Comparative study of the intracellular superoxide anion production in different penaeid species through the NBT-reduction assay

Aquaculture Research

Volumn 41, Issue 7, 2010, Pages 1082-1088

  Guertler, Cristhiane ^a   Schleder, Delano Dias ^a   Barracco, Margherita Anna ^a   Perazzolo, Luciane Maria ^a  

^a FEDERAL UNIVERSITY OF SANTA CATARINA   (Brazil)

Author keywords

Farfantepenaeus paulensis; Immunoparameter; Litopenaeus schmitti; Litopenaeus vannamei; ROI; Shrimp immunity

Indexed keywords

DECAPODA (CRUSTACEA); FARFANTEPENAEUS PAULENSIS; LITOPENAEUS SCHMITTI; LITOPENAEUS VANNAMEI; PENAEIDAE;

EID: 84861221229     PISSN: 1355557X     EISSN: 13652109     Source Type: Journal    
DOI: 10.1111/j.1365-2109.2009.02393.x     Document Type: Article

References (32)

1. Bell K.L. & Smith V.J. (1993) In vitro superoxide production by hyaline cells of the shore crab Carcinus maenas (L.). Developmental and Comparative Immunology 17, 211-219.
2. Bogdan C., Röllinghoff M. & Diefenbac A. (2000) Reactive oxygen and reactive nitrogen intermediates in innate and specific immunity. Current Opinion in Immunology 12, 64-76.
3. Campa-Córdova A.I., Saavedra-Hernández N.Y., Philippis R. & Ascencio F. (2002) Generation of superoxide anion and SOD activity in haemocytes and muscle of American white shrimp (Litopenaeus vannamei) as a response to β-glucan and sulphated polysaccharide. Fish and Shellfish Immunology 12, 353-366.
4. Chang H.F., Chen H.Y., Su M.S. & Liao I.C. (2000) Immunomodulation by dietary β-1, 3-glucan in the brooders of the black tiger shrimp Penaeus monodon. Fish and Shellfish Immunology 10, 505-514.
5. Chang C.C., Lee P.P., Liu C.H. & Winton C. (2006) Trichlorfon, an organophosphorus insecticide, depresses the immune responses and resistence to Lactococcus garvieae of the giant freshwater prawn Macrobrachium rosenbergii. Fish and Shellfish Immunology 20, 574-585.
6. Chang C.F., Su M.S., Chen H.Y.N. & Liao I.C. (2003) Dietary β-1, 3-glucan effectively improves immunity and survival of Penaeus monodon challenged with white spot syndrome virus. Fish and Shellfish Immunology 15, 297-310.
7. Fu Y. W., Hou W. Y., Yeh S.T., Li C.H. & Chen J.C. (2007) The immunostimulatory effects of hot-water extract of Gelidium amansii via immersion, injection and dietary administrations on white shrimp Litopenaeus vannamei and its resistance against Vibrio alginolyticus. Fish and Shellfish Immunology 22, 673-685.
8. Gullian M., Thompson F.E. & Rodriguez J. (2004) Selection of probiotic bacteria and study of their immunostimulatory effect in Penaeus vannamei. Aquaculture 233, 1-14.
9. Jiravanichpaisal P., Lee B.L. & Söderhäll K. (2006) Cell-mediated immunity in arthropods: hematopoiesis, coagulation, melanization and opsonization. Immunobiology 211, 213-236.
10. Klebanoff S.J. (1999) Oxygen metabolites from phagocytes. In: Inflammation: Basic Principles and Clinical Correlates (ed. by J.I. Gallin & R. Snyderman ), pp. 721-768. Lippincott Williams and Wilkins, Philadelphia, PA, USA.
11. Le Moullac G., Soyez C., Saulnier D., Ansquer D., Avarre J.C. & Levy P. (1998) Effect of hypoxic stress on the immune response and the resistance to vibriosis of the shrimp Penaeus stylirostris. Fish and Shellfish Immunology 8, 621-629.
12. Lee S.Y. & Söderhäll K. (2002) Early events in crustacean immunity. Fish and Shellfish Immunology 12, 421-437.
13. Liu C.H. & Chen J.C. (2004) Effect of ammonia on the immune response of white shrimp Litopenaeus vannamei and its susceptibility to Vibrio alginolyticus. Fish and Shellfish Immunology 16, 321-334.
14. Misra C.K., Das B.K., Mukherjee S.C. & Pradhan J. (2007) Effects of dietary vitamin C on immunity, growth and survival of Indian major carp Labeo rohita, fingerlings. Aquaculture Nutrition 13, 35-44.
