Evidence map›Paper›PMID 42426580›Full record

ArticleEnvironmental microbiology reports2026

In Situ Bacterioplankton Growth Partitioning by High-Resolution Metatranscriptomics.

J Cesar Ignacio-Espinoza, Yuxuan Zou, Andrew Long, Shengwei Hou, David M Needham, Jed A Fuhrman

Abstract read
In one paragraph

Article in Environmental microbiology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

J Cesar Ignacio-EspinozaMarine and Environmental Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California, USA.ORCID https://orcid.org/0000-0001-9303-7504
Yuxuan ZouState Key Joint Laboratory of Environmental Simulation and Pollution Control, School of Environment, Beijing Normal University, Beijing, China.
Andrew LongMarine and Environmental Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California, USA.ORCID https://orcid.org/0000-0002-2003-4254
Shengwei HouMarine and Environmental Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California, USA.ORCID https://orcid.org/0000-0002-4474-7443
David M NeedhamMarine and Environmental Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California, USA.ORCID https://orcid.org/0000-0001-7257-2516
Jed A FuhrmanMarine and Environmental Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California, USA.ORCID https://orcid.org/0000-0002-2361-1985

Funding

Gordon and Betty Moore Foundation 3779National Natural Science Foundation of China 42276163National Natural Science Foundation of China 42476109Shenzhen Science and Technology Innovation Program JCYJ20220530115401003Simons Foundation 549943
6 · The paper itself

Abstract

Microbial communities are fundamental to marine trophic webs, elemental cycling and geochemical transformations. Yet we lack high phylogenetic resolution measurements or good indicators of how fast different taxa are actively growing in situ. Here, we use high temporal resolution transcriptomics to phylogenetically disentangle an index of growth before and after a short spring phytoplankton bloom, by quantifying the phylogenetic distribution of the expression of ftsZ, a gene encoding for a protein involved in cell division. We interpret the relative abundances of ftsZ transcripts as a general indicator of how growth was distributed amongst taxa. This expression was also compared to RNase P to estimate how each organism's transcriptional resources were allocated to replication versus other functions. During the time-series, we observed two distinct profiles: prior to and several days after the bloom, ftsZ expression was dominated by Synechococcales, Pelagibacterales and picoeukaryotes, and by Rhodobacterales, SAR92 and SAR86 as the bloom declined. Whilst similar successional patterns have been observed previously, our dataset extends these observations by resolving transcriptional and replication-associated activity at high temporal resolution, enabling the detection of disproportionate contributions during bloom development and turnover. Our approach is scalable and will inform conceptual and mechanistic models of planktonic food webs.

Indexed as

BacteriaPhytoplanktonPlanktonTranscriptomeBacterial ProteinsCytoskeletal ProteinsGene Expression ProfilingPhylogenyBacterial ProteinsCytoskeletal ProteinsFtsZ protein, Bacteria

Identifiers

PMID42426580
PMCPMC13349992

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.