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High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics

Image-based high-throughput screening strategies for quantifying morphological phenotypes have proven widely successful. Here we describe a combined experimental and multivariate image analysis approach for systematic large-scale phenotyping of morphological dynamics in bacteria. Using off-the-shelf...

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Autores principales: Zahir, Taiyeb, Camacho, Rafael, Vitale, Raffaele, Ruckebusch, Cyril, Hofkens, Johan, Fauvart, Maarten, Michiels, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650389/
https://www.ncbi.nlm.nih.gov/pubmed/31341968
http://dx.doi.org/10.1038/s42003-019-0480-9
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author Zahir, Taiyeb
Camacho, Rafael
Vitale, Raffaele
Ruckebusch, Cyril
Hofkens, Johan
Fauvart, Maarten
Michiels, Jan
author_facet Zahir, Taiyeb
Camacho, Rafael
Vitale, Raffaele
Ruckebusch, Cyril
Hofkens, Johan
Fauvart, Maarten
Michiels, Jan
author_sort Zahir, Taiyeb
collection PubMed
description Image-based high-throughput screening strategies for quantifying morphological phenotypes have proven widely successful. Here we describe a combined experimental and multivariate image analysis approach for systematic large-scale phenotyping of morphological dynamics in bacteria. Using off-the-shelf components and software, we established a workflow for high-throughput time-resolved microscopy. We then screened the single‐gene deletion collection of Escherichia coli for antibiotic-induced morphological changes. Using single-cell quantitative descriptors and supervised classification methods, we measured how different cell morphologies developed over time for all strains in response to the β-lactam antibiotic cefsulodin. 191 strains exhibit significant variations under antibiotic treatment. Phenotypic clustering provided insights into processes that alter the antibiotic response. Mutants with stable bulges show delayed lysis, contributing to antibiotic tolerance. Lipopolysaccharides play a crucial role in bulge stability. This study demonstrates how multiparametric phenotyping by high-throughput time-resolved imaging and computer-aided cell classification can be used for comprehensively studying dynamic morphological transitions in bacteria.
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spelling pubmed-66503892019-07-24 High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics Zahir, Taiyeb Camacho, Rafael Vitale, Raffaele Ruckebusch, Cyril Hofkens, Johan Fauvart, Maarten Michiels, Jan Commun Biol Article Image-based high-throughput screening strategies for quantifying morphological phenotypes have proven widely successful. Here we describe a combined experimental and multivariate image analysis approach for systematic large-scale phenotyping of morphological dynamics in bacteria. Using off-the-shelf components and software, we established a workflow for high-throughput time-resolved microscopy. We then screened the single‐gene deletion collection of Escherichia coli for antibiotic-induced morphological changes. Using single-cell quantitative descriptors and supervised classification methods, we measured how different cell morphologies developed over time for all strains in response to the β-lactam antibiotic cefsulodin. 191 strains exhibit significant variations under antibiotic treatment. Phenotypic clustering provided insights into processes that alter the antibiotic response. Mutants with stable bulges show delayed lysis, contributing to antibiotic tolerance. Lipopolysaccharides play a crucial role in bulge stability. This study demonstrates how multiparametric phenotyping by high-throughput time-resolved imaging and computer-aided cell classification can be used for comprehensively studying dynamic morphological transitions in bacteria. Nature Publishing Group UK 2019-07-23 /pmc/articles/PMC6650389/ /pubmed/31341968 http://dx.doi.org/10.1038/s42003-019-0480-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zahir, Taiyeb
Camacho, Rafael
Vitale, Raffaele
Ruckebusch, Cyril
Hofkens, Johan
Fauvart, Maarten
Michiels, Jan
High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics
title High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics
title_full High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics
title_fullStr High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics
title_full_unstemmed High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics
title_short High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics
title_sort high-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650389/
https://www.ncbi.nlm.nih.gov/pubmed/31341968
http://dx.doi.org/10.1038/s42003-019-0480-9
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