对虾白斑综合症抗病力指标的筛选及其应用的研究
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摘要
近年来,中国迅速发展的海水养殖业面临着病害和养殖环境退化等诸多问
    题的困扰,其中对虾养殖业受到白斑综合症病毒(WSSV)的冲击很大。本文针
    对这一问题,系统研究了对虾在白斑综合症病毒感染和环境因子胁迫下先天性免
    疫因子的动态变化过程,筛选出了能够准确反映对虾健康状况的免疫因子,进而
    将其运用到对虾抵抗 WSSV 的机制和环境胁迫对对虾健康状况的影响的研究中。
     在对现有文献进行全面综述的基础上,我们通过实验系统比较了中国对虾
    和日本对虾在摄食感染 WSSV 后的死亡率、免疫学因子和感染病毒的变化情况,
    以及在氨氮胁迫下对虾感染 WSSV 过程中免疫学因子的变化情况。根据各种免
    疫学因子的变化情况,从中筛选出与 WSSV 感染直接相关的免疫学因子,并优
    选出一氧化氮合成酶(NOS)作为反映对虾抗病力的重要指标,它直接反映出了
    两种对虾对白斑综合症病毒抵抗能力的差异,应当是导致其对 WSSV 敏感性差
    异的主要原因之一。其水平也受氨氮胁迫的影响。
     在此基础上,我们建立了对虾血细胞中诱导型一氧化氮合成酶(iNOS)的
    鉴定方法—硝基四氮唑蓝(NBT)还原法和血细胞形态法以及酶活力的测定方法
    —L-瓜氨酸分析法和亚硝酸盐分析法并优化了鉴定和测量条件,结果显示: 对虾
    血细胞在 4oC 下与 L-精氨酸和 LPS 孵育 8h 以及当 L-精氨酸浓度为 2.5mmol l-1,
    LPS 浓度为 100μg ml-1,Ca2+浓度为 2.5mmol l-1 时,iNOS 活力的测定结果最佳。
     我们通过NBT还原法和血细胞形态法在中国对虾和日本对虾血细胞中鉴定
    到了iNOS,并通过亚硝酸盐法和L-瓜氨酸法对比研究了感染WSSV后这两种对虾
    血细胞中iNOS的变化情况,结果显示:在WSSV感染初期,WSSV可以诱导中国
    对虾和日本对虾产生iNOS,且日本对虾比中国对虾的iNOS更容易被LPS所诱导。
    此后随着病毒的增殖,iNOS活性显著降低,对虾也趋于死亡。iNOS活力的差异
    可能是日本对虾较中国对虾对WSSV的抵抗力强的原因之一。
     本文在系统比较两种对虾感染WSSV病毒过程中抗病力指标变化的基础上,
    优选出与WSSV感染直接相关的抗病力指标,并首次对对虾的一氧化氮合成酶进
    行了系统的研究,所得到的结果为深入了解对虾对白班综合症病毒的抗病力机制,
    并建立和发展相应的病害防御措施提供了科学依据。
The rapid development of the mariculture industry in China is now facing
    the problems such as diseases and degradation of mariculture environment, among
    which the shrimp-culture industry is particularly impacted by the disease of white spot
    syndrome virus (WSSV). Focusing on this topic, we studied systematically the
    variation of immune parameters of Chinese shrimp Fenneropenaeus chinensis and
    Kuruma prawn Marsupenaeus japonicus after infection of WSSV by oral route, with
    attention of comparing the immunocompetence of the two species to WSSV infection.
    The immune parameters were also evaluated in Kuruma prawn M. japonicus under the
    stress of ammonia-N and WSSV infection. Based on these works, we discriminated
    the immune parameters closely related to WSSV infection from all the parameters
    used, and found nitric oxide synthase (NOS) a reliable parameter for indicating
    disease resistance ability to WSSV infection.
     Based on these findings, we developed nitro blue tetrazolium (NBT) method and
    cellular morphological approaches to identify the inducible NOS (iNOS) in the
    haemocytes of Kuruma prawn M. japonicus and Chinese shrimp F. chinensis. The
    conditions for NBT method were modified to make them suitable for the analysis of
    iNOS in shrimp blood cells. Results showed that the optimal concentrations of
    L-arginine, lipopolysaccharide (LPS) and Ca2+ for NBT method are 2.5mmol l-1,
    100μg ml-1 and 2.5mmol l-1, respectively. Meanwhile, two methods for iNOS activity
    assay based on the analysis of nitrite and L-citrulline concentrations were also applied
    to study iNOS activity in the haemocytes of shrimp. The results showed that an
    incubation time of 8 hours is most suitable for the analysis of iNOS enzyme activity.
    The four methods could identify iNOS in shrimp haemocytes and analyze the activity
    effectively, thus provide a good way for the further study of role of iNOS in innate
     2
    
    
    对虾抗白斑综合症病毒的免疫学研究
    immunology of shrimps.
     Furthermore, the iNOS was identified in the haemocytes of Chinese shrimp F.
    chinensis and Kuruma prawn M. japonicus, and the methods developed were
    employed to evaluate their immunocompetence to WSSV infection in shrimps. The
    variations of iNOS activity in both penaeid species post-challenge of WSSV were
    assayed with the methods of L-citrulline analysis and nitrite analysis. The result
    showed that iNOS activity in WSSV infected Chinese shrimp F. chinensis and
    Kuruma prawn M. japonicus increased at 12 and 48 hours post-inoculum, but
    decreased sharply after 36 and 72 hours post-inoculum respectively. LPS inducible
    NOS activity also decreased significantly with the time elapsed in WSSV infected
    shrimps. Results of WSSV detection with the Dig-DNA Probe dot blot hybridization
    test showed that WSSV of the two penaeid species couldn’t be detected until iNOS
    started decreasing. It can be concluded that WSSV infection can stimulate the iNOS
    synthesis in shrimps. However, the enzyme activity decreased sharply after the
    proliferation of virus. Therefore, iNOS can be considered as a valuable index for
    indicating the health status of Chinese shrimp F. chinensis and Kuruma prawn M.
    japonicus. In comparison with Chinese shrimp F. chinensis, the iNOS in the
    haemocytes of Kuruma prawn M. japonicus are more inclined to be induced by LPS
    after WSSV infection at early stage of infection, which might account for the
    relatively longer surviving time of M. japonicus after WSSV infection.
     Based on the findings in the comparative study of immune parameters between
    Chinese shrimp Fenneropenaeus chinensis and Kuruma prawn Marsupenaeus
    japonicus, this thesis firstly carry on the researches of iNOS activity in shrimps, and
    find it a reliable parameter for indicating the disease resistance ability in shrimps. The
    results here could offer a sound scientific basis for the better understanding of the
    mechanism of shrimp disease resistance ability to WSSV infection, as well as the
    development of countermeasures for
引文
Acosta F, Ruiz de Galarreta C M, Ellis A E, Díaz R, Gómez V, D Padilla and F Real.
     Activation of the nitric oxide response in gilthead seabream after experimental
     infection with Photobacterium damselae subsp. Piscicida. Fish & Shellfish
     Immunology, 2004(16): 581-588.
    Adams A. Response of penaeid shrimp to exposure to Vibrio species. Fish Sellfish
     Immunol., 1991(1): 59– 70.
    Adams W J, Kimerle R A, & Barnett Jr J W. Sediment criteria and aquatic life
     assessment. Environ. Sci. Technol., 1992 (26): 1865–1875.
    Adams M S, Crumby W D, Greeley M S Jr, et al. Responses of fish populations and
     communities to pulp mill effluents: A holistic assessment. Ecotoxicol. Environ.
     Saf, 1992 (24): 347-360.
    Adema C, van der Knaap M, Sminia W P W. Molluscan haemocyte mediated
     cytotoxicity: the role of reactive oxygen intermediates. Rev. Aquat. Sci., 1991(4):
     201–223.
    Adler H, Beland J L, Del-Pan NC, Kobzik L, Brewer J P, Martin T R, Rimm I J.
     Suppression of herpes simplex virus type 1 (HSV-1)-induced pneumonia in mice
     by inhibition of inducible nitric oxide synthase (iNOS, NOS2). J. Exp. Med.,
     1997(185): 1533-1540.
    Akaike T, & Maeda H. Nitric oxide and virus infection. Immunology,
     2000(101):300-308.
    Amirante G A. 1986. Agglutinins and lectins of Crustacea. In: Gupta.
     A.P.(Ed.),Hemocytic and Hemoral Immunity in Arthropods. Wiley, New York.
     pp. 359-380.
    Arimoto R, Tripp M P. Characterization of bacterial agglutinin in the hemolymph of
     the hard clam Mercenaria meercenaria. J.Invertbr.Pathol. 1977(30): 406-413.
    Ashida M, Soderhall K. The prophenoloxidsae activating system in crayfish. Comp.
     Biochem. Physiol., 1984(77B):21-26.
     93
    
