Evidence map›Paper›PMID 29053148›Full record

ArticleThe ISME journal2018

Stress response of a marine ammonia-oxidizing archaeon informs physiological status of environmental populations.

Wei Qin, Shady A Amin, Rachel A Lundeen, Katherine R Heal, Willm Martens-Habbena, Serdar Turkarslan, Hidetoshi Urakawa, Kyle C Costa, Erik L Hendrickson, Tony Wang and 16 more

Abstract 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 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Ocean warming enhances iron use efficiencies of marine ammonia-oxidizing archaea.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Exploring proteinmBio · 2025
    Article
  8. Article
  9. Cyclization of archaeal membrane lipids impacts membrane protein activity and archaellum formation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Adaptive traits ofmBio · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

26 authors.

Wei QinDepartment of Civil and Environmental Engineering, University of Washington, Seattle, WA, USA.
Shady A AminDepartment of Biology, New York University Abu Dhabi, Abu Dhabi, UAE.
Rachel A LundeenSchool of Oceanography, University of Washington, Seattle, WA, USA.
Katherine R HealSchool of Oceanography, University of Washington, Seattle, WA, USA.
Willm Martens-HabbenaDepartment of Microbiology and Cell Science & Fort Lauderdale Research and Education Center, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL, USA.
Serdar TurkarslanInstitute for Systems Biology, Seattle, WA, USA.
Hidetoshi UrakawaDepartment of Marine and Ecological Sciences, Florida Gulf Coast University, Fort Myers, FL, USA.ORCID 0000-0003-3748-6027
Kyle C CostaDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Erik L HendricksonDepartment of Chemical Engineering and Center for Microbial Proteomics, University of Washington, Seattle, WA, USA.
Tony WangDepartment of Chemical Engineering and Center for Microbial Proteomics, University of Washington, Seattle, WA, USA.
David Ac BeckDepartment of Chemical Engineering and eScience Institute, University of Washington, Seattle, WA, USA.
Sonia M Tiquia-ArashiroDepartment of Natural Sciences, University of Michigan, Dearborn, MI, USA.
Fred TaubDepartment of Chemical Engineering and Center for Microbial Proteomics, University of Washington, Seattle, WA, USA.
Andrew D HolmesDepartment of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA, USA.
Neeraja VajralaBotany and Plant Pathology, Oregon State University, Corvallis, OR, USA.
Paul M BerubeDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Todd M LoweDepartment of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA, USA.
James W MoffettDepartments of Biological Sciences and Earth Sciences and Civil and Environmental Engineering, University of Southern California, Los Angeles, CA, USA.
Allan H DevolSchool of Oceanography, University of Washington, Seattle, WA, USA.
Nitin S BaligaInstitute for Systems Biology, Seattle, WA, USA.
Daniel J ArpBotany and Plant Pathology, Oregon State University, Corvallis, OR, USA.
Luis A Sayavedra-SotoBotany and Plant Pathology, Oregon State University, Corvallis, OR, USA.
Murray HackettDepartment of Chemical Engineering and Center for Microbial Proteomics, University of Washington, Seattle, WA, USA.
E Virginia ArmbrustSchool of Oceanography, University of Washington, Seattle, WA, USA.
Anitra E IngallsSchool of Oceanography, University of Washington, Seattle, WA, USA.
David A StahlDepartment of Civil and Environmental Engineering, University of Washington, Seattle, WA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High representation by ammonia-oxidizing archaea (AOA) in marine systems is consistent with their high affinity for ammonia, efficient carbon fixation, and copper (Cu)-centric respiratory system. However, little is known about their response to nutrient stress. We therefore used global transcriptional and proteomic analyses to characterize the response of a model AOA, Nitrosopumilus maritimus SCM1, to ammonia starvation, Cu limitation and Cu excess. Most predicted protein-coding genes were transcribed in exponentially growing cells, and of ~74% detected in the proteome, ~6% were modified by N-terminal acetylation. The general response to ammonia starvation and Cu stress was downregulation of genes for energy generation and biosynthesis. Cells rapidly depleted transcripts for the A and B subunits of ammonia monooxygenase (AMO) in response to ammonia starvation, yet retained relatively high levels of transcripts for the C subunit. Thus, similar to ammonia-oxidizing bacteria, selective retention of amoC transcripts during starvation appears important for subsequent recovery, and also suggests that AMO subunit transcript ratios could be used to assess the physiological status of marine populations. Unexpectedly, cobalamin biosynthesis was upregulated in response to both ammonia starvation and Cu stress, indicating the importance of this cofactor in retaining functional integrity during times of stress.

Indexed as

Stress, PhysiologicalAmmoniaArchaeaArchaeal ProteinsCarbon CycleCopperOxidation-ReductionOxidoreductasesProteomicsTranscriptomeVitamin B 12Water MicrobiologyAmmoniaammonia monooxygenaseArchaeal ProteinsCopperOxidoreductasesVitamin B 12

Identifiers

PMID29053148
PMCPMC5776466

What OpenQuestion holds

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Read underepoch 390

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.