Effect of moulting and lunar rhythms on the lymphoid organ spheroid (LOS) cells of the black tiger prawn (Penaeus monodon)

Journal of Experimental Marine Biology and Ecology

Volumn 389, Issue 1-2, 2010, Pages 6-12

  Rusaini, G ^a,b   Owens, L ^b  

^a TADULAKO UNIVERSITY   (Indonesia)

^b JAMES COOK UNIVERSITY   (Australia)

Author keywords

Lunar rhythms; Lymphoid organ; Moulting; Penaeus monodon; Spheroid cells

Indexed keywords

ABUNDANCE; CRUSTACEAN; ENVIRONMENTAL CUE; HYDROSTATICS; LABORATORY METHOD; LIGHT INTENSITY; MOLT;

ANIMALIA; DECAPODA (CRUSTACEA); PENAEUS MONODON;

EID: 77954534614     PISSN: 00220981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jembe.2010.04.005     Document Type: Article

References (50)

1. Anantasomboon, G., Poonkhum, R., Sittidilokratna, N., Flegel, T.W., Withyachumnarn-kul, B., 2008. Low viral loads and lymphoid organ spheroids are associated with yellow head virus (YHV) tolerance in whiteleg shrimp Penaeus vannamei. Dev. Comp. Immunol. 32, 613-626.
2. Anggraeni, M.S., 1998. The origin and role of lymphoid organ spheroid cells in the giant tiger prawn, Penaeus monodon. Unpublished MSc thesis, James Cook University, Townsville, North Queensland, pp. 120.
3. Anggraeni, M.S., Owens, L., 2000. The haemocytic origin of lymphoid organ spheroid cells in the penaeid prawn Penaeus monodon. Dis. Aquat. Organ. 40, 85-92.
4. Bell, T.A., Lightner, D.V., 1988. A Handbook of Normal Penaeid Shrimp Histology. World Aquaculture Society, Baton Rouge, Louisiana. pp. 1-6.
5. Bonami, J.R., Lightner, D.V., Redman, R.M., Poulos, B.T., 1992. Partial characterization of a togavirus (LOVV) associated with histopathological changes of the lymphoid organ of penaeid shrimps. Dis. Aquat. Organ. 14, 145-152.
6. Burgents, J.E., Burnett, L.E., Stabb, E.V., Burnett, K.G., 2005. Localization and bacteriostasis of Vibrio introduced into the Pacic white shrimp, Litopenaeus vannamei. Dev. Comp. Immunol. 29, 68-691.
7. Chang, E.S., 1995. Physiological and biochemical changes during the molt cycle in decapod crustaceans: an overview. J. Exp. Mar. Biol. Ecol. 193, 1-14.
8. Chen, J.-C., Cheng, S.-Y., 1993. Studies on haemocyanin and haemolymph protein levels of Penaeus japonicus based on sex, size and moulting cycle. Comp. Biochem. Physiol. B 106, 293-296.
9. Cheng, W., Chen, J.C., 2001. Effect of intrinsic and extrinsic factors on the haemocyte prole of the prawn, Macrobrachium rosenbergii. Fish Shellsh Immunol. 11, 53-63.
10. Cheng, W., Liu, C.H., Yan, D.F., Chen, J.C., 2002. Hemolymph oxyhemocyanin, protein, osmolality, and electrolyte levels of whiteleg shrimp Litopenaeus vannamei in relation to size and molt stage. Aquaculture 211, 325-339.
11. Cheng, W., Juang, F.-M., Li, J.-T., Lin, M.-C., Liu, C.-H., Chen, J.-C., 2003. The immune response of the giant freshwater prawn Macrobrachium rosenbergii and its susceptibility to Lactococcus garvieae in relation to the moult stage. Aquaculture 218, 33-45.
12. Duangsuwan, P., Tinikul, Y., Chotwiwatthanakun, C., Vanichviriyakit, R., Sobhon, P., 2008. Changes in the histological organization and spheroid formation in lymphoid organ of Penaeus monodon infected with yellow head virus. Fish Shellsh Immunol. 25, 560-569.
13. Fraser, C., Owens, L., 1996. Spawner-isolated mortality virus from Australian Penaeus monodon. Dis. Aquat. Organ. 27, 141-148.
14. Grifth, D.R.W., Wigglesworth, J.M., 1993. Growth rhythms in the shrimp Penaeus vannamei and P. schimitti. Mar. Biol. 115, 295-299.
15. Grifths, S.P., 1999. Effects of lunar periodicity on catches of Penaeus plebejus (Hess) in an Australian coastal lagoon. Fish. Res. 42, 195-199.
