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Dose-dependent pathogenicity of a pseudorabies virus variant in pigs inoculated via intranasal route

机译:经鼻内途径接种的猪伪狂犬病病毒变体的剂量依赖性致病性

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Pseudorabies (PR) or Aujeszky's disease (AD), caused by pseudorabies virus (PRV), is an economically important viral disease in many countries. The modified live vaccine Bartha-K61 strain has played an important role in the control of PR in many countries including China. Since late 2011, however, increasing PR outbreaks caused by an emerging PRV variant have been reported in Bartha-K61-vaccinated swine population on many farms in China. Previously, we showed that the PRV variant TJ strain exhibited enhanced pathogenicity in pigs inoculated via intramuscular route. To develop an animal infection model for accurate evaluation of novel vaccines against the emergent PRV variant, we evaluated the pathogenicity of the PRV TJ strain of different doses in pigs infected via intranasal route. Groups (n = 5) of 7-week-old healthy pigs were inoculated intranasally with 10(3), 10(4), 10(5), or 10(6) TCID50 (median tissue culture infective dose) PRV TJ strain. Clinical signs, rectal temperature, virus shedding, pathological changes, and seroconversion were monitored. The results showed that the PRV TJ strain induced varied morbidity and mortality (0/5 to 5/5), clinical signs, and tissue lesions, increasingly correlated with the infection doses, and the median lethal dose (LD50) of the virus was determined to be 10(4.5) TCID50. Together, this study demonstrates the dose-dependent pathogenicity of the PRV variant via the intranasal route of infection, which provides an ideal animal infection model for evaluation of novel vaccines against the emerging PRV variant. (C) 2015 Elsevier B.V. All rights reserved.
机译:由伪狂犬病病毒(PRV)引起的伪狂犬病(PR)或Aujeszky病(AD),在许多国家中是一种经济上重要的病毒性疾病。在包括中国在内的许多国家,改良的活疫苗Bartha-K61菌株在控制PR中发挥了重要作用。然而,自2011年下半年以来,据报道,在中国许多农场中,接种Bartha-K61疫苗的猪群中出现了由新出现的PRV变异引起的PR爆发。先前,我们显示PRV变异TJ株在通过肌肉内途径接种的猪中表现出增强的致病性。为了开发动物感染模型以准确评估针对新兴PRV变体的新型疫苗,我们评估了不同剂量的PRV TJ株在经鼻内感染猪中的致病性。每组7周龄健康猪(n = 5)分别经鼻内接种10(3),10(4),10(5)或10(6)TCID50(中值组织培养感染剂量)PRV TJ株。监测临床体征,直肠温度,病毒脱落,病理变化和血清转化。结果表明,PRV TJ菌株引起各种发病率和死亡率(0/5至5/5),临床体征和组织损伤,与感染剂量越来越相关,并且确定了该病毒的中值致死剂量(LD50)为10(4.5)TCID50。总之,这项研究通过鼻内感染途径证明了PRV变体的剂量依赖性致病性,这为评估针对新兴PRV变体的新型疫苗提供了理想的动物感染模型。 (C)2015 Elsevier B.V.保留所有权利。

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