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Short-term storage of the oocytes affects the ploidy status in the yellowtail tetra Astyanax altiparanae

Published online by Cambridge University Press:  15 January 2018

Matheus Pereira dos Santos*
Affiliation:
Aquaculture Center, São Paulo State University, Jaboticabal, Brazil.
Nivaldo Ferreira do Nascimento
Affiliation:
Aquaculture Center, São Paulo State University, Jaboticabal, Brazil.
George Shigueki Yasui
Affiliation:
National Center for Research and Conservation of Continental Fish, Chico Mendes Institute of Biodiversity Conservation, Pirassununga, Brazil.
Nycolas Levy Pereira
Affiliation:
Aquaculture Center, São Paulo State University, Jaboticabal, Brazil.
Takafumi Fujimoto
Affiliation:
Faculty of Fisheries Sciences, Hokkaido University, Hakodate, Japan.
José Augusto Senhorini
Affiliation:
National Center for Research and Conservation of Continental Fish, Chico Mendes Institute of Biodiversity Conservation, Pirassununga, Brazil.
Laura Satiko Okada Nakaghi
Affiliation:
Aquaculture Center, São Paulo State University, Jaboticabal, Brazil.
*
All correspondence to: Aquaculture Center, São Paulo State University, Jaboticabal, Brazil E-mail: matheusps.pereira@gmail.com

Summary

In fish, many factors can affect reproduction during in vitro fertilization, therefore determination of the factors that affect affecting gamete quality is needed. However, few studies have focused on gamete quality and the ploidy status. This study was conducted to elucidate whether oocyte storage can affect ploidy status, survival, and embryo viability in the characid species Astyanax altiparanae. Oocytes were stored in Dulbecco's phosphate-buffered saline (PBS) at 26°C, then aliquots were fertilized immediately after extrusion (control) and also after 60, 120, 180, and 240 min of storage. Fertilization and hatching rates were measured, and the developmental stages were analyzed at each stage before describing the main abnormalities. Ploidy status was analyzed by flow cytometry and blood smear. In the control group, 100% of the samples were diploid. After treatment for 60 min, 95.56 ± 4.44% samples were diploid and 4.44 ± 4.44% were triploid. After 120 min, 94.44 ± 9.62% of the samples was diploid and 5.56 ± 5.56% were triploid; 100% of the samples were diploid after 180 min and, after 240 min, there was no survival. In other treatments, the highest percentage of hatching was after 60 min (88.93 ± 5.15%; P = 0.015), and treatment with 180 min storage resulted in the highest percentage of abnormal larvae (95.76 ± 12.67%; P = 0.012). These results show that oocyte storage can affect ploidy status and may be an interesting parameter for analysis in studies on chromosome set manipulation and micromanipulation.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2018 

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