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Protection of chickens against very virulent infectious bursal disease virus (IBDV) and Marek's disease virus (MDV) with a recombinant MDV expressing IBDV VP2.

机译:用表达IBDV VP2的重组MDV保护鸡免受强毒传染性法氏囊病病毒(IBDV)和马立克氏病病毒(MDV)的侵害。

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摘要

To develop a herpes virus vaccine that can induce immunity for an extended period, a recombinant Marek's disease (MD) virus (MDV) CVI-988 strain expressing infectious bursal disease virus (IBDV) host-protective antigen VP2 at the US2 site (rMDV) was developed under the control of an SV40 early promoter. Chickens vaccinated with the rMDV showed no clinical signs and no mortality and 55% of the chickens were considered protected histopathologically after challenge with very virulent IBDV (vvIBDV), whereas all of the chickens vaccinated with the conventional IBDV vaccine showed no clinical signs and were protected. Chickens vaccinated with the CVI-988 or chickens in the challenge control showed severe clinical signs and high mortality (70-75%) and none of them were protected. Also, the rMDV conferred full protection to chickens against vvMDV just as the CVI-988 strain did, whereas 90% of the challenge control chickens died of MD. Antibody levels against IBDV and MDV following the vaccination increased continuously for at least 10 weeks. No histopathological lesions in the rMDV-vaccinated chickens and no contact transmission of the rMDV to their penmates were confirmed. These results demonstrate that an effective and safe recombinant herpesvirus-based IBD vaccine could be constructed by expressing the VP2 antigen at the US2 site of the CVI-988 vaccine strain. Copyright 1999 Academic Press.
机译:为了开发可以长时间诱导免疫的疱疹病毒疫苗,重组的马立克氏病(MD)病毒(MDV)CVI-988菌株在US2位点(rMDV)表达传染性法氏囊病病毒(IBDV)宿主保护性抗原VP2在SV40早期启动子的控制下被开发。接种了rMDV的鸡没有任何临床体征,也没有致死率,并且认为55%的鸡在用强力IBDV(vvIBDV)攻击后受到了组织病理学的保护,而所有接种了常规IBDV疫苗的鸡都没有临床体征,并且受到了保护。用CVI-988疫苗接种的鸡或在攻击对照组中的鸡表现出严重的临床体征和高死亡率(70-75%),并且没有受到保护。同样,rMDV就像CVI-988菌株一样,为鸡提供了针对vvMDV的全面保护,而90%的攻击对照鸡死于MD。接种疫苗后,针对IBDV和MDV的抗体水平持续持续至少10周。在接种rMDV的鸡中未发现组织病理学损害,也未确认rMDV与其戊二烯的接触传播。这些结果表明,通过在CVI-988疫苗株的US2位点表达VP2抗原,可以构建有效且安全的基于重组疱疹病毒的IBD疫苗。版权所有1999,学术出版社。

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