    
    参考文献
    Ashida M, Yamazaki H I. Biochemistry of the Phenoloxidase System In Insects: With
     Special Reference to Activation. In: Ishizaki, H. ed., Molting and Metamorphosis.
     Springer Verlag Berlin: Japan Sci Soc Press, 1990: 239-263.
    Babior B M. Oxidants from phagocytes: agents of defense and destruction. Blood,
     1984(64): 959–966.
    Bachère E, Destoumieux D, Bulet P. Penaeidins, antimicrobial peptides of shrimp: a
     comparison with other effectors of innate immunity. Aquaculture, 2000(191):
     71-88.
    Bachère E, Miahle E, Rodriguez J. Identification of defence effectors in the
     haemolymph of crustaceans with particular reference to the shrimp Penaeus
     japonicus (Bate), propects and applications. Fish Shellfish Immunol., 1995a(5):
     597-612.
    Bachère E, Mialhe E, Noel D, Boulo V, Morvan A, Rodriguez J. Knowledge and
     Research Prospects in Marine Mollusk and Crustacean immunology. Aquaculture,
     1995b(132): 17-32.
    Bachère E, Noel T, Mialhe E. Effects of environmental pollutants and
     chemotherapeutic agents on the chemiluminescence of the hemocytes from the
     oyster Crassostrea gigas. Eur. Aquacult. Soc., Spec. Publ., Dublin, 1991: 14–15.
    Bachère E. Shrimp immunity and disease control - Introduction. Aquaculture, 2000
     (191): 3-11.
    Barracco M A, Duvic B, Soderhall K. β-1,3-glucan binding protein from the crayfish
     Pacifastacus leniusculus, when reached with a β 43 man, induces spreading and
     degranulation of crayfish granular cells. Cell Tissue Res., 1991(266): 491-497.
    Bauchau A G. Crustaceans. In: Ratcliffe N A and Rowley A F (editors). Invertebrate
     blood cells. Academic Press, London and New York, 1981, pp.385-420.
    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.
    Benencia F, & Courreges M C. Nitric oxide and macrophage antiviral extrinsic
     activity. Immunology, 1999(98): 363–370.
    Bi Z and Reiss C S. Inhibition of vesicular stomatitis virus infection by nitric oxide. J.
     94
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
     Virol, 1995(69):2208–2213.
    Bishop J M, Gosselink J G & Stone. Oxigen consumption and haemolymph
     osmolality of brown shrimp, Penaeus aztecus. Fisheries Bulletin, 1980(78):
     741-757.
    Bradford M M. A rapid and sensitive method for the quantification of microgram
     quantities of protein utilizing protein-dye binding. Anal. Biochem.,
     1976(72):248-254.
    Bray W A, Lawrence A L, Leung-Trujillo J R. The effect of salinity on growth and
     survival of Penaeus vannamei, with observations on the interaction of IHHN virus
     and salinity. Aquaculture, 1994 (122): 133– 146.
    Bredt D S, Hwang P M, Glatt C E, et al. Cloned and expressed nitric oxide
     synthasestructurally resembles cytochrome P-450 reductase. Nature, 1991(351):
     714–718.
    Bredt D S, Snyder S H. Nitric oxide: a physiology messenger molecule. Annu. Rev.
     Biochem, 1994(63): 175-195.
    Cai S, Huang J, Wang C, Song X, Yu J, Zhang Y, Yang C. Epidermiological studies
     on the explosive epidemic disease of prawn in1993-1994. J. Fish. China, 1995(19):
     112-117.
    Cameron J N. Responses to reversed NH3 and NH+4gradients in a teleost (Ictalurus
     punctatus), an elasmobranch (Raia erinacea) and a crustacean (Callineces capidus):
     Evidence for NH+4/H+ exchange in the teleost and ealsmobranch. J. exp. Zool.,
     1986(239):183-195.
    Campbell I L, Samimi A, and Chiang C S. Expression of the inducible nitric oxide
     synthase: correlation with neuropathology and clinicalfeatures in mice with
     lymphocytic choriomeningitis. J. Immunol, 1994(153):3622–3629.
    Cerenius L, Henttonen P, Lindqvist O V, Soderhall K. The crayfish pathogen
     Psorospermiiiium-haeckeli activates the Prophenoloxidase activating system of
     fresh-water crayfish invitro. Aquaculture, 1991(99): 225-233.
    Chakravortty D, Hensel M. Inducible nitric oxide synthase and control of intracellular
     95
    
    
    参考文献
     bacterial pathogens. Microbes and Infection, 2003(5): 621–627.
    Chang P S, Chen L J, Wang Y C. The effect of ultraviolet irradiation, heat, pH, ozone,
     salinity and chemical disinfectants on the infectivity of white spot syndrome
     baculovirus. Aquaculture, 1998(166): 1-17.
    Chang C F, Su M S, Chen H Y, Liao I C. Dietary β-1,3-glucan effectively improves
     immunity and survival of Penaeus monodon challenged with white spot
     syndrome virus. Fish & Shellfish Immunology, 2003 (15): 297–310.
    Chang C F, Su M S, Chen H Y. A rapid method to quantify total haemocyte count of
     Penaeus monodon using ATP analysis. Fish Pathol, 1999(34):211–212.
    Chen J C, Chen C T, Cheng S Y. Nitrogen excretion and changes of heocyanin, protein
     and amino acid levels in the hemolymph of Penaeus monodon exposed to
     different concentrations of ambient ammonia-N at different salinity levels. Mar.
     Ecol. Prog. Ser., 1994a (10): 85-94.
    Chen J C, Cheng S Y, Chen C T. Changes of haemocyanin, protein and free amino
     acid levels in the haemolymph of Penaeus japonicus exposed to ambient
     ammonia. Comp. Biochem. Physiol., 1994b(109A): 339-347.
    Chen J C, Kou Y Z. Effects of ammonia on growth and molting of Penaeus japonicus
     juveniles. Aquaculture, 1992(104): 249-260.
    Chen J C, Lin C Y. Effect of ammonia on growth and molting of Penaeus mondon
     juveniles. Comp. Biochem. Physiol., 1992a (101C): 449-452.
    Chen J C, Lin C Y. Effect of ammonia on growth of Penaeus penicillatus juveniles.
     Comp. Biochem. Physiol., 1992b (101C): 443-447.
    Chen J C, Lin C Y. Oxygen consumption and ammonia-N excretion of Penaeus
     chinensis juveniles exposed to ambient ammonia at different salinity levels.
     Comp. Biochem. Physiol., 1992c(102C): 287-291.
    Chen J C, Nan F H, Cheng S Y. Effects of ambient ammonia on ammonia-N and
     protein concentration in haemolymoh an ammonia-N excretion of Penaeuse
     chinensis. Mar. Ecol. Pro. Ser., 1993(98): 203-208.
     96
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Cheng W, Chen J C. Effects of pH, temperature and salinity on immune parameters of
     the freshwater prawn Macrobrachium rosenbergii. Fish Shellfish Immunol.,
     2000(10): 387-391.
    Cheng W, Chen J C. The virulence of Enterococcus to freshwater prawn
     Macrobrachium rosenbergii and its immune resistance under ammonia stress.
     Fish& Shellfish Immunology, 2002a(12): 97-109.
    Cheng W, Chen J C. Effects of environmental factors on the immune responses of
     freshwater prawn Macrobrachium rosenbergii and other decapod crustaceans. J.
     Fish. Soc. Taiwan, 2002b(29): 1 –19.
    Cheng T C. In vivo effects of heavy metals on cellular defense mechanisms of
     Crassostrea virginica: phagocytic and endocytotic indices. J. Invertebr. Pathol.,
     1988(51): 215-220.
    Cheng T C and Sullivan J T. Effects of heavy metals on phagocytosis by molluscan
     hemocytes. Bull. Environ. Res., 1984(138): 155-188.
    Cheng T C and Rodirick G E. Lysosome and other enzymes in the haemolymph of
     Crassostrea virgiica and Mercenaria mercenaria. Comp. Biochem. Phsiol.,
     1975(52B): 443-447.
    Chernova O B, Chernov M V, Agarwal M L et al. The role of p53 in regulating
     genomic stability when DNA and RNA synthesis are inhibited. Trends Biochem.
     Sci., 1995(20): 431–434.
    Chisholm J R S, Smith V J. Antibacterial activity in the hemocytes of the shore crab,
     Carcinus maenas. J. Mar. Biol. Assoc. U.K., 1992(72): 529-542.
    Chotigeat W, Tongsupa S, Supamataya K, Phongdara A. Effect of Fucoidan on
     Disease Resistance of Black Tiger Shrimp. Aquaculture, 2004 (233): 23–30.
    Chou H Y, Huang C Y, Wang C H, Chiang H C, Lo C F. Pathogenicity of a
     baculovirus infection causing white spot syndrome in cultured penaeid shrimp in
     Taiwan. Dis. Aquat. Ogan., 1995(23): 165-173.
    Cohen R I, Hassell A M, Ye X B, Marzouk K, and Liu S F. Lipopolysaccharide
     down-regulates inducible nitric oxide synthase expression in swine heart in vivo.
     97
    
