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Rescue of Very Virulent and Mosaic Infectious Bursal Disease Virus from Cloned cDNA: VP2 Is Not the Sole Determinant of the Very Virulent Phenotype

机译:从克隆的cDNA拯救极强毒和镶嵌感染性法氏囊病病毒:VP2不是极强毒表型的唯一决定因素

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摘要

Many recent outbreaks of infectious bursal disease in commercial chicken flocks worldwide are due to the spread of very virulent strains of infectious bursal disease virus (vvIBDV). The molecular determinants for the enhanced virulence of vvIBDV compared to classical IBDV are unknown. The lack of a reverse genetics system to rescue vvIBDV from its cloned cDNA hampers the identification and study of these determinants. In this report we describe, for the first time, the rescue of vvIBDV from its cloned cDNA. Two plasmids containing a T7 promoter and either the full-length A- or B-segment cDNA of vvIBDV (D6948) were cotransfected into QM5 cells expressing T7 polymerase. The presence of vvIBDV could be detected after passage of the transfection supernatant in either primary bursa cells (in vitro) or embryonated eggs (in vivo), but not QM5 cells. Rescued vvIBDV (rD6948) appeared to have the same virulence as the parental isolate, D6948. Segment-reassorted IBDV, in which one of the two genomic segments originated from cDNA of classical attenuated IBDV CEF94 and the other from D6948, could also be rescued by using this system. Segment-reassorted virus containing the A segment of the classical attenuated isolate (CEF94) and the B segment of the very virulent isolate (D6948) is not released until 15 h after an in vitro infection. This indicates a slightly retarded replication, as the first release of CEF94 is already found at 10 h after infection. Next to segment reassortants, we generated and analyzed mosaic IBDVs (mIBDVs). In these mIBDVs we replaced the region of CEF94 encoding one of the viral proteins (pVP2, VP3, or VP4) by the corresponding region of D6948. Analysis of these mIBDV isolates showed that tropism for non-B-lymphoid cells was exclusively determined by the viral capsid protein VP2. However, the very virulent phenotype was not solely determined by this protein, since mosaic virus containing VP2 of vvIBDV induced neither morbidity nor mortality in young chickens.
机译:全球范围内许多商业鸡群最近爆发了传染性法氏囊病,这是由于极强力的传染性法氏囊病病毒(vvIBDV)的传播所致。与经典IBDV相比,vvIBDV毒力增强的分子决定因素尚不清楚。缺乏从克隆的vvIBDV中拯救vvIBDV的反向遗传学系统阻碍了这些决定因素的鉴定和研究。在本报告中,我们首次描述了从克隆的cDNA中拯救vvIBDV。将两个包含T7启动子和vvIBDV全长A或B段cDNA(D6948)的质粒共转染到表达T7聚合酶的QM5细胞中。转染上清液在原囊囊细胞(体外)或胚卵(体内)中传代后,但在QM5细胞中传代后,可检测到vvIBDV的存在。营救的vvIBDV(rD6948)的毒力似乎与亲本隔离株D6948相同。片段重新排列的IBDV,其中两个基因组片段之一来自经典减毒IBDV CEF94 cDNA,另一个来自D6948,也可以使用该系统进行拯救。包含经典减毒分离株的A片段(CEF94)和毒性极强的分离株的B片段(D6948)的片段重组病毒直到体外感染后15小时才释放。这表明复制略有延迟,因为在感染后10小时已经发现CEF94的首次释放。在分段重分类的旁边,我们生成并分析了镶嵌IBDV(mIBDV)。在这些mIBDV中,我们用D6948的相应区域替换了编码其中一种病毒蛋白(pVP2,VP3或VP4)的CEF94区域。对这些mIBDV分离株的分析表明,非B淋巴样细胞的向性完全由病毒衣壳蛋白VP2决定。但是,非常强毒的表型并非仅由该蛋白决定,因为含有vvIBDV VP2的花叶病毒既不会引起雏鸡发病也不会引起死亡。

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