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Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms

Continuous monitoring of large specimens for long durations requires fast volume imaging. This is essential for understanding the processes occurring during the developmental stages of multicellular organisms. One of the key obstacles of fluorescence based prolonged monitoring and data collection is...

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Autores principales: Basumatary, Jigmi, Ara, Tarannum, Mukherjee, Amartya, Dutta, Debanjan, Nongthomba, Upendra, Mondal, Partha Pratim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027194/
https://www.ncbi.nlm.nih.gov/pubmed/33828140
http://dx.doi.org/10.1038/s41598-021-86951-3
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author Basumatary, Jigmi
Ara, Tarannum
Mukherjee, Amartya
Dutta, Debanjan
Nongthomba, Upendra
Mondal, Partha Pratim
author_facet Basumatary, Jigmi
Ara, Tarannum
Mukherjee, Amartya
Dutta, Debanjan
Nongthomba, Upendra
Mondal, Partha Pratim
author_sort Basumatary, Jigmi
collection PubMed
description Continuous monitoring of large specimens for long durations requires fast volume imaging. This is essential for understanding the processes occurring during the developmental stages of multicellular organisms. One of the key obstacles of fluorescence based prolonged monitoring and data collection is photobleaching. To capture the biological processes and simultaneously overcome the effect of bleaching, we developed single- and multi-color lightsheet based OVSS imaging technique that enables rapid screening of multiple tissues in an organism. Our approach based on OVSS imaging employs quantized step rotation of the specimen to record 2D angular data that reduces data acquisition time when compared to the existing light sheet imaging system (SPIM). A co-planar multicolor light sheet PSF is introduced to illuminate the tissues labelled with spectrally-separated fluorescent probes. The detection is carried out using a dual-channel sub-system that can simultaneously record spectrally separate volume stacks of the target organ. Arduino-based control systems were employed to automatize and control the volume data acquisition process. To illustrate the advantages of our approach, we have noninvasively imaged the Drosophila larvae and Zebrafish embryo. Dynamic studies of multiple organs (muscle and yolk-sac) in Zebrafish for a prolonged duration (5 days) were carried out to understand muscle structuring (Dystrophin, microfibers), primitive Macrophages (in yolk-sac) and inter-dependent lipid and protein-based metabolism. The volume-based study, intensity line-plots and inter-dependence ratio analysis allowed us to understand the transition from lipid-based metabolism to protein-based metabolism during early development (Pharyngula period with a critical transition time, [Formula: see text] h post-fertilization) in Zebrafish. The advantage of multicolor lightsheet illumination, fast volume scanning, simultaneous visualization of multiple organs and an order-less photobleaching makes OVSS imaging the system of choice for rapid monitoring and real-time assessment of macroscopic biological organisms with microscopic resolution.
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spelling pubmed-80271942021-04-08 Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms Basumatary, Jigmi Ara, Tarannum Mukherjee, Amartya Dutta, Debanjan Nongthomba, Upendra Mondal, Partha Pratim Sci Rep Article Continuous monitoring of large specimens for long durations requires fast volume imaging. This is essential for understanding the processes occurring during the developmental stages of multicellular organisms. One of the key obstacles of fluorescence based prolonged monitoring and data collection is photobleaching. To capture the biological processes and simultaneously overcome the effect of bleaching, we developed single- and multi-color lightsheet based OVSS imaging technique that enables rapid screening of multiple tissues in an organism. Our approach based on OVSS imaging employs quantized step rotation of the specimen to record 2D angular data that reduces data acquisition time when compared to the existing light sheet imaging system (SPIM). A co-planar multicolor light sheet PSF is introduced to illuminate the tissues labelled with spectrally-separated fluorescent probes. The detection is carried out using a dual-channel sub-system that can simultaneously record spectrally separate volume stacks of the target organ. Arduino-based control systems were employed to automatize and control the volume data acquisition process. To illustrate the advantages of our approach, we have noninvasively imaged the Drosophila larvae and Zebrafish embryo. Dynamic studies of multiple organs (muscle and yolk-sac) in Zebrafish for a prolonged duration (5 days) were carried out to understand muscle structuring (Dystrophin, microfibers), primitive Macrophages (in yolk-sac) and inter-dependent lipid and protein-based metabolism. The volume-based study, intensity line-plots and inter-dependence ratio analysis allowed us to understand the transition from lipid-based metabolism to protein-based metabolism during early development (Pharyngula period with a critical transition time, [Formula: see text] h post-fertilization) in Zebrafish. The advantage of multicolor lightsheet illumination, fast volume scanning, simultaneous visualization of multiple organs and an order-less photobleaching makes OVSS imaging the system of choice for rapid monitoring and real-time assessment of macroscopic biological organisms with microscopic resolution. Nature Publishing Group UK 2021-04-07 /pmc/articles/PMC8027194/ /pubmed/33828140 http://dx.doi.org/10.1038/s41598-021-86951-3 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Basumatary, Jigmi
Ara, Tarannum
Mukherjee, Amartya
Dutta, Debanjan
Nongthomba, Upendra
Mondal, Partha Pratim
Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms
title Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms
title_full Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms
title_fullStr Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms
title_full_unstemmed Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms
title_short Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms
title_sort fluorescence based rapid optical volume screening system (ovss) for interrogating multicellular organisms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027194/
https://www.ncbi.nlm.nih.gov/pubmed/33828140
http://dx.doi.org/10.1038/s41598-021-86951-3
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