首页> 美国卫生研究院文献>Journal of Virology >Evaluation of the Newcastle Disease Virus F and HN Proteins in Protective Immunity by Using a Recombinant Avian Paramyxovirus Type 3 Vector in Chickens
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Evaluation of the Newcastle Disease Virus F and HN Proteins in Protective Immunity by Using a Recombinant Avian Paramyxovirus Type 3 Vector in Chickens

机译:用重组禽副粘病毒3型载体对鸡新城疫病毒F和HN蛋白的保护性免疫评价

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摘要

Newcastle disease virus (NDV) belongs to serotype 1 of the avian paramyxoviruses (APMV-1) and causes severe disease in chickens. Current live attenuated NDV vaccines are not fully satisfactory. An alternative is to use a viral vector vaccine that infects chickens but does not cause disease. APMV serotype 3 infects a wide variety of avian species but does not cause any apparent disease in chickens. In this study, we constructed a reverse-genetics system for recovery of infectious APMV-3 strain Netherlands from cloned cDNAs. Two recombinant viruses, rAPMV3-F and rAPMV3-HN, were generated expressing the NDV fusion (F) and hemagglutinin-neuraminidase (HN) proteins, respectively, from added genes. These viruses were used to immunize 2-week-old chickens by the oculonasal route in order to evaluate the contribution of each protein to the induction of NDV-specific neutralizing antibodies and protective immunity. Each virus induced high titers of NDV-specific hemagglutination inhibition and serum neutralizing antibodies, but the response to F protein was greater. Protective immunity was evaluated by challenging the immunized birds 21 days later with virulent NDV via the oculonasal, intramuscular, or intravenous route. With oculonasal or intramuscular challenge, all three recombinant viruses (rAPMV3, rAPMV3-F, and rAPMV3-HN) were protective, while all unvaccinated birds succumbed to death. These results indicated that rAPMV3 alone can provide cross-protection against NDV challenge. However, with intravenous challenge, birds immunized with rAPMV3 were not protected, whereas birds immunized with rAPMV3-F alone or in combination with rAPMV3-HN were completely protected, and birds immunized with rAPMV3-HN alone were partially protected. These results indicate that the NDV F and HN proteins are independent neutralization and protective antigens, but the contribution by F is greater. rAMPV3 represents an avirulent vaccine vector that can be used against NDV and other poultry pathogens.
机译:新城疫病毒(NDV)属于禽副粘病毒(APMV-1)的血清型1,在鸡中引起严重的疾病。当前的减毒活NDV疫苗并不完全令人满意。一种替代方法是使用能感染鸡但不会引起疾病的病毒载体疫苗。 APMV 3型血清型可感染多种鸟类,但不会在鸡中引起任何明显的疾病。在这项研究中,我们构建了一个反向基因系统,用于从克隆的cDNAs中回收感染性APMV-3菌株荷兰。产生了两种重组病毒,rAPMV3-F和rAPMV3-HN,分别从添加的基因表达NDV融合蛋白(F)和血凝素神经氨酸酶(HN)蛋白。为了评估每种蛋白质对诱导NDV特异性中和抗体和保护性免疫的贡献,使用这些病毒通过眼鼻途径免疫了2周龄的鸡。每种病毒均诱导高滴度的NDV特异性血凝抑制和血清中和抗体,但对F蛋白的反应更大。通过在21天后通过眼鼻,肌内或静脉内途径用强毒NDV攻击免疫的禽类来评估保护性免疫。受到眼鼻或肌内攻击后,所有三种重组病毒(rAPMV3,rAPMV3-F和rAPMV3-HN)都具有保护性,而所有未接种疫苗的禽类均已死亡。这些结果表明,单独的rAPMV3可以提供针对NDV攻击的交叉保护。但是,在进行静脉内攻击时,用rAPMV3免疫的鸟没有受到保护,而单独用rAPMV3-F或与rAPMV3-HN组合免疫的鸟受到了完全保护,而单独用rAPMV3-HN免疫的鸟受到了部分保护。这些结果表明NDV F和HN蛋白是独立的中和和保护性抗原,但是F的贡献更大。 rAMPV3代表一种无毒的疫苗载体,可用于抗NDV和其他家禽病原体。

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