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Comparative study on tetraploid induction of the Fujian oyster Crassostrea angulata utilizing three typical methods

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Abstract

The sterility advantages of triploids make them paramount for oyster aquaculture. Tetraploids are always used as male parents for triploid industrial breeding in current hatcheries, thus they are the core asset for triploid oyster culture. The oyster Crassostrea angulata is the most productive oyster species in China. However, the optimal conditions for tetraploid induction have never been examined. In this study, we investigated the effectiveness of three induction methods (Method I, 2n ♀ × 2n ♂ + inducer abbreviated as DD + ind; Method II, 3n ♀ × 2n ♂ + inducer abbreviated as TrD + ind; Method III, 2n ♀ × 4n ♂ + inducer abbreviated as DT + ind) and three inducers (salinity; cytochalasin B, CB; and 6-dimethylaminopurine, 6-DMAP) for tetraploid induction in C. angulata. The optimal induction conditions for the three induction methods were a CB concentration of 0.5 mg/L treated for 20 min, 0.75 mg/L CB for a constant induction treatment of 20 min and 6-DMAP at a concentration of 100 mg/L for 20 min, respectively. When the optimal induction conditions were applied to a single pair of oysters, the D-larval tetraploid rate for the three methods were 18.93 ± 1.46%, 58.32 ± 1.03% and 51.61 ± 1.37%, respectively. After 30 days, the survival rates of the experimental groups were only 10.36 ± 2.51%, 28.07 ± 2.03% and 21.99 ± 1.27%, respectively, at day 30. The tetraploid rates in DD + ind and DT + ind were both decreased significantly over time, but they still reached 11.81% and 21.99% at 30 days, and 8% and 16% at day 180, respectively. Tetraploid rates in TrD + ind were 58.32 − 71.28% at the larval stage and 80% at day 180. In summary, despite very different induction rates, surviving tetraploids of C. angulata could be obtained in all three methods. Method II (TrD + inducer) was regarded as the optimal method to induce C. angulata tetraploids, and the optimal induction condition was a CB concentration of 0.75 mg/L and treated for 20 min under this method.

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Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request.

References

  • Aileen Tan SH, Teh CP, Chang GO, Yasin Z (2017) Tetraploid induction in tropical oysters, Crassostrea belcheri (Sowerby) and Crassostrea iredalei (Faustino). Aquac Res 48:1406–1412. https://doi.org/10.1111/are.12976

    Article  Google Scholar 

  • Allen SK (1983) Flow cytometry: assaying experimental polyploidy in fish shellfish. Aquaculture 33:317–328

    Article  Google Scholar 

  • Allen SK Jr, Bushek D (1992) Large scale production of triploid Crassostrea virginica (Gmelin) using “stripped” gametes. Aquaculture 103:241–251

    Article  Google Scholar 

  • Allen SK, Downing SL (1986) Performance of triploid Pacific oysters, Crassostrea gigas (Thunberg). I. Survival, growth, glycogen content, and sexual maturation in yearlings. J Exp Mar Biol Ecol 102:197–208. https://doi.org/10.1016/0022-0981(86)90176-0

    Article  Google Scholar 

  • Allen SK, Downing SL, Chew KK (1989) Hatchery manual for producing triploid oysters. Washington Sea Grant Program

  • Allen SK Jr, Shpigel M, Utting S, Spencer B (1994) Incidental production of tetraploid Manila clams, Tapes philippinarum (Adams and Reeve). Aquaculture 128:13–19

    Article  Google Scholar 

  • Barreto-Hernández A, Velasco LA, Winkler FM (2018) Effect of three triploidy induction methods on the growth and survival of larvae and post-larvae of the caribbean scallop Argopecten nucleus Aquac Res 49:1578–1587. https://doi.org/10.1111/are.13612

    Article  CAS  Google Scholar 

  • Benabdelmouna A, Ledu C (2007) Obtention de mollusques bivalves tétraploides á partir de géniteurs diploides. FR patent #2913982-A1

