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Antibiotic Resistance via Bacterial Cell Shape-Shifting
Bacteria have evolved to develop multiple strategies for antibiotic resistance by effectively reducing intracellular antibiotic concentrations or antibiotic binding affinities, but the role of cell morphology in antibiotic resistance remains poorly understood. By analyzing cell morphological data fo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239207/ https://www.ncbi.nlm.nih.gov/pubmed/35616332 http://dx.doi.org/10.1128/mbio.00659-22 |
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author | Ojkic, Nikola Serbanescu, Diana Banerjee, Shiladitya |
author_facet | Ojkic, Nikola Serbanescu, Diana Banerjee, Shiladitya |
author_sort | Ojkic, Nikola |
collection | PubMed |
description | Bacteria have evolved to develop multiple strategies for antibiotic resistance by effectively reducing intracellular antibiotic concentrations or antibiotic binding affinities, but the role of cell morphology in antibiotic resistance remains poorly understood. By analyzing cell morphological data for different bacterial species under antibiotic stress, we find that bacteria increase or decrease the cell surface-to-volume ratio depending on the antibiotic target. Using quantitative modeling, we show that by reducing the surface-to-volume ratio, bacteria can effectively reduce the intracellular antibiotic concentration by decreasing antibiotic influx. The model further predicts that bacteria can increase the surface-to-volume ratio to induce the dilution of membrane-targeting antibiotics, in agreement with experimental data. Using a whole-cell model for the regulation of cell shape and growth by antibiotics, we predict shape transformations that bacteria can utilize to increase their fitness in the presence of antibiotics. We conclude by discussing additional pathways for antibiotic resistance that may act in synergy with shape-induced resistance. |
format | Online Article Text |
id | pubmed-9239207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92392072022-06-29 Antibiotic Resistance via Bacterial Cell Shape-Shifting Ojkic, Nikola Serbanescu, Diana Banerjee, Shiladitya mBio Opinion/Hypothesis Bacteria have evolved to develop multiple strategies for antibiotic resistance by effectively reducing intracellular antibiotic concentrations or antibiotic binding affinities, but the role of cell morphology in antibiotic resistance remains poorly understood. By analyzing cell morphological data for different bacterial species under antibiotic stress, we find that bacteria increase or decrease the cell surface-to-volume ratio depending on the antibiotic target. Using quantitative modeling, we show that by reducing the surface-to-volume ratio, bacteria can effectively reduce the intracellular antibiotic concentration by decreasing antibiotic influx. The model further predicts that bacteria can increase the surface-to-volume ratio to induce the dilution of membrane-targeting antibiotics, in agreement with experimental data. Using a whole-cell model for the regulation of cell shape and growth by antibiotics, we predict shape transformations that bacteria can utilize to increase their fitness in the presence of antibiotics. We conclude by discussing additional pathways for antibiotic resistance that may act in synergy with shape-induced resistance. American Society for Microbiology 2022-05-26 /pmc/articles/PMC9239207/ /pubmed/35616332 http://dx.doi.org/10.1128/mbio.00659-22 Text en Copyright © 2022 Ojkic et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Opinion/Hypothesis Ojkic, Nikola Serbanescu, Diana Banerjee, Shiladitya Antibiotic Resistance via Bacterial Cell Shape-Shifting |
title | Antibiotic Resistance via Bacterial Cell Shape-Shifting |
title_full | Antibiotic Resistance via Bacterial Cell Shape-Shifting |
title_fullStr | Antibiotic Resistance via Bacterial Cell Shape-Shifting |
title_full_unstemmed | Antibiotic Resistance via Bacterial Cell Shape-Shifting |
title_short | Antibiotic Resistance via Bacterial Cell Shape-Shifting |
title_sort | antibiotic resistance via bacterial cell shape-shifting |
topic | Opinion/Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239207/ https://www.ncbi.nlm.nih.gov/pubmed/35616332 http://dx.doi.org/10.1128/mbio.00659-22 |
work_keys_str_mv | AT ojkicnikola antibioticresistanceviabacterialcellshapeshifting AT serbanescudiana antibioticresistanceviabacterialcellshapeshifting AT banerjeeshiladitya antibioticresistanceviabacterialcellshapeshifting |