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Interplay between autotrophic and heterotrophic prokaryotic metabolism in the bathypelagic realm revealed by metatranscriptomic analyses
Srivastava, A.; De Corte, D.; Garcia, J.A.L.; Swan, B.K.; Stepanauskas, R.; Herndl, G.; Sintes, E. (2023). Interplay between autotrophic and heterotrophic prokaryotic metabolism in the bathypelagic realm revealed by metatranscriptomic analyses. Environmental Microbiome 11(1): 239. https://dx.doi.org/10.1186/s40168-023-01688-7
In: Environmental Microbiome. BMC: London. e-ISSN 2524-6372, meer
Peer reviewed article  

Beschikbaar in  Auteurs 

Author keywords
    Metatranscriptome;Gene expression; Bathypelagic; Labrador Sea Water; Thiosulfate; Dissolved organic matter (DOM); Dissolved inorganic carbon (DIC) fixation; Chemoautotrophy; Heterotrophy

Auteurs  Top 
  • Srivastava, A.
  • De Corte, D.
  • Garcia, J.A.L.
  • Swan, B.K.
  • Stepanauskas, R.
  • Herndl, G., meer
  • Sintes, E.

Abstract

    Background

    Heterotrophic microbes inhabiting the dark ocean largely depend on the settling of organic matter from the sunlit ocean. However, this sinking of organic materials is insufficient to cover their demand for energy and alternative sources such as chemoautotrophy have been proposed. Reduced sulfur compounds, such as thiosulfate, are a potential energy source for both auto- and heterotrophic marine prokaryotes.

    Methods

    Seawater samples were collected from Labrador Sea Water (LSW, ~ 2000 m depth) in the North Atlantic and incubated in the dark at in situ temperature unamended, amended with 1 µM thiosulfate, or with 1 µM thiosulfate plus 10 µM glucose and 10 µM acetate (thiosulfate plus dissolved organic matter, DOM). Inorganic carbon fixation was measured in the different treatments and samples for metatranscriptomic analyses were collected after 1 h and 72 h of incubation.

    Results

    Amendment of LSW with thiosulfate and thiosulfate plus DOM enhanced prokaryotic inorganic carbon fixation. The energy generated via chemoautotrophy and heterotrophy in the amended prokaryotic communities was used for the biosynthesis of glycogen and phospholipids as storage molecules. The addition of thiosulfate stimulated unclassified bacteria, sulfur-oxidizing Deltaproteobacteria (SAR324 cluster bacteria), Epsilonproteobacteria (Sulfurimonas sp.), and Gammaproteobacteria (SUP05 cluster bacteria), whereas, the amendment with thiosulfate plus DOM stimulated typically copiotrophic Gammaproteobacteria (closely related to Vibrio sp. and Pseudoalteromonas sp.).

    Conclusions

    The gene expression pattern of thiosulfate utilizing microbes specifically of genes involved in energy production via sulfur oxidation and coupled to CO2 fixation pathways coincided with the change in the transcriptional profile of the heterotrophic prokaryotic community (genes involved in promoting energy storage), suggesting a fine-tuned metabolic interplay between chemoautotrophic and heterotrophic microbes in the dark ocean.


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