Evidence map›Paper›PMID 31462715›Full record

ArticleThe ISME journal2019

Expansion of Thaumarchaeota habitat range is correlated with horizontal transfer of ATPase operons.

Baozhan Wang, Wei Qin, Yi Ren, Xue Zhou, Man-Young Jung, Ping Han, Emiley A Eloe-Fadrosh, Meng Li, Yue Zheng, Lu Lu and 15 more

Abstract read
In one paragraph

Article in The ISME journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

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  8. DPANN Archaea and CPR Bacteria: insights into early cellular evolution?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
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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

25 authors.

Baozhan Wang *State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China.
Wei Qin *School of Oceanography, University of Washington, Seattle, WA, USA.
Yi Ren *Shanghai Majorbio Bio-pharm Biotechnology Co., Ltd, Shanghai, China.
Xue ZhouState Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China.
Man-Young JungCentre for Microbiology and Environmental Systems Science, Department of Microbiology and Ecosystem Science, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-5244-5197
Ping HanCentre for Microbiology and Environmental Systems Science, Department of Microbiology and Ecosystem Science, University of Vienna, Vienna, Austria.
Emiley A Eloe-FadroshMarine Biology Research Division, Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-8162-1276
Meng LiInstitute for Advanced Study, Shenzhen University, Shenzhen, China.
Yue ZhengCAS Key Laboratory of Urban Pollutant Conversion, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen, China.
Lu LuState Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China.
Xin YanCollege of Life Sciences, Nanjing Agricultural University, Nanjing, China.
Junbin JiCollege of Life Sciences, Nanjing Agricultural University, Nanjing, China.
Yang LiuInstitute for Advanced Study, Shenzhen University, Shenzhen, China.
Linmeng LiuShanghai Majorbio Bio-pharm Biotechnology Co., Ltd, Shanghai, China.
Cheryl HeinerPacific Biosciences, Menlo Park, CA, USA.
Richard HallPacific Biosciences, Menlo Park, CA, USA.
Willm Martens-HabbenaDepartment of Microbiology and Cell Science & Fort Lauderdale Research and Education Center, University of Florida, Gainesville, FL, USA.
Craig W HerboldCentre for Microbiology and Environmental Systems Science, Department of Microbiology and Ecosystem Science, University of Vienna, Vienna, Austria.
Sung-Keun RheeDepartment of Microbiology, Chungbuk National University, Cheongju, South Korea.
Douglas H BartlettMarine Biology Research Division, Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA, USA.
Li HuangState Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Anitra E IngallsSchool of Oceanography, University of Washington, Seattle, WA, USA.
Michael WagnerCentre for Microbiology and Environmental Systems Science, Department of Microbiology and Ecosystem Science, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-9778-7684
David A StahlDepartment of Civil and Environmental Engineering, University of Washington, Seattle, WA, USA.
Zhongjun JiaState Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China. Jia@issas.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thaumarchaeota are responsible for a significant fraction of ammonia oxidation in the oceans and in soils that range from alkaline to acidic. However, the adaptive mechanisms underpinning their habitat expansion remain poorly understood. Here we show that expansion into acidic soils and the high pressures of the hadopelagic zone of the oceans is tightly linked to the acquisition of a variant of the energy-yielding ATPases via horizontal transfer. Whereas the ATPase genealogy of neutrophilic Thaumarchaeota is congruent with their organismal genealogy inferred from concatenated conserved proteins, a common clade of V-type ATPases unites phylogenetically distinct clades of acidophilic/acid-tolerant and piezophilic/piezotolerant species. A presumptive function of pumping cytoplasmic protons at low pH is consistent with the experimentally observed increased expression of the V-ATPase in an acid-tolerant thaumarchaeote at low pH. Consistently, heterologous expression of the thaumarchaeotal V-ATPase significantly increased the growth rate of E. coli at low pH. Its adaptive significance to growth in ocean trenches may relate to pressure-related changes in membrane structure in which this complex molecular machine must function. Together, our findings reveal that the habitat expansion of Thaumarchaeota is tightly correlated with extensive horizontal transfer of atp operons.

Indexed as

Gene Transfer, HorizontalOperonAdenosine TriphosphatasesAmmonium CompoundsArchaeaArchaeal ProteinsEcosystemEscherichia coliHydrogen-Ion ConcentrationOxidation-ReductionPhylogenySoil MicrobiologyAdenosine TriphosphatasesAmmonium CompoundsArchaeal Proteins

Identifiers

PMID31462715
PMCPMC6863869

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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.