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This article is part of the supplement: 22nd European Workshop for Rheumatology Research

Meeting abstract

A simple system for rapid generation of recombinant adenoviruses by ligation

J Dudler1, R Salvi1, R Driscoll1 and AK So2

Author affiliations

1 CHUV, Lausanne, Switzerland

2 Service de Rhumatologie, Lausanne, Switzerland

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Citation and License

Arthritis Res 2002, 4(Suppl 1):112  doi:10.1186/ar448


The electronic version of this article is the complete one and can be found online at:


Received:15 January 2002
Published:4 February 2002

©

Meeting abstract

Recombinant adenoviruses provide a versatile tool for gene expression, and both ease of production and ability to infect non dividing cells have led to their widespread use in arthritis models. Classically, their construction is time-consuming, requires homologous recombination in permissive cells, and, despite recent technical improvements such as homologous recombination in bacteria, their construction remains often difficult with manipulation of cosmids or large plasmids containing full-length adenoviral genome. We have designed and constructed a system where recombinant adenoviruses are constructed by a simple ligation. Ad-P-EGFP is a recombinant first generation E1-deleted adenovirus where a unique and rare restriction site (PacI) has been engineered at 3.7 mu. The shuttle vector (pC5) also contains a PacI site 3 prime of a CMV-driven expression cassette. pC5 only contains the left ITR and packaging signal from wild-type adenovirus serotype 5, but no regions for homologous recombination. This strategy allows for a much smaller shuttle than usual, making manipulation and sub-cloning of transgenes easier. Once the gene of interest is cloned in the expression cassette of pC5, the resulting plasmid is digested with PacI and SwaI (another rare cutter engineered just in front of the left ITR) to free a fragment containing all the necessary elements for the construction of a recombinant adenovirus (left ITR, packaging signal and expression cassette). Another engineered PacI site in the backbone of pC5 allows for easier purification. This fragment is then ligated overnight to unpurified PacI restricted and dephosphorylated Ad-P-EGFP viral DNA. The mixture is then directly lipofected without further manipulation in 293 cells. Cells are covered with an overlay and, after 5 to 10 days, plaques are screened under a fluorescent microscope and non fluorescent plaques picked and amplified. Typical ratios for fluorescent to non fluorescent plaques are between 1:4 to 1:20. This system allows for rapid generation of recombinant adenoviruses, uses common techniques such as ligation and lipofection, and doesn't need homologous recombination, special bacteria, extraction of large DNA fragments or manipulation of cosmids. This system has allowed us to construct more than 15 different viruses lately, viruses that will be ultimately used in animal models.