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An interbacterial DNA deaminase toxin directly mutagenizes surviving target populations
Journal article   Open access   Peer reviewed

An interbacterial DNA deaminase toxin directly mutagenizes surviving target populations

Marcos H. de Moraes, FoSheng Hsu, Dean Huang, Dustin E Bosch, Jun Zeng, Matthew C. Radey, Noah Simon, Hannah E. Ledvina, Jacob P Frick, Paul A. Wiggins, …
eLife, Vol.10, e62967
01/01/2021
DOI: 10.7554/eLife.62967
PMCID: PMC7901873
PMID: 33448264
url
https://doi.org/10.7554/eLife.62967View
Published (Version of record) Open Access

Abstract

When bacterial cells come in contact, antagonism mediated by the delivery of toxins frequently ensues. The potential for such encounters to have long-term beneficial consequences in recipient cells has not been investigated. Here, we examined the effects of intoxication by DddA, a cytosine deaminase delivered via the type VI secretion system (T6SS) of Burkholderia cenocepacia. Despite its killing potential, we observed that several bacterial species resist DddA and instead accumulate mutations. These mutations can lead to the acquisition of antibiotic resistance, indicating that even in the absence of killing, interbacterial antagonism can have profound consequences on target populations. Investigation of additional toxins from the deaminase superfamily revealed that mutagenic activity is a common feature of these proteins, including a representative we show targets single-stranded DNA and displays a markedly divergent structure. Our findings suggest that a surprising consequence of antagonistic interactions between bacteria could be the promotion of adaptation via the action of directly mutagenic toxins.
Bacteria Developmental Biology DNA Microbiology Urogenital System Adaptation Antagonism basic medicine Burkholderia Burkholderia cenocepacia Cytosine deaminase food and beverages fungi humanities medical and health sciences reproductive and urinary physiology Toxin Type VI secretion system

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