  • Benabdelmouna A, Ledu C (2015) Autotetraploid Pacific oysters (Crassostrea gigas) obtained using normal diploid eggs: induction and impact on cytogenetic stability. Genome 58:333–348. https://doi.org/10.1139/gen-2015-0014

    Article  PubMed  Google Scholar 

  • Benabdelmouna A, Ledu C, Gérard A (2007) Obtention de mollusques bivalves tétraploides á partir du croisement de femelles diploädes et de males tétraploides. FR patent #2913983-A1

  • Bodenstein S, Callam BR, Walton WC et al (2023) Survival and growth of triploid eastern oysters, Crassostrea virginica, produced from wild diploids collected from low-salinity areas. Aquaculture 564:739032. https://doi.org/10.1016/j.aquaculture.2022.739032

    Article  CAS  PubMed  Google Scholar 

  • Brake J, Evans F, Langdon C (2004) Evidence for genetic control of pigmentation of shell and mantle edge in selected families of Pacific oysters, Crassostrea gigas Aquaculture 229:89–98. https://doi.org/10.1016/S0044-8486(03)00325-9

    Article  Google Scholar 

  • Buestel D, Ropert M, Prou J, Goulletquer P (2009) History, status, and future of oyster culture in France. J Shellfish Res 28:813–820

    Article  Google Scholar 

  • Callam BR, Allen SK, Frank-Lawale A (2016) Genetic and environmental influence on triploid Crassostrea virginica grown in Chesapeake Bay: growth. Aquaculture 452:97–106. https://doi.org/10.1016/j.aquaculture.2015.10.027

    Article  Google Scholar 

  • Cheng G, Jiang G, Xu C et al (2023) A comparative study in inducing tetraploid Crassostrea gigas “Haida No.2” by three pathways. unpublished data

  • Comai L (2005) The advantages and disadvantages of being polyploid. Nat Rev Genet 6:836–846. https://doi.org/10.1038/nrg1711

    Article  CAS  PubMed  Google Scholar 

  • Desrosiers RR, Gérard A, Peignon J-M et al (1993) A novel method to produce triploids in bivalve molluscs by the use of 6-dimethylaminopurine. J Exp Mar Biol Ecol 170:29–43. https://doi.org/10.1016/0022-0981(93)90127-A

    Article  CAS  Google Scholar 

  • Dufresne L, Néant I, St-Pierre J, Dubé F, Guerrier P (1991) Effects of 6- dimethylaminopurine on microtubules and putative intermediate filaments in sea urchin embryos. J Cell Sci 99:721–730

    Article  CAS  PubMed  Google Scholar 

  • Eudeline B, Allen SK, Guo X (2000a) Optimization of tetraploid induction in Pacific oysters, Crassostrea gigas, using first polar body as a natural indicator. Aquaculture 187:73–84. https://doi.org/10.1016/S0044-8486(00)00302-1

    Article  Google Scholar 

  • Eudeline B, Allen SK, Guo X (2000b) Delayed meiosis and polar body release in eggs of triploid Pacific oysters, Crassostrea gigas, in relation to tetraploid production. J Exp Mar Biol Ecol 248:151–161. https://doi.org/10.1016/S0022-0981(00)00158-1

    Article  CAS  PubMed  Google Scholar 

  • Gérard A, Naciri Y, Peignon JM, Ledu C, Phelipot P (1994) Optimization of triploid induction by the use of 6-DMAP for the oyster Crassostrea gigas (Thuneberg). Aquacult Fish Manage 25:709–719

    Google Scholar 

  • Gérard A, Ledu C, Phélipot P, Naciri-Graven Y (1999) The induction of MI and MII triploids in the Pacific oyster Crassostrea gigas with 6-DMAP or CB. Aquaculture 174:229–242. https://doi.org/10.1016/S0044-8486(99)00032-0

