Alnus firma supplementation diet on haematology and innate immune response in olive flounder against Tenacibaculum maritimum

• Autorzy: Harikrishnan R. , Kim M. C. , Kim J. S. , Kim D. H. , Hong S. H. , Heo M. S.
• Języki publikacji: EN

Abstrakty

EN

The effect of 0%, 0.01%, 0.1%, and 1.0% supplementation of diets with Alnus firma on haematological and innate immune parameters in olive flounder (Paralichthys olivaceus) against Tenacibaculum maritimum infection was investigated. The supplemented diets were given for 30 d and then the fish were infected with T. maritimum. The particular diets were continued for 1, 2, and 4 weeks after the infection. The white blood cell count did not significantly change after any diet in the first week, whereas in 2nd and 4th week it was significantly increased in fish fed 0.1% and 1.0% supplementation diets. The number of red blood cells did not significantly change in fish fed 0.01% and 0.1% supplementation diets in any weeks but it was significantly increased in 1.0% supplementation diet. The haemoglobin and haematocrit levels did not significantly change after any diet in the first week; however, significantly increased in fish fed 0.1%, and 1.0% supplementation diets for 2 and 4 weeks. The biochemical parameters such as total protein and cholesterol levels significantly increased in fish fed 0.1% and 1.0% supplementation diets in the 2nd and 4th week, whereas in case of calcium levels the changes were observed from weeks 1 to 4. The glucose level significantly increased in all diets in weeks 2 and 4. The respiratory burst activity and lysozyme activity significantly were enhanced in 0.1% and 1.0% supplementation diets from weeks 1 to 4 compared to 0% diet. The cumulative mortality was lower in groups fed 0.1% and 1.0% supplemented diets than in the 0.01% diet. This study reported that 0.1% and 1.0% Alnus firma-supplemented diet protected the olive flounder against T. maritimum infection due to positive haematological, biochemical, and innate immune parameter changes.

• Wydawca: -
• Czasopismo: Bulletin of the Veterinary Institute in Puławy
• Rocznik: 2011
• Tom: 55
• Numer: 4
• Opis fizyczny: p.649-655,fig.,ref.

Twórcy

autor

Harikrishnan R.

• Marine Applied Microbes and Aquatic Organism Disease Control Laboratory, Department of Aquatic Biomedical Sciences, School of Marine Biomedical Sciences, College of Ocean Sciences and Marine and Environmental Research Institute, Jeju National University, Jeju 690-756, South Korea

autor

Kim M. C.

autor

Kim J. S.

autor

Kim D. H.

autor

Hong S. H.

autor

Heo M. S.

