无特定病原中国对虾的培育技术
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摘要
白斑综合征病毒(White spot syndrome virus, WSSV)是造成中国对虾暴发性流行病的主要病原,迄今没有能有效控制WSSV疫情的技术措施。为预防和减少WSSV对中国对虾造成的损失,本文比较了3种PCR方法检测WSSV灵敏度的差异,对中国对虾WSSV携带量与繁殖、存活及育种值进行相关性分析,取得
     主要结果如下:
     1、三种PCR方法检测白斑综合征病毒(WSSV)的灵敏度比较
     分别利用TaqMan实时定量PCR、世界动物卫生组织(Office International Des Epizooties, OIE)公布的巢式PCR引物(简称OIE巢式PCR)及本研究室设计的引物(简称GB巢式PCR)和OIE巢式PCR及GB巢式PCR对应的一步法PCR等三种方法对不同白斑综合征病毒(White spot syndrome virus,WSSV)含量的中国对虾样品进行灵敏度比较。结果显示,当使用已知病毒含量的标准品进行检测时,TaqMan实时定量PCR方法可以检测到10个WSSV copies,OIE巢式PCR与GB巢式PCR方法分别可检测到10~4和10~3个WSSV copies。分别使用OIE巢式PCR的外引物和内引物扩增时,可检测到5×10~4和2.5×10~4个WSSV copies;分别使用GB巢式PCR的外引物和内引物扩增时,可检测到10~4和5×10~3个WSSV copies。使用上述PCR方法对44份未知WSSV含量的样品进行验证,定量PCR方法检测阳性率为84.09%,OIE巢式PCR与GB巢式PCR方法检测的阳性率分别为18.18%和27.27%。分别使用OIE巢式PCR的外引物和内引物扩增检测的阳性率均为15.91%,分别使用GB巢式PCR的外引物和内引物扩增检测的阳性率分别为18.18%和20.45%。根据以上结果,这三种方法检测WSSV的灵敏度由高到低依次为:TaqMan实时定量PCR、巢式PCR、一步法PCR。
     2、不同饵料组合对越冬对虾WSSV携带量及繁殖特征的影响
     对越冬对虾使用的2种饵料菲律宾蛤仔和沙蚕进行WSSV检测,显示携带量分别为17.79±3.71 copies/ng DNA和19.06±4.31 copies/ng DNA。设计三种饵料组合,即高锰酸钾消毒的菲律宾蛤仔足肌+沙蚕+配饵(消毒组),菲律宾蛤仔足肌+沙蚕+配饵(对照组)及配饵(配饵组),分别投喂对虾60天。结果表明:越冬期间投喂消毒组、对照组和配饵组这3种饵料组合的对虾体重量分别降低了1.48±0.86g、0.39±0.63g和1.71±0.91g,投喂三种饵料的对虾存活率分别为52.53%、79.75%和46.01%。投喂消毒组、对照组与配饵组饵料的对虾越冬前WSSV携带量分别为7.63±6.24 copies/ng DNA、10.58±7.34 copies/ng DNA和11.97±9.32 copies/ng DNA,越冬后分别为11.69±9.18 copies/ng DNA、9.31±6.95 copies/ng DNA和16.87±14.47 copies/ng DNA,越冬前后变化差异不显著(P>0.05)。亲虾在产卵量、受精率和孵化率三个指标上的排序均为对照组>消毒组>配饵组,且均呈显著差异(P<0.05)。研究结果表明,菲律宾蛤仔和沙蚕不同程度的携带WSSV,利用对照组饵料投喂亲虾,可获得较高的产卵量、受精率和孵化率,但投喂上述三组饵料,越冬前后对虾体内的WSSV携带量变化差异不显著。
     3、不同饵料组合对中国对虾幼体WSSV携带量及存活率的影响
     采用单胞藻(SA)、配合饵料(AF)、轮虫(BP)和卤虫幼体(BS)4种饵料,设计了SA+AF、SA+AF+BP、SA+AF+BS和SA+AF+BP+BS等4种饵料组合并用于对虾苗种培育,其中投喂SA+AF饵料组合的受精卵分设“碘伏”消毒及未消毒组,投喂其它饵料组合的受精卵均为“碘伏”消毒组。观察和分析各期幼体成活率,结果表明,N-Z期间,受精卵消毒与否及投喂不同饵料组合对对虾的成活率差异均不显著(P>0.05);Z-P期间,投喂BP的成活率明显高于未投喂BP组(P<0.01);饵料组合SA+AF+BS在M-P期间幼体成活率与其它饵料组差异极显著(P<0.01)。对P_(10)幼体体重测量结果表明,投喂SA+AF+BP的虾苗平均体重小于投喂SA+AF+BP+BS的幼体(P<0.01)。P_(10)仔虾WSSV携带量检测结果表明, SA+AF消毒组仔虾WSSV携带量为10.52±3.3 copies/ng DNA,显著低于其它各组饵料培育的仔虾WSSV携带量(P<0.05)。
     在P_(11)-P60培育期间,分别投喂菲律宾蛤仔足肌(CF)+配饵(AF)、~(60)Coγ辐照菲律宾蛤仔足肌(RCF)+配饵(AF)、高锰酸钾消毒菲律宾蛤仔足肌(DCF)+配饵(AF)和配饵(AF)4种饵料组合。结果表明, CF+AF组对虾体重和体长增长最大,但与AF组差异不显著,而CF+AF组和AF组与其余两组差异显著(P<0.05);CF+AF组存活率最高,但与其余3组差异不显著(P>0.05)。WSSV人工感染实验结果表明,四种饵料投喂的对虾累积死亡率都在90%以上(P>0.05),显示~(60)Coγ辐照(RCF)和高锰酸钾消毒后的菲律宾蛤仔足肌(DCF)投喂P_(11)-P_(60)对虾幼体,对感染WSSV后的对虾存活率无显著影响。
     4、中国对虾的WSSV携带量与生长及抗WSSV育种值的相关性分析
