Lai C J, Zhao B T, Hori H, Bray M
Molecular Viral Biology Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5139-43. doi: 10.1073/pnas.88.12.5139.
Dengue virus is an enveloped positive-strand RNA virus with a genome approximately 11 kilobases in length. The four serotypes of dengue virus are currently the most important members of the flavivirus family in terms of geographical distribution and the incidence of infection in humans. In this communication we describe successful cloning of a stable full-length cDNA copy of dengue type 4 virus that can be used as the template for in vitro transcription of infectious RNA. Evidence is presented that dengue virus recovered from permissive cells transfected with the in vitro RNA transcripts retained a mutation that was engineered into full-length cDNA. The properties of the virus produced by cells transfected with infectious RNA transcripts of dengue cDNA resembled those of the virus from which the cDNA clone was derived. The dengue virus recombinant DNA system should prove helpful in gaining a better understanding of the molecular biology of dengue viruses and should facilitate the development of a safe and effective live vaccine for use in humans.
登革病毒是一种有包膜的正链RNA病毒,基因组长度约为11千碱基。就地理分布和人类感染发病率而言,登革病毒的四种血清型目前是黄病毒科最重要的成员。在本通讯中,我们描述了登革4型病毒稳定全长cDNA拷贝的成功克隆,该拷贝可作为传染性RNA体外转录的模板。有证据表明,从用体外RNA转录本转染的允许细胞中回收的登革病毒保留了一个被设计到全长cDNA中的突变。用登革病毒cDNA的传染性RNA转录本转染的细胞产生的病毒特性类似于从中获得cDNA克隆的病毒。登革病毒重组DNA系统应有助于更好地理解登革病毒的分子生物学,并应促进开发用于人类的安全有效的活疫苗。