    
    参考文献
     Biochemical and Biophysical Research Communications, 2003(307): 451–458.
    Cominetti M R, Marques M R F, Lorenzini D M, L?fgren S E, S Daffre and M A
     Barracco. Characterization and partial purification of a lectin from the hemolymph
     of the white shrimp Litopenaeus schmitti. Developmental & Comparative
     Immunology, 2002(26): 715-721.
    Conte A, Ottavian E. Nitric oxide synthase activity in molluscan hemocytes. FEBS
     Letters, 1995(365): 120-124.
    Curtin J F, Donovan M, Cotter T G. Regulation and measurement of oxidative stress
     in apoptosis. Journal of Immunological Methods, 2002(265): 49–72.
    Cuthbertson B J, Shepard E F, Chapman R W, Gross P S. Diversity of the penaeidin
     antimicrobial peptides in two shrimp species. Immunogenetics, 2002(54):
     442-445.
    Davies S A. Nitric oxide signalling in insects. Insect Biochemistry and Molecular
     Biology, 2000 (30): 1123–1138.
    Dawson T M, Bredt D S, Fotuhi M, Hwang P M, Snyder S H. Nitric oxide and
     NADPH-diaphorase are identical in brain and peripheral tissue. Proc Natl Acad
     Sci USA, 1991 (88):7797–7801.
    De Groote M A, Testerman T, Xu Y, Stauffer G, Fang FC. Homocysteine antagonism
     of nitric oxide-related cytostasis in Salmonella typhimurium. Science, 1996(272):
     414–417.
    de Murcia G, and de Murcia J M. Poly (ADP-ribose) polymerase: a molecular
     nick-sensor. Trends Biochem. Sci., 1994(19): 172–176.
    Destoumieux D, Bulet P, Loew D, Dorsselaer AV, Rodriguez J, Bachère E.
     Penaeidins, a new family of antimicrobial peptides in the shrimp Penaeus
     vannamei (Decapoda). J Biol Chem., 1997(272):28398-28406.
    Destoumieux D, Munoz M, Bulet P, Bachère E. Penaeidins, a family of antimicrobial
     peptides from penaeid shrimp (Crustacea, Decapoda). Cell. Mol. Life. Sci., 2000a
     (57): 1260-1271.
     98
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Destoumieux D, Munoz M, Cosseau C, Rodriguez J, Bulet P, Comps M, Bachère E.
     Penaeidins, antimicrobial peptides with chitin-binding activity, are produced and
     stored in shrimp granulocytes and released after microbial challenge. J. Cell. Sci.,
     2000b (113): 461-469.
    Dikkeboom R, van der Knaap W P W, Meuleman E A. Hemocytes of the pond snail
     Lymnaea stagnalis generates reactive forms of oxygen. J. Invertebr. Pathol.,
     1987(49): 321–331.
    Dimopoulos G, Müller H-M, Levashina E A, et al. Innate immune defense against
     malaria infection in the mosquito. Current Opinion in Immunology, 2001(13):
     79–88.
    Donovan M, Carmody R J, Cotter TG. Light-induced photoreceptor apoptosis in vivo
     requires nNOS and guanylate cyclase activity and is caspase-3 independent. J.
     Biol. Chem., 2001 (276): 23000-23008
    Enoch T and Norbury C. Cellular responses to DNA damage: cell-cycle checkpoints,
     apoptosis and the roles of p53 and ATM. Trends Biochem. Sci., 1995 (20):
     426–430.
    Feelish M R and Noack E. The in vivo metabolism of nitrovasodilators and their
     conversion in to vasoactive species. In: Heart Failure-Mechanisms and
     Management, eds, Lewis B S and Kimchi A, 1991: 241-255. Springer Verlag,
     Berlin.
    Flegel T W, Alday-Sanz V. The crisis in Asian shrimp aquaculture: current status and
     future needs. J APPL ICHTHYOL., 1998(14): 269-273.
    Franchi R I B, Fauquet C M, Knudson D I, Brown F (Eds). Classification and
     nomenclature of viruses. Arch. Virol. Suppl., 1991(2): 117-123.
    Franchini A, Conte A, Ottaviani E. Nitric oxide: An ancestral immunocyte effector
     molecule. Adv. Neuroimmunol, 1995a (5): 463-478.
    Franchini A, Fontanili P, Ottaviani E. Invertebrate immunocytes – relationship
     between phagocytosis and nitric oxide production. Comp. Biochem. Physiol.,
     1995b (110 B): 403-407.
     99
    
    
    参考文献
    Friedman N, Tsokos M, Samuni A, et al. Nitric oxide potentiates hydrogen
     peroxide-induced killing of Escherichia coli. J. Exp. Med., 1995(182):
     1469–1479.
    Fries C R and Tripp M R. Depression of phagocytosis in Mercenaria mercenaria
     following chemical stress. Dev. Comp. Immunol., 1980 (4): 233-244.
    Gaudy R & Slone L. Effect of salinity on oxygen consumption in postlavae of the
     penaeid shrimp Peneaus monodon and P. stylirostris without and with
     acclimation. Marine Biology, 1981(65): 297-301.
    Gillespie J P, Kanost M R, Trenczek T. Biological mediators of insect immunity. Annu.
     Rev. Entomol., 1997(42): 611-643.
    Gollas-Galván T, Hernández-López J and Vargas-Albores F. Prophenoloxidase from
     brown shrimp (Penaeus californiensis) hemocytes. Comparative Biochemistry
     and Physiology, 1999(122 B): 77-82.
    Gollas-Galván T, Hernández-López J and Vargas-Albores F. Effect of Calcium on the
     Prophenoloxidase System Activation of the Brown Shrimp (Penaeus
     californiensis, Holmes). Comparative Biochemistry and Physiology, 1997(117A):
     419-425.
    Gopalakrishna R, Chen Z H and Gundimeda U. Nitric oxide and nitric
     oxide-generating agents induce a reversible inactivation of protein kinase C
     activity and phorbol ester binding. J. Biol. Chem., 1993(268): 27180–27185.
    Gourdon I, Gue?in M-C, Torreilles J, et al. Nitric Oxide Generation by Hemocytes of
     the Mussel Mytilus galloprovincialis. NITRIC OXIDE: Biology and Chemistry,
     2001(5): 1–6.
    Grundy M M, Moore M N, Howell S M and Ratcliffe N A. Phagocytic reduction and
     effects on lysosomal membranes by polycyclic aromatic hydrocarbons, in
     haemocytes of Mytilus edulis. Aquatic Toxicology, 1996(34): 273-290.
    Guan Y Q, Yu Z M and Li C W, The effects of temperature on white spot syndrome
     infections in Marsupenaeus japonicus, Journal of Invertebrate Pathology, 2003
     (83): 257–260.
     100
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Hall M, Wang R, Antwerpen R K, Sottrup-Jensen L, S?derh?ll K. The crayfish plasma
     clotting: a vitellogenin-related protein responsible for clot formation in
     crustacean blood. Proc. Natl. Acad. Sci. U.S.A., 1999(96): 1965-1970.
    Hall M R, van Ham E H. The effects of different types of stress on blood glucose in
     the giant tiger prawn Penaeus monodon. Journal of the world aquaculture society,
     1998(29): 290-299.
    Hervio D, Bachère E, Mialhe E, et al. Chemiluminescent responses of Ostrea edulis
     and Crassostrea gigas hemocytes to Bonamia ostrea Ascetospora. Dev. Comp.
     Immunol., 1989(13): 449.
    Hoffmann J A, Kafatos F C, Janeway Jr C A, Ezekowitz R A B. Phylogenetic
     perspectives in innate immunity. Science, 1999(284):1313–1318.
    Hogg N, Kalyanaraman B. Nitric oxide and lipid peroxidation. Biochimica et
     Biophysica Acta, 1999(1411): 378-384.
    Holmblad T, S?derh?ll K. Cell adhesion molecules and antioxidative enzymes in a
     crustacean, possible role in immunity. Aquaculture, 1999(172): 111–123.
    Holscher, C. Nitric oxide, the enigmatic neuronal messenger: its role in synaptic
     plasticity. Trends Neurosci., 1997(20): 298–303.
    Hope B T, Michael G J, Knigge K M, Vincent S R. Neuronal NADPH diaphorase is a
     nitric oxide synthase. Proc Natl Acad Sci USA, 1991(88):2881–2814.
    Hose J E, Lightne D V, Redman R M. and Danald D A. Observations on the
     pathogenesis of the imperfect fungus, Fusarium solani, in the Californian brown
     shrimp, Penaeus californiensis. Journal of Invertebrate Pathology, 1984 (44):
     292-303.
    Howe D, Barrows L F, Lindstrom N M, Heinzen R A. Nitric oxide inhibits Coxiella
     burnetii replication and parasitophorous vacuole maturation. Infect. Immun.,
     2002(70): 5140-5147.
    Huang J, Song X L, Yu J, Zhang L J. The components of an inorganic physiological
     buffer for Penaeus chinensis. Methods Cell Sci. 1999(21): 225–230.
    Incze K, Farkas J, Mihalyi V, et al. Antibacterial effect of cysteine-nitrosothiol and
     possible percursors thereof . Appl. Microbiol., 1974(27): 202–205.
     101
    
