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  4. A method to disentangle and quantify host anabolic turnover in photosymbiotic holobionts with subcellular resolution
 
research article

A method to disentangle and quantify host anabolic turnover in photosymbiotic holobionts with subcellular resolution

Gibbin, Emma Mary  
•
Banc-Prandi, Guilhem
•
Fine, Maoz
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January 8, 2020
Communications Biology

A wide range of organisms host photosynthesizing symbionts. In these animals the metabolic exchange between host and symbionts has prevented in situ host anabolic turnover to be studied without the confounding effect of translocated photosynthates. Using the symbiotic coral Stylophora pistillata as a model organism and [1-13C]-pyruvate and [2,3-13C]-pyruvate in different incubation conditions (light, light + DCMU, and darkness), we employed NanoSIMS isotopic imaging to quantify host anabolism, with and without translocated metabolites from their photosynthesizing dinoflagellate symbionts. Under our experimental conditions, host de novo lipid synthesis accounted for ~40% of the total holobiont lipid reserve, and dinoflagellate recycling of metabolic 13CO2 enhanced host tissue 13C-enrichment by 13–22% in the epidermis, 40–58% in the gastrodermis, and 135–169% in host lipid bodies. Furthermore, we show that host anabolic turnover in different tissue structures differs, in a manner consistent with the localisation, function and cellular composition of these structures.

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Type
research article
DOI
10.1038/s42003-019-0742-6
Author(s)
Gibbin, Emma Mary  
Banc-Prandi, Guilhem
Fine, Maoz
Comment, Arnaud
Meibom, Anders  
Date Issued

2020-01-08

Published in
Communications Biology
Volume

3

Issue

1

Start page

14

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGB  
Available on Infoscience
January 16, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/164631
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