共查询到18条相似文献,搜索用时 62 毫秒
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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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小反刍兽疫是一种传染性极强的病毒性疾病,主要影响家养及野生的小反刍动物。该病的主要特征是发热、口腔炎、结膜炎、肠胃炎和肺炎,是世界动物卫生组织(World Organization for Animal Health,OIE)规定必须上报的疾病之一。文章对该病的流行与传播、诊断方法及防控措施进行了综述。 相似文献
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小反刍兽疫是一种传染性极强的病毒性疾病,主要影响家养以及野生的小反刍动物。该病的主要特征是发热、口腔炎、结膜炎、肠胃炎和肺炎。小反刍兽疫也是世界动物卫生组织(0IE)规定必须上报的法定疾病之一。文章对该病的流行、传播方式、诊断方法以及防控措施进行了综述。 相似文献
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小反刍兽疫研究现状 总被引:1,自引:0,他引:1
小反刍兽疫(Peste des petits ruminants,PPR)是由小反刍兽疫病毒(Peste des petits ruminants virus,PPRV)引起的一种主要感染小反刍动物的急性、接触性传染病,发病率、死亡率高.近年来,小反刍兽疫(PPR)呈扩散的趋势,成为重要的跨国动物传染病之一,我国周边国家频繁器发该病.2007年7月25日暴发于西藏自治区日土县的我国首例小反刍尊疫疫情,更是对我国如何做好该病的防控工作提出了新的要求和挑战.为了增强广大兽医工作者和相关人士对本病的认识,文中就小反刍兽疫的病原学、流行病学、临床症状、病理特征以及诊断方法等方面的研究现状进行了综述. 相似文献
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Dan Liu Lingxia Li Xiaoan Cao Jinyan Wu Guoyu Du Youjun Shang 《Journal of veterinary science (Suw?n-si, Korea)》2021,22(4)
BackgroundPeste des petits ruminants (PPR) is an infectious disease caused by the peste des petits ruminants virus (PPRV) that mainly produces respiratory symptoms in affected animals, resulting in great losses in the world''s agriculture industry every year. Single-domain variable heavy chain (VHH) antibody fragments, also referred to as nanobodies, have high expression yields and other advantages including ease of purification and high solubility.ObjectivesThe purpose of this study is to obtain a single-domain antibody with good reactivity and high specificity against PPRV.MethodsA VHH cDNA library was established by immunizing camels with PPRV vaccine, and the capacity and diversity of the library were examined. Four PPRV VHHs were selected, and the biological activity and antigen-binding capacity of the four VHHs were identified by western blot, indirect immunofluorescence, and enzyme-linked immunosorbent assay (ELISA) analyses. ELISA was used to identify whether the four VHHs were specific for PPRV, and VHH neutralization tests were carried out. ELISA and western blot analyses were used to identify which PPRV protein was targeted by VHH2.ResultsThe PPRV cDNA library was constructed successfully. The library capacity was greater than 2.0 × 106 cfu/mL, and the inserted fragment size was approximately 400 bp to 2000 bp. The average length of the cDNA library fragment was about 1000 bp, and the recombination rate was approximately 100%. Four single-domain antibody sequences were selected, and proteins expressed in the supernatant were obtained. The four VHHs were shown to have biological activity, close affinity to PPRV, and no cross-reaction with common sheep diseases. All four VHHs had neutralization activity, and VHH2 was specific to the PPRV M protein.ConclusionsThe results of this preliminary research of PPRV VHHs showed that four screened VHH antibodies could be useful in future applications. This study provided new materials for inclusion in PPRV research. 相似文献