Metagenomics of the MAST-3 stramenopile, , and its associated microbiome reveals unexpected metabolic attributes and extensive nutrient dependencies.

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Autori principali: Absolon, Dominic E, Jackson, Victoria L N, Monier, Adam, Smith, Alison G, Helliwell, Katherine E
Natura: Artículo científico
Lingua:en
Pubblicazione: Microbial genomics 2025
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author Absolon, Dominic E
Jackson, Victoria L N
Monier, Adam
Smith, Alison G
Helliwell, Katherine E
author_facet Absolon, Dominic E
Jackson, Victoria L N
Monier, Adam
Smith, Alison G
Helliwell, Katherine E
Absolon, Dominic E
Jackson, Victoria L N
Monier, Adam
Smith, Alison G
Helliwell, Katherine E
collection PubMed - marine biology
contents Metagenomics of the MAST-3 stramenopile, , and its associated microbiome reveals unexpected metabolic attributes and extensive nutrient dependencies. Absolon, Dominic E Jackson, Victoria L N Monier, Adam Smith, Alison G Helliwell, Katherine E Metagenomics Microbiota Stramenopiles Bacteria Phylogeny Protists are polyphyletic single-celled eukaryotes that underpin global ecosystem functioning, particularly in the oceans. Most remain uncultured, limiting the investigation of their physiology and cell biology. MArine STramenopiles (MASTs) are heterotrophic protists that, although related to well-characterized photosynthetic diatoms and parasitic oomycetes, are poorly studied. The Nanomonadea (MAST-3) species has been maintained in co-culture with a bacterial consortium, offering opportunities to investigate the metabolic attributes and nutritional dependencies of the community. Employing a metagenomics approach, the 68 Mbp haploid genome of was retrieved to an estimated completeness of 93%, representing the most complete MAST genome so far. We also characterized the diversity of, and assembled genomes for, 23 co-cultured bacteria. Auxotrophy of for B vitamins (B, B, B, B and B), but not vitamins C, B, B and B, was predicted. Several bacteria also lacked complete B-vitamin biosynthesis pathways, suggesting that vitamins and/or their precursors are exchanged in the consortium. Moreover, lacked the ability to synthesize half the protein amino acids, although genes encoding the complete urea cycle were identified, like diatoms; this may play a role in recycling organic nitrogen compounds. Unexpectedly, we also identified the gene for dimethylsulphoniopropionate biosynthesis. Biosynthesis of this important stress protectant and bacterial chemoattractant is typically found in photosynthetic eukaryotes and has not been identified before in heterotrophic stramenopiles. Together, our study reveals the metabolic attributes of a hitherto understudied organism, advancing knowledge of the evolution and adaptations of the stramenopiles and informing future culturing efforts.
format Artículo científico
id pubmed_41231233
institution PubMed
language en
publishDate 2025
publisher Microbial genomics
record_format pubmed
spellingShingle Metagenomics of the MAST-3 stramenopile, , and its associated microbiome reveals unexpected metabolic attributes and extensive nutrient dependencies.
Absolon, Dominic E
Jackson, Victoria L N
Monier, Adam
Smith, Alison G
Helliwell, Katherine E
Metagenomics
Microbiota
Stramenopiles
Bacteria
Phylogeny
Metagenomics of the MAST-3 stramenopile, , and its associated microbiome reveals unexpected metabolic attributes and extensive nutrient dependencies. Absolon, Dominic E Jackson, Victoria L N Monier, Adam Smith, Alison G Helliwell, Katherine E Metagenomics Microbiota Stramenopiles Bacteria Phylogeny Protists are polyphyletic single-celled eukaryotes that underpin global ecosystem functioning, particularly in the oceans. Most remain uncultured, limiting the investigation of their physiology and cell biology. MArine STramenopiles (MASTs) are heterotrophic protists that, although related to well-characterized photosynthetic diatoms and parasitic oomycetes, are poorly studied. The Nanomonadea (MAST-3) species has been maintained in co-culture with a bacterial consortium, offering opportunities to investigate the metabolic attributes and nutritional dependencies of the community. Employing a metagenomics approach, the 68 Mbp haploid genome of was retrieved to an estimated completeness of 93%, representing the most complete MAST genome so far. We also characterized the diversity of, and assembled genomes for, 23 co-cultured bacteria. Auxotrophy of for B vitamins (B, B, B, B and B), but not vitamins C, B, B and B, was predicted. Several bacteria also lacked complete B-vitamin biosynthesis pathways, suggesting that vitamins and/or their precursors are exchanged in the consortium. Moreover, lacked the ability to synthesize half the protein amino acids, although genes encoding the complete urea cycle were identified, like diatoms; this may play a role in recycling organic nitrogen compounds. Unexpectedly, we also identified the gene for dimethylsulphoniopropionate biosynthesis. Biosynthesis of this important stress protectant and bacterial chemoattractant is typically found in photosynthetic eukaryotes and has not been identified before in heterotrophic stramenopiles. Together, our study reveals the metabolic attributes of a hitherto understudied organism, advancing knowledge of the evolution and adaptations of the stramenopiles and informing future culturing efforts.
title Metagenomics of the MAST-3 stramenopile, , and its associated microbiome reveals unexpected metabolic attributes and extensive nutrient dependencies.
topic Metagenomics
Microbiota
Stramenopiles
Bacteria
Phylogeny
url https://pubmed.ncbi.nlm.nih.gov/41231233/