References
- Anderson, D. P., T. Moritomo and R. de Grooth. 1992. Neutrophil, glass-adherent, nitroblue tetrazolium assay gives early indication of immunization effectiveness in rainbow trout. Vet. Immunol. Immunop. 30:419-429 https://doi.org/10.1016/0165-2427(92)90110-C
- Association of Official Analytical Chemists (AOAC). 1995. Official methods of analysis, 16th edition, Arlington VA. Association of Official Analytical Chemists
- Bromage, E. S. and L. Owens. 2002. Infection of barramundi Lates calcarifer with Streptococcus iniae: effects of different routes of exposure. Dis. Aquat. Organ. 52:199-205 https://doi.org/10.3354/dao052199
- Castro, R., I. Zarra and J. Lamas. 2004. Water soluble extracts modulate the respiratory burst activity of turbot phagocytes. Aquaculture 229:67-78 https://doi.org/10.1016/S0044-8486(03)00401-0
- Chen, Y. J., O. S. Kwon, B. J. Min, K. S. Son, J. H. Cho, J. W. Hong and I. H. Kim. 2005. The effects of dietary Biotite V supplementation as an alternative substance to antibiotics in growing pigs. Asian-Aust. J. Anim. Sci. 18:1642-1645 https://doi.org/10.5713/ajas.2005.1642
- Choi, S. M., X. Wang, G. J. Park, S. R. Lim, K. W. Kim, S. C. Bai and I.-S. Shin. 2004. Dietary de-hulled soybean meal as replacement for fish meal in fingerling and growing olive flounder Paralichthys olivaceus (Temminck et Schlegel). Aquac. Res. 35:410-418 https://doi.org/10.1111/j.1365-2109.2004.01046.x
- Couso, N., R. Castro, B. Magarinos, A. Obach and J. Lamas. 2003. Effect of oral administration of glucans on the resistance of gilthead seabream to pasteurellosis. Aquaculture 219:99-109 https://doi.org/10.1016/S0044-8486(03)00019-X
- Eldar, A. and C. Ghittino. 1999. Lactococcus garvieae and Streptococcus iniae infections in rainbow trout Oncorhyncus mykiss: similar, but different diseases. Dis. Aquat. Organ. 36:227-231 https://doi.org/10.3354/dao036227
-
Heo, M. S., C. B. Song, J. Lee, I. I. Yeo, J. Y. Jeon, J. J. Lee, S. C. Chung, K. W. Lee, S. Rho, K. S. Choi and Y. D. Lee. 2001. Characteristics of
$\beta$ -Streptococcus spp. isolated in cultured flounder (Paralichthys olivaceus) of Jeju Island. J. Kor. Fish Soc. 34:365-369 - Hose, S., J. S. Zigler Jr. and D. Sinha. 2005. A novel rat model to study the functions of macrophages during normal development and pathophysiology of the eye. Immunol. Lett. 96:299-302 https://doi.org/10.1016/j.imlet.2004.09.017
- Hume, D. A. 2006. The mononuclear phagocyte system. Curr. Opin. Immunol. 18:49-53 https://doi.org/10.1016/j.coi.2005.11.008
- Karawita, R., N. Siriwardhana, K. W. Lee, M. S. Heo, I. K. Yeo, Y. D. Lee and Y. J. Jeon. 2004. Reactive oxygen species scavenging, metal chelating, reducing power and lipid peroxidation inhibition properties of different solvent fractions from Hizikia fusiformis. Eur. Food Res. Technol. 220:363-371 https://doi.org/10.1007/s00217-004-1044-9
- Kim, K. W., X. J. Wang and S. C. Bai. 2002. Optimum dietary protein level for maximum growth of juvenile olive flounder Paralichthys olivaceus (Temminck et Schlegel). Aquac. Res. 33:673-679 https://doi.org/10.1046/j.1365-2109.2002.00704.x
- Lahav, D., M. Eyngor, A. Hurvitz, C. Ghittino, A. Lublin and L. Eldar. 2004. Streptococcus iniae type infections in rainbow trout Oncorhynchus mykiss. Dis. Aquat. Organ. 62:177-180 https://doi.org/10.3354/dao062177
- Lee, D. J. and G. B. Putman. 1973. The response of rainbow trout to varying protein/energy ratios in a test diet. J. Nutr. 103:916- 922 https://doi.org/10.1093/jn/103.6.916
- Li, P., D. H. Lewis, M. Delbert and D. M. Gatlin III. 2004. Dietary oligonucleotides from yeast RNA influence immune responses and resistance of hybrid striped bass (Morone chrysops x Morone saxatilis) to Streptococcus iniae infection. Fish Shellfish Immun. 16:561-569 https://doi.org/10.1016/j.fsi.2003.09.005
