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Article: Metatranscriptomics-guided genome-scale metabolic reconstruction reveals the carbon flux and trophic interaction in methanogenic communities

TitleMetatranscriptomics-guided genome-scale metabolic reconstruction reveals the carbon flux and trophic interaction in methanogenic communities
Authors
KeywordsAnaerobic digestion
Long reads
Omics
Reverse electron transfer
Syntrophic bacteria
Issue Date5-Jul-2024
PublisherBioMed Central
Citation
Microbiome, 2024, v. 12, n. 1 How to Cite?
Abstract

Background

Despite rapid advances in genomic-resolved metagenomics and remarkable explosion of metagenome-assembled genomes (MAGs), the function of uncultivated anaerobic lineages and their interactions in carbon mineralization remain largely uncertain, which has profound implications in biotechnology and biogeochemistry.

Results

In this study, we combined long-read sequencing and metatranscriptomics-guided metabolic reconstruction to provide a genome-wide perspective of carbon mineralization flow from polymers to methane in an anaerobic bioreactor. Our results showed that incorporating long reads resulted in a substantial improvement in the quality of metagenomic assemblies, enabling the effective recovery of 132 high-quality genomes meeting stringent criteria of minimum information about a metagenome-assembled genome (MIMAG). In addition, hybrid assembly obtained 51% more prokaryotic genes in comparison to the short-read-only assembly. Metatranscriptomics-guided metabolic reconstruction unveiled the remarkable metabolic flexibility of several novel Bacteroidales-affiliated bacteria and populations from Mesotoga sp. in scavenging amino acids and sugars. In addition to recovering two circular genomes of previously known but fragmented syntrophic bacteria, two newly identified bacteria within Syntrophales were found to be highly engaged in fatty acid oxidation through syntrophic relationships with dominant methanogens Methanoregulaceae bin.74 and Methanothrix sp. bin.206. The activity of bin.206 preferring acetate as substrate exceeded that of bin.74 with increasing loading, reinforcing the substrate determinantal role.

Conclusion

Overall, our study uncovered some key active anaerobic lineages and their metabolic functions in this complex anaerobic ecosystem, offering a framework for understanding carbon transformations in anaerobic digestion. These findings advance the understanding of metabolic activities and trophic interactions between anaerobic guilds, providing foundational insights into carbon flux within both engineered and natural ecosystems.


Persistent Identifierhttp://hdl.handle.net/10722/353810
ISSN
2023 Impact Factor: 13.8
2023 SCImago Journal Rankings: 3.802
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYan, Weifu-
dc.contributor.authorWang, Dou-
dc.contributor.authorWang, Yubo-
dc.contributor.authorWang, Chunxiao-
dc.contributor.authorChen, Xi-
dc.contributor.authorLiu, Lei-
dc.contributor.authorWang, Yulin-
dc.contributor.authorLi, Yu-You-
dc.contributor.authorKamagata, Yoichi-
dc.contributor.authorNobu, Masaru K-
dc.contributor.authorZhang, Tong-
dc.date.accessioned2025-01-25T00:35:26Z-
dc.date.available2025-01-25T00:35:26Z-
dc.date.issued2024-07-05-
dc.identifier.citationMicrobiome, 2024, v. 12, n. 1-
dc.identifier.issn2049-2618-
dc.identifier.urihttp://hdl.handle.net/10722/353810-
dc.description.abstract<h3>Background</h3><p>Despite rapid advances in genomic-resolved metagenomics and remarkable explosion of metagenome-assembled genomes (MAGs), the function of uncultivated anaerobic lineages and their interactions in carbon mineralization remain largely uncertain, which has profound implications in biotechnology and biogeochemistry.</p><h3>Results</h3><p>In this study, we combined long-read sequencing and metatranscriptomics-guided metabolic reconstruction to provide a genome-wide perspective of carbon mineralization flow from polymers to methane in an anaerobic bioreactor. Our results showed that incorporating long reads resulted in a substantial improvement in the quality of metagenomic assemblies, enabling the effective recovery of 132 high-quality genomes meeting stringent criteria of minimum information about a metagenome-assembled genome (MIMAG). In addition, hybrid assembly obtained 51% more prokaryotic genes in comparison to the short-read-only assembly. Metatranscriptomics-guided metabolic reconstruction unveiled the remarkable metabolic flexibility of several novel <em>Bacteroidales</em>-affiliated bacteria and populations from <em>Mesotoga</em> sp. in scavenging amino acids and sugars. In addition to recovering two circular genomes of previously known but fragmented syntrophic bacteria, two newly identified bacteria within <em>Syntrophales</em> were found to be highly engaged in fatty acid oxidation through syntrophic relationships with dominant methanogens <em>Methanoregulaceae</em> bin.74 and <em>Methanothrix</em> sp. bin.206. The activity of bin.206 preferring acetate as substrate exceeded that of bin.74 with increasing loading, reinforcing the substrate determinantal role.</p><h3>Conclusion</h3><p>Overall, our study uncovered some key active anaerobic lineages and their metabolic functions in this complex anaerobic ecosystem, offering a framework for understanding carbon transformations in anaerobic digestion. These findings advance the understanding of metabolic activities and trophic interactions between anaerobic guilds, providing foundational insights into carbon flux within both engineered and natural ecosystems.</p>-
dc.languageeng-
dc.publisherBioMed Central-
dc.relation.ispartofMicrobiome-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAnaerobic digestion-
dc.subjectLong reads-
dc.subjectOmics-
dc.subjectReverse electron transfer-
dc.subjectSyntrophic bacteria-
dc.titleMetatranscriptomics-guided genome-scale metabolic reconstruction reveals the carbon flux and trophic interaction in methanogenic communities-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s40168-024-01830-z-
dc.identifier.scopuseid_2-s2.0-85197801216-
dc.identifier.volume12-
dc.identifier.issue1-
dc.identifier.eissn2049-2618-
dc.identifier.isiWOS:001262971000001-
dc.identifier.issnl2049-2618-

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