Immune response of Litopenaeus vannamei after infection with Vibrio harveyi

Aquaculture

Volumn 406-407, Issue , 2013, Pages 115-120

  Huang, Hai Hong ^a   Liu, Xiao Lin ^a   Xiang, Jian Hai ^b   Wang, Ping ^c  

^a NORTHWEST A F UNIVERSITY   (China)

^b INSTITUTE OF OCEANOLOGY   (China)

^c Nanjiang Marine Biotechnology Company Limited   (China)

Author keywords

AMPs; Hemocyanin; Litopenaeus vannamei; Phenoloxidase; PO; SOD; SSS; Superoxide dismutase; TCBS; THC; Total hemocyte count; TSB; Vibrio harveyi; WSSV

Indexed keywords

BACTERIAL DISEASE; ENZYME ACTIVITY; IMMUNE RESPONSE; INFECTIOUS DISEASE; SHRIMP CULTURE;

DECAPODA (CRUSTACEA); LITOPENAEUS VANNAMEI; SHRIMP WHITE SPOT SYNDROME VIRUS; VIBRIO; VIBRIO HARVEYI;

EID: 84878523003     PISSN: 00448486     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aquaculture.2013.05.010     Document Type: Article

References (31)

1. Adams A. Response of penaeid shrimp to exposure to Vibrio species. Fish & Shellfish Immunology 1991, 1:59-70.
2. Amparyup P., Charoensapsri W., Tassanakajon A. Two prophenoloxidases are important for the survival of Vibrio harveyi challenged shrimp Penaeus monodon. Developmental and Comparative Immunology 2009, 33:247-256.
3. Amparyup P., Charoensapsri W., Tassanakajon A. Prophenoloxidase system and its role in shrimp immune responses against major pathogens. Fish & Shellfish Immunology 2013, 34:990-1001.
4. Antony S.P., Singh I., Jose R.M., Kumar P., Philip R. Antimicrobial peptide gene expression in tiger shrimp, Penaeus monodon in response to gram-positive bacterial probionts and white spot virus challenge. Aquaculture 2011, 316:6-12.
5. Argue B., Arce S., Lotz J., Moss S. Selective breeding of Pacific white shrimp (Litopenaeus vannamei) for growth and resistance to Taura Syndrome Virus. Aquaculture 2002, 204:447-460.
6. Boman H.G., Nilsson-Faye I., Paul K., Rasmuson T. Insect immunity I. Characteristics of an inducible cell-free antibacterial reaction in hemolymph of Samia cynthia pupae. Infection and Immunity 1974, 10:136-145.
7. De Lorgeril J., Gueguen Y., Goarant C., Goyard E., Mugnier C., Fievet J., Piquemal D., Bachere E. A relationship between antimicrobial peptide gene expression and capacity of a selected shrimp line to survive a Vibrio infection. Molecular Immunology 2008, 45:3438-3445.
8. Flegel T., Sritunyalucksana K. Shrimp molecular responses to viral pathogens. Marine Biotechnology 2011, 13:587-607.
9. Fontaine C., Lightner D. Observations on the phagocytosis and elimination of carmine particles injected into the abdominal musculature of the white shrimp, Penaeus setiferus. Journal of Invertebrate Pathology 1974, 24:141-148.
10. Fukui Y., Sawabe T. Improved one-step colony PCR detection of Vibrio harveyi. Microbes and Environments 2007, 22:1-10.
11. García J.C., Reyes A., Salazar M., Granja C.B. Differential gene expression in White Spot Syndrome Virus (WSSV)-infected naïve and previously challenged Pacific white shrimp Penaeus (Litopenaeus) vannamei. Aquaculture 2009, 289:253-258.
12. Garcia-Carreno F.L., Cota K., Navarrete del Toro M.A. Phenoloxidase activity of hemocyanin in whiteleg shrimp Penaeus vannamei: conversion, characterization of catalytic properties, and role in postmortem melanosis. Journal of Agricultural and Food Chemistry 2008, 56:6454-6459.
13. Gauger E.J., Gomez-Chiarri M. 16S ribosomal DNA sequencing confirms the synonymy of Vibrio harveyi and V. carchariae. Diseases of Aquatic Organisms 2002, 52:39-46.
14. Gómez-Anduro G.A., Ascencio-Valle F., Peregrino-Uriarte A.B., Angel C.C., Yepiz-Plascencia G. Cytosolic manganese superoxide dismutase genes from the white shrimp Litopenaeus vannamei are differentially expressed in response to lipopolysaccharides, white spot virus and during ontogeny. Comparative Biochemistry and Physiology. B 2012, 162:120-125.
