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Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography

Our understanding of metabolic interactions between small symbiotic animals and bacteria or parasitic eukaryotes that reside within their bodies is extremely limited. This gap in knowledge originates from a methodological challenge, namely to connect histological changes in host tissues induced by b...

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Autores principales: Geier, Benedikt, Oetjen, Janina, Ruthensteiner, Bernhard, Polikarpov, Maxim, Gruber-Vodicka, Harald R., Liebeke, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300811/
https://www.ncbi.nlm.nih.gov/pubmed/34183413
http://dx.doi.org/10.1073/pnas.2023773118
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author Geier, Benedikt
Oetjen, Janina
Ruthensteiner, Bernhard
Polikarpov, Maxim
Gruber-Vodicka, Harald R.
Liebeke, Manuel
author_facet Geier, Benedikt
Oetjen, Janina
Ruthensteiner, Bernhard
Polikarpov, Maxim
Gruber-Vodicka, Harald R.
Liebeke, Manuel
author_sort Geier, Benedikt
collection PubMed
description Our understanding of metabolic interactions between small symbiotic animals and bacteria or parasitic eukaryotes that reside within their bodies is extremely limited. This gap in knowledge originates from a methodological challenge, namely to connect histological changes in host tissues induced by beneficial and parasitic (micro)organisms to the underlying metabolites. We addressed this challenge and developed chemo-histo-tomography (CHEMHIST), a culture-independent approach to connect anatomic structure and metabolic function in millimeter-sized symbiotic animals. CHEMHIST combines chemical imaging of metabolites based on mass spectrometry imaging (MSI) and microanatomy-based micro-computed X-ray tomography (micro-CT) on the same animal. Both high-resolution MSI and micro-CT allowed us to correlate the distribution of metabolites to the same animal’s three-dimensional (3D) histology down to submicrometer resolutions. Our protocol is compatible with tissue-specific DNA sequencing and fluorescence in situ hybridization for the taxonomic identification and localization of the associated micro(organisms). Building CHEMHIST upon in situ imaging, we sampled an earthworm from its natural habitat and created an interactive 3D model of its physical and chemical interactions with bacteria and parasitic nematodes in its tissues. Combining MSI and micro-CT, we present a methodological groundwork for connecting metabolic and anatomic phenotypes of small symbiotic animals that often represent keystone species for ecosystem functioning.
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spelling pubmed-83008112021-07-28 Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography Geier, Benedikt Oetjen, Janina Ruthensteiner, Bernhard Polikarpov, Maxim Gruber-Vodicka, Harald R. Liebeke, Manuel Proc Natl Acad Sci U S A Biological Sciences Our understanding of metabolic interactions between small symbiotic animals and bacteria or parasitic eukaryotes that reside within their bodies is extremely limited. This gap in knowledge originates from a methodological challenge, namely to connect histological changes in host tissues induced by beneficial and parasitic (micro)organisms to the underlying metabolites. We addressed this challenge and developed chemo-histo-tomography (CHEMHIST), a culture-independent approach to connect anatomic structure and metabolic function in millimeter-sized symbiotic animals. CHEMHIST combines chemical imaging of metabolites based on mass spectrometry imaging (MSI) and microanatomy-based micro-computed X-ray tomography (micro-CT) on the same animal. Both high-resolution MSI and micro-CT allowed us to correlate the distribution of metabolites to the same animal’s three-dimensional (3D) histology down to submicrometer resolutions. Our protocol is compatible with tissue-specific DNA sequencing and fluorescence in situ hybridization for the taxonomic identification and localization of the associated micro(organisms). Building CHEMHIST upon in situ imaging, we sampled an earthworm from its natural habitat and created an interactive 3D model of its physical and chemical interactions with bacteria and parasitic nematodes in its tissues. Combining MSI and micro-CT, we present a methodological groundwork for connecting metabolic and anatomic phenotypes of small symbiotic animals that often represent keystone species for ecosystem functioning. National Academy of Sciences 2021-07-06 2021-06-28 /pmc/articles/PMC8300811/ /pubmed/34183413 http://dx.doi.org/10.1073/pnas.2023773118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Geier, Benedikt
Oetjen, Janina
Ruthensteiner, Bernhard
Polikarpov, Maxim
Gruber-Vodicka, Harald R.
Liebeke, Manuel
Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography
title Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography
title_full Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography
title_fullStr Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography
title_full_unstemmed Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography
title_short Connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography
title_sort connecting structure and function from organisms to molecules in small-animal symbioses through chemo-histo-tomography
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300811/
https://www.ncbi.nlm.nih.gov/pubmed/34183413
http://dx.doi.org/10.1073/pnas.2023773118
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