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通过体外连接产生的全长cDNA模板转录传染性黄热病毒RNA。

Transcription of infectious yellow fever RNA from full-length cDNA templates produced by in vitro ligation.

作者信息

Rice C M, Grakoui A, Galler R, Chambers T J

机构信息

Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110-1093.

出版信息

New Biol. 1989 Dec;1(3):285-96.

PMID:2487295
Abstract

Yellow fever (YF) virus is the prototype member of the flavivirus family, a diverse group of human and animal pathogens. A live-attenuated strain of YF virus, called 17D, has been used successfully for human vaccination for more than 50 years. In this report we describe the construction of full-length YF 17D cDNA templates that can be transcribed in vitro to yield infectious YF virus RNA. Because of the instability of full-length YF cDNA clones and their toxic effects on Escherichia coli, we developed a strategy in which full-length templates for transcription were constructed by in vitro ligation of appropriate restriction fragments. The YF virus recovered from cDNA was indistinguishable from the parental virus by several criteria. This system should facilitate the molecular genetic analysis of flavivirus replication and attenuation and may allow YF 17D to be used as a carrier for immunologically important epitopes from other disease agents.

摘要

黄热病(YF)病毒是黄病毒科的原型成员,该科包含多种人类和动物病原体。一种减毒活的YF病毒株,称为17D,已成功用于人类疫苗接种50多年。在本报告中,我们描述了全长YF 17D cDNA模板的构建,该模板可在体外转录以产生传染性YF病毒RNA。由于全长YF cDNA克隆的不稳定性及其对大肠杆菌的毒性作用,我们开发了一种策略,通过体外连接适当的限制性片段构建转录的全长模板。从cDNA中回收的YF病毒在几个标准上与亲本病毒没有区别。该系统应有助于黄病毒复制和减毒的分子遗传学分析,并可能使YF 17D用作来自其他病原体的免疫重要表位的载体。

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