16. Hasson, K.W., Lightner, D.V., Mohney, L.L., Redman, R.M., White, B.M., 1999. Role of lymphoid organ spheroids in chronic Taura syndrome virus (TSV) infections in Penaeus vannamei. Dis. Aquat. Organ. 38, 93-105.
17. Hauton, C., Hawkins, L.E., Williams, J.A., 1995. Circatidal rhythmicity in the activity of the phenoloxidase enzyme in the common shore crab, Carcinus maenas. Comp. Biochem. Physiol. B 111, 347-352.
18. Hawkins, L.E., Brooks, J.D., Brooks, S., Hutchinson, S., 1993. The effect of tidal exposure on aspects of metabolic and immunological activity in the hard clam Mercenaria mercenaria (Linnaeus). Comp. Biochem. Physiol. 104, 225-228.
19. Ho, P.-Y., Cheng, C.-H., Cheng, W., 2009. Identication and cloning of the alpha 2-macroglobulin of giant freshwater prawn Macrobrachium rosenbergii and its expression in relation with the molt stage and bacteria injection. Fish Shellsh Immunol. 26, 459-466.
20. Hose, J.E., Martin, G.G., Nguyen, V.A., Lucas, J., Rosenstein, T., 1987. Cytochemical features of shrimp hemocytes. Biol. Bull. 173, 178-187.
21. Hose, J.E., Martin, G.G., Tiu, S., McKrell, N., 1992. Patterns of hemocyte production and release throughout the molt cycle in the penaeid shrimp Sicyonia ingentis. Biol. Bull. 183, 185-199.
22. Kondo, M., Itami, T., Takahashi, Y., Fujii, R., Tomonaga, S., 1994. Structure and function of the lymphoid organ in the kuruma prawn. Dev. Comp. Immunol. 18 (Supplement 1), S109.
23. Le Moullac, G., Le Groumellec, M., Ansquer, D., Froissard, S., Levy, P., Aquacop, 1997. Haematological and phenoloxidase activity changes in the shrimp Penaeus stylirostris in relation with the moult cycle: protection against vibriosis. Fish Shellsh Immunol. 7, 227-234.
24. Liu, C.-H., Yeh, S.-T., Cheng, S.-Y., Chen, J.-C., 2004. The immune response of the white shrimp Litopenaeus vannamei and its susceptibility to Vibrio infection in relation with the moult cycle. Fish Shellsh Immunol. 16, 151-161.
25. Liu, C.-H., Tseng, D.-Y., Lai, C.-Y., Cheng, W., Kuo, C.-M., 2006. Molecular cloning and characterisation of prophenoloxidase cDNA from haemocytes of the giant freshwater prawn, Macrobrachium rosenbergii, and its transcription in relation with the moult stage. Fish Shellsh Immunol. 21, 60-69.
26. Liu, C.-H., Yeh, S.-P., Hsu, P.-Y., Cheng, W., 2007. Peroxinectin gene transcription of the giant freshwater prawn Macrobrachium rosenbergii under intrinsic, immunostimulant, and chemotherapeutant inuences. Fish Shellsh Immunol. 22, 408-417.
27. Martin, G.G., Hose, J.E., Minka, G., Rosenberg, S., 1996. Clearance of bacteria injected into the hemolymph of the ridgeback prawn, Sicyonia ingentis (Crustacea: Decapoda): role of hematopoietic tissue. J. Morphol. 227, 227-233.
28. Nakamura, K., 1987. Lymphoid organ and its developmental property of larval prawn Penaeus japonicus. Mem. Fac. Fish. Kagoshima Univ. 36, 215-220.
29. Owens, L., Hall-Mendellin, S., 1990. Recent advances in Australian prawns diseases and pathology. Advances in Tropical Aquaculture: Actes de Colloque, 9. Aquacop, I FREMER, Tahiti, pp. 103-112.
30. Owens, L., Beer, S.D., Smith, J., 1991. Lymphoidal parvovirus-like particles in Australian penaeid prawns. Dis. Aquat. Organ. 11, 129-134.
31. Phlippen, M., Webster, S., Chung, J., Dircksen, H., 2000. Ecdysis of decapod crustaceans is associated with a dramatic release of crustacean cardioactive peptide into the haemolymph. J. Exp. Biol. 203, 521-536.
