Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/111639
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Title: Starvation-induced mutagenesis in rhsC and ybfD genes extends bacterial tolerance to various stresses by boosting efflux function
Authors: Wan, Y 
Ye, L 
Zheng, J 
Tang, Y 
Chan, EWC 
Chen, S 
Issue Date: Jun-2025
Source: Microbiological research, Jun. 2025, v. 295, 128106
Abstract: Recent evidence showed that bacteria actively maintained a range of physiological functions to enhance survival fitness under adverse growth conditions. In this study, we investigated whether bacteria need to undergo active genetic changes for stress-protection purposes if environmental stress persists. Our results revealed that mutations became detectable at specific sites in several genes in E. coli after encountering starvation conditions for six days. This discovery is groundbreaking since bacteria are not known to undergo site-specific mutagenesis during prolonged starvation when most physiological activities are down-regulated. The genes in which mutations were consistently detected in the tolerant population were ybfD and rhsC within the ybf gene cluster, which are predicted to encode components of a transporter. To assess the impact of these mutations on bacterial survival, mutants with single or double mutations in these genes were generated and tested. The results demonstrated that these mutations caused significant increase in tolerance to antibiotics, heat, and oxidative stresses. Functional analysis indicated that the E. coli BW25113
Keywords: Antibiotic tolerance
Efflux
Genetic changes
Mutagenesis
Tolerant subpopulations
Journal: Microbiological research 
DOI: 10.1016/j.micres.2025.128106
Rights: © 2025 The Author(s). Published by Elsevier GmbH. This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/).
The following publication Wan, Y., Ye, L., Zheng, J., Tang, Y., Chan, E. W. C., & Chen, S. (2025). Starvation-induced mutagenesis in rhsC and ybfD genes extends bacterial tolerance to various stresses by boosting efflux function. Microbiological Research, 128106 is available at https://10.1016/j.micres.2025.128106.
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