    Article  Google Scholar 

  • Guo X (1991) Studies on tetraploid induction in the Pacific oyster, Crassostrea gigas (Thuneberg). Ph.D. dissertation, University of Washington, Seattle, Wash

  • Guo XM, Allen SK (1994a) Viable tetraploids in the Pacific oyster (Crassostrea gigas Thunberg) produced by inhibiting polar body I in eggs from triploids. Mol Mar Biol Biotechnol 3:42–50

    Google Scholar 

  • Guo XM, Allen SK (1994b) Sex determination and polyploid gigantism in the dwarf surfclam (Mulinia lateralis Say). Genetics 138:1199–1206

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Guo X, Cooper K, Hershberger WK, Chew KK (1992a) Genetic consequences of blocking polar body I with cytochalasin B in fertilized eggs of the Pacific Oyster, Crassostrea gigas: I. Ploidy of Resultant embryos. Biol Bull 183:381–386. https://doi.org/10.2307/1542013

    Article  CAS  PubMed  Google Scholar 

  • Guo XM, Hershberger WK, Cooper K, Chew KK (1992b) Genetic consequences of blocking polar body I with cytochalasin B in fertilized eggs of the Pacifc oyster, Crassostrea gigas: II. Segregation of chromosomes. Bio Bullet 183:387–393

    Article  CAS  Google Scholar 

  • Guo X, DeBrosse GA, Allen SK (1996) All-triploid Pacific oysters (Crassostrea gigas Thunberg) produced by mating tetraploids and diploids. Aquaculture 142:149–161. https://doi.org/10.1016/0044-8486(95)01243-5

    Article  Google Scholar 

  • Guo XM, Wang J, Landau BJ, Li L, DeBrosse GA, Buono KD (2002) The successful production of tetraploid eastern oyster, Crassostrea virginica Gmelin. J Shellfish Res 21:380–381 (abstract)

  • Ibarra AM, Ascencio-Michel R, Ramirez JL et al (2017) Performance of diploid and triploid Crassostrea gigas (thunberg, 1793) grown in tropical versus temperate natural environmental conditions. J Shellfish Res 36:119–139. https://doi.org/10.2983/035.036.0113

    Article  Google Scholar 

  • Jeung H-D, Keshavmurthy S, Lim H-J et al (2016) Quantification of reproductive effort of the triploid Pacific oyster, Crassostrea gigas raised in intertidal rack and bag oyster culture system off the west coast of Korea during spawning season. Aquaculture 464:374–380. https://doi.org/10.1016/j.aquaculture.2016.07.010

    Article  Google Scholar 

  • Jouaux A, Heude-Berthelin C, Sourdaine P, Mathieu M, Kellner K (2010) Gametogenic stages in triploid oysters Crassostrea gigas: irregular locking of gonial proliferation and subsequent reproductive effort. J Exp Mar Biol Ecol 395:162–170. https://doi.org/10.1016/j.jembe.2010.08.030

    Article  Google Scholar 

  • Komaru A, Wada KT (1990) Gametogenesis of triploid japanese pearl oyster, Pinctada fucata martensii. In: Hoshi M, Yamashita O (eds) Advances in Invertebrate Reproduction. Elsevier, Amsterdam, pp 469–474

  • Kong J, Wang ZP, Yu RH, Liu J, Zhang YH (2011) Triploid induction in Pacific oyster (Crassostrea gigas) by hypotonic treatment and comparison with other induction methods. J Fish Sci China 18:581–587 (in Chinese)

    Google Scholar 

  • Ledu C, Mccombie H (2003) Effects of cytochalasin B on fertilization and ploidy in the Pacific oyster Crassostrea gigas Invertebrate Reprod Dev 44:131–137. https://doi.org/10.1080/07924259.2003.9652563

