Evidence map›Paper›PMID 27458440›Full record

ArticleFrontiers in microbiology2016

Diversity and Expression of Bacterial Metacaspases in an Aquatic Ecosystem.

Johannes Asplund-Samuelsson, John Sundh, Chris L Dupont, Andrew E Allen, John P McCrow, Narin A Celepli, Birgitta Bergman, Karolina Ininbergs, Martin Ekman

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.5field-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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Novel endolithic bacteria of phylumApplied and environmental microbiology · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

9 authors at 3 institutions in 2 countries.

Johannes Asplund-SamuelssonScience for Life Laboratory, Department of Ecology, Environment and Plant Sciences, Stockholm University Solna, Sweden.
John SundhScience for Life Laboratory, Department of Biology and Environmental Science, Linnaeus University Solna, Sweden.
Chris L DupontMicrobial and Environmental Genomics, J. Craig Venter Institute San Diego, CA, USA.
Andrew E AllenMicrobial and Environmental Genomics, J. Craig Venter Institute San Diego, CA, USA.
John P McCrowMicrobial and Environmental Genomics, J. Craig Venter Institute San Diego, CA, USA.
Narin A CelepliScience for Life Laboratory, Department of Ecology, Environment and Plant Sciences, Stockholm University Solna, Sweden.
Birgitta BergmanScience for Life Laboratory, Department of Ecology, Environment and Plant Sciences, Stockholm University Solna, Sweden.
Karolina IninbergsScience for Life Laboratory, Department of Ecology, Environment and Plant Sciences, Stockholm University Solna, Sweden.
Martin EkmanScience for Life Laboratory, Department of Ecology, Environment and Plant Sciences, Stockholm University Solna, Sweden.
J. Craig Venter Institute · USScience for Life Laboratory · SEStockholm University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metacaspases are distant homologs of metazoan caspase proteases, implicated in stress response, and programmed cell death (PCD) in bacteria and phytoplankton. While the few previous studies on metacaspases have relied on cultured organisms and sequenced genomes, no studies have focused on metacaspases in a natural setting. We here present data from the first microbial community-wide metacaspase survey; performed by querying metagenomic and metatranscriptomic datasets from the brackish Baltic Sea, a water body characterized by pronounced environmental gradients and periods of massive cyanobacterial blooms. Metacaspase genes were restricted to ~4% of the bacteria, taxonomically affiliated mainly to Bacteroidetes, Alpha- and Betaproteobacteria and Cyanobacteria. The gene abundance was significantly higher in larger or particle-associated bacteria (>0.8 μm), and filamentous Cyanobacteria dominated metacaspase gene expression throughout the bloom season. Distinct seasonal expression patterns were detected for the three metacaspase genes in Nodularia spumigena, one of the main bloom-formers. Clustering of normalized gene expression in combination with analyses of genomic and assembly data suggest functional diversification of these genes, and possible roles of the metacaspase genes related to stress responses, i.e., sulfur metabolism in connection to oxidative stress, and nutrient stress induced cellular differentiation. Co-expression of genes encoding metacaspases and nodularin toxin synthesis enzymes was also observed in Nodularia spumigena. The study shows that metacaspases represent an adaptation of potentially high importance for several key organisms in the Baltic Sea, most prominently Cyanobacteria, and open up for further exploration of their physiological roles in microbes and assessment of their ecological impact in aquatic habitats.

Indexed as

bacterial communitiesBaltic SeacaspasesCyanobacteriametacaspasesmetagenomicsmetatranscriptomicsNodularia spumigena

Identifiers

PMID27458440
PMCPMC4933709
OpenAlexW2461579438

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.