Mutational spectra are associated with bacterial niche

As observed in cancers, individual mutagens and defects in DNA repair create distinctive mutational signatures that combine to form context-specific spectra within cells. We reasoned that similar processes must occur in bacterial lineages, potentially allowing decomposition analysis to detect both d...

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Bibliographic Details
Published in:	Nature communications 2023-11, Vol.14 (1), p.7091-7091, Article 7091
Main Authors:	Ruis, Christopher, Weimann, Aaron, Tonkin-Hill, Gerry, Pandurangan, Arun Prasad, Matuszewska, Marta, Murray, Gemma G R, Lévesque, Roger C, Blundell, Tom L, Floto, R Andres, Parkhill, Julian
Format:	Article
Language:	eng ; nor
Subjects:	Bacteria Cancer Context Defects DNA Mutational Analysis - methods DNA repair DNA Repair - genetics Exposure Humans Mutagens Mutation Neoplasms - genetics Niches Phylogeny Replication Signatures Spectra
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Summary:	As observed in cancers, individual mutagens and defects in DNA repair create distinctive mutational signatures that combine to form context-specific spectra within cells. We reasoned that similar processes must occur in bacterial lineages, potentially allowing decomposition analysis to detect both disruption of DNA repair processes and exposure to niche-specific mutagens. Here we reconstruct mutational spectra for 84 clades from 31 diverse bacterial species and find distinct mutational patterns. We extract signatures driven by specific DNA repair defects using hypermutator lineages, and further deconvolute the spectra into multiple signatures operating within different clades. We show that these signatures are explained by both bacterial phylogeny and replication niche. By comparing mutational spectra of clades from different environmental and biological locations, we identify niche-associated mutational signatures, and then employ these signatures to infer the predominant replication niches for several clades where this was previously obscure. Our results show that mutational spectra may be associated with sites of bacterial replication when mutagen exposures differ, and can be used in these cases to infer transmission routes for established and emergent human bacterial pathogens.
ISSN:	2041-1723 2041-1723