    Article  CAS  Google Scholar 

  • Li Q, Wang Q, Liu S, Kong L (2011) Selection response and realized heritability for growth in three stocks of the Pacific oyster Crassostrea gigas. Fish Sci 77:643–648. https://doi.org/10.1007/s12562-011-0369-0

  • Li HK, Zhang Z, Yu RH, Wang YW, Li LW, Ma PZ (2021) A comparative study on the effectiveness of 6-DMAP and different salinities in inducing tetraploid Crassostrea gigas “Haida No.1”. J Ocean Univ China 51:136–145 (in Chinese)

    Google Scholar 

  • Li H, Yu R, Li Q, Ma P (2022) Evaluation of advantages in the growth, survival and reproductive aspects of triploid hybrids derived from Crassostrea gigas tetraploids and C. ariakensis diploids in northern China. Aquaculture 548:737675. https://doi.org/10.1016/j.aquaculture.2021.737675

    Article  Google Scholar 

  • Maclean-Fletcher S, Pollard TD (1980) Mechanism of action of cytochalasin B on actin. Cell 20:329–341

    Article  CAS  PubMed  Google Scholar 

  • Matt JL, Allen SK (2021) A classification system for gonad development in triploid Crassostrea virginica Aquaculture 532:735994. https://doi.org/10.1016/j.aquaculture.2020.735994

    Article  CAS  Google Scholar 

  • McCombie H, Ledu C, Phelipot P et al (2005) A complementary method for production of tetraploid Crassostrea gigas using crosses between diploids and tetraploids with cytochalasin B treatments. Mar Biotechnol 7:318–330. https://doi.org/10.1007/s10126-004-0440-2

    Article  CAS  Google Scholar 

  • McCombie H, Cornette F, Beaumont AR (2009) Short sharp shock produces viable tetraploids in crosses of diploid blue mussels Mytilus edulis Aquac Res 40:1680–1682. https://doi.org/10.1111/j.1365-2109.2009.02273.x

    Article  Google Scholar 

  • Melo EMC, Sühnel S, de Oliveira ACS et al (2020) Growth, mortality and reproductive traits of diploid and triploid Pacific oysters (Crassostrea gigas, THUNBERG, 1793) in Southern Brazil. Aquac Res 51:3631–3640. https://doi.org/10.1111/are.14713

    Article  CAS  Google Scholar 

  • Ministry of Agriculture and Rural Affairs of the People’s Republic of China, National Fisheries Technology Extension Center, China Society of Fisheries (2021) China fishery statistical yearbook. China Agriculture Press, pp 1–144

  • Nell JA (2002) Farming triploid oysters. Aquaculture 210:69–88. https://doi.org/10.1016/S0044-8486(01)00861-4

    Article  Google Scholar 

  • Nell JA, Hand RE, Goard LJ, McAdam SP, Maguire GB (1996) Studies on triploid oysters in Australia: evaluation of cytochalasin B and 6-dimethylaminopurine for triploidy induction in Sydney rock oysters Saccostrea commercialis (Iredale and Roughley). Aquaculture Res 27:689–698. https://doi.org/10.1111/j.1365-2109.1996.tb01304.x

    Article  Google Scholar 

  • Normand J, Le Pennec M, Boudry P (2008) Comparative histological study of gametogenesis in diploid and triploid Pacific oysters (Crassostrea gigas) reared in an estuarine farming site in France during the 2003 heatwave. Aquaculture 282:124–129. https://doi.org/10.1016/j.aquaculture.2008.06.026

    Article  Google Scholar 

  • Peachey BL, Allen SK (2016) Evaluation of cytochalasin B and 6-dimethylaminopurine for tetraploidy induction in the Eastern oyster, Crassostrea virginica Aquaculture 450:199–205. https://doi.org/10.1016/j.aquaculture.2015.07.034

    Article  CAS  Google Scholar 

  • Piferrer F, Beaumont A, Falguière J-C et al (2009) Polyploid fish and shellfish: production, biology and applications to aquaculture for performance improvement and genetic containment. Aquaculture 293:125–156. https://doi.org/10.1016/j.aquaculture.2009.04.036

