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首页> 外文期刊>Journal of Clinical Microbiology >Rapid Phenotypic Characterization Method for Herpes Simplex Virus and Varicella-Zoster Virus Thymidine Kinases To Screen for Acyclovir-Resistant Viral Infection
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Rapid Phenotypic Characterization Method for Herpes Simplex Virus and Varicella-Zoster Virus Thymidine Kinases To Screen for Acyclovir-Resistant Viral Infection

机译:单纯疱疹病毒和水痘-带状疱疹病毒胸苷激酶的快速表型表征方法以筛选抗阿昔洛韦的病毒感染

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摘要

A rapid phenotypic screening method for herpes simplex virus (HSV) and varicella-zoster virus (VZV) thymidine kinase (TK) genes was developed for monitoring acyclovir-resistant viruses. This method determines the biochemical phenotype of the TK polypeptide, which is synthesized in vitro from viral DNA using a procedure as follows. The TK gene of each sample virus strain is amplified and isolated under the control of a T7 promoter by PCR. The PCR products are transcribed with T7 RNA polymerase and translated in a rabbit reticulocyte lysate. Using this method, enzymatic characteristics and the size of the TK polypeptides encoding HSV and VZV DNA were defined in less than 2 days without virus isolation. The assay should be a powerful tool in monitoring drug-resistant viruses, especially in cases in which virus isolation is difficult.
机译:建立了一种针对单纯疱疹病毒(HSV)和水痘带状疱疹病毒(VZV)胸苷激酶(TK)基因的快速表型筛选方法,以监测抗阿昔洛韦的病毒。该方法确定了TK多肽的生化表型,其是使用以下步骤从病毒DNA体外合成的。通过PCR,在T7启动子的控制下扩增并分离出每种样品病毒株的TK基因。 PCR产物用T7 RNA聚合酶转录并在兔网织红细胞裂解物中翻译。使用这种方法,可以在不到2天的时间内无需病毒分离的情况下定义编码HSV和VZV DNA的TK多肽的酶学特征和大小。该测定法应该是监测耐药病毒的有力工具,尤其是在病毒分离困难的情况下。

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