Jiang Hongbing, Franz Carl J, Wang David
Departments of Molecular Microbiology and Pathology & Immunology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Departments of Molecular Microbiology and Pathology & Immunology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA
J Virol. 2014 Oct;88(20):11774-81. doi: 10.1128/JVI.01630-14. Epub 2014 Jul 30.
The recent identification of Orsay virus, the first virus that is capable of naturally infecting Caenorhabditis elegans, provides a unique opportunity to explore host-virus interaction studies in this invaluable model organism. A key feature of this system is the robust genetic tractability of the host, C. elegans, which would ideally be complemented by the ability to genetically manipulate Orsay virus in parallel. To this end, we developed a plasmid-based reverse genetics system for Orsay virus by creating transgenic C. elegans strains harboring Orsay virus cDNAs. Both wild-type and mutant Orsay viruses, including a FLAG epitope-tagged recombinant Orsay virus, were generated by use of the reverse genetics system. This is the first plasmid-based virus reverse genetics system in the metazoan C. elegans. The Orsay virus reverse genetics we established will serve as a fundamental tool in host-virus interaction studies in the model organism C. elegans. Importance: To date, Orsay virus is the first and the only identified virus capable of naturally infecting Caenorhabditis elegans. C. elegans is a simple multicellular model organism that mimics many fundamental features of human biology and has been used to define many biological properties conserved through evolution. Thus, the Orsay virus-C. elegans infection system provides a unique opportunity to study host-virus interactions. In order to take maximal advantage of this system, the ability to genetically engineer mutant forms of Orsay virus would be highly desirable. Most efforts to engineer viruses have been done with cultured cells. Here we describe the creation of mutant viruses directly in the multicellular organism C. elegans without the use of cell culture. We engineered a virus expressing a genetically tagged protein that could be detected in C. elegans. This provides proof of concept for modifying Orsay virus, which will greatly facilitate studies in this experimental system.
最近发现的奥赛病毒是第一种能够自然感染秀丽隐杆线虫的病毒,这为在这种极具价值的模式生物中探索宿主 - 病毒相互作用研究提供了独特的机会。该系统的一个关键特征是宿主秀丽隐杆线虫强大的遗传易操作性,理想情况下,这需要同时具备对奥赛病毒进行基因操作的能力作为补充。为此,我们通过创建携带奥赛病毒cDNA的转基因秀丽隐杆线虫品系,开发了一种基于质粒的奥赛病毒反向遗传学系统。利用该反向遗传学系统,我们产生了野生型和突变型奥赛病毒,包括一种带有FLAG表位标签的重组奥赛病毒。这是后生动物秀丽隐杆线虫中首个基于质粒的病毒反向遗传学系统。我们建立的奥赛病毒反向遗传学将成为在模式生物秀丽隐杆线虫中进行宿主 - 病毒相互作用研究的基础工具。重要性:迄今为止,奥赛病毒是第一种也是唯一一种被鉴定出能够自然感染秀丽隐杆线虫的病毒。秀丽隐杆线虫是一种简单的多细胞模式生物,模拟了人类生物学的许多基本特征,并已被用于定义许多进化过程中保守的生物学特性。因此,奥赛病毒 - 秀丽隐杆线虫感染系统为研究宿主 - 病毒相互作用提供了独特的机会。为了充分利用这个系统,对奥赛病毒的突变形式进行基因工程改造的能力将非常有必要。大多数病毒工程改造工作都是在培养细胞中进行的。在这里,我们描述了直接在多细胞生物秀丽隐杆线虫中创建突变病毒的方法,而无需使用细胞培养。我们构建了一种表达可在秀丽隐杆线虫中检测到的基因标签蛋白的病毒。这为修饰奥赛病毒提供了概念验证,将极大地促进该实验系统中的研究。