    Article  Google Scholar 

  • Qin Y, Zhang Y, Mo R et al (2019) Influence of ploidy and environment on grow-out traits of diploid and triploid Hong Kong oysters Crassostrea hongkongensis in southern China. Aquaculture 507:108–118. https://doi.org/10.1016/j.aquaculture.2019.04.017

    Article  Google Scholar 

  • Qin Y, Noor Z, Li X et al (2021) Tetraploid induction of Crassostrea hongkongensis and C. sikamea by inhibiting the polar body 1 release in diploid fertilized eggs. Mar Life Sci Technol 3:463–473. https://doi.org/10.1007/s42995-021-00107-w

  • Stanley JG, Allen SK, Hidu H (1981) Polyploidy induced in the american oyster, Crassostrea virginica, with cytochalasin B. Aquaculture 23:1–10. https://doi.org/10.1016/0044-8486(81)90002-8

    Article  CAS  Google Scholar 

  • Tan K, Deng L, Zheng H (2021) Effects of stocking density on the aquaculture performance of diploid and triploid, pacific oyster Crassostrea gigas and portuguese oyster C. angulata in warm water aquaculture. Aquac Res 52(12):6268–6279

    Article  CAS  Google Scholar 

  • Wadsworth P, Wilson AE, Walton WC (2019) A meta-analysis of growth rate in diploid and triploid oysters. Aquaculture 499:9–16. https://doi.org/10.1016/j.aquaculture.2018.09.018

    Article  Google Scholar 

  • Wang ZP, Zhao T, Yu RH, Zhang CC (2009) A new method for triploid induction by hypotonic treatment in scallop Patinopecten yessoensis J Ocean Univ China 39:193–196 (in Chinese)

    ADS  Google Scholar 

  • Wang Y, Gan Y, Zhang J et al (2022) Performance of triploid Haliotis discus hannai cultured in a subtropical area using sea-based suspended systems. Aquaculture 548:737722. https://doi.org/10.1016/j.aquaculture.2021.737722

    Article  Google Scholar 

  • Yang H, Zhang F, Guo X (2000) Triploid and tetraploid Zhikong scallop, Chlamys farreri Joene et Preston, produced by inhibiting polar body I. Mar Biotechnol 2:466–475

    Article  CAS  Google Scholar 

  • Zhang Y, Qin Y, Yu Z (2022) Comparative study of tetraploid-based reciprocal triploid portuguese oysters, Crassostrea angulata, from seed to marketsize. Aquaculture 547:737523. https://doi.org/10.1016/j.aquaculture.2021.737523

    Article  Google Scholar 

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Funding

This work was supported by grants from the National Key R&D Program of China (2022YFD2400305), the China Agriculture Research System Project (CARS-49), and Shandong Province (2021ZLGX03, 2021LZGC027).

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Yuanxin Liang: Conceptualization, supervision, resources, project admi. Geng Cheng: Resources. Xianchao Bai: Resources. Jianmin Zhou: Conceptualization, supervision. Haining Zhang: Supervision. Yong Chi: Resources. Gaowei Jiang: Conceptualization. Chengxun Xu: Resources. Qi Li: Conceptualization, supervision, resources, project admi.All authors reviewed the manuscript.

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Correspondence to Qi Li.

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The present study was performed according to the standard operation procedures (SOPs) of the Guide for the Use of Experimental Animals of the Ocean University of China. All animal care and use procedures were approved by the Institutional Animal Care and Use Committee of Ocean University of China.

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Liang, Y., Cheng, G., Bai, X. et al. Comparative study on tetraploid induction of the Fujian oyster Crassostrea angulata utilizing three typical methods. Aquacult Int 32, 593–612 (2024). https://doi.org/10.1007/s10499-023-01174-9

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