    
    参考文献
    Itami T, Takahasshi Y, Tsuchihiea E, Igusa H, Kondo M. Enhancement of disease
     resistance of kuruma shrimp, Penaeus japonicus and increase in phagocytic
     activity of prawn hemocytes after oral administration of β-1,3-glucan
     (Schizophyllan). In: Chou, L.M., Munro, A.D., Lam, T.J., Chen, T.W., Cheong,
     L.K.K., Ding, J.K., Hooi, K.K., Khoo, H.W., Phang, V.P.E., Shim, K.F., Tan,
     C.H.(Eds.),The 3rd Asian Fisheries Forum. Asian Fisheries Society, Manila,
     Philippines, 1994, pp. 375-378.
    James F, Curtin L, Maryanne D, et al. Regulation and measurement of oxidative stress
     in apoptosis. Journal of Immunological Methods, 2002(265): 49–72.
    Johansson M W, S?derh?ll K. Cellular immunity in crustaceans and the proPO system.
     Parasitol Today, 1989(5):171–176.
    Kandemir O, Polat A, and Kaya A, Inducible nitric oxide synthase expression in
     chronic viral hepatitis and its relation with histological severity of disease.
     Journal of Viral Hepatitis, 2002(9): 419–423.
    Kang C J, Wang J X, Zhao X, Yang X M, Shao H L and Xiang J H. Molecular cloning
     and expression analysis of Ch-penaeidin, an antimicrobial peptide from Chinese
     shrimp, Fenneropenaeus chinensis. Fish & Shellfish Immunology, 2004(16):
     513-525
    Karupiah, G., et al. Inhibition of Viral Replication by Interferon-γ-Induced Nitric
     Oxide Synthase. Science, 1993 (261): 1445-1448.
    Kautsky N, Ronnback P, Tedengren M, Troell M. Ecosystem perspectives on
     management of disease in shrimp pond farming. Aquaculture, 2000(191):
     145-161.
    Kawabata S I, Muta T, Iwanaga S. The clotting cascade and defense molecules found
     in the hemolymph of the horseshoe crab. In: Soderhall, K., Iwanaga, S., Vasta,
     G.R. (Eds.), New Directions in Invertebrate Immunology. SOS Publications,
     Fair Haven, 1996, pp. 255-283.
    Kandemir ?, Polat A and Kaya A Inducible nitric oxide synthase expression in
     chronic viral hepatitis and its relation with histological severity of disease.
     Journal of Viral Hepatitis, 2002(9): 419–423.
     102
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Kiemer A K, Müller C and Vollmar A M. Inhibition of LPS-induced nitric oxide and
     TNF-α production by α-lipoic acid in rat Kupffer cells and in RAW 264.7
     murine macrophages. Immunology and Cell Biology, 2002(80): 550–557.
    Kim Y M, Bergonia H A, Muller C, et al. Loss and degradation of enzyme-bound
     heme induced by cellular nitric oxide synthesis. J. Biol. Chem., 1995(270):
     5710–5713.
    KimY J, Choi W C, Kim H R, Jung S J, Oh M J. Changes in Penaeus chinensis
     haemocytes during white spot baculovirus (WSBV) infections. Bull. Eur. Assn.
     Fish. P., 1999(19): 213-215.
    Kinne O. Cultivation of marine organism: Water quality management and technology.
     In Marine Ecology, 1976, Vol. Ⅲ , Part 1 (Edited by Kinne O.), pp.
     79-300.Wiley-Interscience, New York.
    Kitano T, Matsumura S, Seki T, Hikida T, Sakimura K, Naganoe T, Mishina M,
     Nakanishi S, Ito S. Characterization of N-methyl-d-aspartate receptor subunits
     involved in acute ammonia toxicity. Neurochemistry International, 2004(44):
     83–90
    Kopacek P, Hall M, S?derh?ll K. Characterization of clotting of a clotting protein
     isolated from plasma of the fresh crayfish Pacifastacus leniusculus. Eur. J.
     Biochem., 1993(62): 459-463.
    Kou Y Z, Chen J C. Acute toxicity off ammonia to Penaeus japonicus Bate juveniles.
     Aquacult. Fish. Manage., 1991(22): 259-263.
    Kreil T R, and Eibl M M. Nitric oxide and viral infection: no antiviral activity against
     a flavivirus in vitro and evidence for contribution to pathogenesis in
     experimental infection in vivo. Virology, 1996(219):304–306.
    Kr?ncke K D, Fehsel K, and Kolb-Bachofen V. Nitric Oxide: Cytotoxicity versus
     Cytoprotection—How, Why, When, and Where?. NITRIC OXIDE: Biology and
     Chemistry, 1997(1): 107–120.
    Lackie A M. Invertebrate immunity. Parasitology, 1980(80): 393-412.
    Laing K J, Grabowski P S, Belosevic M, Secombes C J. A partial sequence for nitric
     oxide synthase from a goldfish Carassius auratus macrophagecell line.
     103
    
