First transcriptome of the copepod Gladioferens pectinatus subjected to chronic contaminant exposures.


Journal

Aquatic toxicology (Amsterdam, Netherlands)
ISSN: 1879-1514
Titre abrégé: Aquat Toxicol
Pays: Netherlands
ID NLM: 8500246

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 27 08 2021
revised: 19 11 2021
accepted: 21 12 2021
pubmed: 31 12 2021
medline: 28 1 2022
entrez: 30 12 2021
Statut: ppublish

Résumé

Contaminants are often at low concentrations in ecosystems and their effects on exposed organisms can occur over long periods of time and across multiple generations. Alterations to subcellular mechanistic pathways in response to exposure to contaminants can provide insights into mechanisms of toxicity that methods measuring higher levels of biological may miss. Analysis of the whole transcriptome can identify novel mechanisms of action leading to impacts in exposed biota. The aim of this study was to characterise how exposures to copper, benzophenone and diclofenac across multiple generations altered molecular expression pathways in the marine copepod Gladioferens pectinatus. Results of the study demonstrated differential gene expression was observed in cultures exposure to diclofenac (569), copper (449) and benzophenone (59). Pathways linked to stress, growth, cellular and metabolic processes were altered by exposure to all three contaminants with genes associated with oxidative stress and xenobiotic regulation also impacted. Protein kinase functioning, cytochrome P450, transcription, skeletal muscle contraction/relaxation, mitochondrial phosphate translocator, protein synthesis and mitochondrial methylation were all differentially expressed with all three chemicals. The results of the study also suggested that using dimethyl sulfoxide as a dispersant influenced the transcriptome and future research may want to investigate it's use in molecular studies. Data generated in this study provides a first look at transcriptomic response of G. pectinatus exposed to contaminants across multiple generations, future research is needed to validate the identified biomarkers and link these results to apical responses such as population growth to demonstrate the predictive capacity of molecular tools.

Identifiants

pubmed: 34968986
pii: S0166-445X(21)00329-5
doi: 10.1016/j.aquatox.2021.106069
pii:
doi:

Substances chimiques

Water Pollutants, Chemical 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106069

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Andrew Barrick (A)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand. Electronic address: Andrew.barrick@cawthron.org.nz.

Olivier Laroche (O)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand.

Michael Boundy (M)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand.

John K Pearman (JK)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand.

Tanja Wiles (T)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand.

Juliette Butler (J)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand.

Xavier Pochon (X)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand; Institute of Marine Science, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.

Kirsty F Smith (KF)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand; School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.

Louis A Tremblay (LA)

Cawthron Institute, 98 Halifax Street East, Nelson 7010, New Zealand; School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.

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Classifications MeSH