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1.
Mol Microbiol ; 119(6): 659-676, 2023 06.
Article in English | MEDLINE | ID: mdl-37066636

ABSTRACT

Bacteria often grow into matrix-encased three-dimensional (3D) biofilm communities, which can be imaged at cellular resolution using confocal microscopy. From these 3D images, measurements of single-cell properties with high spatiotemporal resolution are required to investigate cellular heterogeneity and dynamical processes inside biofilms. However, the required measurements rely on the automated segmentation of bacterial cells in 3D images, which is a technical challenge. To improve the accuracy of single-cell segmentation in 3D biofilms, we first evaluated recent classical and deep learning segmentation algorithms. We then extended StarDist, a state-of-the-art deep learning algorithm, by optimizing the post-processing for bacteria, which resulted in the most accurate segmentation results for biofilms among all investigated algorithms. To generate the large 3D training dataset required for deep learning, we developed an iterative process of automated segmentation followed by semi-manual correction, resulting in >18,000 annotated Vibrio cholerae cells in 3D images. We demonstrate that this large training dataset and the neural network with optimized post-processing yield accurate segmentation results for biofilms of different species and on biofilm images from different microscopes. Finally, we used the accurate single-cell segmentation results to track cell lineages in biofilms and to perform spatiotemporal measurements of single-cell growth rates during biofilm development.


Subject(s)
Deep Learning , Cell Lineage , Imaging, Three-Dimensional/methods , Algorithms , Biofilms , Bacteria , Image Processing, Computer-Assisted/methods
3.
Nat Microbiol ; 6(2): 151-156, 2021 02.
Article in English | MEDLINE | ID: mdl-33398098

ABSTRACT

Biofilms are microbial communities that represent a highly abundant form of microbial life on Earth. Inside biofilms, phenotypic and genotypic variations occur in three-dimensional space and time; microscopy and quantitative image analysis are therefore crucial for elucidating their functions. Here, we present BiofilmQ-a comprehensive image cytometry software tool for the automated and high-throughput quantification, analysis and visualization of numerous biofilm-internal and whole-biofilm properties in three-dimensional space and time.


Subject(s)
Biofilms , Image Cytometry/methods , Imaging, Three-Dimensional/methods , Microbiota , Software , Bacteria/cytology , Bacteria/genetics , Bacteria/growth & development , Spatio-Temporal Analysis
4.
Biol Chem ; 401(12): 1365-1374, 2020 11 26.
Article in English | MEDLINE | ID: mdl-32990640

ABSTRACT

Biofilms are a ubiquitous mode of microbial life and display an increased tolerance to different stresses. Inside biofilms, cells may experience both externally applied stresses and internal stresses that emerge as a result of growth in spatially structured communities. In this review, we discuss the spatial scales of different stresses in the context of biofilms, and if cells in biofilms respond to these stresses as a collection of individual cells, or if there are multicellular properties associated with the response. Understanding the organizational level of stress responses in microbial communities can help to clarify multicellular functions of biofilms.


Subject(s)
Bacteria/metabolism , Biofilms , Bacteria/cytology , Humans , Stress, Physiological
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