    
    参考文献
     Immunol. Cell Biol., 1996, (74): 374-379.
    Laing K J, Hardie L J, Aartsen W, et al. Expression of an inducible nitric oxide
     synthase gene in rainbow trout Oncorhynchus mykiss. Developmental and
     Comparative Immunology, 1999, (23): 71-85.
    Lane T E, Paoletti A D, and Buchmeier M J. Disassociation between the in vitro and
     in vivo effects of nitric oxide on a neurotropic murine coronavirus. J. Virol,
     1997(71): 2202–2210.
    Larson K G, Roberson B S, Hetrick F M. Effect of environmental pollutants on the
     chemiluminescence of hemocytes from the American oyster Crassostrea
     ?irginica. Dis. Aquat. Org., 1989(6): 131–136.
    Le Gall G, Bachére E, Mialhe E. Chemiluminescence analysis of the activity of
     Pecten maximus hemocytes stimulated with zymosan and host-specific
     Rickettsiales-like organisms. Dis. Aquat. Org., 1991(11): 181–186.
    Leake L D, Moroz L L.Putative nitric oxide synthase (NOS)-containing cells in the
     central nervous system of the leech, Hirudo medicinalis: NADPH-diaphorase
     histochemistry. Brain Research, 1996(723): 115-124.
    Lee S Y, Soderhall K. Early events in crustacean innate immunity. Fish & Shellfish
     Immunology, 2002(12): 421-437.
    LeMoullac G, LeGroumellec M, Ansquer D, Froissard S, Levy P, Aquacop.
     Haematological and phenoloxidase activity changes in the shrimp Penaeus
     stylirostris in relation with the moult cycle: Protection against vibriosis. Fish
     Shellfish Immunol., 1997 (4): 227-234.
    LeMoullac G, Soyez C, Saulnier D, Ansquer D, Avarre J C, Levy P. Effect of hypoxic
     stress on the immune response and the resistance to vibriosis of the shrimp
     Penaeus stylirostris. Fish & Shellfish Immunology, 1998 (8): 621-629.
    LeMoullac G, Haffner P. Environmental factors affecting immune responses in
     Crustacea. Aquaculture, 2000(191): 121-131.
    Lepoivre, M., et al. Alterations of Ribonucleotide Reductase Activity Following
     Induction of the Nitrite-generating pathway in adenocarcinoma cell. J. Biol.
     Chem., 1990(265):14143-14149.
     104
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Lightner D V. A Handbook of Shrimp Pathology and Diagnostic Procedures for
     Diseases of Cultured Penaeid Shrimp. World Aquaculture Society, Baton Rouge,
     1996, pp. 305. L A.
    Lightner D V, Redman R M. Strategies for the control of viral diseases of shrimp in
     the Americas. Fish. Pathol., 1998(33):165-180.
    Lindahl T, Satoh M S, Poirier G G, and Klungland A. Post-translational modification
     of poly(ADP-ribose) polymerase induced by DNA strand breaks. Trends
     Biochem. Sci, 1995(20): 405–411.
    Liu C-H, Chen J-C. Effect of ammonia on the immune response of white shrimp
     Litopenaeus vannamei and its susceptibility to Vibrio alginolyticus. Fish &
     Shellfish Immunology, 2004(16): 321–334.
    López-Guerrero J A, Carrasco L. Effect of nitric oxide on poliovirus infection of two
     human cell lines. J. Virol., 1998(72): 2538-2540.
    Luckhart S, Li K.Transcriptional complexity of the Anopheles stephensi nitric oxide
     synthase gene. Insect Biochemistry and Molecular Biology, 2001(31): 249–256.
    Luckhart S, Rosenberg R. Gene structure and polymorphism of an invertebrate nitric
     oxide synthase gene. Gene, 1999(232): 25–34.
    Luckhart S, Vodovotz Y, Cui L, and Rosenberg R. The mosquito Anopheles stephensi
     limits malaria parasite development with inducible synthesis of nitric oxide.
     Proc. Natl. Acad. Sci. USA, 1998(95): 5700–5705.
    Mabuchi T, Matsumura S, Okuda-Ashitaka E, Kitano T, Kojima T, Nagano T,
     Minami T, Ito S. Attenuation of neuropathic pain by nociceptin/orphanin FQ
     antagonist is mediated by inhibition of nitric oxide production. Eur. J. Neurosci.,
     2003 (171): 384–1392.
    Maheswari R, P Mullainadhan and M Arumugam. Isolation and characterization of an
     acetyl group-recognizing agglutinin from the serum of the Indian white shrimp
     Fenneropenaeus indicus. Archives of Biochemistry and Biophysics, 2002(402):
     65-76.
     105
    
    
    参考文献
    Malagoli D, Conte A, Ottaviani E. Protein kinases mediate nitric oxide-induced
     apoptosis in the insect cell line IPLB-LdFB. Cell. Mol. Life. Sci., 2002(59):
     894-901.
    Marletta M A. Nitric oxide: biosynthesis and biological significance.Trends Biochem.
     Sci., 1989(14): 488–492.
    Marques M R F, Barracco M A. Lectins, as non-self-recognition factors, in
     crustaceans. Aquaculture, 2000(191): 23-44.
    Martin G G, Hose J E, Omori S, Chong C, Hoodbhoy T, McKrell N. Localization and
     roles of coagulogen and transglutaminase in hemolymph coagulation in decapod
     crustaceans. Comp Biochem Physiol, 1991(100B):517–22.
    Marzinzig M, Nussler A K, Stadler J, Marzinzig E, Barthlen W, Nussler N C, Beger H
     G, Morris Jr S M and Bruckner U B. Improved Methods to Measure End
     Products of Nitric Oxide in Biological Fluids: Nitrite, Nitrate, and S-Nitrosothiols.
     NITRIC OXIDE: Biology and Chemistry, 1997(1): 177–189.
    Mayer B. Regulation of nitric oxide synthase and soluble guanylate cylase. Cell.
     Biochem. Function, 1994(12): 167–177.
    Montano-Perez K, Yepiz-Plascencia G, Higuera-Ciapara I, Vargas-Albores F.
     Purification and characterization of the clotting protein from the white shrimp
     Penaeus vannamei . Comp. Biochem. Physiol., 1999(122B): 381-387.
    Moormann A M, Koenig R J, and Meshnick S R. Effects of hydrogen peroxide, nitric
     oxide and antioxidants on NF-kappa B. Redox Report, 1996(2): 249–256.
    Mulero V and J Meseguer. Functional characterisation of a macrophage-activating
     factor produced by leucocytes of gilthead seabream (Sparus aurata L.). Fish &
     Shellfish Immunology, 1998, 8: 143-156.
    Mulcahy M F, Twomey E, Peterson A and Maye C T. Pathobiology of estuarine fish
     and shellfish in relation to pollution. In: Biological Indicators of Pollution,
     edited by D.H.S. Richardson. Royal Irish Academy, Dublin, (1987) pp.
     201-210.
    Mu?oz M, Cede?o R, Rodríguez J, et al. Measurement of reactive oxygen
     intermediate production in haemocytes of the penaeid shrimp, Penaeus
     106
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
     Vannamei. Aquaculture, 2000(191): 89–107.
    Mu?oz M, Vandenbulcke F, Saulnier D, Bachère E. Expression and distribution of
     penaeidin antimicrobial peptides are regulated by haemocyte reactions in
     microbial challenged shrimp. Eur. J. Biochem., 2002(269): 2678-2689.
    Nakatsuboa N, Kojimaa H, Kikuchia K, Nagoshib H, Hiratab Y, Maedaa D, Imaia Y,
     Irimuraa T, Naganoa T. Direct evidence of nitric oxide production from bovine
     aortic endothelial cells using new fluorescence indicators: diaminofluoresceins
     FEBS Letters, 1998(427): 263-266.
    Nappi A J, Vass E, Frey F, et al. Nitric Oxide Involvement in Drosophila Immunity.
     NITRIC OXIDE: Biology and Chemistry, 2000 (4): 423-430.
    Naviner M, Berge J-P, Durand P, LeBris H. Antibacteral activit of marine diatom
     Skeletonema costatum against aquacultural pathogens. Aquaculture, 1999 (174):
     15-24.
    Neumann N F, Belosovic M. Deactivation of primed respiratory burst response of
     goldfish macrophages by leukocyte-derived macrophage activating factor(s).
     Developmental and Comparative Immunology, 1996(20): 427-439.
    Neumann N F, D R Barreda and Miodrag Belosevic. Generation and functional
     analysis of distinct macrophage sub-populations from goldfish (Carassius
     auratus L.) kidney leukocyte cultures. Fish & Shellfish Immunology, 2000, 10(1):
     1-20.
    Neumeister B, Bach W, Faigle M, et al. Induction of NOS in human monocytes
     infected with different Legionella species. FEMS Microbiol Letters, 2001(202):
     31-38 .
    Nishida K J, Ohta Y S J and Ishiguro I. Relation of Inducible Nitric Oxide Synthase
     Activity to Lipid Peroxidation and Nonprotein Sulfhydryl Oxidation in the
     Development of Stress-Induced Gastric Mucosal Lesions in Rats. Nitric Oxide,
     1998 (2): 215-223.
    Novas A, Cao A, Barcia R, et al. Nitric oxide release by hemocytes of the mussel
     Mytilus galloprovincialis Lmk was provoked by interleukin-2 but not by
     lipopolysaccharide. The International Journal of Biochemistry & Cell Biology,
     107
    