- Lin, M. -F. and S.-Y. Shiau. 2005a. Requirements of vitamin C (Lascorbyl- 2-sulphate and L-ascorbyl-2-polyphosphate) and its effects on non-specific immune responses of grouper, Epinephelus malabaricus. Aquacult. Nutr. 11:183-189 https://doi.org/10.1111/j.1365-2095.2005.00336.x
- Lin, Y. -H. and S.-Y. Shiau. 2005b. Dietary vitamin E requirements of grouper, Epinephelus malabaricus, at two lipid levels, and their effects on immune responses. Aquaculture 248:235-244 https://doi.org/10.1016/j.aquaculture.2005.04.020
- Liu, J. N., Y. Yoshida, M. Q. Wang, Y. Okai and U. Yamashita. 1997. B cell stimulating activity of seaweeds extracts. Int. J. Immunopharmaco. 19:135-142 https://doi.org/10.1016/S0192-0561(97)00016-7
- Magnado'ttir, B. 2006. Innate immunity of fish (overview). Fish Shellfish Immun. 20:137-151 https://doi.org/10.1016/j.fsi.2004.09.006
- Ministry of Maritime Affairs and Fisheries. 2002. Statistical Year Book of Agriculture and Fisheries. Seoul, Korea
- Nakatsugawa, T. 1983. Streptococcus disease of cultured flounder. Fish Pathol. 17:281-285 https://doi.org/10.3147/jsfp.17.281
- Nguyen, H. T. and K. Kanai. 1999. Selective agars for the isolation of Streptococcus iniae from Japanese flounder, Paralychthys olivaceus, and its cultural environment. J. Appl. Microbiol. 86:769-776. https://doi.org/10.1046/j.1365-2672.1999.00724.x
- Nguyen, H. T., K. Kanai and K. Yoshikoshi. 2002. Ecological investigation of Streptococcus iniae in culture Japanese flounder (Paralichthys olivaceus) using selective isolation procedures. Aquaculture 205:7-17 https://doi.org/10.1016/S0044-8486(01)00667-6
- Nikoskelainen, S., S. Verho, K. Airas and E.-M. Lilius. 2005. Adhesion and ingestion activities of fish phagocytes induced by bacterium Aeromonas salmonicida can be distinguished and directly measured from highly diluted whole blood of fish. Dev. Comp. Immunol. 29:525-537 https://doi.org/10.1016/j.dci.2004.10.006
- Okai, Y., K. H. Okai, S. Ishizaka and U. Yamashita. 1997. Enhancing effect of polysaccharides from an edible brown alga, Hijikia fusiformes (Hijikia), on release of tumor necrosis factor alpha from macrophages of endotoxin-nonresponder C3H/HeJ mice. Nutr. Cancer 27:74-79 https://doi.org/10.1080/01635589709514505
- Okai, Y., K. H. Okai, S. Ishizaka, K. Ohtani, I. M. Yuasa and U. Yamashita. 1998. Possible immunomodulating activities in an extract of edible brown algae, Hijikia fusiformes (Hijikia). J. Sci. Food Agric. 76:56-62 https://doi.org/10.1002/(SICI)1097-0010(199801)76:1<56::AID-JSFA927>3.0.CO;2-L
- Panigrahi, A., V. Kiron, J. Puangkaew, T. Kobayashi, S. Satoh and H. Sugita. 2005. The viability of probiotic bacteria as a factor influencing the immune response in rainbow trout Oncorhynchus mykiss. Aquaculture 243:241-254 https://doi.org/10.1016/j.aquaculture.2004.09.032
- Perera, R. P., S. K. Johnson, M. D. Collins and D. H. Lewis. 1994. Streptococcus iniae associated with mortality of Tilapia nilotica x T. aurea hybrids. J. Aquat. Anim. Health 6:335-340 https://doi.org/10.1577/1548-8667(1994)006<0335:SIAWMO>2.3.CO;2
- Peres, H., C. Lim and P. H. Klesius. 2004. Growth, chemical composition and resistance to Streptococcus iniae challenge of juvenile Nile tilapia (Oreochromis niloticus) fed graded levels of dietary inositol. Aquaculture 235:423-432 https://doi.org/10.1016/j.aquaculture.2003.09.021
- Pier, G. B. and S. H. Madin. 1976. Streptococcus iniae sp. Nov., a beta-hemolytic streptococcus isolated from an Amazon freshwater dolphin, Inia geoffrensis. Int. J. Syst. Bacteriol. 26:545-553 https://doi.org/10.1099/00207713-26-4-545
