Evidence map›Paper›PMID 29222443›Full record

ArticleThe ISME journal2018

Metabolic versatility of small archaea Micrarchaeota and Parvarchaeota.

Lin-Xing Chen, Celia Méndez-García, Nina Dombrowski, Luis E Servín-Garcidueñas, Emiley A Eloe-Fadrosh, Bao-Zhu Fang, Zhen-Hao Luo, Sha Tan, Xiao-Yang Zhi, Zheng-Shuang Hua and 8 more

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 135 citations in OpenAlex.

  1. Article
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  3. Diversity of Archaea.Progress in molecular and subcellular biology · 2026
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  9. Resilience of deep aquifer microbial communities to seasonal hydrological fluctuations.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  15. Article
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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

18 authors at 10 institutions in 5 countries.

Lin-Xing ChenState Key Laboratory of Biocontrol, Guangdong Key Laboratory of Plant Resources, College of Ecology and Evolution, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.ORCID http://orcid.org/0000-0003-2774-1952
Celia Méndez-GarcíaDepartamento de Biología Funcional-IUBA, Universidad de Oviedo, Oviedo, Spain.ORCID http://orcid.org/0000-0002-8587-0114
Nina DombrowskiDepartment of Marine Science, University of Texas Austin, Marine Science Institute, Port Aransas, TX, 78373, USA.ORCID http://orcid.org/0000-0003-1917-2577
Luis E Servín-GarcidueñasLaboratory of Microbiomics, National School of Higher Studies Morelia, National University of Mexico, Morelia, Michoacan, 58190, Mexico.
Emiley A Eloe-FadroshDepartment of Energy Joint Genome Institute, Walnut Creek, CA, 94598, USA.
Bao-Zhu FangState Key Laboratory of Biocontrol, Guangdong Key Laboratory of Plant Resources, College of Ecology and Evolution, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Zhen-Hao LuoState Key Laboratory of Biocontrol, Guangdong Key Laboratory of Plant Resources, College of Ecology and Evolution, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Sha TanState Key Laboratory of Biocontrol, Guangdong Key Laboratory of Plant Resources, College of Ecology and Evolution, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Xiao-Yang ZhiYunnan Institute of Microbiology, Yunnan University, Kunming, 650091, People's Republic of China.
Zheng-Shuang HuaState Key Laboratory of Biocontrol, Guangdong Key Laboratory of Plant Resources, College of Ecology and Evolution, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Esperanza Martinez-RomeroDepartment of Ecological Genomics, Center for Genomic Sciences, National University of Mexico, Cuernavaca, Morelos, 62210, Mexico.
Tanja WoykeDepartment of Energy Joint Genome Institute, Walnut Creek, CA, 94598, USA.
Li-Nan HuangState Key Laboratory of Biocontrol, Guangdong Key Laboratory of Plant Resources, College of Ecology and Evolution, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Jesús SánchezDepartamento de Biología Funcional-IUBA, Universidad de Oviedo, Oviedo, Spain.
Ana Isabel PeláezDepartamento de Biología Funcional-IUBA, Universidad de Oviedo, Oviedo, Spain.
Manuel FerrerInstitute of Catalysis, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Brett J BakerDepartment of Marine Science, University of Texas Austin, Marine Science Institute, Port Aransas, TX, 78373, USA. acidophile@gmail.com.
Wen-Sheng ShuSchool of Life Sciences, South China Normal University, Guangzhou, 510631, People's Republic of China. shuws@mail.sysu.edu.cn.
Sun Yat-sen University · CNIstituto di Scienze Marine del Consiglio Nazionale delle Ricerche · ITJoint Genome Institute · USUniversidad de Oviedo · ESConsejo Superior de Investigaciones Científicas · ESNational Institute of Genomic Medicine · MXSouth China Normal University · CNUniversidad de Morelia · MXUniversity of Illinois Urbana-Champaign · USYunnan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small acidophilic archaea belonging to Micrarchaeota and Parvarchaeota phyla are known to physically interact with some Thermoplasmatales members in nature. However, due to a lack of cultivation and limited genomes on hand, their biodiversity, metabolisms, and physiologies remain largely unresolved. Here, we obtained 39 genomes from acid mine drainage (AMD) and hot spring environments around the world. 16S rRNA gene based analyses revealed that Parvarchaeota were only detected in AMD and hot spring habitats, while Micrarchaeota were also detected in others including soil, peat, hypersaline mat, and freshwater, suggesting a considerable higher diversity and broader than expected habitat distribution for this phylum. Despite their small genomes (0.64-1.08 Mb), these archaea may contribute to carbon and nitrogen cycling by degrading multiple saccharides and proteins, and produce ATP via aerobic respiration and fermentation. Additionally, we identified several syntenic genes with homology to those involved in iron oxidation in six Parvarchaeota genomes, suggesting their potential role in iron cycling. However, both phyla lack biosynthetic pathways for amino acids and nucleotides, suggesting that they likely scavenge these biomolecules from the environment and/or other community members. Moreover, low-oxygen enrichments in laboratory confirmed our speculation that both phyla are microaerobic/anaerobic, based on several specific genes identified in them. Furthermore, phylogenetic analyses provide insights into the close evolutionary history of energy related functionalities between both phyla with Thermoplasmatales. These results expand our understanding of these elusive archaea by revealing their involvement in carbon, nitrogen, and iron cycling, and suggest their potential interactions with Thermoplasmatales on genomic scale.

Indexed as

Amino AcidsArchaeaBiodiversityBiological EvolutionCarbonFresh WaterGenome, ArchaealGenomicsHot SpringsIronNitrogenNitrogen CyclePhylogenyRNA, Ribosomal, 16SAmino AcidsCarbonIronNitrogenRNA, Ribosomal, 16S

Identifiers

PMID29222443
PMCPMC5864196
OpenAlexW2771168186

What OpenQuestion holds

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LicenceCC BY
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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.