Evolution via recombination: Cell-to-cell contact facilitates larger recombination events in Streptococcus pneumoniae

• Published in: PLoS genetics 2018-06, Vol.14 (6), p.e1007410-e1007410
• Main Authors: Cowley, Lauren A, Petersen, Fernanda C, Junges, Roger, Jimson D Jimenez, Med, Morrison, Donald A, Hanage, William P
• Format: Article
• Language: English
• Subjects: Antibiotics; Biofilms; Bioinformatics; Biology and life sciences; Cell Communication - genetics; Cell Communication - physiology; Cell culture; Cloning; Deoxyribonucleic acid; DNA; DNA - genetics; DNA - physiology; Epidemiology; Evolution; Evolution, Molecular; Evolutionary genetics; Gene Rearrangement - genetics; Genetic aspects; Genetic recombination; Genetic research; Genetic transformation; Genome, Bacterial - genetics; Genomes; Homologous recombination; Homologous Recombination - genetics; Medicine and Health Sciences; Microbiological research; Peptides; Pheromones; Polymorphism, Single Nucleotide - genetics; Population; Public health; Recombinants; Recombination, Genetic - genetics; Research and analysis methods; Single-nucleotide polymorphism; Streptococcus infections; Streptococcus pneumoniae; Streptococcus pneumoniae - genetics; Whole Genome Sequencing - methods
• ISSN: 1553-7404; 1553-7390; 1553-7404
• DOI: 10.1371/journal.pgen.1007410

Homologous recombination in the genetic transformation model organism Streptococcus pneumoniae is thought to be important in the adaptation and evolution of this pathogen. While competent pneumococci are able to scavenge DNA added to laboratory cultures, large-scale transfers of multiple kb are rare under these conditions. We used whole genome sequencing (WGS) to map transfers in recombinants arising from contact of competent cells with non-competent 'target' cells, using strains with known genomes, distinguished by a total of ~16,000 SNPs. Experiments designed to explore the effect of environment on large scale recombination events used saturating purified donor DNA, short-term cell assemblages on Millipore filters, and mature biofilm mixed cultures. WGS of 22 recombinants for each environment mapped all SNPs that were identical between the recombinant and the donor but not the recipient. The mean recombination event size was found to be significantly larger in cell-to-cell contact cultures (4051 bp in filter assemblage and 3938 bp in biofilm co-culture versus 1815 bp with saturating DNA). Up to 5.8% of the genome was transferred, through 20 recombination events, to a single recipient, with the largest single event incorporating 29,971 bp. We also found that some recombination events are clustered, that these clusters are more likely to occur in cell-to-cell contact environments, and that they cause significantly increased linkage of genes as far apart as 60,000 bp. We conclude that pneumococcal evolution through homologous recombination is more likely to occur on a larger scale in environments that permit cell-to-cell contact.