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首页> 外文期刊>Microbiology and Immunology >A unique transcription mode of rabies virus high egg passage-Flury strain detected in infected baby hamster kidney-21 cells.
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A unique transcription mode of rabies virus high egg passage-Flury strain detected in infected baby hamster kidney-21 cells.

机译:在感染的小仓鼠肾21细胞中检测到狂犬病病毒高卵子传代Flury株的独特转录模式。

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摘要

The transcription mode of rabies virus high egg passage-Flury (HEP) strain was examined and compared with that of Evelyn Rokitniki Abelseth (ERA) strain by northern blot analysis using rabies virus gene-specific probes. The ERA strain was shown to exclusively produce monocistronic mRNAs in transcription. All combinations of multicistronic transcripts, including five monocistronic mRNAs, were detected in the viral RNA transcripts of HEP strain. It was concluded that the unique transcription mode is not due to the nucleotide structure of the genome RNA template, but rather to the viral RNA polymerase of HEP strain. The viral polymerase of HEP strain read through the gene junction at a high frequency. The HEP strain has been passaged many times in chick embryo and cultured cells, and has adapted to propagate well in the baby hamster kidney-21 (BHK-21) cells. Through these passages in various hosts, the HEP strain has acquired a unique transcription mode that might have an advantage in amplification of the virus
机译:使用狂犬病病毒基因特异性探针,通过Northern印迹分析检查了狂犬病病毒高卵子传代Flury(HEP)菌株的转录模式,并将其与Evelyn Rokitniki Abelseth(ERA)的转录模式进行了比较。 ERA菌株显示出在转录中仅产生单顺反子mRNA。在HEP株的病毒RNA转录物中检测到多顺反子转录物的所有组合,包括5个单顺反子mRNA。结论是独特的转录方式不是由于基因组RNA模板的核苷酸结构,而是由于HEP株的病毒RNA聚合酶。 HEP菌株的病毒聚合酶通过基因接头高频率读取。 HEP菌株已在鸡胚和培养的细胞中多次传代,并已适应在小仓鼠肾21(BHK-21)细胞中良好繁殖。通过在各种宿主中的传代,HEP菌株获得了独特的转录模式,可能在病毒的扩增中具有优势

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