Bibliografia

• 1. Alexander J.B., Ingram G.A.: Noncellular nonspecific defense mechanisms of fish. Annu Rev Fish Dis 1992, 2, 249-279.
• 2. Amend D.: Potency testing of fish vaccines. Dev Biol Stand 1981, 49, 447-454.
• 3. Asakawa Y.: Chemical constituents of Alnusfirma (Betulaceae). I. Phenyl propane derivatives isolated from Alnus firma. Bull Chem Soc Jpn 1982, 43, 2223-2229.
• 4. Avendano-Herrera R., Toranzo A.E., Magarinos B.: Tenacibaculosis infection in marine fish caused by Tenacibaculum maritimum: a review. Dis Aquat Org 2006, 71, 255-266.
• 5. Avendaño-Herrera R., Magariños B., López-Romalde S., Romalde J.L., Toranzo A.E.: Phenotypic characterization and description of two major O-serotypes in Tenacibaculum maritimum strains isolated from marine fishes. Dis Aquat Org 2004, 58, 1-8.
• 6. Avendaño-Herrera R., Rodriguez J., Magariños B., Romalde J.L., Toranzo A.E.: Intraspecific diversity of the marine fish pathogen Tenacibaculum maritimum as determined by randomly amplified polymorphic DNA-PCR. J Appl Microbiol 2004, 96, 871-877.
• 7. Baxa D.V., Kawai K., Kusuda R.: Characteristics of gliding bacteria isolated from diseased cultured flounder, Paralichthys olivaceous. Fish Pathol 1986, 21, 251-258.
• 8. Bernardet J.F., Campbell A.C., Buswell J.A.: Flexibacter maritimus is the agent of black patch necrosis in Dover sole in Scotland. Dis Aquat Org 1990, 8, 233-237.
• 9. Bernardet J.-F., Kerouault B., Michel C.: Comparative study on Flexibacter maritimus strains isolated from farmed sea bass (Dicentrarchus labrax) in France. Fish Pathol 1994, 29, 105-111.
• 10. Brenden S.A., Huizinga H.W.: Pathophysiology of experimental Aeromonas hydrophila infection in goldfish, Carassius auratus (L.). J Fish Dis 1986, 9, 163-167.
• 11. Campbell T.W.: Hematology of lower vertebrates. In: Proceedings of the 55th Annual meeting of the American College of Veterinary Pathologists (ACUPC). www.ivis.org/proceedings/ACVP/2004/Campbell/ivis.pdf; 2004.
• 12. Chung S., Secombes C.J.: Analysis of events occurring within teleost macrophages during the respiratory burst. Comp Biochem Physiol 1988, 89B, 539-543.
• 13. Cipriano R.C., Novak B.M., Flint D.E., Cutting D.C.: Reappraisal of the federal fish health recommendation for disinfecting eggs of Atlantic salmon in iodophor. J Aquat Anim Health 2001, 13, 320-327.
• 14. Costello M.J., Grant A., Davies I.М., Cecchini S., Papoutsoglou S., Quigley D., Saroglia M.: The control of chemicals used in aquaculture in Europe. J Appl Ichthyol 2001, 17, 173-180.
• 15. Derksen, J.A., Ostland, V.E., Ferguson, H.W.: Effects of hydrogen peroxide on clearance of formalin-killed Flavobacterium branchiophilum from the gills of rainbow trout, Oncorhynchus mykiss (Walbaum). J Fish Dis 1999, 22, 59-67.
• 16. Ellis A.E.: Lysozyme assays. In: Stolen J.S., Fletcher T.C., Anderson D.P., Roberson B.S., van Muiswinkel W.B. (Eds.), Techniques in fish immunology. SOS Publications Fair Haven, USA, 1990, pp. 101-103.
• 17. Ellsaesser C.F., Clem L.W.: Haematological and immunological changes in channel catfish stressed by handling and transport. J Fish Biol 1986, 28, 511-521.
• 18. Fearon D.T., Locksley R.M.: The instructive role of innate immunity in the acquired immune response. Science 1996, 272, 50-54.
• 19. Gollock M.J., Kennedy C.R., Quabius E.S., Brown J.A.: The effect of parasitism of European eels with the nematode, Anguillicola crassus on the impact of netting and aerial exposure. Aquaculture 2004, 233, 45-54.
• 20. Handlinger J., Soltani H., Percival V.: The pathology of Flexibacter maritimus in aquaculture species of Tasmania, Australia. J Fish Dis 1997, 20, 159-168.
