4.7 Article

Seasonal changes and endocrine regulation of gonadal development in hatchery-produced Pacific bluefin tuna Thunnus orientalis broodstock in sea cages

Journal

AQUACULTURE
Volume 545, Issue -, Pages -

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ELSEVIER
DOI: 10.1016/j.aquaculture.2021.737199

Keywords

Pacific bluefin tuna; Broodstock management; Oogenesis; Spermatogenesis; Gonadotropin

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The reproductive season of hatchery-produced Pacific bluefin tuna peaks between June and July, in agreement with wild-caught juveniles. Furthermore, the percentage of hatchery-reared females reaching late vitellogenesis was higher than that of wild-caught captive-reared females reported in previous literature.
We examined the annual reproductive cycle of both female and male hatchery-produced Pacific bluefin tuna (PBT, Thunnus orientalis) broodstock at 3 years of age, including the associated changes in plasma levels of sex steroid hormones and the gene expression of key endocrine factors. The females progressed to vitellogenesis in April, and approximately 50% of the females were observed in late vitellogenesis between June and July at water temperatures between 24.1 degrees C and 29.0 degrees C. Approximately 90% of the males were in spermiation for at least 7 months between April and October, which included the period when vitellogenic females were present. Furthermore, the gonadosomatic index of both females and males peaked between June and July. These results indicate that the reproductive season of hatchery-produced PBT peaks between June and July, which is in agreement with the reproductive season reported for PBT broodstock originating from wild-caught juveniles. Furthermore, the percentage of hatchery-reared females that reached late vitellogenesis in the present study was higher than that in wild-caught captive-reared females reported in previous literature. Analysis of plasma sex steroid levels and gene expression profiles suggested that oocyte and ovarian development were associated with 17 beta-estradiol (E2) control, whereas spermatogonial differentiation towards meiosis seemed to be mediated by 11-ketotestosterone (11-KT). Furthermore, the production of E2 and 11-KT is likely regulated by luteinizing hormone and follicle-stimulating hormone, respectively, via their related receptors. The findings of this study are expected to contribute to improvements of technologies for obtaining fertilized eggs from hatchery-produced PBT broodstock.

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