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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6650389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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