Measuring single-cell susceptibility to antibiotics within monoclonal bacterial populations.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 19 02 2024
accepted: 30 04 2024
medline: 1 8 2024
pubmed: 1 8 2024
entrez: 1 8 2024
Statut: epublish

Résumé

The emergence of new resistant bacterial strains is a worldwide challenge. A resistant bacterial population can emerge from a single cell that acquires resistance or persistence. Hence, new ways of tackling the mechanism of antibiotic response, such as single cell studies are required. It is necessary to see what happens at the single cell level, in order to understand what happens at the population level. To date, linking the heterogeneity of single-cell susceptibility to the population-scale response to antibiotics remains challenging due to the trade-offs between the resolution and the field of view. Here we present a platform that measures the ability of individual E. coli cells to form small colonies at different ciprofloxacin concentrations, by using anchored microfluidic drops and an image and data analysis pipelines. The microfluidic results are benchmarked against classical microbiology measurements of antibiotic susceptibility, showing an agreement between the pooled microfluidic chip and replated bulk measurements. Further, the experimental likelihood of a single cell to form a colony is used to provide a probabilistic antibiotic susceptibility curve. In addition to the probabilistic viewpoint, the microfluidic format enables the characterization of morphological features over time for a large number of individual cells. This pipeline can be used to compare the response of different bacterial strains to antibiotics with different action mechanisms.

Identifiants

pubmed: 39088440
doi: 10.1371/journal.pone.0303630
pii: PONE-D-24-06332
doi:

Substances chimiques

Anti-Bacterial Agents 0
Ciprofloxacin 5E8K9I0O4U

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0303630

Informations de copyright

Copyright: © 2024 Le Quellec et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Lena Le Quellec (L)

Institut Pasteur, Université Paris Cité, Physical Microfluidics and Bioengineering, Paris, France.
LadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.

Andrey Aristov (A)

Institut Pasteur, Université Paris Cité, Physical Microfluidics and Bioengineering, Paris, France.

Salomé Gutiérrez Ramos (S)

Institut Pasteur, Université Paris Cité, Physical Microfluidics and Bioengineering, Paris, France.
LadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.

Gabriel Amselem (G)

Institut Pasteur, Université Paris Cité, Physical Microfluidics and Bioengineering, Paris, France.
LadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.

Julia Bos (J)

Institut Pasteur, Université Paris Cité, CNRS UMR3525, Bacterial Genome Plasticity Unit, Paris, France.

Zeynep Baharoglu (Z)

Institut Pasteur, Université Paris Cité, CNRS UMR3525, Bacterial Genome Plasticity Unit, Paris, France.

Didier Mazel (D)

Institut Pasteur, Université Paris Cité, CNRS UMR3525, Bacterial Genome Plasticity Unit, Paris, France.

Charles N Baroud (CN)

Institut Pasteur, Université Paris Cité, Physical Microfluidics and Bioengineering, Paris, France.
LadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.

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Classifications MeSH