     对130个中国对虾家系进行生长及抗WSSV能力测试。根据统计软件分析结果,选择出生长育种值最大的5个家系和最小的5个家系,以及抗WSSV育种值最大的5个家系和最小的5个家系,分别检测上述20个家系的亲虾以及养殖50 d和170 d时对虾的WSSV携带量。结果表明,亲虾、50 d对虾及170 d对虾的WSSV携带量分别为0.1908 copies /ng DNA、0.2866 copies /ng DNA和0.2329 copies /ng DNA,三者之间差异均不显著(P>0.05)。亲虾、50 d对虾和170 d对虾的WSSV携带量与对虾的生长育种值相关系数分别为0.021、0.363和0.185(P>0.05),亲虾、50 d对虾和170 d对虾的WSSV携带量与抗WSSV育种值相关性分别为0.033、0.048和0.019(P>0.05),显示中国对虾的生长育种值和抗WSSV育种值与对虾体内的WSSV携带量均无显著的相关性。
     5、结论及研究的意义
     三种PCR方法检测WSSV的灵敏度由高到低依次为:TaqMan实时定量PCR、巢式PCR、一步法PCR;中国对虾WSSV携带量与其繁殖和育种值之间均无显著相关性,与其存活率之间存在一定的相关性。本研究为中国对虾WSSV疫情的预防及治理提供了理论及实际基础。
The epidemic pathogenic of Fenneropenaeus chinensis is main caused by White spot syndrome virus(WSSV), no effectively technical measures could control the WSSV epidemic so far. For the purpose of prevention and decrease of WSSV loss to F. chinensis, first of all we compared the sensitivity of three PCR methods on detecting the white spot syndrome virus (WSSV); and then we focused on analysing the correlation of WSSV load and reproduction、survival and breeding value in F. chinensis. The results are as following:
     1、Sensitivity comparison of three different kinds of PCR-based methods in white spot syndrome virus (WSSV) test
     In this part, we compared the sensitivity of several PCR methods, including TaqMan real-time PCR, Office International Des Epizooties (OIE) and Genetic resource and Our Lab-designed nested PCR (GB) and two corresponding one-step PCR methods, with standard samples of serial known WSSV load of F. chinensis. As a result, TaqMan real-time PCR could detect with certainty 10 WSSV copies per reaction while 10~4, 10~3 copies were needed for OIE and GB nested PCR; 5×10~4, 2.5×10~4 copies were needed for the outer primer and inner primer amplification separately of OIE nested PCR; and 10~4, 5×10~3 copies were needed for that of the GB nested PCR. 44 F. chinensis samples which we did not know the WSSV load were tested with these PCR methods to validate the sensitivity, the positive ratio of TaqMan real-time PCR was 84.09 %, and that of the OIE and the GB nested PCR were 18.18% and 27.27%, respectively; the positive ratio of the outer primer and inner primer amplification separately of OIE nested PCR both were 15.91%; and that of the GB nested PCR were 18.18% and 20.45%. According to the results, the sensitivity of PCR detected the WSSV from high to low are: TaqMan real-time PCR, nested PCR, one-step PCR.