    
    参考文献
     2004(36): 390-394.
    Olafsen J A. Invertebrate lectins: biochemical heterogeneity as a possible key to their
     biological function. In: Breh é lin. M (Ed.), Immunity in Invertebrates.
     Springer-Verlag, Berlin. 1986, pp.94-111.
    Olafsen J A. Role of lectins in invertebrate humoral defence. Am. Fish. Soc. Sp. Publ.,
     1988(18): 189-205.
    Ott S R, and Burrows M. NADPH Diaphorase Histochemistry in the Thoracic Ganglia
     of Locusts, Crickets, and Cockroaches: Species Differences and the Impact of
     Fixation. The Journal of Comparative Neurology, 1999(410):387–397.
    Ottaviani E, Barbieri D, Malagoli D, Franchini A. Nitric oxide induces apoptosis in
     the fat body cell line IPLB-LdFB from the insect Lymantria dispar. Comparative
     Biochemistry and Physiology, 2001(128B): 247-254.
    Ottaviani E, Franchini A, Cassanelli S, et al. Cytokines and invertebrate immune
     responses . Biol. Cell., 1995(85): 87-91.
    Ottaviani E, Paeman L R, Cadet P, et al. Evidence for nitric oxide production and
     utilization as a bacteriocidal agent by invertebrate immunocytes. Eur. J.
     Pharmacol., 1993 (248): 319-324.
    Ouellet H, Ouellet Y, Richard C, Labarre M, Wittenberg B, Wittenberg J, Guertin M.
     Truncated hemoglobin HbN protects Mycobacterium bovis from nitric oxide. Proc.
     Natl. Acad. Sci. USA, 2002 (99): 5902–5907.
    Pacelli R, Wink D A, Cook J A, Krishna M C, DeGraff W, Friedman N, Tsokos M,
     Samuni A, Mitchell J B. Nitric oxide potentiates hydrogen peroxide-induced
     killing of Escherichia coli, J. Exp. Med. 1995 (182): 1469–1479.
    Palmer R M, Ferrige A G, Moncada S. Nitric oxide release accounts for the biological
     activity of endothelium-derived relaxing factor. Nature, 1987(327): 524–526.
    Panikkar N K. Osmotic behaviour of shrimps and prawn\ in relation to their biology
     and culture. FAO Fish. Rep., 1968(57): 527-538.
    Peng S E, Lo C F, Ho C H, Chang C F, Kou G H. Detection of white spot baculovirus
     (WSBV) in giant freshwater prawn, Macrobrachium rosenbergii, using
     polymerase chain reaction. Aquaculture, 1998(164): 253-262.
     108
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Pequeux A and Gills R. Na+ fluxes across isolated perfused gills off the Chinese crab
     Eriocheir sinensis. J. exp. Biol., 1981(92): 173-186.
    Persson M, Cerenius L, Soderhall K. The influence of haemocytes number on the
     resistance of the freshwater crayfish, Pacifatacus leniusculus Dana, to the
     parasitic fungus Aphanomices astaci. J. Fish Dis., 1987(10): 471-477.
    Pfarr K M, Qazi S, and Fuhrman J A. Nitric oxide synthase in Filariae: Demonstration
     of nitric oxide production by embryos in Brugia malayi and Acanthocheilonema
     viteae. Experimental Parasitology, 2001(97): 205-214.
    Pickwell G V and Steinert S A Serum biochemical and cellular responses to
     experimental cupric ion exchange in mussels. Mar. Environ. Res., 1984 (14):
     245-265.
    Prayitno S B, Latchford J W. Experimental infections of crustaceans with luminous
     bacteria related to Photobacterium and Vibrio. Effect of salinity and pH on
     infectiosity. Aquaculture, 1995 (132): 105-l 12.
    Pressley T A, Graves J S, Krall A R. Amiloride-sensitive ammonium and sodium ion
     transport in the blue crab. Am. J. physiol., 1981(241): 370-378.
    Quaroni L, Reglinski J, Wolf R, et al. Interaction of nitrogen monoxide with
     cytochrome P-450 monitored by surface-enhanced resonance Raman scattering.
     Biochim. Biophys. Acta, 1996(1296): 5–8.
    Raber J, Toggas S M, Lee S, Bloom F E, Epstein C J, and Mucke L. Central nervous
     system expression of HIV-1 Gp120 activates the hypothalamic pituitary-adrenal
     axis: evidence for involvement of NMDA receptors and nitric oxide synthase.
     Virology, 1996(226):362–373.
    Regnault M. Nitrogen excretion in marine and freshwater-water crustacea. Bio. Rev.,
     1987(62): 1-24.
    Regulski M and Tully T. Molecular and biochemical characterization of dNOS: A
     Drosophila Ca2+/calmodulindependent nitric oxide synthase. Proc. Natl. Acad. Sci.
     USA, 1995(92): 90722–90726.
    Reiss C S and Komatsu T. Does Nitric Oxide Play a Critical Role in Viral Infections? .
     J. Virology, 1998(72): 4547–4551.
     109
    
    
    参考文献
    Reyes-Izquierdo T and Vargas-Albores F. Proteinase Activity in the White Shrimp
     (Penaeus vannamei) Clotting Protein. Biochemical and Biophysical Research
     Communications, 2001(287): 332-336.
    Robinson N M K, Zhang H Y, Bevan A L, de Belder A J, Moncada S, Martin J F, and
     Archard L C. Induction of myocardial nitric oxide synthase by Coxsackie B3
     virus in mice. European Journal of Clinical Investigation, 1999(29): 700–707.
    Roch P. Defense mechanisms and disease prevention in farmed marine invertebrates.
     Aquaculture, 1999(172): 125-145.
    Rodríguez J, Le Moullac G. State of the art of immunological tools and health control
     of penaeid shrimp. Aquaculture, 2000(191): 109-119.
    Rolff J and Siva-Jothy M T. Invertebrate Ecological Immunology. Science,
     2003(301):472-475.
    Rojtinnakorn J, Hirono I, Itami T, Takahashi Y, Aoki T. Gene expression in haemocytes
     of kuruma prawn, Penaeus japonicus, in response to infection with WSSV by EST
     approach. Fish & Shellfish Immunology, 2002(13): 69-83.
    Rosselli M, Keller P J, Dubey R K. Role of nitric oxide in the biology, physiology and
     pathophysiology of reproduction. Human Reprod. Update, 1998(4): 3–24.
    Saeij J PJ, Stet R J M, Groeneveld A, Verburg-van Kemenade B M L, van-Muiswinkel
     W B, Wiegertjes G F. Molecular and functional characterization of a fish
     inducible-type nitric oxide synthase. Immunogenetics, 2000(51): 339-346.
    Sahul Hameed A S, Xavier C M, Anilkumar M, Tolerance of Macrobrachium
     rosenbergii to white spot syndrome virus. Aquaculture, 2000(183): 207–213.
    Saleh D, Barnes P J, Giaid A. Increased prodiction of the potent oxidant peroxynitrite
     in the lungs of patients with idiopathic pulmonary fribrosis. Am J Crit Care Med,
     1997(155):1763-1769.
    Salzet M, Breton C, Bisogno T, and Marzo V D. Comparative biology of the
     endocannabinoid system-possible role in the immune response. Eur. J. Biochem,
     2000(267): 4917-4927.
    Sami S, Faisal M and Huggett R J. Effects oflaboratory exposure to sediments
     contaminated with polycyclic aromatic hydrocarbons on hemocytes of the
     110
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
     American oyster, Crassostrea virginica. Mar.Environ. Res., 1993 (35): 131-135.
    Sanders S P, Sierkierski E S, Porter J D, Richards S M, and Proud D. Nitric oxide
     inhibits rhinovirus-induced cytokine production and viralreplication in a human
     respiratory epithelial cell line. J. Virol, 1998(72): 934–942.
    Scharsack J P, Steinhagen D, Kleczka C, Schmidt J O, Korting W, Michael R D,
     Leibold W, and Schuberth H J.The haemoflagellate Trypanoplasma borreli
     induces the production of nitric oxide, which is associated with modulation of
     carp (Cyprinus carpio L.) leucocyte functions. Fish & Shellfish Immunology,
     2003 (14): 207–222.
    Schulz S, Chinkers M, Garbers D L. The guanylate cyclase/receptor family of proteins.
     FASEB J., 1989(3): 2026–2035.
    Secombes C J, Wang T, Hong S, Peddie S, Crampe M, Laing K J, Cunningham C, Zou
     J. Cytokines and immunity of fish. Developmental and Comparative Immunology,
     2001(25): 713-723.
    Sellers V M, Johnson M K and Dailey H A. Function of the [2FE-2S] cluster in
     mammalian ferrochelatase: a possible role as a nitric oxide sensor. Biochemistry,
     1996(35): 2699–2704.
    Selvin J, Huxley A J, Lipton A P.Immunomodulatory potential of marine secondary
     metabolites against bacterial diseases of shrimp. Aquaculture, 2004 (230):
     241–248.
    Sharon N, Lis H. Lectin: Cell—agglutinin and sugar—specific proteins. Science,
     1972(177): 949-959.
    Sindermann C J. Pollution associated diseases and abnormalities of fish and shellfish:
     a review. Fish. Bull., 1979(76): 717-749.
    Sindermann C J and Rosenfield A. Principal diseases of commercially important
     bivalve mollusks and crustaceans. Fish. Bull., 1967 ( 66): 335-384.
    Smith V J. Invertebrate immunology: phylogenetic, ecotoxicological and biomedical
     implications. Comp. Haematol. lnt., 1991 (1): 61-76.
    Smith V J, Brown J H and Hauton C. Immunostimulation in crustaceans: does it really
     111
    