15. Huang Y.C., Ai H.S., Yin Z.X., Huang X.D., Li S.D., Weng S.P., He J.G. Studies on WSSV-resistant and immune characteristics of the 4th generation selective breeding families for resistance to the white spot syndrome virus (WSSV) of Litopenaeus vannamei. Journal of Fisheries of China 2010, 34:1549-1558. (in Chinese).
16. Huang Y.C., Yin Z.X., Ai H.S., Huang X.D., Li S.D., Weng S.P., He J.G. Characterization of WSSV resistance in selected families of Litopenaeus vannamei. Aquaculture 2011, 311:54-60.
17. Hultmark D., Steiner H., Rasmuson T., Boman H.G. Insect immunity. Purification and properties of three inducible bactericidal proteins from hemolymph of immunized pupae of Hyalophora cecropia. European Journal of Biochemistry 1980, 106:7-16.
18. Iwanaga S., Lee B. Recent advances in the innate immunity of invertebrate animals. Journal of Biochemistry and Molecular Biology 2005, 38:128-150.
19. Ji P.F., Yao C.L., Wang Z.Y. Immune response and gene expression in shrimp (Litopenaeus vannamei) hemocytes and hepatopancreas against some pathogen-associated molecular patterns. Fish & Shellfish Immunology 2009, 27:563-570.
20. Johansson M.W., Keyser P., Sritunyalucksana K., Söderhäll K. Crustacean haemocytes and haematopoiesis. Aquaculture 2000, 191:45-52.
21. Lee S.Y., Lee B.L., Söderhäll K. Processing of an antibacterial peptide from hemocyanin of the freshwater crayfish Pacifastacus leniusculus. The Journal of Biological Chemistry 2003, 278:7927-7933.
22. Li F., Xiang J. Recent advances in researches on the innate immunity of shrimp in China. Developmental and Comparative Immunology 2012, 1-2:11-26.
23. Li C.C., Yeh S.T., Chen J.C. The immune response of white shrimp Litopenaeus vannamei following Vibrio alginolyticus injection. Fish & Shellfish Immunology 2008, 25:853-860.
24. Muňoz M., Vandenbulcke F., Garnier J., Gueguen Y., Bulet P., Saulnier D., Bachère E. Involvement of penaeidins in defense reactions of the shrimp Litopenaeus stylirostris to a pathogenic Vibrio. Cellular and Molecular Life Sciences 2004, 61:961-972.
25. Nickerson K.W., Van Holde K.E. A comparison of molluscan and arthropod hemocyanin-I. Circular dichroism and absorption spectra. Comparative Biochemistry and Physiology. B 1971, 39:855-872.
26. Pan Z., He J., Weng S., Yin Z., Fu X., Li S. Changes in mortality and immunological variables of Litopenaeus vannamei parents and their filial families infected with white spot syndrome under different experimental conditions. Fish & Shellfish Immunology 2008, 25:459-471.
27. Song Y.L., Yu C.I., Lien T.W., Huang C.C., Lin M.N. Haemolymph parameters of Pacific white shrimp (Litopenaeus vannamei) infected with Taura syndrome virus. Fish & Shellfish Immunology 2003, 14:317-331.
28. Van de Braak C., Botterblom M., Huisman E., Rombout J., Van der Knaap W. Preliminary study on haemocyte response to white spot syndrome virus infection in black tiger shrimp Penaeus monodon. Diseases of Aquatic Organisms 2002, 51:149-155.
29. Van de Braak C., Botterblom M., Taverne N., Van Muiswinkel W., Rombout J., Van der Knaap W. The roles of haemocytes and the lymphoid organ in the clearance of injected Vibrio bacteria in Penaeus monodon shrimp. Fish & Shellfish Immunology 2002, 13:293-309.
30. Wang X.W., Zhang X.W., Xu W.T., Zhao X.F., Wang J.X. A novel C-type lectin (FcLec4) facilitates the clearance of Vibrio anguillarum in vivo in Chinese white shrimp. Developmental and Comparative Immunology 2009, 33:1039-1047.
31. Zhang X.B., Huang C.H., Qin Q.W. Antiviral properties of hemocyanin isolated from shrimp Penaeus monodon. Antiviral Research 2004, 61:93-99.