     2、Effect of different diets on the WSSV loads and reproduction of F. chinensis over winter
     Based on the detecting result of WSSV loads of two kinds of prawn overwinter diets , Ruditapes philippinarum and clamworm, which were 17.79±3.71 copies/ng DNA and 19.06±4.31 copies/ng DNA, respectively, three kinds of diet combinations were designed as 1) disinfected Ruditapes philippinarum musle + disinfected clamworm + artificial diets (disinfected group); 2) R. philippinarum musle + clamworm + artificial diets (control group) ; 3) artificial diets (artificial group). After 60 days it was showed that the loss of weight of prawn in three groups was 1.48±0.86g、0.39±0.63g and 1.71±0.91g; and the survival rate of each group was 52.53%、79.75% and 46.01%. The WSSV loads of prawn before and after overwinter were 7.63±6.24 copies/ng DNA、10.58±7.34 copies/ng DNA、11.97±9.32 copies/ng DNA and 11.69±9.18 copies/ng DNA、9.31±6.95 copies/ng DNA、16.87±14.47 copies/ng DNA, respectively, showing no significant difference (P>0.05). The fecundity、the rates of fertilization and hatching of the brookstock from high to low were group of feeding control group、disinfected group and artificial group, showing significant difference (P<0.05). It was indicated that the R. philippinarum and clamworm can carry small amount of WSSV, Besides this, the brookstock can gain high fecundity、high rates of fertilization and hatching when feeding on control group diet combination over winter, the WSSV load of prawn feeding on three diet combinations is showing no significant difference overwinter.
     3、Effect by feeding different diets on the WSSV load and survival rate of F. chinensis.
     Based on single-cell algae (SA), artificial feed (AF), brachionus plicatilis (BP) and brine shrimp larva (BS), four groups of diet combination were designed as SA + AF, SA + AF + BP, SA + AF + BS, SA + AF + BP + BS , and used to the cultivation of F. chinensis larval, the oosperm which feeding on the group SA+AF divided into disinfected and undisinfected group, other groups’oosperm all were disinfected group. The survival rate of each stage was compared in different groups. It was showed that there was no significant difference from each other in the survival rate of N-Z by diet different diet combination (P>0.05). The survival rate of Z-P fed BP was higher than others (P<0.01) and the survival rate of M-P fed SA + AF + BS was significant difference (P<0.01) from others. The body weight of 10-day post larva by diet SA + AF + BP was less than that by diet SA + AF + BP + BS (P<0.01). The result of detecting WSSV load of 10-day post larva were disinfection Group SA + AF WSSV larva carrying the lowest load of 10.52±3.3 WSSV copies / ng DNA, which lower than other diet groups (P<0.05 ).
     During the stage of P11-P60, R. philippinarum foot muscle (CF) + artificial feed (AF), 60Coγradiated R. philippinarum foot muscle (RCF) + artificial feed (AF), potassium-permanganate-disinfected R. philippinarum foot muscle (DCF) + artificial feed (AF) and artificial feed (AF), which four diet groups were feeding to prawn. Shrimp of group CF + AF gained the largest increase of body weight and body length and showed no significantly difference (P>0.05) from group AF, but showed significantly difference (P<0.05) from the other two groups. The survival rate of group CF + AF was highest, (P>0.05) The result of WSSV artificial infection experiment showed that all groups of shrimp accumulated mortality were higher than 90% (P>0.05). It was concluded that shrimp larval feeding on 60Coγradiated R. philippinarum foot muscle (RCF) and potassium-permanganate-disinfected R. philippinarum foot muscle (DCF) could not caused significant effect of survival rate.
     4、The relationship between viral loads and growth & WSSV resistance
     After testing the growth and WSSV resistance of 130 F. chinnensis families, According to the results of statistics software analysis, we choosed the five families each of largest and smallest growth breeding value, five families each of largest and smallest WSSV-resistance breeding value.We detecting the WSSV load of these broodstock, 50 d shrimp and 170 d shrimp of 20 families. The mean WSSV load of broodstock, 50 d shrimp and 170 d shrimp of 20 families were 0.1908, 0.28662 and 0.2329 copies / ng DNA, respectively, which showed no significant difference (P>0.05). The correlation coefficient between WSSV-resistance breeding value and WSSV load of broodstock, 50 d shrimp and 170 d shrimp were 0.021, 0.463 and 0.185, respectively; and that between growth breeding value and WSSV load of broodstock, 50 d shrimp and 170 d shrimp were 0.033, 0.048 and 0.019, respectively. The results shows that the relationship between growth breeding value, WSSV-resistance breeding value and the WSSV load of shrimp were not significant (P>0.05).
     5.Conclusion and research implications
     The sensitivity of PCR detected the WSSV from high to low are: TaqMan real-time PCR, nested PCR, one-step PCR; The correlation of WSSV load and reproduction、breeding value in F. chinensis all showing no significant difference, The correlation of WSSV load and suivival is showing certain significant difference. This research provided the theoretical and practical basis in the prevention and management WSSV epidemic of F. chinnensis.