    
    参考文献
     protect against infection?. Fish & Shellfish Immunology, 2003(15): 71-90.
    Smith V J, Johnston P A. Differential hemotoxic effect of PCB congeners in the
     common shrimp, Crangon crangon. Comp. Biochem. Physiol., 1992(101C):
     641-649.
    Smith V J, S?derh?ll K. A comparison of phenoloxidase activity in the blood of
     marine invertebrates. Dev. Comp. Immunol., 1991(15): 251-261.
    Smith V J, Swindlehurst R J, Johnston P A, Vethaak A D. Disturbance of host defense
     capability in the common shrimp, Crangon crangonI, by exposure to harbor
     dredge spoils. Aquatic Toxicology, 1995(32): 43-58.
    S?derh?ll K. Fungal cell wall β-1,3-glucans induce clotting and phenoloxidase
     attachment to foreign surface of crayfish hemocyte lysate. Dev. Comp.
     Immunol., 1981(5): 565-573.
    S?derh?ll K. Editorial. Dev. Comp. Immunol., 1999(23): 263-266.
    S?derh?l K, Cerenius L. Crustacean immunity. Annual Review of Fish Disease,
     1992(2):3-23.
    S?derh?l K, Cerenius L. Role of the prophenoloxidase-activating system in
     invertebrate I- mmunity. Curr. Opin. Immunol, 1998(10): 23-28.
    S?derh?l K, Hall L. Lipopolysaccharide induced actvation of the prophenoloxidase
     activating system in crayfish haemocyte. Biochem. Biophys. Acta., 1984(797):
     99-104.
    S?derh?l K, Smith V J. Separation of the haemocyte of populations of Carcinus
     maenas and other marine decapods, and prophenoloxidase distribution. Dev.
     Comp. Immunol, 1983(7): 229-239.
    S?derh?l K, Smith V J. The prophenolaxidase activating system: the biochemistry of
     its activating and role in arthropod cellular immunity with special reference to
     Crustacea. In Breheline, M. (Ed.), Immunity in Invertebrates.
     Springer-Verlag.Berlin, 1986, pp.208-223.
    Song Y L, Hsieh Y T. Immunostmulation of tiger shrimp (Penaeus monodon)
     hemocytes for generation of microbicidal substances-analysis of reactive oxygen
     species. Dev. Comp. Immunol, 1994(18): 201-209.
     112
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Song Y L, Yu C-I, Lien T-W, Huang C-C and Lin M-N. Haemolymph parameters of
     Pacific white shrimp (Litopenaeus vannamei) infected with Taura syndrome virus.
     Fish & Shellfish Immunology, 2003(14): 317-331.
    Sritunyalucksana K, Cerenius L and S?derh?ll K. Molecular cloning and
     characterization of prophenoloxidase in the black tiger shrimp, Penaeus monodon.
     Developmental & Comparative Immunology, 1999(23): 179-186.
    Sritunyalucksana K, Sithisarn P, Withayachumnarnkul B and Flegel T W. Activation of
     prophenoloxidase, agglutinin and antibacterial activity in haemolymph of the
     black tiger prawn, Penaeus monodon, by immunostimulants. Fish & Shellfish
     Immunology, 1999a (9): 21-30.
    Sritunyalucksana K, S?derh?ll K. The proPO and clotting system in crustaceans.
     Aquaculture, 2000(191): 53-69.
    Stefano G B, Ottaviani E. The biochemical substrate of nitric oxide signaling is
     present in primitive non-cognitive organisms. Brain. Res., 2002(924): 82-89.
    Stewart J E, Arie B, Zwicker B M and Dingle J R. Gaffkemia, a bacterial disease of
     the lobster, Homarus americanus: effects of the pathogen, Gaffkemia homari, on
     the physiology of the host. Canadian Journal of Microbiology 1969 (15): 925-932.
    Sung H H, Chang H J, Her C H, Chang J C and Song Y L. Phenoloxidase Activity of
     Hemocytes Derived from Penaeus monodon and Macrobrachium rosenbergii.
     Journal of Invertebrate Pathology, 1998(71): 26-33.
    Suresh K and Mohandas A. Hemolymph acid phosphatase activity pattern in copper
     stressed crabs. J. Invertebr. Pathol., 1990 (55): 118-125.
    Tafalla C, Gómez-León J, Novoa B, et al. Nitric oxide production by carpet shell clam
     (Ruditapes decussatus) hemocytes. Developmental and Comparative
     Immunology, 2003(27): 197–205.
    Tafalla C, Novoa B. Requirements for nitric oxide production by turbot
     (Scophthalmus maximus ) head kidney macrophages. Developmental and
     Comparative Immunology, 2000(24): 623-631.
    Tafalla C, Figueras A, Novoa B. Role of nitric oxide on the replication of
     haemorrhagic septicemia virus (VHSV), a fish rhabdovirus. Veterinary
     113
    
    
    参考文献
     Immunology and immunopathology, 1999(72): 249-256.
    Torreilles J and Gueurin M C. Production of peroxynitrite by zymosan stimulation of
     Mytilus galloprovincialis haemocytes in vitro. Fish & Shellfish Immunology,
     1999(9): 509–518.
    Truscott R, White K N. The influence of metal and temperature stress on the immune
     system of crabs. Funct. Ecol., 1990 (4): 455–461.
    Vaandrager A B, De Jonge H R. Signalling by cGMP-dependent protein kinases. Mol.
     Cell. Biochem., 1996(157): 23–30.
    Van Hulten M C, Wittevel Peters S, Kloosterboer N, Tarchini R, Fiers M, Sandbrink
     H, Lankhorst R K, Vlak J M. The white spot syndrome virus DNA genome
     sequence. Virology, 2001(286): 7– 22.
    Van de Braak C B T, Botterblom M H A, Huisman E A, et al. Preliminary study on
     haemocyte response to white spot syndrome virus infection in black tiger
     shrimp Penaeus monodon. Dis. aquat. organ., 2002(51): 149-155.
    Vargas-Albores F, Guzmán M A, Ochoa J L. An anticoagulant solution for hemolymph
     collection and prophenolaxidase studies of penaeid shrimp (Penaeus
     californiensis). Comp. Biochem. Physiol., 1993 (106A): 299-303.
    Vargas-Albores F, Guzmán M A and Ochoa J L. A lipopolysaccharide-binding
     agglutinin isolated from brown shrimp (Penaeus californiensis Holmes)
     haemolymph. Comparative Biochemistry and Physiology, 1993a(104B):
     407-413.
    Vargas-Albores F, Hinojosa-Baltazar P, Portillo-Clark G, Magallon-Barajas F.
     Influence of temperature and salinity on the yellowleg shrimp, Penaeus
     californiensis Holmes, prophenoloxidase system. Aquacult. Res., 1998(29):
     549-553.
    Vargas-Albores F, Monta?o-Pérez K, Reyes-Izquierdo T, Higuera-Ciapara I and
     Yepiz-Plascencia G. The shrimp coagulation system. Developmental &
     Comparative Immunology, 1997 (21): 213.
    Vargas-Albores F, Yepiz-Plascencia G. Beta glucan binding protein and its role in
     shrimp immune response. Aquaculture, 2000(191): 13-21.
     114
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    Vethaak A D and Rheinallt T. Fish disease as a monitor for marine pollution: the case
     of the North Sea. Rev. Fish Biol. Fish., 1992 (2): 1-32.
    Vici V, Singh I S B, Bhat S G. Application of bacterins and yeast Acremonium
     dyosporii to protect the larvae of Macrobrachium rosenbergii from vibriosis.
     Fish Shellfish Immunol., 2000(10): 559-563.
    Vogan C L, Rowley A F. Effects of shell disease syndrome on the haemocytes and
     humoral defences of the edible crab, Cancer pagurus. Aquaculture, 2002(205):
     237-252.
    Volety A K, Chu F L E. Suppression of chemiluminescence of eastern oyster
     Crassostrea ?irginica hemocytes by the protozoan parasite Perkinsus marinus.
     Dev. Comp. Immunol., 1995(19): 135–142.
    Wang T, Ward M, Grabowski P S, Secombes C J, Molecular cloning, gene
     organization and expression of rainbow trout inducible nitric oxide synthase
     (iNOS) gene. EMBL accession No. AJ 295231: 2000.
    Wang C H, Lo C F, Leu J H, Chou C M, Yeh P Y, Chou H Y, Tung M C, Chang C F,
     Su M S, Kou G H. Purification and genomic analysis of baculovirus associated
     with white spot syndrome WSBV of Penaeus monodon. Dis. Aquat. Org.,
     1995(23): 239–242.
    Weeks-Perkins B A, Chansue N, Wong-Verelle D. Assay of immune function in shrimp
     phagcytes: Techniques used as indicators of pesticide exposure. In: Stolen, J.S.,
     Fletcher, T.C.,Smith, S.A.,Zelikoff, J.T., Kaattari, S.L., Anderson, R. S.,
     S?derh?ll, K., Weekss-Perkins, B. A. (Ed.), Techniques in fish Immunology-4.
     SOS Publications, Fair Haven, N J, USA, 1995. pp.223-231.
    Weiske J and Wiesner A. Stimulation of NO Synthase Activity in the
     Immune-Competent Lepidopteran Estigmene acraea Hemocyte Line. NITRIC
     OXIDE: Biology and Chemistry, 1999(3): 123-131.
    Wilcox D E and Smith R P. Detection and quantification of nitric oxide using electron
     magnetic resonance spectroscopy. Methods: a companion to methods in
     enzymology, 1995(7): 59-70.
    Wink D A and Ford P C. Nitric oxide reactions important to biological systems: a
     115
    
