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An Engineered Virus Library as a Resource for the Spectrum-wide Exploration of Virus and Vector Diversity.

Authors :
Zhang W
Fu J
Liu J
Wang H
Schiwon M
Janz S
Schaffarczyk L
von der Goltz L
Ehrke-Schulz E
Dörner J
Solanki M
Boehme P
Bergmann T
Lieber A
Lauber C
Dahl A
Petzold A
Zhang Y
Stewart AF
Ehrhardt A
Source :
Cell reports [Cell Rep] 2017 May 23; Vol. 19 (8), pp. 1698-1709.
Publication Year :
2017

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.<br /> (Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2211-1247
Volume :
19
Issue :
8
Database :
MEDLINE
Journal :
Cell reports
Publication Type :
Academic Journal
Accession number :
28538186
Full Text :
https://doi.org/10.1016/j.celrep.2017.05.008