15. Muñoz M., Cedeño R., Rodríguez J., Van Der Knaap W. P. W., Mialhe E. & Bachère E. (2000) Measurement of reactive oxygen intermediate production in haemocytes of the penaeid shrimp, Penaeus vannamei. Aquaculture 191, 89-107.
16. Murphy R. & DeCoursey T. (2006) Charge compensation during the phagocyte respiratory burst. Biochimica et Biophysica Acta 1757, 996-1011.
17. Pérez-Farfante J. & Kensley B. (1997) Penaeoid and sergestoid shrimps and prawns of the world, key and diagnosis for the species and genera. Mémoires Muséum National d Histoire Naturelle, Zoologia, Tome, 175, 235pp.
18. Pipe R.K. (1992) Generation of reactive oxygen metabolites by the haemocytes of the mussel Mytilus edulis. Developmental and Comparative Immunology 16, 111-122.
19. Raman T., Arumugam M. & Mullainadhan P. (2008) Agglutinin-mediated phagocytosis-associated generation of superoxide anion and nitric oxide by the hemocytes of the giant freshwater prawn Macrobrachium rosenbergii. Fish and Shellfish Immunology 24, 337-345.
20. Rosas C., Cooper E.L., Pascual C., Brito R., Gelabert R., Moreno T., Miranda G. & Sánchez A. (2004) Indicators of physiological and immunological status of Litopenaeus setiferus wild populations (Crustacea, Penaeidae). Marine Biology 145, 401-413.
21. Schleder D.D., Kayser M., Sühnel S., Ferreira J.F., Rupp G.S. & Barracco M.A. (2008) Evaluation of hematoimmunological parameters during the reproductive cycle of the scallop Nodipecten nodosus in association with a carotenoid-enriched diet. Aquaculture 280, 256-263.
22. Secombes C.J., Cheng S. & Jeffries A.H. (1988) Superoxide anion production by rainbow trout macrophages detected by the reduction of ferricytochrome C. Developmental and Comparative Immunology 12, 201-206.
23. Sierra C., Lascurain R., Pereya A., Guevara J., Martínez G., Agundis C., Zenteno E. & Vázquez L. (2005) Participation of serum and membrane lectins on the oxidative burst regulation in Macrobrachium rosenbergii hemocytes. Developmental and Comparative Immunology 29, 113-121.
24. Song Y.L. & Hsieh Y.T. (1994) Immunostimulation of tiger shrimp (Penaeus monodon) hemocytes for generation of microbicidal substances: analysis of reactive oxygen species. Developmental and Comparative Immunology 18, 201-209.
25. Song Y.L., Yu C., Lien T. W., Huang C.C. & Lin M.N. (2003) Haemolymph parameters of Pacific white shrimp (Litopenaeus vannamei) infected with Taura syndrome virus. Fish and Shellfish Immunology 14, 317-331.
26. Sung H.H., Yang Y.L. & Song Y.L. (1996) Enhancement of microbicidal activity in the tiger shrimp Penaeus monodon via immunostimulation. Journal of Crustacean Biology 16, 278-284.
27. Thiagarajan R., Gopalakrishnan S. & Thilagam H. (2006) Immunomodulation in the marine green mussel Perna viridis exposed to sub-lethal concentrations of Cu and Hg. Archives of Environmental Contamination and Toxicology 51, 392-399.
28. Vargas-Albores F., Guzmán M.A. & Ochoa J.L. (1993) An anticoagulant solution for haemolymph collection and prophenoloxidase studies of penaeid shrimp (Penaeus californiensis). Comparative Biochemistry and Physiology 106, 299-303.
29. Vidya N., Thiagarajan R. & Arumugam M. (2007) In vitro generation of superoxide anion by the hemocytes of Macrobrachium rosenbergii: possible mechanism and pathways. Journal of Experimental Zoology 307, 383-396.
30. Wang L.U. & Chen J.C. (2005) The immune response of white shrimp Litopenaeus vannamei and its susceptibility to Vibrio alginolyticus at different salinity levels. Fish and Shellfish Immunology 18, 269-278.
31. Warner H.R. (1994) Superoxide dismutase, aging, and degenerative disease. Free Radical Biology and Medicine 3, 249-258.
32. Yeh S.T., Lee C.S. & Chen J.C. (2006) Administration of hot-water extract of brown seaweed Sargassum duplicatum via immersion and injection enhances the immune resistance of white shrimp Litopenaeus vannamei. Fish and Shellfish Immunology 20, 332-345.