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Detection of prostaglandin E2 in polychaete Perinereis sp. and its effect on Penaeus monodon oocyte development in vitro

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Abstract

Prostaglandins are involved in the reproductive processes in a variety of animals, including crustaceans. It was found that polychaetes, the best maturation diet for shrimp broodstock, possessed the greatest variation of prostaglandin E2 (PGE2) when compared with other live feeds. The level of PGE2 varied according to sizes, feed intake, sources and type of polychaete. The matured and also larger sand polychaete Perinereis sp. contained higher PGE2 levels than younger and smaller sand polychaetes (18.16 ± 5.82 ng PGE2 mg−1 protein for polychaetes at an average length of 10 cm up to 160.8 ± 37.09 ng PGE2 mg−1 protein for polychaetes at an average length of 17 cm). The PGE2 levels in ovaries and haemolymph of female shrimp fluctuated with the developmental stage of the ovaries. The highest concentration of PGE2 in haemolymph was at stage 3 of ovarian development, whereas the highest concentration of PGE2 in shrimp ovaries was at stage 4. In vitro incubation of Penaeus monodon pre-vitellogenic oocytes with polychaete extract and synthetic PGE2 demonstrated that both PGE2s enhanced oocyte development, especially during late development and ovulation. The putative role of PGE2 from polychaetes or the presence of PGE2 in polychaetes may be a factor in their role as a dietary constituent required for shrimp oocyte development.

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References

  1. Reddy PS, Reddy PR, Nagaraju GPC (2004) The synthesis and effects of prostaglandins on the ovary of the crab Oziotelphusa senex senex. Gen Comp Endocrinol 135:35–41

    Article  CAS  PubMed  Google Scholar 

  2. Middleditch BS, Missler RS, Ward DG, McVey JP, Brown A, Lawrence AL (1979) Development of penaeid shrimp: dietary fatty acids. Proc World Mar Soc 10:472–476

    Google Scholar 

  3. Lytle JS, Lytle TF, Ogle JT (1990) Polyunsaturated fatty acid profiles as a comparative tool in assessing development diets of Penaeus vannamei. Aquaculture 89:287–299

    Article  CAS  Google Scholar 

  4. Rouse GW, Fauchald K (1995) The articulation of annelids. Zool Scr 24:269–302

    Article  Google Scholar 

  5. Andreis JC (2001) Endocrine and environmental control of reproduction in polychaete. Can J Zool 79:254–270

    Article  Google Scholar 

  6. Oumi T, Ukena K, Matsushima O, Ikeda T, Fujita T, Minakata H, Nomoto K (1996) Annetocin, an annelid oxytocin-related peptide, induces egg-laying behavior in the earthworm, Eisenia foetida. J Exp Zool 276(2):151–156

    Article  CAS  PubMed  Google Scholar 

  7. Fujino Y, Nagahama T, Oumi T, Ukena K, Morishita F, Furukawa Y, Matsushima O, Ando M, Takahama H, Satake H, Minakata H, Nomoto K (1999) Possible functions of oxytocin/vasopressin-superfamily peptides in annelids with special reference to reproduction and osmoregulation. J Exp Zool 284(4):401–406

    Article  CAS  PubMed  Google Scholar 

  8. Porchet M, Spik G (1978) Biochemical analysis of nereidae gametogenesis—I. Evolution of glycocojugates during natural oogenesis of Perinereis cultrifera Grube (Polychaete Annelid). Comp Biochem Phys 59b:175–181

    Article  CAS  Google Scholar 

  9. Hardege JD, Bartel-Hardege HD, Yang Y, Wu BL, Zhu MY, Zeek E (1994) Environmental control of reproduction of Perinereis nuntia var. brevicirrus. J Mar Biol Assoc UK 74:903–918

    Google Scholar 

  10. Zeeck E, Harder T, Beckmann M (1998) Uric acid: the sperm-release pheromone of the marine polychaete Platynereis dumerilii. J Chem Ecol 24(1):13–22

    Article  CAS  Google Scholar 

  11. Salzet M (2001) The neuroendocrinology systems of annelids. Can J Zool 79:175–191

    Article  CAS  Google Scholar 

  12. Meunpol O, Iam-Pai S, Suthikrai W, Piyatiratitivorakul S (2007) Identification of progesterone and 17α-hydroxyprogesterone in polychaetes (Perinereis sp.) and the effects of hormone extracts on penaeid oocyte development in vitro. Aquaculture 270:485–492

    Article  CAS  Google Scholar 

  13. Meunpol O, Meejing P, Piyatiratitivorakul S (2005) Maturation diet based on fatty acid content for male Penaeus monodon (Fabricius) broodstock. Aquac Res 36:1216–1225