• 21. Haney D.C., Hursh D.A., Mix M.C., Winton J.R.: Physiological and hematological changes in chum salmon artificially infected with erythrocytic necrosis virus. J Aquat Animal Health 1992, 4, 48-57.
• 22. Hawk P.B., Oser B.L., Summersion H.W.: Practical Physiological Chemistry. Ed. McGraw-Hill, New York, 1954, p. 1439.
• 23. Hill B.J.: Infectious pancreatic necrosis virus and its virulence. In: Roberts R.J. (Ed), Microbial Diseases of Fish. Academic Press, New York, 1982, pp. 91-114.
• 24. Holeton G.F., Randall D.J.: The effect of hypoxia upon the partial pressure of gasses in the blood and water afferent and efferent to the gills of rainbow trout. J Exp Biol 1967, 46, 317-327.
• 25. Houston A.H.: Blood and circulation. In: Schreck C.B., Moyle P.B. (Eds.), Methods for Fish Biology. American Fisheries Society , Maryland, USA, 1990, pp. 273-334.
• 26. Jian J., Wu Z.: Effects of traditional Chinese medicine on nonspecific immunity and disease resistance of large yellow croaker Pseudosciaena crocea (Richardson). Aquaculture 2003, 218, 1-9.
• 27. Kim T.J.: Korean resources plants. Vol. 1. Seoul National University Press, Seoul, 1996, p. 94.
• 28. Larsen H.N., Snieszko S.F.: Modification of the microhematocrit technique with trout blood. Trans Am Fish Soc 1961, 90, 139-142.
• 29. Lee E.H., Kim K.H.: CpG-ODN increases resistance of olive flounder (Paralichthys olivaceus) against Philasterides dicentrachi (Ciliophora: Scuticociliatia) infection. Fish Shellfish Immunol 2009, 26, 29-32.
• 30. Lee M., Lee H.K., Kim S.H., Kim Y.C., Sung S.H.: Chemical constituents of Alnus firma and their inhibitory activity on lipopolysaccharide-induced nitric oxide production in BV2 microglia. Planta Med 2010, 76, 1007-1010.
• 31. Lumsden J.S., Ostland V.E., Ferguson H.W.: Use of hydrogen peroxide to treat experimentally induced bacterial gill disease in rainbow trout. J Aquat Anim Health 1998, 10, 230-240.
• 32. Martinez-Silvestre A., Mateo J.A., Silveira L.S.: Presencia de protozoos intraeritrocitarios en el lagarto gigante de La Gomera (Gallotia simonyi gomerana). Bol Asoc Herpetol Espan 2001, 12, 90-92.
• 33. Powell M.D., Carson J., van Gelderen R.: Experimental induction of gill disease in Atlantic salmon Salmo salar smolts with Tenacibaculum maritimum. Dis Aquat Org 2004, 61, 179-185.
• 34. Rath R.K.: Freshwater Aquaculture, Scientific Publishers, Jodhpur, India, 2000.
• 35. Scott A.L., Rogers W.A.: Hematological effects of prolonged sublethal hypoxia on channel catfish Ictalurus punctatus (Rafinesque). J Fish Biol 1981, 18, 591-601.
• 36. Siwicki A.K., Anderson D.P., Rumsey G.L.: Dietary intake of immunostimulants by rainbow trout affects non-specific immunity and protection against furunculosis. Vet Immunol Immunopathol 1994, 41, 125-139.
• 37. Tendencia E.A.: Effect of iodine disinfection on the bacterial flora and hatching rate of grouper, Epinephelus coioides eggs at the cleavage and eyed stages. Bull Eur Assoc Fish Pathol 2001, 21, 160-163.
• 38. Toranzo A.E., Magariños B., Romalde J.L.: A review of the main bacterial fish diseases in mariculture system. Aquaculture 2005, 246, 37-61.
• 39. Wakabayashi H., Hikida H., Masumura K.: Flexibacler maritimus sp. nov., a pathogen of marine fishes. Int J System Bacteriol 1986, 36, 396-398.
• 40. Wright P.A., Perry S.F., Moon T.W.: Regulation of hepatic gluconeogenesis and glycogenolysis by catecholamines in rainbow trout during environmental hypoxia. J Exp Biol 1989, 147, 169-188.
• 41. Yu Y.B., Miyashiro H., Nakamura N., Hattori M., Park J.C.: Effects of triterpenoids and flavonoids isolated from Alnus firma on HIV-1 viral enzymes. Arch Pharm Res 2007, 30, 820-826.

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