Evidence map›Paper›PMID 34996355›Full record

ArticleBMC ecology and evolution2022

Cardiac physiology and metabolic gene expression during late organogenesis among F. heteroclitus embryo families from crosses between pollution-sensitive and -resistant parents.

Goran Bozinovic, Zuying Feng, Damian Shea, Marjorie F Oleksiak

Open access · goldAbstract read
In one paragraph

Article in BMC ecology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Goran BozinovicBoz Life Science Research and Teaching Institute, San Diego, CA, USA. gbozinovic@ucsd.edu.ORCID 0000-0001-8934-7884
Zuying FengBoz Life Science Research and Teaching Institute, San Diego, CA, USA.
Damian SheaDepartment of Biological Sciences, North Carolina State University, Raleigh, NC, USA.
Marjorie F OleksiakDepartment of Biological Sciences, North Carolina State University, Raleigh, NC, USA.
Fleet Science Center · USNorth Carolina State University · US

Funding

Zebrafish as a Detector of Organophosphate ExposureP42ES010356 · NIEHS · DUKE UNIVERSITY · PI AMY H HERRING · 2000 to 2026
$56.2M
Training CoreP42ES007381 · NIEHS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MONTI, STEFANO · 1995 to 2019
$46.1M
Microarray Analyses of Polluted Natural PopulationsR01ES011588 · NIEHS · UNIVERSITY OF MIAMI ROSENTEIL SCHOOL · PI OLEKSIAK, MARJORIE F · 2004 to 2008
$1.5M
NIEHS NIH HHS P42 ES007381NIEHS NIH HHS P42 ES010356NIEHS NIH HHS R01 ES011588NIH HHS 2P42 ES010356NIH HHS P42 ES007381NIH HHS R01 ES011588
6 · The paper itself

Abstract

backgroundThe teleost fish Fundulus heteroclitus inhabit estuaries heavily polluted with persistent and bioaccumulative chemicals. While embryos of parents from polluted sites are remarkably resistant to toxic sediment and develop normally, embryos of parents from relatively clean estuaries, when treated with polluted sediment extracts, are developmentally delayed, displaying deformities characteristic of pollution-induced embryotoxicity. To gain insight into parental effects on sensitive and resistant phenotypes during late organogenesis, we established sensitive, resistant, and crossed embryo families using five female and five male parents from relatively clean and predominantly PAH-polluted estuaries each, measured heart rates, and quantified individual embryo expression of 179 metabolic genes.

resultsPollution-induced embryotoxicity manifested as morphological deformities, significant developmental delays, and altered cardiac physiology was evident among sensitive embryos resulting from crosses between females and males from relatively clean estuaries. Significantly different heart rates among several geographically unrelated populations of sensitive, resistant, and crossed embryo families during late organogenesis and pre-hatching suggest site-specific adaptive cardiac physiology phenotypes relative to pollution exposure. Metabolic gene expression patterns (32 genes, 17.9%, at p < 0.05; 11 genes, 6.1%, at p < 0.01) among the embryo families indicate maternal pollutant deposition in the eggs and parental effects on gene expression and metabolic alterations.

conclusionHeart rate differences among sensitive, resistant, and crossed embryos is a reliable phenotype for further explorations of adaptive mechanisms. While metabolic gene expression patterns among embryo families are suggestive of parental effects on several differentially expressed genes, a definitive adaptive signature and metabolic cost of resistant phenotypes is unclear and shows unexpected sensitive-resistant crossed embryo expression profiles. Our study highlights physiological and metabolic gene expression differences during a critical embryonic stage among pollution sensitive, resistant, and crossed embryo families, which may contribute to underlying resistance mechanisms observed in natural F. heteroclitus populations living in heavily contaminated estuaries.

Indexed as

FundulidaeWater Pollutants, ChemicalAnimalsEmbryo, NonmammalianFemaleGene ExpressionHumansMaleOrganogenesisWater Pollutants, ChemicalAdaptationDevelopmentGene expressionHeart physiologyMetabolism

Identifiers

PMID34996355
PMCPMC8739662
OpenAlexW4206667546

What Socratic holds

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LicenceCC BY
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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 Socratic graph.