine virus (PPRV Sungri/96) belongs to Asian lineage have been determined and the deduced amino acid sequences were compared with another vaccine strain PPRV/Nigeria75/1 and with those of the other morbilliviruses. The 1652 nucleotides of the P gene encode a phosphoprotein of 509 amino acid residues (from nucleotide numbers 60 to 1587), which is 91% identical to that of PPRV/Nigeria75/1. The C protein consists of 177 amino acid residues and is 91% identical with that of PPRV/Nigeria75/1. The conserved mRNA editing site (5'TTAAAAGGGCACAG) was present at positions 742-756 in the P gene, which is conserved in all other morbilliviruses. The CTT trinucleotide sequence is present at the N/P and P/M intergenic region, which is totally conserved in morbilliviruses. This will be the third sequence for the P gene of PPRV since that of the vaccine strain and a wild-type Turkish isolate has been published already. 相似文献
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Post vaccination and colostral peste des petits ruminants antibody dynamics in research flocks of Kirdi goats and Foulbe sheep of north Cameroon 总被引:2,自引:0,他引:2
We studied Kirdi goats and Foulbe sheep kept on-station at the Institute of Agricultural Research for Development (IRAD), Garoua to look at their immunological response following vaccination with a specific peste des petits ruminant (PPR) virus vaccine. Pre-vaccination PPR antibody seroprevalences were 44 and 29% in goats and sheep, respectively. Seroprevalences following vaccination were 100% in both species. Titres remained above the protection threshold level (1:10) in both species at 12 months. Maternal antibodies in young animals were detectable to up to 6 months of age but fell below the protection threshold level at 3.5 and 4.5 months in lambs and kids, respectively. Kids and lambs from immunised or exposed dams should be vaccinated at 4 and 5 months of age, respectively. 相似文献
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《Veterinary microbiology》2015,175(1):132-138
Nucleoprotein (NP) is the most abundant and highly immunogenic protein of morbillivirus, and is presently the basis of most diagnostic assays for peste des petits ruminants virus (PPRV). In this study, fine epitope mapping and conservation analysis of linear B-cell epitopes on the PPRV NP has been undertaken using biosynthetic peptides. Nineteen linear B-cell epitopes were identified and their corresponding minimal motifs were located on the NP of PPRV China/Tibet/Geg/07-30. Conservation analysis indicated that ten of the 19 minimal motifs were conserved among 46 PPRV strains. Peptides containing the minimal motifs were recognized using anti-PPRV serum from a goat immunized with PPRV vaccine strain Nigeria 75/1. Identified epitopes and their motifs improve our understanding of the antigenic characteristics of PPRV NP and provide a basis for the development of epitope-based diagnostic assays. 相似文献
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Seroprevalence of, and risk factors for, peste des petits ruminants in sheep and goats in Northern Jordan 总被引:1,自引:0,他引:1
Peste des petits ruminants (PPR) is an economically important disease that affect sheep and goat industry in Asia and Africa. In this study, we investigated the seroprevalence, and risk factors, of PPR in sheep and goat flocks from five different governorates (Irbid, Jarash, Ajloun, Mafraq and Zarka) located in Northern Jordan. Serum samples from 929 and 400 sheep and goats, respectively, corresponding to 122 sheep flock and 60 goats flock were collected. Seroprevalence was determined using PPR competitive ELISA. Health status and management information were collected using a semi-structured pre-tested questionnaire. The individual true prevalence of PPR in sheep and goats was 29 and 49%, respectively. The flock level true prevalence of PPR was 60 and 74% in sheep and goats, respectively. In both sheep and goat flocks, large flock size, visiting live animals market and inadequate veterinary services were identified as risk factors for PPR seropositivity. Mixed (sheep and goats) raising was identified as a risk factor for PPR seropositivity in sheep flocks only. 相似文献