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Non-invasive single-cell morphometry in living bacterial biofilms

Fluorescence microscopy enables spatial and temporal measurements of live cells and cellular communities. However, this potential has not yet been fully realized for investigations of individual cell behaviors and phenotypic changes in dense, three-dimensional (3D) bacterial biofilms. Accurate cell...

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Autores principales: Zhang, Mingxing, Zhang, Ji, Wang, Yibo, Wang, Jie, Achimovich, Alecia M., Acton, Scott T., Gahlmann, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708432/
https://www.ncbi.nlm.nih.gov/pubmed/33262347
http://dx.doi.org/10.1038/s41467-020-19866-8
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author Zhang, Mingxing
Zhang, Ji
Wang, Yibo
Wang, Jie
Achimovich, Alecia M.
Acton, Scott T.
Gahlmann, Andreas
author_facet Zhang, Mingxing
Zhang, Ji
Wang, Yibo
Wang, Jie
Achimovich, Alecia M.
Acton, Scott T.
Gahlmann, Andreas
author_sort Zhang, Mingxing
collection PubMed
description Fluorescence microscopy enables spatial and temporal measurements of live cells and cellular communities. However, this potential has not yet been fully realized for investigations of individual cell behaviors and phenotypic changes in dense, three-dimensional (3D) bacterial biofilms. Accurate cell detection and cellular shape measurement in densely packed biofilms are challenging because of the limited resolution and low signal to background ratios (SBRs) in fluorescence microscopy images. In this work, we present Bacterial Cell Morphometry 3D (BCM3D), an image analysis workflow that combines deep learning with mathematical image analysis to accurately segment and classify single bacterial cells in 3D fluorescence images. In BCM3D, deep convolutional neural networks (CNNs) are trained using simulated biofilm images with experimentally realistic SBRs, cell densities, labeling methods, and cell shapes. We systematically evaluate the segmentation accuracy of BCM3D using both simulated and experimental images. Compared to state-of-the-art bacterial cell segmentation approaches, BCM3D consistently achieves higher segmentation accuracy and further enables automated morphometric cell classifications in multi-population biofilms.
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spelling pubmed-77084322020-12-03 Non-invasive single-cell morphometry in living bacterial biofilms Zhang, Mingxing Zhang, Ji Wang, Yibo Wang, Jie Achimovich, Alecia M. Acton, Scott T. Gahlmann, Andreas Nat Commun Article Fluorescence microscopy enables spatial and temporal measurements of live cells and cellular communities. However, this potential has not yet been fully realized for investigations of individual cell behaviors and phenotypic changes in dense, three-dimensional (3D) bacterial biofilms. Accurate cell detection and cellular shape measurement in densely packed biofilms are challenging because of the limited resolution and low signal to background ratios (SBRs) in fluorescence microscopy images. In this work, we present Bacterial Cell Morphometry 3D (BCM3D), an image analysis workflow that combines deep learning with mathematical image analysis to accurately segment and classify single bacterial cells in 3D fluorescence images. In BCM3D, deep convolutional neural networks (CNNs) are trained using simulated biofilm images with experimentally realistic SBRs, cell densities, labeling methods, and cell shapes. We systematically evaluate the segmentation accuracy of BCM3D using both simulated and experimental images. Compared to state-of-the-art bacterial cell segmentation approaches, BCM3D consistently achieves higher segmentation accuracy and further enables automated morphometric cell classifications in multi-population biofilms. Nature Publishing Group UK 2020-12-01 /pmc/articles/PMC7708432/ /pubmed/33262347 http://dx.doi.org/10.1038/s41467-020-19866-8 Text en © The Author(s) 2020 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
Zhang, Mingxing
Zhang, Ji
Wang, Yibo
Wang, Jie
Achimovich, Alecia M.
Acton, Scott T.
Gahlmann, Andreas
Non-invasive single-cell morphometry in living bacterial biofilms
title Non-invasive single-cell morphometry in living bacterial biofilms
title_full Non-invasive single-cell morphometry in living bacterial biofilms
title_fullStr Non-invasive single-cell morphometry in living bacterial biofilms
title_full_unstemmed Non-invasive single-cell morphometry in living bacterial biofilms
title_short Non-invasive single-cell morphometry in living bacterial biofilms
title_sort non-invasive single-cell morphometry in living bacterial biofilms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708432/
https://www.ncbi.nlm.nih.gov/pubmed/33262347
http://dx.doi.org/10.1038/s41467-020-19866-8
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