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Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation

Advances in microscopy hold great promise for allowing quantitative and precise measurement of morphological and molecular phenomena at the single-cell level in bacteria; however, the potential of this approach is ultimately limited by the availability of methods to faithfully segment cells independ...

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Autores principales: Cutler, Kevin J., Stringer, Carsen, Lo, Teresa W., Rappez, Luca, Stroustrup, Nicholas, Brook Peterson, S., Wiggins, Paul A., Mougous, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636021/
https://www.ncbi.nlm.nih.gov/pubmed/36253643
http://dx.doi.org/10.1038/s41592-022-01639-4
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author Cutler, Kevin J.
Stringer, Carsen
Lo, Teresa W.
Rappez, Luca
Stroustrup, Nicholas
Brook Peterson, S.
Wiggins, Paul A.
Mougous, Joseph D.
author_facet Cutler, Kevin J.
Stringer, Carsen
Lo, Teresa W.
Rappez, Luca
Stroustrup, Nicholas
Brook Peterson, S.
Wiggins, Paul A.
Mougous, Joseph D.
author_sort Cutler, Kevin J.
collection PubMed
description Advances in microscopy hold great promise for allowing quantitative and precise measurement of morphological and molecular phenomena at the single-cell level in bacteria; however, the potential of this approach is ultimately limited by the availability of methods to faithfully segment cells independent of their morphological or optical characteristics. Here, we present Omnipose, a deep neural network image-segmentation algorithm. Unique network outputs such as the gradient of the distance field allow Omnipose to accurately segment cells on which current algorithms, including its predecessor, Cellpose, produce errors. We show that Omnipose achieves unprecedented segmentation performance on mixed bacterial cultures, antibiotic-treated cells and cells of elongated or branched morphology. Furthermore, the benefits of Omnipose extend to non-bacterial subjects, varied imaging modalities and three-dimensional objects. Finally, we demonstrate the utility of Omnipose in the characterization of extreme morphological phenotypes that arise during interbacterial antagonism. Our results distinguish Omnipose as a powerful tool for characterizing diverse and arbitrarily shaped cell types from imaging data.
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spelling pubmed-96360212022-11-06 Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation Cutler, Kevin J. Stringer, Carsen Lo, Teresa W. Rappez, Luca Stroustrup, Nicholas Brook Peterson, S. Wiggins, Paul A. Mougous, Joseph D. Nat Methods Article Advances in microscopy hold great promise for allowing quantitative and precise measurement of morphological and molecular phenomena at the single-cell level in bacteria; however, the potential of this approach is ultimately limited by the availability of methods to faithfully segment cells independent of their morphological or optical characteristics. Here, we present Omnipose, a deep neural network image-segmentation algorithm. Unique network outputs such as the gradient of the distance field allow Omnipose to accurately segment cells on which current algorithms, including its predecessor, Cellpose, produce errors. We show that Omnipose achieves unprecedented segmentation performance on mixed bacterial cultures, antibiotic-treated cells and cells of elongated or branched morphology. Furthermore, the benefits of Omnipose extend to non-bacterial subjects, varied imaging modalities and three-dimensional objects. Finally, we demonstrate the utility of Omnipose in the characterization of extreme morphological phenotypes that arise during interbacterial antagonism. Our results distinguish Omnipose as a powerful tool for characterizing diverse and arbitrarily shaped cell types from imaging data. Nature Publishing Group US 2022-10-17 2022 /pmc/articles/PMC9636021/ /pubmed/36253643 http://dx.doi.org/10.1038/s41592-022-01639-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cutler, Kevin J.
Stringer, Carsen
Lo, Teresa W.
Rappez, Luca
Stroustrup, Nicholas
Brook Peterson, S.
Wiggins, Paul A.
Mougous, Joseph D.
Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation
title Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation
title_full Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation
title_fullStr Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation
title_full_unstemmed Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation
title_short Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation
title_sort omnipose: a high-precision morphology-independent solution for bacterial cell segmentation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636021/
https://www.ncbi.nlm.nih.gov/pubmed/36253643
http://dx.doi.org/10.1038/s41592-022-01639-4
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