HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Free via Open Access: OA OA Free Full Text Full Text (PDF) Supplementary Figure Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via CrossRef Citing Articles via Google Scholar Google Scholar Articles by van der Walt, E. Articles by Martin, D. P. Search for Related Content PubMed PubMed Citation Articles by van der Walt, E. Articles by Martin, D. P. Agricola Articles by van der Walt, E. Articles by Martin, D. P.

Rapid host adaptation by extensive recombination

¹ Department of Molecular and Cell Biology, University of Cape Town, Cape Town, South Africa
² Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa
³ Electron Microscope Unit, University of Cape Town, Cape Town, South Africa
⁴ Department of Plant Pathology, University of Florida, Gainesville, FL 32611, USA
⁵ Department of Microbiology, University of Washington, Seattle, Washington, USA

Correspondence
Edward P. Rybicki
ed.rybicki{at}uct.ac.za

Experimental investigations into virus recombination can provide valuable insights into the biochemical mechanisms and the evolutionary value of this fundamental biological process. Here, we describe an experimental scheme for studying recombination that should be applicable to any recombinogenic viruses amenable to the production of synthetic infectious genomes. Our approach is based on differences in fitness that generally exist between synthetic chimaeric genomes and the wild-type viruses from which they are constructed. In mixed infections of defective reciprocal chimaeras, selection strongly favours recombinant progeny genomes that recover a portion of wild-type fitness. Characterizing these evolved progeny viruses can highlight both important genetic fitness determinants and the contribution that recombination makes to the evolution of their natural relatives. Moreover, these experiments supply precise information about the frequency and distribution of recombination breakpoints, which can shed light on the mechanistic processes underlying recombination. We demonstrate the value of this approach using the small single-stranded DNA geminivirus, maize streak virus (MSV). Our results show that adaptive recombination in this virus is extremely efficient and can yield complex progeny genomes comprising up to 18 recombination breakpoints. The patterns of recombination that we observe strongly imply that the mechanistic processes underlying rolling circle replication are the prime determinants of recombination breakpoint distributions found in MSV genomes sampled from nature.

A supplementary figure is available with the online version of this paper.