Integrated transcriptomic and metabolomic analysis reveals the response of pearl oyster (Pinctada fucata martensii) to long-term hypoxia.

Hypoxic stress Metabolome Pearl oyster Transcriptome

Journal

Marine environmental research
ISSN: 1879-0291
Titre abrégé: Mar Environ Res
Pays: England
ID NLM: 9882895

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 07 04 2023
revised: 27 07 2023
accepted: 09 08 2023
pubmed: 17 8 2023
medline: 17 8 2023
entrez: 16 8 2023
Statut: ppublish

Résumé

The frequency at which organisms are exposed to hypoxic conditions in aquatic environments is increasing due to coastal eutrophication and global warming. To reveal the effects of long-term hypoxic stress on metabolic changes of pearl oyster, commonly known as Pinctada (Pinctada fucata martensii), the present study performed the integrated analysis of transcriptomics and metabolomics to investigate the global changes of genes and metabolites following 25 days hypoxia challenge. Transcriptome analysis detected 1108 differentially expressed genes (DEGs) between the control group and the hypoxia group. The gene ontology (GO) analysis of DEGs revealed that they are significantly enriched in functions such as "microtubule-based process", "histone (H3-K4, H3-K27, and H4-K20) trimethylation", "histone H4 acetylation", "kinesin complex", and "ATPase activity", and KEGG pathway functions, such as "DNA replication", "Apoptosis", and "MAPK signaling pathways". Metabolome analysis identified 68 significantly different metabolites from all identified metabolites, and associated with 25 metabolic pathways between the control and hypoxia groups. These pathways included aminoacyl-tRNA biosynthesis, arginine and proline metabolism, and phenylalanine metabolism. Our integrated analysis suggested that pearl oysters were subject to oxidative stress, apoptosis, immune inhibition, and neuronal excitability reduction under long-term hypoxic conditions. We also found a remarkable depression in a variety of biological functions under long-term hypoxia, including metabolic rates, biomineralization activities, and the repression of reorganization of the cytoskeleton and cell metabolism. These findings provide a basis for elucidating the mechanisms used by marine bivalves to cope with long-term hypoxic stress.

Identifiants

pubmed: 37586225
pii: S0141-1136(23)00261-1
doi: 10.1016/j.marenvres.2023.106133
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106133

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing interest No conflicts of interest, financial or otherwise, are declared by the authors.

Auteurs

Chuangye Yang (C)

Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.

Hailing Wu (H)

Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.

Jiayi Chen (J)

Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.

Yongshan Liao (Y)

Guangdong Science and Innovation Center for Pearl Culture, Zhanjiang, 524088, China; Pearl Breeding and Processing Engineering Technology Research Centre of Guangdong Province, Zhanjiang, 524088, China.

Robert Mkuye (R)

Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.

Yuewen Deng (Y)

Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China; Guangdong Science and Innovation Center for Pearl Culture, Zhanjiang, 524088, China; Pearl Breeding and Processing Engineering Technology Research Centre of Guangdong Province, Zhanjiang, 524088, China; Guangdong Provincial Key Laboratory of Aquatic Animal Disease Control and Healthy Culture, Zhanjiang, 524088, China; Guangdong Marine Ecology Early Warning and Monitoring Laboratory, Zhanjiang, 524088, China. Electronic address: dengyw@gdou.edu.cn.

Xiaodong Du (X)

Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.

Classifications MeSH