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Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients

Spatiotemporal structures and heterogeneities are common in natural habitats, yet their role in the evolution of antibiotic resistance is still to be uncovered. We applied a microfluidic gradient generator device to study the emergence of resistant bacteria in spatial ciprofloxacin gradients. We obs...

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Autores principales: Nagy, Krisztina, Dukic, Barbara, Hodula, Orsolya, Ábrahám, Ágnes, Csákvári, Eszter, Dér, László, Wetherington, Miles T., Noorlag, Janneke, Keymer, Juan E., Galajda, Péter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981919/
https://www.ncbi.nlm.nih.gov/pubmed/35391738
http://dx.doi.org/10.3389/fmicb.2022.820738
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author Nagy, Krisztina
Dukic, Barbara
Hodula, Orsolya
Ábrahám, Ágnes
Csákvári, Eszter
Dér, László
Wetherington, Miles T.
Noorlag, Janneke
Keymer, Juan E.
Galajda, Péter
author_facet Nagy, Krisztina
Dukic, Barbara
Hodula, Orsolya
Ábrahám, Ágnes
Csákvári, Eszter
Dér, László
Wetherington, Miles T.
Noorlag, Janneke
Keymer, Juan E.
Galajda, Péter
author_sort Nagy, Krisztina
collection PubMed
description Spatiotemporal structures and heterogeneities are common in natural habitats, yet their role in the evolution of antibiotic resistance is still to be uncovered. We applied a microfluidic gradient generator device to study the emergence of resistant bacteria in spatial ciprofloxacin gradients. We observed biofilm formation in regions with sub-inhibitory concentrations of antibiotics, which quickly expanded into the high antibiotic regions. In the absence of an explicit structure of the habitat, this multicellular formation led to a spatial structure of the population with local competition and limited migration. Therefore, such structures can function as amplifiers of selection and aid the spread of beneficial mutations. We found that the physical environment itself induces stress-related mutations that later prove beneficial when cells are exposed to antibiotics. This shift in function suggests that exaptation occurs in such experimental scenarios. The above two processes pave the way for the subsequent emergence of highly resistant specific mutations.
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spelling pubmed-89819192022-04-06 Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients Nagy, Krisztina Dukic, Barbara Hodula, Orsolya Ábrahám, Ágnes Csákvári, Eszter Dér, László Wetherington, Miles T. Noorlag, Janneke Keymer, Juan E. Galajda, Péter Front Microbiol Microbiology Spatiotemporal structures and heterogeneities are common in natural habitats, yet their role in the evolution of antibiotic resistance is still to be uncovered. We applied a microfluidic gradient generator device to study the emergence of resistant bacteria in spatial ciprofloxacin gradients. We observed biofilm formation in regions with sub-inhibitory concentrations of antibiotics, which quickly expanded into the high antibiotic regions. In the absence of an explicit structure of the habitat, this multicellular formation led to a spatial structure of the population with local competition and limited migration. Therefore, such structures can function as amplifiers of selection and aid the spread of beneficial mutations. We found that the physical environment itself induces stress-related mutations that later prove beneficial when cells are exposed to antibiotics. This shift in function suggests that exaptation occurs in such experimental scenarios. The above two processes pave the way for the subsequent emergence of highly resistant specific mutations. Frontiers Media S.A. 2022-03-22 /pmc/articles/PMC8981919/ /pubmed/35391738 http://dx.doi.org/10.3389/fmicb.2022.820738 Text en Copyright © 2022 Nagy, Dukic, Hodula, Ábrahám, Csákvári, Dér, Wetherington, Noorlag, Keymer and Galajda. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Nagy, Krisztina
Dukic, Barbara
Hodula, Orsolya
Ábrahám, Ágnes
Csákvári, Eszter
Dér, László
Wetherington, Miles T.
Noorlag, Janneke
Keymer, Juan E.
Galajda, Péter
Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients
title Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients
title_full Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients
title_fullStr Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients
title_full_unstemmed Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients
title_short Emergence of Resistant Escherichia coli Mutants in Microfluidic On-Chip Antibiotic Gradients
title_sort emergence of resistant escherichia coli mutants in microfluidic on-chip antibiotic gradients
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981919/
https://www.ncbi.nlm.nih.gov/pubmed/35391738
http://dx.doi.org/10.3389/fmicb.2022.820738
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