Administration of the hot-water extract of Spirulina platensis enhanced the immune response of white shrimp Litopenaeus vannamei and its resistance against Vibrio alginolyticus

Fish and Shellfish Immunology

Volumn 28, Issue 5-6, 2010, Pages 764-773

  Tayag, Carina Miranda ^a   Lin, Yong Chin ^a   Li, Chang Che ^a   Liou, Chyng Hwa ^a   Chen, Jiann Chu ^a  

^a NATIONAL TAIWAN OCEAN UNIVERSITY   (Taiwan)

Author keywords

Challenge test; Clearance efficiency; Hot water extract; Innate immunity; Litopenaeus vannamei; Phagocytic activity; Spirulina platensis; Vibrio alginolyticus

Indexed keywords

DECAPODA (CRUSTACEA); LITOPENAEUS VANNAMEI; SPIRULINA PLATENSIS; VIBRIO ALGINOLYTICUS;

EID: 77951129731     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2010.01.023     Document Type: Article

References (40)

1. Sarathi M., Ishaq Ahmed V.P., Venkatesan C., Balasubramanian G., Prabavathy J., and Sahul Hameed A.S. Comparative study on immune response of Fenneropenaeus indicus to Vibrio alginolyticus and white spot syndrome virus. Aquaculture 271 (2007) 8-20
2. Jiravanichpaisal P., Lee B.L., and Söderhäll K. Cell-mediated immunity in arthropods: hematopoiesis, coagulation, melanization and opsonization. Immunobiology 211 (2006) 213-236
3. Lightner D.V., and Redman R.M. Strategies for the control of viral diseases of shrimp in the Americas. Fish Pathol 33 (1998) 165-180
4. Liu C.H., Cheng W., Hsu J.P., and Chen J.C. Vibrio alginolyticus infection in the white shrimp Litopenaeus vannamei confirmed by polymerase chain reaction and 16S rDNA sequencing. Dis Aquat Org 61 (2004) 169-174
5. Raa J. The use of immunostimulatory substances in fish and shellfish farming. Rev Fish Sci 4 (1996) 288-299
6. Sakai M. Current research status of fish immunostimulant. Aquaculture 172 (1999) 63-92
7. Smith V.J., Brown J.H., and Hauton C. Immunostimulation in crustaceans: does it really protect against infection?. Fish Shellfish Immunol 15 (2004) 71-90
8. Miranda M.S., Cintra R.G., Barros S.B.M., and Mancini-Filho J. Antioxidant activity of the microalga Spirulina maxima. Braz J Med Biol Res 31 (1998) 1075-1079
9. Belay A. The potential application of Spirulina (Arthrospira) as a nutritional and therapeutic supplement in health management. J Am Nutraceut Assoc 5 (2002) 26-46
10. Hayashi O., Hirahashi T., Katoh T., Miyajima H., Hirano T., and Okuwaki Y. Class specific influence of dietary Spirulina platensis on antibody production in mice. J Nutr Sci Vitaminol (Tokyo) 44 (1998) 841-851
11. Duncan P., and Klesius P. Effects of Spirulina on specific and non-specific immune responses of channel catfish. J Aquat Anim Health 8 (1996) 308-313
12. Watanuki H., Ota H., Tassakka A.C.M.A.R., Kato T., and Sakai M. Immunostimulant effects of dietary Spirulina platensis on carp, Cyprinus carpio. Aquaculture 258 (2006) 157-163
13. Lee Y.K., Chew P.F., Soh B.S., and Tham L.Y. Enhancing phagocytic activity of hemocytes and disease resistance in the prawn Penaeus merguieneis by feeding Spirulina platensis. J Appl Phycol 15 (2003) 279-287
14. Rahman M.M., Escobedo-Bonilla C.M., Wille M., Alday Sanz V., Audoorn L., Neyts J., et al. Clinical effect of cidofovir and a diet supplemented with Spirulina platensis in white spot syndrome virus (WSSV) infected specific pathogen-free Litopenaeus vannamei juveniles. Aquaculture 255 (2006) 600-605
15. Yeh S.T., and Chen J.C. White shrimp Litopenaeus vannamei that received the hot-water extract of Gracilaria tenuistipitata showed earlier recovery in immunity after a Vibrio alginolyticus injection. Fish Shellfish Immunol 26 (2009) 724-730
16. Fujiki K., Matsuyama H., and Yano T. Effect of hot-water extracts from marine algae on resistance of carp and yellowtail against bacterial infections. Sci Bull 47 (1992) 137-141 Faculty of Agriculture, Kyushu University
17. Dubois M., Gilles K.A., Hamilton J.K., Rebers P.A., and Smith F. Colorimetric method for determination of sugars and related substances. Anal Chem 28 (1956) 350-356
18. Bradford M.M. A rapid and sensitive method for the determination of microgem quantities of protein utilizing the principles of protein-dye binding. Anal Chem 72 (1976) 248-254
