Vitellogenin receptor and fatty acid profiles of individual lipid classes of oocytes from wild and captive-reared greater amberjack (Seriola dumerili) during the reproductive cycle.


Journal

Theriogenology
ISSN: 1879-3231
Titre abrégé: Theriogenology
Pays: United States
ID NLM: 0421510

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 29 03 2019
revised: 26 07 2019
accepted: 12 08 2019
pubmed: 30 8 2019
medline: 9 4 2020
entrez: 30 8 2019
Statut: ppublish

Résumé

The greater amberjack Seriola dumerili (Risso, 1810) is a large migratory pelagic fish occurring in tropical and temperate waters with a great potential for the world aquaculture industry. Previous studies showed that wild-caught female greater amberjack reared in sea cages and handled during the reproductive season, underwent extensive ovarian atresia. This atresia, however, was not related to an insufficient liver transcription or oocyte uptake of vitellogenin (Vtg). In the present study, the structure of two greater amberjack vitellogenin receptors, namely Vtgr (Lr8-) and Lrp13, was characterized. Moreover, vtgr and lrp13 gene expression and the fatty acid profiles of specific phospholipids and neutral lipids were compared in the ovaries of wild and captive-reared greater amberjack during different phases of the reproductive cycle (i.e. early gametogenesis, advanced gametogenesis and spawning). Ovarian vtgr and lrp13 transcription was more active during early gametogenesis, suggesting that vitellogenin receptor transcripts were synthesized by previtellogenic oocytes and remained in the cellular mRNA pool until oocytes resumed meiosis and entered into secondary growth (i.e. vitellogenesis). Rearing of wild-caught greater amberjack in captivity together with handling during the reproductive season was associated with a reduced vtgr and lrp13 transcription and with a diminished capacity of oocytes in the early phase of gametogenesis (primary oocyte growth) to enter into vitellogenesis. During early gametogenesis, remarkable differences in the fatty acid composition were observed between wild and captive-reared individuals: all phospholipids of captive fish displayed dramatic increases of saturates (16:0 and 18:0) and decreases of arachidonic acid (ARA) and docosahexaenoic acid (DHA). The present study confirms the susceptibility of greater amberjack reproductive function to handling stress and suggests that the consequent extensive atresia of vitellogenic follicles originated during the primary oocytes growth when the capacity of oocytes to synthesize vitellogenin receptors was reduced. The study also suggests that this reduced capacity was associated with an altered oocyte phospholipid fatty acid composition during early gametogenesis.

Identifiants

pubmed: 31465910
pii: S0093-691X(19)30354-1
doi: 10.1016/j.theriogenology.2019.08.014
pii:
doi:

Substances chimiques

Egg Proteins 0
Fatty Acids 0
Receptors, Cell Surface 0
vitellogenin receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

73-83

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Chrysovalentinos Pousis (C)

Department of Emergency and Organ Transplantation, Section of Veterinary Clinics and Animal Production, University of Bari Aldo Moro, S.P. per Casamassima km. 3, I-70010, Valenzano, Bari, Italy.

Covadonga Rodríguez (C)

Departamento de Biología Animal, Edafología y Geología, Facultad de Ciencias, Universidad de La Laguna, Avda. Astrofísico Francisco Sánchez s/n, La Laguna, Tenerife, 38071, Spain.

Pasquale De Ruvo (P)

Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari Aldo Moro, Via E. Orabona, 4-70124, Bari, Italy.

Caterina De Virgilio (C)

Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari Aldo Moro, Via E. Orabona, 4-70124, Bari, Italy.

José A Pérez (JA)

Departamento de Biología Animal, Edafología y Geología, Facultad de Ciencias, Universidad de La Laguna, Avda. Astrofísico Francisco Sánchez s/n, La Laguna, Tenerife, 38071, Spain.

Constantinos C Mylonas (CC)

Institute of Marine Biology, Biotechnology and Aquaculture, Hellenic Center for Marine Research, P.O. Box 2214, Heraklion, 71003, Crete, Greece.

Rosa Zupa (R)

Department of Emergency and Organ Transplantation, Section of Veterinary Clinics and Animal Production, University of Bari Aldo Moro, S.P. per Casamassima km. 3, I-70010, Valenzano, Bari, Italy.

Letizia Passantino (L)

Department of Emergency and Organ Transplantation, Section of Veterinary Clinics and Animal Production, University of Bari Aldo Moro, S.P. per Casamassima km. 3, I-70010, Valenzano, Bari, Italy.

Nicoletta Santamaria (N)

Department of Emergency and Organ Transplantation, Section of Veterinary Clinics and Animal Production, University of Bari Aldo Moro, S.P. per Casamassima km. 3, I-70010, Valenzano, Bari, Italy.

Luisa Valentini (L)

Department of Emergency and Organ Transplantation, Section of Veterinary Clinics and Animal Production, University of Bari Aldo Moro, S.P. per Casamassima km. 3, I-70010, Valenzano, Bari, Italy.

Aldo Corriero (A)

Department of Emergency and Organ Transplantation, Section of Veterinary Clinics and Animal Production, University of Bari Aldo Moro, S.P. per Casamassima km. 3, I-70010, Valenzano, Bari, Italy. Electronic address: aldo.corriero@uniba.it.

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Classifications MeSH