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Characterization of interleukin-1 beta mRNA expression in chicken macrophages in response to avian reovirus

机译:Characterization of interleukin-1 beta mRNa expression in chicken macrophages in response to avian reovirus

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摘要

Inhibitors of viral disassembly or RNA and protein synthesis, viral disassembly intermediates (infectious subviral particles, ISVP), binary ethylenimine-inactivated virions, and viral particles lacking genomic double-stranded (ds) RNA (empty particles) were used to assess the expression of interleukin-1 beta (IL-1 beta) mRNA in chicken (chIL-1 beta) macrophages in response to avian reovirus. The results demonstrate that two distinct expression patterns of chIL-1 beta mRNA mediated by different steps in viral replication were found. Viral disassembly was required for the induction of a rapid, transient expression pattern of chIL-1 beta mRNA that was rapidly induced at 30 min, with maximal levels reached by 2 h, and fell to a low level within 6 h post-inoculation, while viral RNA synthesis rather than protein translation, which was subsequent to membrane penetration, was required to induce a stable, sustained expression pattern of chIL-1 beta mRNA that occurred at and after 6 h post-inoculation. In addition, the induction of chIL-1 beta mRNA expression by the empty particles and ISVP was extremely weak, compared with the active dsRNA(+) virions or binary ethylenimine-inactivated virions, suggesting that the presence of dsRNA, even if transcriptionally inactive, may be an important factor in this response.
机译:病毒分解或RNA和蛋白质合成的抑制剂,病毒分解中间体(传染性亚病毒颗粒,ISVP),二元乙炔亚胺灭活的病毒体和缺乏基因组双链(ds)RNA的病毒颗粒(空颗粒)被用于评估鸡巨噬细胞(chIL-1 beta)中白介素-1 beta(IL-1 beta)mRNA响应禽呼肠孤病毒。结果表明,发现了由不同的病毒复制步骤介导的chIL-1βmRNA的两种不同表达模式。需要病毒分解才能诱导chIL-1βmRNA的快速,瞬时表达模式,该模式在30分钟时被快速诱导,最大水平在2 h内达到最高水平,而在接种后6 h内降至较低水平,而需要病毒RNA合成而不是膜穿透后的蛋白质翻译来诱导chIL-1βmRNA的稳定,持续表达模式,这种模式发生在接种后6小时及之后。此外,与活性dsRNA(+)病毒体或二元乙炔亚胺灭活的病毒体相比,空颗粒和ISVP对chIL-1 beta mRNA表达的诱导作用极弱,这表明存在dsRNA,即使在转录上无活性,可能是这种反应的重要因素。

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