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Characterisation of experimental infections of domestic pigs with genotype 2.1 and 3.3 isolates of classical swine fever virus.

机译:基因型为2.1和3.3的经典猪瘟病毒分离株的家猪实验感染的特征。

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摘要

The early identification of classical swine fever epizootics is hampered by difficulties in recognising early signs of infection, due to a lack of specific clinical signs. In addition many textbook descriptions of CSF are based on observations of disease caused by historic, mainly genotype 1, strains. Our objective was to improve our knowledge of the diverse range of signs that different CSFV strains can cause by characterising the experimental infection of domestic pigs with both a recent strain of CSFV and a divergent strain. Conventional pigs were inoculated with a genotype 2.1 isolate, that caused an outbreak in the UK in 2000, and a genotype 3.3 strain that is genetically divergent from European strains. This latter strain is also antigenically distinct as it is only poorly recognised by the CSFV-specific monoclonal antibody, WH303. Transmission was monitored by use of in-contact animals. Clinical, virological and haematological parameters were observed and an extended macro- and histopathological scoring system allowed detailed characterisation of pathological lesions. Infection with the genotype 2.1 isolate resulted in a similar outcome to other recent genotype 2 European strains, whereas the genotype 3.3 strain produced fewer and delayed clinical signs, notably with little fever. This strain would therefore be particularly difficult to detect in the early stages of infection and highlights the importance of encouraging early submission of samples for laboratory diagnosis. As representatives of recent and divergent CSFV isolates, these strains are good candidates to study the pathogenesis of current CSFV isolates and as challenge models for vaccine development.
机译:由于缺乏特定的临床体征,难以识别感染的早期体征,阻碍了经典猪瘟流行病的早期识别。另外,许多关于脑脊液的教科书描述都是基于对历史性的,主要是基因型1的菌株引起的疾病的观察。我们的目标是通过表征近期感染CSFV株和发散株的家猪的实验感染,来提高对不同CSFV株可能引起的各种迹象的认识。传统的猪接种了2.1型基因分离株,该菌株在2000年在英国引起了大流行,并接种了与欧洲菌株遗传不同的3.3型基因株。后一种菌株在抗原上也不同,因为它仅能被CSFV特异性单克隆抗体WH303识别。通过使用接触动物监测传播。观察到临床,病毒学和血液学参数,并扩展了宏观和组织病理学评分系统,可以对病理性病变进行详细表征。基因型2.1分离株的感染导致的结果与最近的其他欧洲基因型2菌株相似,而基因型3.3菌株产生较少且延迟的临床体征,尤其是很少发烧。因此,这种菌株在感染的早期阶段将特别难以检测,并强调了鼓励尽早提交样品进行实验室诊断的重要性。作为近期和不同的CSFV分离株的代表,这些菌株是研究当前CSFV分离株的发病机理以及疫苗开发挑战模型的良好候选者。

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