White shrimp Litopenaeus vannamei immersed in seawater containing Sargassum hemiphyllum var. chinense powder and its extract showed increased immunity and resistance against Vibrio alginolyticus and white spot syndrome virus

Fish and Shellfish Immunology

Volumn 31, Issue 2, 2011, Pages 286-293

  Huynh, Truong Giang ^a   Yeh, Su Tuen ^a   Lin, Yong Chin ^a   Shyu, Jeng Feng ^b   Chen, Li Li ^a   Chen, Jiann Chu ^a  

^a NATIONAL TAIWAN OCEAN UNIVERSITY   (Taiwan)

^b NATIONAL PENGHU UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Taiwan)

Author keywords

Immune response; Litopenaeus vannamei; Sargassum hemiphyllum var. chinense; Vibrio alginolyticus; White spot syndrome virus (WSSV)

Indexed keywords

DECAPODA (CRUSTACEA); LITOPENAEUS VANNAMEI; SARGASSUM; SARGASSUM HEMIPHYLLUM; SHRIMP WHITE SPOT SYNDROME VIRUS; VIBRIO ALGINOLYTICUS;

EID: 79959781848     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2011.05.014     Document Type: Article

References (46)

1. Jiravanichpaisal P., Lee B.L., Söderhäll K. Cell-mediated immunity in arthropods: hematopoiesis, coagulation, melanization and opsonization. Immunobiology 2006, 211:213-236.
2. Rodríguez J., Le Moullac G. State of the art of immunological tools and health control of penaeid shrimp. Aquaculture 2000, 191:109-119.
3. Lightner D.V., Redman R.M. Strategies for the control of viral diseases of shrimp in the Americas. Fish Pathol 1998, 33:165-180.
4. Lavilla-Pitogo C.R., Leaño E.M., Paner M.G. Mortalities of pond-cultured juvenile shrimp, Penaeus monodon, associated with dominance of luminescent vibrios in the rearing environment. Aquaculture 1998, 164:337-349.
5. Raa J. The use of immunostimulatory substances in fish and shellfish farming. Rev Fish Sci 1996, 4:288-299.
6. Sakai M. Current research status of fish immunostimulant. Aquaculture 1999, 172:63-92.
7. Smith V.J., Brown J.H., Hauton C. Immunostimulation in crustaceans: does it really protect against infection?. Fish Shellfish Immunol 2004, 15:71-90.
8. Zhang H.L., Zhang Z.E., Wu P.P. Study on the effective ingredients and anti-tumor in Sargassum fusiforme. J Mar Drugs 1988, 4:1-8.
9. Zhuang C., Itoh H., Mizuno T., Ito H. Antitumor active fucoidan from the brown seaweed Umitorano (Sargassum thunbergii). Biosci Biotechnol Biochem 1995, 59:563-567.
10. Asker M.M.S., Mohamed S.F., Ali F.M., El-Sayed O.H. Chemical structure and antiviral activity of water-soluble sulphated polysaccharides from Sargassum latifolium. J Appl Sci Res 2007, 3:1178-1185.
11. Hellio C., de La Broise D., Dufossé L., Le Gal Y., Bourgougnon N. Inhibition of marine bacteria by extracts of macroalgae: potential use for environmentally friendly antifouling paints. Mar Environ Res 2001, 52:231-247.
12. Huang X., Zhou H., Zhang H. The effect of Sargassum fusiforme polysaccharide extracts on vibriosis resistance and immune activity of the shrimp Fenneropenaeus chinensis. Fish Shellfish Immunol 2006, 20:750-757.
13. Yeh S.T., Lee C.S., Chen J.C. Administration of hot-water extract of brown seaweed Sargassum duplicatum via immersion and injection enhances the immune resistance of white shrimp Litopenaeus vannamei. Fish Shellfish Immunol 2006, 20:332-345.
14. Chotigeat W., Tongsupa S., Supamataya K., Phongdara A. Effect of fucoidan on disease resistance of black tiger shrimp. Aquaculture 2004, 233:23-30.
15. Liu C.H., Cheng W., Hsu J.P., Chen J.C. Vibrio alginolyticus infection in the white shrimp Litopenaeus vannamei confirmed by polymerase chain reaction and 16S rDNA sequencing. Dis Aquat Org 2004, 61:169-174.
16. Yeh S.T., 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 2009, 26:724-730.
17. Chen K.Y., Hsu T.C., Huang P.Y., Kang S.T., Lo C.F., Huang W.P., et al. Penaeus monodon chitin-binding protein (PmCBP) is involved in white spot syndrome virus (WSSV) infection. Fish Shellfish Immunol 2009, 27:460-465.
18. Dubois M., Gilles K.A., Hamilton J.K., Rebers P.A., Smith F. Colorimetric method for determination of sugars and related substances. Anal Chem 1956, 28:350-356.
19. Terho T.T., Hartiala K. Method for determination of the sulfate content of glycosaminoglycans. Anal Biochem 1971, 41:471-476.
20. Chan S.M., Rankin S.M., Keeley L.L. Characterization of the molt stages in Penaeus vannamei: setogenesis and hemolymph levels of total protein ecdysteroids, and glucose. Biol Bull 1988, 175:185-192.
21. Smith V.J., Söderhäll K. β-1,3-glucan activation of crustacean hemocytes in vitro and in vivo. Biol Bull 1983, 164:299-314.
