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Synthesis of Reassortant Infectious Bursal Disease Virus in Chickens Injected Directly with Infectious Clones from Different Virus Strains

机译:直接注射来自不同病毒株的传染性克隆的鸡重配传染性法氏囊病病毒的合成

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The infectious bursal disease virus (IBDV), a member of the Birnaviridae family, containing a bisegmented double-stranded RNA genome, encodes four structural viral proteins, VP1, VP2, VP3, and VP4, as well as a non-structural protein, VP5. In the present paper, the segment A from two IBDV strains, field isolate ZJ2000 and attenuated strain HZ2, were inserted into one NaeI site by site-directed silent mutagenesis and subcloned into the eukaryotic expression plasmid pCI under the control of the human cytomegalovirus (hCMV) immediate early enhancer and promoter to construct the recombinant plasmids pCI-AKZJ2000 and pCI-AKHZ2, respectively. Each of the two recombinants was combined with another recombinant pCI plasmid containing the marked segment B of strain HZ2 (pCI-mB), and injected intramuscularly into nonimmunized chickens. Two chimeric IBDV strains were recovered from the chickens. Two out of eight chickens in each of two groups showed the bursal histopathological change. The reassortant virus derived from pCI-AKZJ2000/pCI-mB can infect chicken embryos and shows relatively low virulence. We have developed a novel virus reverse genetic approach for the study of IBDV. The results also form the basis for investigating the role of VP1 in viral replication and pathogenecity.
机译:传染性法氏囊病病毒(IBDV)是Birnaviridae家族的成员,包含双链双链RNA基因组,编码四个结构病毒蛋白VP1,VP2,VP3和VP4,以及非结构蛋白VP5 。本文通过定点沉默诱变将来自现场分离株ZJ2000和减毒株HZ2的两个IBDV株的A段通过定点沉默诱变插入一个NaeI位点,并在人巨细胞病毒(hCMV)的控制下亚克隆到真核表达质粒pCI中。立即早期增强子和启动子分别构建重组质粒pCI-AKZJ2000和pCI-AKHZ2。将这两个重组体中的每一个与另一个包含菌株HZ2的标记片段B的重组pCI质粒(pCI-mB)合并,然后肌肉注射到未免疫的鸡中。从鸡中回收了两种嵌合的IBDV菌株。两组中的八只鸡中有两只显示了法氏囊病理变化。源自pCI-AKZJ2000 / pCI-mB的重配病毒可以感染鸡胚,并显示出较低的毒力。我们已经为IBDV的研究开发了一种新型的病毒反向遗传方法。这些结果也为研究VP1在病毒复制和致病性中的作用奠定了基础。

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