Evidence map›Paper›PMID 35810262›Full record

ArticleThe ISME journal2022

Expanding the phylogenetic distribution of cytochrome b-containing methanogenic archaea sheds light on the evolution of methanogenesis.

Ya-Fei Ou, Hong-Po Dong, Simon J McIlroy, Sean A Crowe, Steven J Hallam, Ping Han, Jens Kallmeyer, Rachel L Simister, Aurele Vuillemin, Andy O Leu and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  4. Targeted isolation of HNature protocols · 2026
    Review
  5. Diversity of Archaea.Progress in molecular and subcellular biology · 2026
    Review
  6. Article
  7. International journal of systematic and evolutionary microbiology · 2025
    Article
  8. International journal of systematic and evolutionary microbiology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Electron transport chains as a window into the earliest stages of evolution.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 5 countries.

Ya-Fei Ou *State Key Laboratory of Estuarine and Coastal Research, East China Normal University, Shanghai, 200241, China.
Hong-Po Dong *State Key Laboratory of Estuarine and Coastal Research, East China Normal University, Shanghai, 200241, China. hpdong@sklec.ecnu.edu.cn.ORCID http://orcid.org/0000-0002-7172-794X
Simon J McIlroyCentre for Microbiome Research, School of Biomedical Sciences, Queensland University of Technology (QUT), Translational Research Institute, Woolloongabba, QLD, 4102, Australia.
Sean A CroweEcosystem Services, Commercialization Platforms, and Entrepreneurship (ECOSCOPE) Training Program, University of British Columbia, Vancouver, BC, Canada.ORCID http://orcid.org/0000-0001-8071-2144
Steven J HallamDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, BC, Canada.ORCID http://orcid.org/0000-0002-4889-6876
Ping HanKey Laboratory of Geographic Information Science, Ministry of Education, East China Normal University, Shanghai, 200241, China.ORCID http://orcid.org/0000-0001-6025-1651
Jens KallmeyerGFZ German Research Centre for Geosciences, Section Geomicrobiology, Potsdam, Germany.
Rachel L SimisterEcosystem Services, Commercialization Platforms, and Entrepreneurship (ECOSCOPE) Training Program, University of British Columbia, Vancouver, BC, Canada.ORCID http://orcid.org/0000-0002-9807-8652
Aurele VuilleminGFZ German Research Centre for Geosciences, Section Geomicrobiology, Potsdam, Germany.ORCID http://orcid.org/0000-0002-7724-8931
Andy O LeuCentre for Microbiome Research, School of Biomedical Sciences, Queensland University of Technology (QUT), Translational Research Institute, Woolloongabba, QLD, 4102, Australia.
Zhanfei LiuMarine Science Institute, The University of Texas at Austin, Port Aransas, TX, 78373, USA.
Yan-Ling ZhengKey Laboratory of Geographic Information Science, Ministry of Education, East China Normal University, Shanghai, 200241, China.ORCID http://orcid.org/0000-0002-8041-2843
Qian-Li SunState Key Laboratory of Estuarine and Coastal Research, East China Normal University, Shanghai, 200241, China.
Min LiuKey Laboratory of Geographic Information Science, Ministry of Education, East China Normal University, Shanghai, 200241, China.
Gene W TysonCentre for Microbiome Research, School of Biomedical Sciences, Queensland University of Technology (QUT), Translational Research Institute, Woolloongabba, QLD, 4102, Australia.ORCID http://orcid.org/0000-0001-8559-9427
Li-Jun HouState Key Laboratory of Estuarine and Coastal Research, East China Normal University, Shanghai, 200241, China. ljhou@sklec.ecnu.edu.cn.ORCID http://orcid.org/0000-0002-5001-1707
Shanghai Estuarine & Coastal Science Research Center · CNEast China Normal University · CNTranslational Research Institute · AUUniversity of British Columbia · CAGFZ Helmholtz Centre for Geosciences · DEThe University of Texas at Austin · US

Funding

National Natural Science Foundation of China (National Science Foundation of China) 41725002National Natural Science Foundation of China (National Science Foundation of China) 42030411
6 · The paper itself

Abstract

Methane produced by methanogenic archaea has an important influence on Earth's changing climate. Methanogenic archaea are phylogenetically diverse and widespread in anoxic environments. These microorganisms can be divided into two subgroups based on whether or not they use b-type cytochromes for energy conservation. Methanogens with b-type cytochromes have a wider substrate range and higher growth yields than those without them. To date, methanogens with b-type cytochromes were found exclusively in the phylum "Ca. Halobacteriota" (formerly part of the phylum Euryarchaeota). Here, we present the discovery of metagenome-assembled genomes harboring methyl-coenzyme M reductase genes reconstructed from mesophilic anoxic sediments, together with the previously reported thermophilic "Ca. Methylarchaeum tengchongensis", representing a novel archaeal order, designated the "Ca. Methylarchaeales", of the phylum Thermoproteota (formerly the TACK superphylum). These microorganisms contain genes required for methyl-reducing methanogenesis and the Wood-Ljundahl pathway. Importantly, the genus "Ca. Methanotowutia" of the "Ca. Methylarchaeales" encode a cytochrome b-containing heterodisulfide reductase (HdrDE) and methanophenazine-reducing hydrogenase complex that have similar gene arrangements to those found in methanogenic Methanosarcinales. Our results indicate that members of the "Ca. Methylarchaeales" are methanogens with cytochromes and can conserve energy via membrane-bound electron transport chains. Phylogenetic and amalgamated likelihood estimation analyses indicate that methanogens with cytochrome b-containing electron transfer complexes likely evolved before diversification of Thermoproteota or "Ca. Halobacteriota" in the early Archean Eon. Surveys of public sequence databases suggest that members of the lineage are globally distributed in anoxic sediments and may be important players in the methane cycle.

Indexed as

EuryarchaeotaHydrogenaseArchaeaCytochromesCytochromes bMethanePhylogenyCytochromesCytochromes bHydrogenaseMethane

Identifiers

PMID35810262
PMCPMC9478090
OpenAlexW4284975309

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.