    
    参考文献
     survey of some kinetics investigations. Methods: a companion to methods in
     enzymology, 1995(7): 14-20.
    Wongprasert K, Khanobdee K, Glunukarn S S, Meeratana P, Withyachumnarnkul B.
     Time-course and levels of apoptosis in various tissues of black tiger shrimp
     Penaeus monodon infected with white-spot syndrome virus. Dis. Aquat. Org.,
     2003(55): 3-10.
    Yeh M S, Chen Y L, Tsai I H. The hemolymph clottable protein of tiger shrimp
     Penaeus monodon, and related species. Comp. Biochem. Phsiol., 1998(121b):
     169-176.
    Yepiz-Plascencia G, Jimenez-Vega F, Romo-Figueroa M G, Sotelo-Mundo R R,
     Vargas-Albores F. Molecular characterization of the bifunctional VHDL-CP
     from the hemolymph of white shrimp Penaeus vannamei.Comparative
     Biochemistry and Physiology , 2002(132 B): 585–592.
    Yuda M, Hirai M, Hirai K, et al. cDNA cloning, expression and characterization of
     nitric oxide synthase from the salivary glands of the blood-sucking insect
     Rhodnius prolixus. Eur. J. Biochem., 1996(242): 807–8
    Zhang X B, Huang C H and Qin Q W. Antiviral properties of hemocyanin isolated
     from shrimp Penaeus monodon. Antiviral Research, 2004(61): 93-99.
    陈昌生,黄标,叶兆弘、纪得华等.南美白对虾摄食、生长及存活与温度的关系.
     集美大学学报(自然科学版),2001,6(4),296-300.
    陈皓文,孙丕喜,宋庆云.外源凝集素—水产动物御敌的有利武器. 黄渤海海洋,
     1995(13): 61-70.
    樊廷俊, 汪小锋. 中国对虾(Penaeus chinensis)酚氧化酶的分离纯化及其部分
     生物化学性质. 生物化学与生物物理学报, 2002(34): 589-594.
    何建国,周化民,姚伯等. 白斑综合症杆状病毒的传染途径和宿主种类. 中山大
     学学报(自然版),1999(38): 65-69.
    黄倢,宋晓玲,于佳,杨丛海.杆状病毒性的皮下造血组织坏死—对虾暴发性流
     行病的病原和病理学.海洋水产研究, 1995(16):1-7.
     116
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
    江晓路,牟海津.对虾免疫系统及免疫机理的研究方法: 管华诗,海水养殖动物
     的免疫、细胞培养和病害研究.山东.山东科学技术出版社. 1999:1-31.
    李光友,王青.中国对虾血细胞及其免疫研究. 海洋与湖沼, 1995(26): 591-597.
    李光友. 中国对虾疾病与免疫机制.海洋科学,1995(4): 1-3.
    李才文,管越强,俞志明. 盐度变化对日本虾暴发白斑综合症病毒病的影响. 海
     洋环境科学,2002(21):6-9,33.
    林林,丁美丽,孙舰军,朱谨钊,李光友. 有机污染提高对虾对病原菌的易感性
     研究.海洋学报,1998(20):90-93.
    刘晓云,张志峰,马洪明.中国对虾血细胞酶细胞化学的初步研究. 青岛海洋大
     学学报, 2002(32):259-265.
    孟凡伦,张玉臻,孔健,马桂荣. 甲壳动物中的酚氧化酶原激活系统研究评价.
     海洋与湖沼,1999(30):110-115.
    史成银,宋晓玲,黄倢,杨丛海.核酸斑点杂交分析方法检测对虾皮下及造血组
     织坏死杆状病毒(HHNBV). 海洋与湖沼,1999(30):486-490.
    孙 舰 军 , 丁 美 丽 . 氨 氮 对 中 国 对 虾 抗 病 力 的 影 响 . 海 洋 与 湖
     沼,1999(30):267-271.
    王宝杰, 王雷.中国对虾血细胞吞噬活动中超氧阴离子(O2 )的产生. 中国水产
     ?–
     科学, 2003(10): 14-18.
    王鑫,马桂荣,郑宝灿等. SL—益生素对小白鼠体重及其单核吞噬细胞功能的影
     响. 微生物学报, 1995(35): 455-459.
    叶燕玲,陈宽智.中国对虾(Penaeus chinensis)血细胞超微结构、分类及计数. 青
     岛海洋大学学报, 1993(23): 35-41.
    朱忠勇. 实用医学检验学. 北京. 人民军医出版社,1997: 368-378.
    姜国建,于仁诚,王云峰,颜天,周名江. 对虾血细胞中一氧化氮合成酶鉴定与
    分析方法研究.中国水产科学,2004(11):177-184.
    姜国建,于仁诚,王云峰,颜天,周名江.中国明对虾血细胞中一氧化氮合成酶
    的鉴定及其在白斑综合症病毒感染过程中的变化. 海洋与湖沼,2004(35):
    346-352.
     117
    
    
    对虾白斑综合症抗病力指标的筛选及其应用的研究
     文章的完成和发表情况
    1)姜国建,于仁诚,王云峰,颜天,周名江. 对虾血细胞中一氧化氮合成酶鉴
     定与分析方法研究.中国水产科学,2004(11):177-184.
    2)姜国建,于仁诚,王云峰,颜天,周名江.中国明对虾血细胞中一氧化氮合成
     酶的鉴定及其在白斑综合症病毒感染过程中的变化. 海洋与湖沼,2004(35):
     346-352.
    3) Jiang Guanjian, Yu Rencheng, Zhou Mingjiang. Modulatory Effects of
     Ammonia-N on the Immune System of Penaeus japonicus to Virulence of White
     Spot Syndrome Virus (WSSV).Disease of aquatic organisms (in review).
    4) Jiang Guojian, Yu Rencheng, Zhou Mingjiang. Comparative Studies of Nitric
     Oxide Synthase in shrimps Fenneropenaeus chinensis and Marsupenaeus
     japonicus against White Spot Syndrome Virus Infection. Fish and shellfish
     immunology (in review).
    5) Yu Rencheng, Jiang Guojian, Li Jun, Wangyun Feng, Zhou Mingjiang.
     Comparison of Disease Resistance Ability to White Spot Syndrome Virus
     (WSSV) Between Fenneropenaeus chinensis and Penaeus japonicus: An
     Immunological Approach. (submitted to Aquaculture).
    6) Jiang Guojian, Yu Rencheng, Zhou Mingjiang. A try to understand the roles of
     phytoplankton and bacteria in white spot syndrome disease. (Complete)
    7) 姜国建,于仁诚.活性氮中间体作为抗病力因子的研究进展.投稿“海洋科
     学”.

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