Heterogeneity in responses to ribosome-targeting antibiotics mediated by bacterial RNA repair

RNA repair is critical for cellular function. The Rtc system maintains RNA integrity within the translational machinery of bacteria. In E. coli, Rtc expression enables cells to rescue growth and survive treatment by conferring transient resistance to ribosome-targeting antibiotics, yet the mechanisms underpinning this resistance remain obscure. Here, we present a computational model of Rtc-regulated repair of translational RNAs. Integrating model predictions with experimental validations, we uncover notable cell-to-cell heterogeneity in rtc expression that impacts on translational capacity, indicating that rtc may induce a form of heteroresistance. We moreover identify Rtc targets that may reduce the translational capacity of cells and so potentiate antibiotic effects. Our findings elucidate a complex response underpinning resistance conferred by Rtc, offering alternate routes for addressing resistance in E. coli and other relevant pathogens.

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Publication Details

Journal
Nature Communications
Published
2025-11-11
DOI
https://doi.org/10.1038/s41467-025-64759-3
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Heterogeneity in responses to ribosome-targeting antibiotics mediated by bacterial RNA repair

Ioly Kotta‐Loizou, Andrea Y. Weiße, Martin Buck, Andrei Sapelkin et al.
Nature Communications
RNA and protein synthesis mechanisms
article

Heterogeneity in responses to ribosome-targeting antibiotics mediated by bacterial RNA repair

Ioly Kotta‐Loizou, Andrea Y. Weiße, Martin Buck, Andrei Sapelkin, Shafagh Moradian, Christoph Engl, Hollie J. Hindley, Maria Giuliano, Z.C. Gong
article en

Abstract

RNA repair is critical for cellular function. The Rtc system maintains RNA integrity within the translational machinery of bacteria. In E. coli, Rtc expression enables cells to rescue growth and survive treatment by conferring transient resistance to ribosome-targeting antibiotics, yet the mechanisms underpinning this resistance remain obscure. Here, we present a computational model of Rtc-regulated repair of translational RNAs. Integrating model predictions with experimental validations, we uncover notable cell-to-cell heterogeneity in rtc expression that impacts on translational capacity, indicating that rtc may induce a form of heteroresistance. We moreover identify Rtc targets that may reduce the translational capacity of cells and so potentiate antibiotic effects. Our findings elucidate a complex response underpinning resistance conferred by Rtc, offering alternate routes for addressing resistance in E. coli and other relevant pathogens.

Nature CommunicationsVol. 16(1)
University of Hertfordshire (GB), Scuola Superiore Sant'Anna (IT), Queen Mary University of London (GB), Imperial College London (GB), University of Edinburgh (GB)
Wellcome Trust, Leverhulme Trust, China Scholarship Council, Directorate for Biological Sciences, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 70%
RNA and protein synthesis mechanisms
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