Evidence map›Paper›PMID 40569035›Full record

ArticleThe ISME journal2025

Cell type-specific immune regulation under symbiosis in a facultatively symbiotic coral.

Maria Valadez-Ingersoll, Hanny E Rivera, Jeric Da-Anoy, Matthew R Kanke, Kelly Gomez-Campo, M Isabel Martinez Rugerio, Sebastian Metz, Michael Sweet, Julian Kwan, Ryan Hekman and 3 more

Abstract read
In one paragraph

Article in The ISME journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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

13 authors.

Maria Valadez-IngersollDepartment of Biology, Boston University, Boston, MA 02215, United States.ORCID 0000-0002-2884-5350
Hanny E RiveraDepartment of Biology, Boston University, Boston, MA 02215, United States.ORCID 0000-0003-4747-1339
Jeric Da-AnoyDepartment of Biology, Boston University, Boston, MA 02215, United States.ORCID 0000-0002-9342-7200
Matthew R KankeAmgen, Research Biomics, South San Francisco, CA 94080, United States.ORCID 0000-0002-7227-3054
Kelly Gomez-CampoDepartment of Biology, State College, Pennsylvania State University, PA 16801, United States.ORCID 0000-0003-4560-111X
M Isabel Martinez RugerioDepartment of Biology, State College, Pennsylvania State University, PA 16801, United States.ORCID 0000-0001-9860-1207
Sebastian MetzAquatic Research Facility, Nature-based Solutions Research Centre, University of Derby, Derby, United Kingdom.
Michael SweetAquatic Research Facility, Nature-based Solutions Research Centre, University of Derby, Derby, United Kingdom.
Julian KwanDepartment of Biochemistry, Boston University Chobanian & Avedisian School of Medicine, Boston, MA 02118, United States.ORCID 0000-0002-9199-1828
Ryan HekmanDepartment of Biochemistry, Boston University Chobanian & Avedisian School of Medicine, Boston, MA 02118, United States.
Andrew EmiliDepartment of Biology, Boston University, Boston, MA 02215, United States.ORCID 0000-0001-8995-246X
Thomas D GilmoreDepartment of Biology, Boston University, Boston, MA 02215, United States.ORCID 0000-0002-1910-768X
Sarah W DaviesDepartment of Biology, Boston University, Boston, MA 02215, United States.ORCID 0000-0002-1620-2278

Funding

National Science Foundation Graduate Research Fellowship and a National Science Foundation NRT DGE 1735087Wellcome Trust
6 · The paper itself

Abstract

Many cnidarians host single-celled algae within gastrodermal cells, yielding a mutually beneficial exchange of nutrients between host and symbiont, and dysbiosis can lead to host mortality. Previous research has uncovered symbiosis tradeoffs, including suppression of immune pathways in hosts, and correlations between symbiotic state and pathogen susceptibility. Here, we used a multiomic approach to characterize symbiotic states of the facultatively symbiotic coral Oculina arbuscula by generating genotype-controlled fragments of symbiotic and aposymbiotic tissue. 16S rRNA gene sequencing showed no difference in bacterial communities between symbiotic states. Whole-organism proteomics revealed differential abundance of proteins related to immunity, confirming immune suppression during symbiosis. Single-cell RNAseq identified diverse cell clusters within seven cell types across symbiotic states. Specifically, the gastrodermal cell clusters containing algal-hosting cells from symbiotic tissue had higher expression of nitrogen cycling and lipid metabolism genes than aposymbiotic gastrodermal cells. Furthermore, differential enrichment of immune system gene pathways and lower expression of genes involved in immune regulation were observed in these gastrodermal cells from symbiotic tissue. However, there were no differences in gene expression in the immune cell cluster between symbiotic states. We conclude that there is evidence for compartmentalization of immune system regulation in specific gastrodermal cells in symbiosis. This compartmentalization may limit symbiosis tradeoffs by dampening immunity in algal-hosting cells while simultaneously maintaining general organismal immunity.

Indexed as

AnthozoaSymbiosisAnimalsProteomicsRNA, Ribosomal, 16SRNA, Ribosomal, 16Scoralimmunityproteomicssingle-cell RNA-sequencingsymbiosis

Identifiers

PMID40569035
PMCPMC12278269

What OpenQuestion holds

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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 OpenQuestion graph.