32. Promwikorn, W., Kirirat, P., Thaweethamsewee, P., 2004. Index of moult staging in the black tiger shrimp (Penaeus monodon). Songklanakarin J. Sci. Technol. 26, 765-772.
33. Rajendran, K.V., Cowley, J.A., McCulloch, R.J., Walker, P.J., 2006. A TaqMan real-time RT-PCR for quantifying Mourilyan virus infection levels in penaeid shrimp tissues. J. Virol. Methods 137, 265-271.
34. Rodríguez, J., Bayot, B., Amano, Y., Panchana, F., de Blas, I., Alday, V., Calderón, J., 2003. White spot syndrome virus infection in cultured Penaeus vannamei (Boone) in Ecuador with emphasis on histopathology and ultrastructure. J. Fish Dis. 26, 439-450.
35. Rusaini, Owens, L., 2007. Validation of quantitative analysis of the LOS cells in prawns. Agroland 14, 72-76.
36. Sarda, F., Cros, M.L., Sese, B., 1989. Ca balance during moulting in the prawn Aristeus antennatus (Risso, 1816): the role of cuticle calcication in the life cycle of decapod crustaceans. J. Exp. Mar. Biol. Ecol. 129, 161-171.
37. Scheer, B.T., 1960. Aspect of the intermoult cycle in natantians. Comp. Biochem. Physiol. 1, 3-18.
38. Sequeira, T., Vilanova, M., Lobo-da-Cunha, A., Baldaia, L., Arala-Chaves, M., 1995. Flow cytometric analysis of molt-related changes in hemocyte type in male and female Penaeus japonicus. Biol. Bull. 189, 376-380.
39. Shao, M.Y., Zhang, Z.F., Kang, K.H., Chen, Z.T., Kim, J.M., 2004. The study on the cytology and histochemistry of lymphoid organ spheroids in Penaeus chinensis. Aquaculture 240, 463-471.
40. Smith, D.M., Dall, W., 1985. Moult staging the tiger prawn Penaeus esculentus. In: Rothlisberg, P.C., Hill, B.J., Staples, D.J. (Eds.), Proc. 2nd Aust. Natl. Prawn Sem. Cleveland, Brisbane, pp. 85-93.
41. Spann, K.M., Vickers, J.E., Lester, R.J.G., 1995. Lymphoid organ virus of Penaeus monodon from Australia. Dis. Aquat. Organ. 23, 127-134.
42. Spann, K.M., Cowley, J.A., Walker, P.J., Lester, R.J.G., 1997. A yellow-head-like virus from Penaeus monodon Culture in Australia. Dis. Aquat. Organ. 31, 169-179.
43. Stevenson, J.R., 1972. Changing activities of the crustacean epidermis during the molting cycle. Am. Zool. 12, 373-380.
44. Travis, D.F., 1955. The molting cycle of the spiny lobster, Panulirus argus Latreille. II. pre- ecdysial histological and histochemical changes in the hepatopancreas and integumental tissue. Biol. Bull. (Woods Hole) 107, 88-112.
45. Travis, D.F., 1957. The molting cycle of the spiny lobster, Panulirus argus Latreille. IV. post-ecdysial histological and histochemical changes in the hepatopancreas and integumental tissues. Biol. Bull. (Woods Hole) 113, 451-479.
46. Truscott, R., White, K.N., 1990. The inuence of metal and temperature stress on the immune system of crabs. Funct. Ecol. 4, 455-461.
47. van de Braak, C.B.T., Botterblom, M.H.A., Taverne, N., van Muiswinkel, W.B., Rombout, J. H.W.M., van der Knaap, W.P.W., 2002. The roles of haemocytes and the lymphoid organ in the clearance of injected Vibrio bacteria in Penaeus monodon shrimp. Fish Shellsh Immunol. 13, 293-309.
48. Wassenberg, T.J., Hill, B.J., 1994. Laboratory study of the effect of light on the emergence behaviour of eight species of commercially important adult penaeid prawns. Aust. J. Mar. Freshwater Res. 45, 43-50.
49. Withers, P.C., 1992. Comparative Animal Physiology. Brooks/Cole-Thomson Learning. Pacic Grove, California. pp. 80-85.
50. Yeh, M.-S., Lai, C.-Y., Liu, C.-H., Kuo, C.-M., Cheng, W., 2009. A second proPO present in white shrimp Litopenaeus vannamei and expression of the proPOs during a Vibrio alginolyticus injection, molt stage, and oral sodium alginate ingestion. Fish Shellsh Immunol. 26, 49-55.