    Article  CAS  Google Scholar 

  14. Primavera JH (1988) Biology and culture of Penaeus monodon. Brackishwater aquaculture information system. Aquaculture Department, Southeast Asian Fisheries Development Center, Tigbauan

    Google Scholar 

  15. Bradford M (1976) A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 28:350–356

    Google Scholar 

  16. Tahara D, Yano I (2003) Development of hemolymph prostaglandins assay systems and their concentration variations during ovarian development in the kuruma shrimp, Penaeus japonicus. Aquaculture 220:791–800

    Article  CAS  Google Scholar 

  17. Curtis GH, Macnaughton WK, Wallace JL (1995) Intraluminal pH modulates gastric prostaglandin synthesis. Can J Physiol Pharmacol 73:130–134

    CAS  PubMed  Google Scholar 

  18. Webster SG (1986) Neurohormonal control of ecdysteroid biosynthesis by Carcinus maenas Y-organ in vitro and preliminary characterization of the putative moult-inhibiting hormone. Gen Comp Endocrinol 61:237–247

    Article  CAS  PubMed  Google Scholar 

  19. Tsukimura B, Kamemoto FI (1991) In vitro stimulation of oocytes by presumptive mandibular secretions in the shrimp Penaeus vannamei. Aquaculture 92:59–66

    Article  Google Scholar 

  20. Bell TA, Lightner DV (1988) A handbook of normal penaeid shrimp histology. The World Aquaculture Society, Baton Rouge

    Google Scholar 

  21. Tan-Fermin JD, Pudadera RA (1989) Ovarian development stages of the wild Giant tiger shrimp, Penaeus monodon Fabricius. Aquaculture 77:229–242

    Article  Google Scholar 

  22. Zar JH (1996) Biostatistical analysis, 3rd edn. Prentice-Hall, New Jersey

    Google Scholar 

  23. Golding DW (1967) The diversity of secretory neurons in the brain of Nereis. Z Zellforsch 82:321–344

    Article  CAS  PubMed  Google Scholar 

  24. Yano I (1988) Oocyte development in the kuruma shrimp Penaeus japonica. Mar Biol 99(4):547–553

    Article  Google Scholar 

  25. Quackenbush LS (1992) Yolk synthesis in the marine shrimp, Penaeus vannamei. Comp Biochem Physiol 103A:711–714

    Article  Google Scholar 

  26. Clark WH Jr, Yudin AI, Lynn JW, Griffin FJ, Pillai MC (1990) Jelly layer formation in penaeoidean shrimp eggs. Biol Bull 178:295–299

    Article  Google Scholar 

  27. Anderson SL, Chang ES, Clark WH Jr (1984) Timing of postvitellogenic ovarian change in the ridgeback shrimp Sicyonia ingentis determined by ovarian biopsy. Aquaculture 42:257–271

    Article  Google Scholar 

  28. Clark WH Jr, Lynn JW (1977) A Mg2+ dependent cortical reaction in the eggs of penaeid shrimp. J Exp Zool 200:177–183

    Article  CAS  Google Scholar 

  29. Spaziani EP, Hinsch GW, Edwards SC (1993) Changes in prostaglandin E(2) and F2-alpha during vitellogenesis in the Florida crayfish Procambarus paeninsulanus. J Comp Physiol 163:541–545

    CAS  Google Scholar 

  30. D’Croz L, Wong LV, Justine G, Gupta M (1988) Prostaglandins and related compounds from the polychaete worm Americonuphis reesi Fauchald (Onuphidae) as possible inducers of gonad development in penaeid shrimps. Rev Biol Trop 36:331–332

    Google Scholar 

  31. Tahara D, Yano I (2004) Development-related variations in prostaglandin and fatty acid content of ovary in the kuruma shrimp (Marsupenaeus japonicus). Comp Biochem Phys 137A:631–637

    CAS  Google Scholar 

Download references

Acknowledgments

This work was funded by the National Research Council of Thailand to O. Meunpol. Many thanks to First Farm and Sam Dao Farm for providing P. monodon broodstock, the CP Group of Companies for some polychaete samples, CENTEX and Mahidol University, Bangkok, for histology facilities.

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Meunpol, O., Duangjai, E., Yoonpun, R. et al. Detection of prostaglandin E2 in polychaete Perinereis sp. and its effect on Penaeus monodon oocyte development in vitro. Fish Sci 76, 281–286 (2010). https://doi.org/10.1007/s12562-009-0208-8

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  • DOI: https://doi.org/10.1007/s12562-009-0208-8

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