Evidence map›Paper›PMID 42853848›Full record

ArticlePloS one2026

Gene transcriptional profiling of osmoregulatory stress response in salmonids: Development and assessment of high-throughput multispecies assays.

Nicolas Tugui, Shahinur S Islam, Daniel D Heath

Abstract read
In one paragraph

Article in PloS one, 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
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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

3 authors.

Nicolas TuguiDepartment of Biology, University of Windsor, Ontario, Canada.
Shahinur S IslamGreat Lakes Institute for Environmental Research, University of Windsor, Ontario, Canada.ORCID https://orcid.org/0000-0001-8475-3381
Daniel D HeathDepartment of Biology, University of Windsor, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osmoregulatory stress is a critical factor in the welfare and performance of salmonids under captive rearing for aquaculture and conservation, and characterizing cellular responses to that stress may foster better husbandry. One approach for early detection of osmotic stress is gene transcriptional profiling, where a suite of qPCR assays designed for related-function genes is used to determine patterns of transcriptional responses to stress. This study describes the development, assessment and application of 28 Taqman qPCR assays for use on the OpenArray® platform as an osmoregulatory stress transcriptional profiling (OSTP) chip. The assays include key genes involved in osmoregulation (twelve), stress response (four), immune function (five), growth/metabolism (four) and endogenous controls (three). Here, using gill and liver tissues from eight salmonid species across four genera, the OSTP chip's performance was evaluated. While results showed both tissue- and species-specific transcriptional differences, the OSTP chip has considerable utility for characterizing molecular stress responses. As a test application of the OSTP chip, we performed a 24-hour saltwater challenge with Chinook salmon and applied the chip to control and challenged fish. This test confirmed the OSTP chip's capacity to detect acute osmotic stress-induced molecular genetic signatures. This OSTP chip will be useful for aquaculture practices by fostering better husbandry as well as providing a valuable tool for future studies of the osmoregulatory response of salmonid fishes to environmental stress.

Indexed as

Gene Expression ProfilingOsmoregulationSalmonidaeStress, PhysiologicalAnimalsGillsLiver

Identifiers

PMID42853848
PMCPMC13652239

What OpenQuestion holds

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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.