- Selvaraj, V., K. Sampath and V. Sekar. 2005. Administration of yeast glucan enhances survival and some non-specific and specific immune parameters in carp (Cyprinus carpio) infected with Aeromonas hydrophyla. Fish Shellfish Immun. 19:293- 306 https://doi.org/10.1016/j.fsi.2005.01.001
- Shan, B. E., Y. Yoshida, E. Koroda and U. Yamashita. 1999. Immunomodulating activity of seaweed extract on human lymphocytes in vitro. Int. J. Immunopharmaco. 21:59-70 https://doi.org/10.1016/S0192-0561(98)00063-0
- Shelby, R. A., P. H. Klesius, C. A. Shoemaker and J. J. Evans. 2002. Passive immunization of tilapia, Oreochromis niloticus (L.) with anti-Streptococcus iniae whole sera. J. Fish Dis. 25:1-6 https://doi.org/10.1046/j.1365-2761.2002.00327.x
- Shoemaker, C. A., J. J. Evans and P. H. Klesius. 2000. Density and dose: factors affecting mortality of Streptococcus iniae infected tilapia (Oreochromis niloticus). Aquaculture 188:229- 235 https://doi.org/10.1016/S0044-8486(00)00346-X
- Shoemaker, C. and P. H. Klesius. 1997. Streptococcal diseases problems and control- a review. In: (Ed. K. Fitzsimmons), Tilapia Aquaculture, vol. 2. Northeast Regional Agricultural Engineering Service, Ithaca, New York. pp. 671-682
- Siriwardhana, N., K. W. Lee and Y. J. Jeon. 2005. Radical scavenging potential of hydrophilic phlorotannins of Hizikia fusiformis. Algae 20:69-75 https://doi.org/10.4490/ALGAE.2005.20.1.069
- Siriwardhana, N., K. W. Lee, S. H. Kim, J. H. Ha and Y. J. Jeon. 2003a. Antioxidant activity of Hizikia fusiformis on reactive oxygen species scavenging and lipid peroxidation inhibition. Food Sci. Technol. Int. 9:339-348 https://doi.org/10.1177/1082013203039014
- Siriwardhana, N., K. W. Lee, S. H. Kim, J. H. Ha, G. T. Park and Y. J. Jeon. 2003b. Lipid peroxidation inhibitory effects of Hizikia fusiformis methanolic extract on fish oils and linoleic acid. Food Sci. Technol. Int. 10:65-72 https://doi.org/10.1177/1082013204043883
- Siriwardhana, N., Y. J. Jeon, S. H. Kim, J. H. Ha, S. J. Heo and K. W. Lee. 2004. Enzymatic hydrolysis for effective extraction of antioxidative compounds from Hizikia fusiformis. Algae 19:59-68 https://doi.org/10.4490/ALGAE.2004.19.1.059
- Skerget, M., P. Kotnik, M. Hadolin, A. R. Hras, M. Simonic and Z. Knez. 2005. Phenols, proanthocyanidins, flavones and flavonols in some plant materials and the antioxidant activities. Food Chem. 89:191-198 https://doi.org/10.1016/j.foodchem.2004.02.025
- Stasiak, S. A. and P. C. Bauman. 1996. Neutrophil activity as a potential bioindicator for contaminant analysis. Fish Shellfish Immun. 6:537-539 https://doi.org/10.1006/fsim.1996.0050
- Stoffregen, D. A., S. C. Backman, R. E. Perham, P. R. Bowser and J. G. Babish. 1996. Initial disease report of Streptococcus iniae infection in hybrid stripped (sunshine) bass and successful therapeutic intervention with the flouroquinolone antibacterial enrofloxacin. J. World Aquacult. Soc. 27:420-434 https://doi.org/10.1111/j.1749-7345.1996.tb00626.x
- Tosi, M. F. 2006. Innate immune responses to infection. J. Allergy Clin. Immun. 116:241-249
- Yeh, S. T., C. S. Lee and J. C. Chen. 2006. Administration of hotwater extract of brown seaweed Sargassum duplicatum via immersion and injection enhances the immune resistance of white shrimp Lipopenaeus vannamei. Fish Shellfish Immun. 20:332-345 https://doi.org/10.1016/j.fsi.2005.05.008
-
Zhou, J., X.-L. Song, J. Huang and X.-H. Wang. 2006. Effects of dietary supplementation of A3
$\alpha$ -peptidoglycan on innate immune responses and defense activity of Japanese flounder (Paralichthys oilvaceus). Aquaculture 251:172-181 https://doi.org/10.1016/j.aquaculture.2005.06.015 - Zlotkin, A., H. Hershko and A. Eldar. 1998. Possible transmission of Streptococcus iniae from wild fish to cultured marine fish. Appl. Environ. Microb. 64:4065-4067
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