| Literature DB >> 28538186 |
Wenli Zhang1, Jun Fu2, Jing Liu1, Hailong Wang2, Maren Schiwon1, Sebastian Janz1, Lukas Schaffarczyk1, Lukas von der Goltz1, Eric Ehrke-Schulz1, Johannes Dörner1, Manish Solanki1, Philip Boehme1, Thorsten Bergmann1, Andre Lieber3, Chris Lauber4, Andreas Dahl5, Andreas Petzold5, Youming Zhang6, A Francis Stewart7, Anja Ehrhardt8.
Abstract
Adenoviruses (Ads) are large human-pathogenic double-stranded DNA (dsDNA) viruses presenting an enormous natural diversity associated with a broad variety of diseases. However, only a small fraction of adenoviruses has been explored in basic virology and biomedical research, highlighting the need to develop robust and adaptable methodologies and resources. We developed a method for high-throughput direct cloning and engineering of adenoviral genomes from different sources utilizing advanced linear-linear homologous recombination (LLHR) and linear-circular homologous recombination (LCHR). We describe 34 cloned adenoviral genomes originating from clinical samples, which were characterized by next-generation sequencing (NGS). We anticipate that this recombineering strategy and the engineered adenovirus library will provide an approach to study basic and clinical virology. High-throughput screening (HTS) of the reporter-tagged Ad library in a panel of cell lines including osteosarcoma disease-specific cell lines revealed alternative virus types with enhanced transduction and oncolysis efficiencies. This highlights the usefulness of this resource.Entities:
Keywords: Red/ET homologous recombination; adenovirus; engineered adenovirus library; large double-stranded DNA viruses; natural virus diversity; resource; therapy; translation; vector
Mesh:
Year: 2017 PMID: 28538186 DOI: 10.1016/j.celrep.2017.05.008
Source DB: PubMed Journal: Cell Rep Impact factor: 9.995