4.8 Article

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

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2023773118

关键词

X-ray micro-CT imaging; 3D reconstruction; metabolomics; symbiosis; multimodal mass spectrometry imaging

资金

  1. Gordon and Betty Moore Foundation Marine Microbiology Initiative Investigator Award [GBMF3811]
  2. Max Planck Society

向作者/读者索取更多资源

We developed a new method CHEMHIST to connect anatomical structure and metabolic function in millimeter-sized symbiotic animals, addressing the limited understanding of metabolic interactions between these animals. By combining MSI and micro-CT, we successfully correlated the distribution of metabolites with the 3D histology of the animals, providing a methodological groundwork for understanding the roles of these symbiotic animals in ecosystem functioning.
Our understanding of metabolic interactions between small symbi-otic 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 histologi -cal 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 spectrom-etry 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 metab-olites 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 hybridiza-tion for the taxonomic identification and localization of the associ-ated micro(organisms). Building CHEMHIST upon in situ imaging, we sampled an earthworm from its natural habitat and created an in-teractive 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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