Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution
ABSTRACT Mechanisms of evolution and evolution of antibiotic resistance are both fundamental and world health problems. Stress-induced mutagenesis defines mechanisms of mutagenesis upregulated by stress responses, which drive adaptation when cells are maladapted to their environments—when stressed....
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Format: | Article |
Language: | English |
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American Society for Microbiology
2022-06-01
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Series: | mBio |
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Online Access: | https://journals.asm.org/doi/10.1128/mbio.01074-22 |
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author | John P. Pribis Yin Zhai P. J. Hastings Susan M. Rosenberg |
author_facet | John P. Pribis Yin Zhai P. J. Hastings Susan M. Rosenberg |
author_sort | John P. Pribis |
collection | DOAJ |
description | ABSTRACT Mechanisms of evolution and evolution of antibiotic resistance are both fundamental and world health problems. Stress-induced mutagenesis defines mechanisms of mutagenesis upregulated by stress responses, which drive adaptation when cells are maladapted to their environments—when stressed. Work in mutagenesis induced by antibiotics had produced tantalizing clues but not coherent mechanisms. We review recent advances in antibiotic-induced mutagenesis that integrate how reactive oxygen species (ROS), the SOS and general stress responses, and multichromosome cells orchestrate a stress response-induced switch from high-fidelity to mutagenic repair of DNA breaks. Moreover, while sibling cells stay stable, a mutable “gambler” cell subpopulation is induced by differentially generated ROS, which signal the general stress response. We discuss other evolvable subpopulations and consider diverse evolution-promoting molecules as potential targets for drugs to slow evolution of antibiotic resistance, cross-resistance, and immune evasion. An FDA-approved drug exemplifies “stealth” evolution-slowing drugs that avoid selecting resistance to themselves or antibiotics. |
first_indexed | 2024-04-12T12:22:52Z |
format | Article |
id | doaj.art-08449f6d585a4eefad9f76f7706d6fd2 |
institution | Directory Open Access Journal |
issn | 2150-7511 |
language | English |
last_indexed | 2024-04-12T12:22:52Z |
publishDate | 2022-06-01 |
publisher | American Society for Microbiology |
record_format | Article |
series | mBio |
spelling | doaj.art-08449f6d585a4eefad9f76f7706d6fd22022-12-22T03:33:14ZengAmerican Society for MicrobiologymBio2150-75112022-06-0113310.1128/mbio.01074-22Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced EvolutionJohn P. Pribis0Yin Zhai1P. J. Hastings2Susan M. Rosenberg3The Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas, USADepartment of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas, USADepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USADepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USAABSTRACT Mechanisms of evolution and evolution of antibiotic resistance are both fundamental and world health problems. Stress-induced mutagenesis defines mechanisms of mutagenesis upregulated by stress responses, which drive adaptation when cells are maladapted to their environments—when stressed. Work in mutagenesis induced by antibiotics had produced tantalizing clues but not coherent mechanisms. We review recent advances in antibiotic-induced mutagenesis that integrate how reactive oxygen species (ROS), the SOS and general stress responses, and multichromosome cells orchestrate a stress response-induced switch from high-fidelity to mutagenic repair of DNA breaks. Moreover, while sibling cells stay stable, a mutable “gambler” cell subpopulation is induced by differentially generated ROS, which signal the general stress response. We discuss other evolvable subpopulations and consider diverse evolution-promoting molecules as potential targets for drugs to slow evolution of antibiotic resistance, cross-resistance, and immune evasion. An FDA-approved drug exemplifies “stealth” evolution-slowing drugs that avoid selecting resistance to themselves or antibiotics.https://journals.asm.org/doi/10.1128/mbio.01074-22antibiotic resistanceantibioticscell subpopulationsevolvabilityevolutionstress-induced mutagenesis |
spellingShingle | John P. Pribis Yin Zhai P. J. Hastings Susan M. Rosenberg Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution mBio antibiotic resistance antibiotics cell subpopulations evolvability evolution stress-induced mutagenesis |
title | Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution |
title_full | Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution |
title_fullStr | Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution |
title_full_unstemmed | Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution |
title_short | Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution |
title_sort | stress induced mutagenesis gambler cells and stealth targeting antibiotic induced evolution |
topic | antibiotic resistance antibiotics cell subpopulations evolvability evolution stress-induced mutagenesis |
url | https://journals.asm.org/doi/10.1128/mbio.01074-22 |
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