19. Hernández-López J., Gollas-Galván T.S., and Vargas-Albores F. Activation of the prophenoloxidase system of the brown shrimp (Penaeus californiensis Holmes). Comp Biochem Physiol C 113 (1996) 61-66
20. Su B.K., and Chen J.C. Effect of saponin immersion on enhancement of the immune response of white shrimp Litopenaeus vannamei and its resistance against Vibrio alginolyticus. Fish Shellfish Immunol 24 (2008) 74-81
21. Biagini G., Sala D., and Zini I. Diethyldithiocarbamate, a superoxide dismutase inhibitor, counteracts the maturation of ischemic-like lesions caused by endothelin-1 intrastriatal injection. Neurosci Lett 90 (1995) 212-216
22. Paglia D.E., and Valentine W.N. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 70 (1967) 248-254
23. Minagawa S., Hikima J., Hirono I., and Aoki T. Expression of Japanese flounder cDNA in insect cells. Dev Comp Immunol 25 (2001) 439-445
24. Sotelo-Mundo R.R., Islas-Osuna M.J., de-la-Re-Vega E., Hernández-López J., Vargas-Albores F., and Yepiz-Plascencia G. cDNA cloning of the lysozyme of the white shrimp Penaeus vannamei. Fish Shellfish Immunol 15 (2003) 325-331
25. Söderhäll I., Banyeekhn E., Mayo S., and Söderhäll K. Hemocyte production and maturation in an invertebrate animal; proliferation and gene expression in hematopoietic stem cell of Pacifastacus leniusculus. Dev Comp Immunol 27 (2003) 661-672
26. Van De Braak C.B.T., Botterblom M.H.A., Liu W., Taverne N., Van Der Knnap W.P.W., and Rombout J.H.W.M. The role of the haemopoietic tissue in haemocyte production and maturation in the black tiger shrimp (Penaeus monodon). Fish Shellfish Immunol 12 (2002) 253-272
27. Sequeira T., Tavares D., and Arala-Chaves M. Evidence for circulating hemocytes proliferation in the shrimp Penaeus japonicus. Dev Comp Immunol 20 (1996) 97-104
28. Holmblad T., and Söderhäll K. Cellular adhesion molecules and antioxidative enzymes in a crustacean, possible role in immunity. Aquaculture 172 (1999) 111-123
29. Campa-Córdova A.I., Hernández-Saavedra N.Y., De Philippis R., and Ascencio F. 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 Shellfish Immunol 12 (2002) 353-366
30. Cerenius L., Lee B.L., and Söderhäll K. The proPO-system: pros and cons for its role in invertebrate immunity. Trends Immunol 29 (2008) 263-271
31. Robertsen B. Modulation of the non-specific defense of fish by structurally conserved microbial polymers. J Fish Dis 9 (1999) 269-290
32. Engstad R.E., and Robertsen B. Recognition of yeast cell wall glucan by Atlantic salmon (Salmo salar) macrophages. Dev Comp Immunol 17 (1993) 253-261
33. Ainsworth A.J. A β-glucan inhibitable zymosan receptors on channel catfish neutrophils. Vet Immunol Immunopathol 41 (1994) 141-152
34. Hayashi T., Hayashi K., Maeda M., and Kojima I. Calcium spirulan, an inhibitor of enveloped virus replication, from a blue green alga Spirulina platensis. J Nutr Sci Vitaminol (Tokyo) 559 (1996) 83-87
35. Aubrey S.M. Spirulina: answer for the hungry (2006). www.familyhealthnews.com
36. Lin Y.C., Vaseeharan B., and Chen J.C. Identification and phylogenetic analysis on lipopolysaccharide and β-1,3-glucan binding protein (LGBP) of kuruma shrimp Marsupenaeus japonicus. Dev Comp Immunol 32 (2008) 1260-1269
37. Kim Y.S., Ryu J.H., Han S.J., Choi K.H., Nam K.B., Jang I.H., et al. Gram-negative bacteria-binding protein, a pattern recognition receptor for lipopolysaccharide and β-1,3-glucan protein that mediates the signaling for the induction of innate immune gene in Drosophila melanogaster cells. J Biol Chem 275 (2000) 32721-32727
38. Lee S.Y., and Söderhäll K. Early events in crustacean innate immunity. Fish Shellfish Immunol 12 (2002) 421-437
39. Liu C.H., Cheng W., Kuo C.M., and Chen J.C. Molecular cloning and characterisation of a cell adhesion molecule, peroxinectin from the white shrimp Litopenaeus vannamei. Fish Shellfish Immunol 17 (2004) 13-26
40. Cheng W., Liu C.H., Tsai C.H., and Chen J.C. Molecular cloning and characterization of a pattern recognition molecule, lipopolysaccharide- and β-1,3-glucan binding protein (LGBP) from the white shrimp Litopenaeus vannamei. Fish Shellfish Immunol 18 (2005) 297-310