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Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination

Heteroresistance refers to phenotypic heterogeneity of microbial clonal populations under antibiotic stress, and it has been thought to be an allocation of a subset of “resistant” cells for surviving in higher concentrations of antibiotic. The assumption fits the so-called bet-hedging strategy, wher...

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Autores principales: Wang, Xiaorong, Kang, Yu, Luo, Chunxiong, Zhao, Tong, Liu, Lin, Jiang, Xiangdan, Fu, Rongrong, An, Shuchang, Chen, Jichao, Jiang, Ning, Ren, Lufeng, Wang, Qi, Baillie, J. Kenneth, Gao, Zhancheng, Yu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950525/
https://www.ncbi.nlm.nih.gov/pubmed/24520060
http://dx.doi.org/10.1128/mBio.00942-13
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author Wang, Xiaorong
Kang, Yu
Luo, Chunxiong
Zhao, Tong
Liu, Lin
Jiang, Xiangdan
Fu, Rongrong
An, Shuchang
Chen, Jichao
Jiang, Ning
Ren, Lufeng
Wang, Qi
Baillie, J. Kenneth
Gao, Zhancheng
Yu, Jun
author_facet Wang, Xiaorong
Kang, Yu
Luo, Chunxiong
Zhao, Tong
Liu, Lin
Jiang, Xiangdan
Fu, Rongrong
An, Shuchang
Chen, Jichao
Jiang, Ning
Ren, Lufeng
Wang, Qi
Baillie, J. Kenneth
Gao, Zhancheng
Yu, Jun
author_sort Wang, Xiaorong
collection PubMed
description Heteroresistance refers to phenotypic heterogeneity of microbial clonal populations under antibiotic stress, and it has been thought to be an allocation of a subset of “resistant” cells for surviving in higher concentrations of antibiotic. The assumption fits the so-called bet-hedging strategy, where a bacterial population “hedges” its “bet” on different phenotypes to be selected by unpredicted environment stresses. To test this hypothesis, we constructed a heteroresistance model by introducing a bla(CTX-M-14) gene (coding for a cephalosporin hydrolase) into a sensitive Escherichia coli strain. We confirmed heteroresistance in this clone and that a subset of the cells expressed more hydrolase and formed more colonies in the presence of ceftriaxone (exhibited stronger “resistance”). However, subsequent single-cell-level investigation by using a microfluidic device showed that a subset of cells with a distinguishable phenotype of slowed growth and intensified hydrolase expression emerged, and they were not positively selected but increased their proportion in the population with ascending antibiotic concentrations. Therefore, heteroresistance—the gradually decreased colony-forming capability in the presence of antibiotic—was a result of a decreased growth rate rather than of selection for resistant cells. Using a mock strain without the resistance gene, we further demonstrated the existence of two nested growth-centric feedback loops that control the expression of the hydrolase and maximize population growth in various antibiotic concentrations. In conclusion, phenotypic heterogeneity is a population-based strategy beneficial for bacterial survival and propagation through task allocation and interphenotypic collaboration, and the growth rate provides a critical control for the expression of stress-related genes and an essential mechanism in responding to environmental stresses.
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spelling pubmed-39505252014-03-12 Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination Wang, Xiaorong Kang, Yu Luo, Chunxiong Zhao, Tong Liu, Lin Jiang, Xiangdan Fu, Rongrong An, Shuchang Chen, Jichao Jiang, Ning Ren, Lufeng Wang, Qi Baillie, J. Kenneth Gao, Zhancheng Yu, Jun mBio Research Article Heteroresistance refers to phenotypic heterogeneity of microbial clonal populations under antibiotic stress, and it has been thought to be an allocation of a subset of “resistant” cells for surviving in higher concentrations of antibiotic. The assumption fits the so-called bet-hedging strategy, where a bacterial population “hedges” its “bet” on different phenotypes to be selected by unpredicted environment stresses. To test this hypothesis, we constructed a heteroresistance model by introducing a bla(CTX-M-14) gene (coding for a cephalosporin hydrolase) into a sensitive Escherichia coli strain. We confirmed heteroresistance in this clone and that a subset of the cells expressed more hydrolase and formed more colonies in the presence of ceftriaxone (exhibited stronger “resistance”). However, subsequent single-cell-level investigation by using a microfluidic device showed that a subset of cells with a distinguishable phenotype of slowed growth and intensified hydrolase expression emerged, and they were not positively selected but increased their proportion in the population with ascending antibiotic concentrations. Therefore, heteroresistance—the gradually decreased colony-forming capability in the presence of antibiotic—was a result of a decreased growth rate rather than of selection for resistant cells. Using a mock strain without the resistance gene, we further demonstrated the existence of two nested growth-centric feedback loops that control the expression of the hydrolase and maximize population growth in various antibiotic concentrations. In conclusion, phenotypic heterogeneity is a population-based strategy beneficial for bacterial survival and propagation through task allocation and interphenotypic collaboration, and the growth rate provides a critical control for the expression of stress-related genes and an essential mechanism in responding to environmental stresses. American Society of Microbiology 2014-02-11 /pmc/articles/PMC3950525/ /pubmed/24520060 http://dx.doi.org/10.1128/mBio.00942-13 Text en Copyright © 2014 Wang et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Xiaorong
Kang, Yu
Luo, Chunxiong
Zhao, Tong
Liu, Lin
Jiang, Xiangdan
Fu, Rongrong
An, Shuchang
Chen, Jichao
Jiang, Ning
Ren, Lufeng
Wang, Qi
Baillie, J. Kenneth
Gao, Zhancheng
Yu, Jun
Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination
title Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination
title_full Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination
title_fullStr Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination
title_full_unstemmed Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination
title_short Heteroresistance at the Single-Cell Level: Adapting to Antibiotic Stress through a Population-Based Strategy and Growth-Controlled Interphenotypic Coordination
title_sort heteroresistance at the single-cell level: adapting to antibiotic stress through a population-based strategy and growth-controlled interphenotypic coordination
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950525/
https://www.ncbi.nlm.nih.gov/pubmed/24520060
http://dx.doi.org/10.1128/mBio.00942-13
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