Efficient Inference of Recombination Hot Regions in Bacterial Genomes

• Published in: Molecular biology and evolution Vol. 31; no. 6; pp. 1593 - 1605
• Main Authors: Yahara, Koji, Didelot, Xavier, Ansari, M. Azim, Sheppard, Samuel K., Falush, Daniel
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01.06.2014
• Subjects: Algorithms; Bacteria; Bacterial Proteins - genetics; Campylobacter jejuni; Campylobacter jejuni - genetics; Chromosome Painting; Computational Biology; Deoxyribonucleic acid; Deviation; DNA; E coli; Escherichia coli; Escherichia coli - genetics; Eukaryotes; Genome, Bacterial; Genomes; Genomics; Haplotypes; Membrane proteins; Membrane Proteins - genetics; Membranes; Methods; Models, Genetic; Population studies; Prokaryotes; Recombination hot spots; Recombination, Genetic; Simulation; Venus; recombination hotspot; population genomics; chromosome painting; recombination hot region; homologous recombination; selection
• ISSN: 0737-4038; 1537-1719; 1537-1719
• DOI: 10.1093/molbev/msu082

In eukaryotes, detailed surveys of recombination rates have shown variation at multiple genomic scales and the presence of “hotspots” of highly elevated recombination. In bacteria, studies of recombination rate variation are less developed, in part because there are few analysis methods that take into account the clonal context within which bacterial evolution occurs. Here, we focus in particular on identifying “hot regions” of the genome where DNA is transferred frequently between isolates. We present a computationally efficient algorithm based on the recently developed “chromosome painting” algorithm, which characterizes patterns of haplotype sharing across a genome. We compare the average genome wide painting, which principally reflects clonal descent, with the painting for each site which additionally reflects the specific deviations at the site due to recombination. Using simulated data, we show that hot regions have consistently higher deviations from the genome wide average than normal regions. We applied our approach to previously analyzed Escherichia coli genomes and revealed that the new method is highly correlated with the number of recombination events affecting each site inferred by ClonalOrigin, a method that is only applicable to small numbers of genomes. Furthermore, we analyzed recombination hot regions in Campylobacter jejuni by using 200 genomes. We identified three recombination hot regions, which are enriched for genes related to membrane proteins. Our approach and its implementation, which is downloadable from https://github.com/bioprojects/orderedPainting, will help to develop a new phase of population genomic studies of recombination in prokaryotes.