Inferring bacterial recombination rates from large-scale sequencing datasets.
basic_science · Level V
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- Record sourced from PubMed, PMID 30664775.
- Also identified by DOI 10.1038/s41592-018-0293-7.
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Abstract
We present a robust, computationally efficient method ( https://github.com/kussell-lab/mcorr ) for inferring the parameters of homologous recombination in bacteria, which can be applied in diverse datasets, from whole-genome sequencing to metagenomic shotgun sequencing data. Using correlation profiles of synonymous substitutions, we determine recombination rates and diversity levels of the shared gene pool that has contributed to a given sample. We validated the recombination parameters using data from laboratory experiments. We determined the recombination parameters for a wide range of bacterial species, and inferred the distribution of shared gene pools for global Helicobacter pylori isolates. Using metagenomics data of the infant gut microbiome, we measured the recombination parameters of multidrug-resistant Escherichia coli ST131. Lastly, we analyzed ancient samples of bacterial DNA from the Copper Age 'Iceman' mummy and from 14th century victims of the Black Death, obtaining measurements of bacterial recombination rates and gene pool diversity of earlier eras.
Medical subject headings
- Computational Biology
- DNA, Ancient
- Drug Resistance, Bacterial
- Metagenomics
- Recombination, Genetic
- Sequence Analysis, DNA