22. Bell K.L., Smith V.J. In vitro superoxide production by hyaline cells of the shore crab Carcinus maenas (L.). Dev Comp Immunol 1993, 17:211-219.
23. Ellis A.E. Lysozyme assay. Technique in fish immunology-1 1990, 101-103. SOS Publications, Fair Haven, NJ. J.S. Stolen, T.C. Fletcher, D.P. Anderson, B.S. Roberson, W.B. van Muiswinkel (Eds.).
24. Tayag C.M., Lin Y.C., Li C.C., Liou C.H., Chen J.C. 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 Shellfish Immunol 2010, 28:764-773.
25. Lanz H., Hernandez S., Garrido-Guerrero E., Tsuysumi V., Arechiqat H. Prophenoloxidase system activation in the crayfish Procambarus clarki. Dev Comp Immunol 1993, 17:399-406.
26. Song Y.L., Hsieh Y.T. Immunostimulation of tiger shrimp (Penaeus monodon) hemocytes for generation of microbicidal substances: analysis of reactive oxygen species. Dev Comp Immunol 1994, 18:201-209.
27. Söderhäll K., Cerenius L., Johansson M.W. The prophenoloxidase activating system and its role in invertebrate defense. Ann N Y Acad Sci 1994, 712:155-161.
28. Perazzolo L.M., Barracco M.A. The prophenoloxidase activating system of the shrimp Penaeus paulensis and associated factors. Dev Comp Immunol 1997, 21:385-395.
29. Söderhäll I., Banyeekhn E., Mayo S., Söderhäll K. Hemocyte production and maturation in an invertebrate animal; proliferation and gene expression in hematopoietic stem cell of Pacifastacus leniusculus. Dev Comp Immunol 2003, 27:661-672.
30. Sequeira T., Tavares D., Arala-Chaves M. Evidence for circulating hemocytes proliferation in the shrimp Penaeus japonicus. Dev Comp Immunol 1996, 20:97-104.
31. Van de Braak C.B.T., Botterblom M.H.A., Liu W., Taverne N., Van der Knnap W.P.W., 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 2002, 12:253-272.
32. Painter T.J. Algal polysaccharides. The polysaccharide 1983, vol. 2:195-285. Academic Press, New York, NY. G.O. Aspinall (Ed.).
33. Lin Y.C., Vaseeharan B., 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 2008, 32:1260-1269.
34. Lee S.Y., Wang R., Söderhäll K. A lipopolysaccharide- and β-1,3-glucan-binding protein from hemocytes of the freshwater crayfish Pacifastacus leniusculus. J Biol Chem 2000, 275:1337-1343.
35. Sritunyalucksana K., Lee S.Y., Söderhäll K. A β-1,3-glucan binding protein from the black tiger shrimp Penaeus monodon. Dev Comp Immunol 2002, 26:237-245.
36. Wang Y.C., Chang P.S., Chen H.Y. Differential time-series expression of immune-related genes of pacific white shrimp Litopenaeus vannamei in response to dietary inclusion of β-1,3-glucan. Fish Shellfish Immunol 2008, 24:113-121.
37. Luo T., Zhang X., Shao Z., Xu X. PmAV, a novel gene involved in virus resistance of shrimp Penaeus monodon. FEBS Lett 2003, 551:53-57.
38. Ma T.H.T., Tiu S.H., He J.G., Chan S.M. Molecular cloning of a C-type lectin (LvLT) from the shrimp Litopenaeus vannamei: early gene down-regulation after WSSV infection. Fish Shellfish Immunol 2007, 23:430-437.
39. Lee S.Y., Söderhäll K. Early events in crustacean innate immunity. Fish Shellfish Immunol 2002, 12:421-437.
40. Paulsen B.S. Biologically active polysaccharides as possible lead compounds. Phytochem Rev 2001, 1:379-387.
41. Smit A. Medicinal and pharmaceutical uses of seaweed natural products: a review. J Appl Phycol 2004, 16:245-262.
42. Takahashi Y., Uehara K., Watanabe R., Okumura T., Yamashita T., Omura H. Efficacy of oral administration shrimp in Japan. Advance in shrimp biotechnology 1998, 171-173. National Center for Genetic Engineering and Biotechnology, Bangkok. T.W. Flegel (Ed.).
43. Witvrouw M., de Clerq E. Sulfated polysaccharides extracted from sea algae as potential antiviral drugs. Gen Pharmacol 1997, 29:497-511.
44. Zhu W., Ooi V.E.C., Chan P.K.S., Ang P.O. Inhibitory effect of extracts of marine algae from Hong Kong against Herpes simplex virus. Proceedings of the 17th international seaweed symposium 2003, 159-164. Oxford University Press, Oxford. A.R.O. Chapman, R.J. Anderson, V.J. Vreeland, I.R. Davison (Eds.).
45. Robalino J., Payne G., Parnell P., Shepard E., Grimes A.C., Metz A. Inactivation of White Spot Syndrome Virus (WSSV) by normal rabbit serum: implications for the role of the envelope protein VP28 in WSSV infection of shrimp. Virus Res 2006, 118:55-61.
46. Tsai J.M., Wang H.C., Leu J.H., Kou G.H., Lo C.F., Hsiao H.H., et al. Genomic and proteomic analysis of thirty-nine structural proteins of shrimp white spot syndrome virus. J Virol 2004, 78:1136-11370.