引文
[1]程水生,陈光华.我国SPF鸡和SPF鸡胚生产及应用现状[J].中国兽药杂志, 2002, 36(7): 6-8
    [2]程水生,陈洪岩,李昌文,等.关于我国SPF鸡卵生产情况的调查报告[J].中国预防兽医学报, 2006, 28(5): 606-608
    [3]李纪平,钱学敏SPF猪规模化生产的防疫措施. 2003, 39(5): 60-61
    [4] CARPENTER N. BROCK J A. Growth and survival of virus infected and SPF Penaeus vannamei on a shrimp farm in Hawaii [M]. The Oceanic Institute, Waimanalo, Hawaii, 1992:285-294
    [5] WYBAN J A. SWINGLE J S, SWEENEY J N, et a1. Specific pathogen free Penaeus vannamei [J]. World Aquaculture,1993, 24: 39-45
    [6] BEDIER E. Book of abstracts of the 1996 annual meeting of the World Aquaculture Society[C]. Bangkok,Thailand,1996: 32
    [7]李健,牟乃海,孙修涛,等.无特定病原中国对虾种群选育的研究[J].海洋科学, 2001, 25(12): 30-33
    [8] HENNIG O L,ARCE SM,MOSS SM,el a1. Developmenl of a specific pathogen free population of the Chinese fleshy prawn, Fenneropenaeus chinensis Part II. Secondary quarantine[J]. Aquaculture, 2005, 250: 579-585
    [9] PANTOJA C R, SONG X L, LEE x, et a1. Development of a specific pathogen free(SPF)population of the Chinese tleshy prawn Fenneropenaeus chinensis, Part l:Disease Prescreening arid Primary qarantine[J]. Aquaculture, 2005, 250: 573-578
    [10]张庆文,孔杰,刘龙常,等.无白斑综合症病毒对虾苗种生产技术.中国:发明专利, 02135494, 2005
    [11]孔杰,张庆文,柳学周,等.对虾胚胎白斑综合症病毒脱毒方法.中国:发明专利, 01107747, 2005
    [12]孔杰,张天时,罗坤,等.无特定病原中国对虾零换水苗种生产方法.中国:发明专利, 200710115011, 2008
    [13]张家松,董双林,田相利,等.浮游微藻携带和传播WSSV的研究.海洋环境科学. 2007, 26(3): 221-224
    [14]邓灯,张庆文,王伟继,等.中国对虾几个产卵场群体携带白斑综合征病毒状况调查.水产学报, 2005, 29(1): 74-78
    [15]何建国,周化民,姚泊,等.白斑综合症杆状病毒的感染途径和宿主种类[J].中山大学学报, 1999, 14(4): 358-361
    [16]黄倢,于佳,宋晓玲,等. 1994年浙江省对虾暴发性流行病病原及传播途径的初步调[J].海洋水产研究, 1995, 16(1): 91-98
    [17]何建国,莫福.对虾白斑综合症病毒暴发流行与传播途径、气候和水体理化因子的关系及其控制措施[J].中国水产, 1999, (7): 34-37
    [18] Corsin F, Tumbull J F, Hao N V, etc.. Risk factors associated with white spot syndrome virus infection in a Vietnamese rice-shrimp farming system[J]. Dis. Aquat. Org., 2001, 47:1-12
    [19] Zhan W B, Wang Y H. White spot syndrome virus infection of cultured shrimp in China[J]. J. A quat. Anim. Health., 1998, 10:405-410
    [20]战文斌,王远红,铃木信一,等.白斑症病毒在日本对虾体内的感染增殖[J].水产学报,1999, 23(3): 278-282
    [21] Yan D C, Dong S L, Huang J, etc.. White spot syndrome virus (WSSV) detected by PCR in rotifers and rotifer resting eggs from shrimp pond sediments[J]. Diseases of Aquatic Organisms, 2004, 45:78-84
    [22] Vijayan K K, Stalin V, Raj C P, etc. Polychaete worms-a vector for white syndrome virus (WSSV) [J]. Diseases ofAquatic organisms, 2005, 63: 107-111
    [23]Nakano H., Koube H., Oseko N., etc. Mass mortalities of cultured kuruma shrimp Penaeus japonicus in Japan in 1993: Epizootiological survey and infection trails. Fish Pathology, 1994,29 (2): 135-139
    [24] Lo C.F., Ho C.H., Chen C.H., Liu K.F., etc.. Detection and tissue tropism of white spot syndrome baculovirus (WSBV) in captured brooders of Penaeus monodon with a special emphasis on reproductive organs[J]. Dis. Aquat. Org.1997, 30: 53-72
    [25] Nunan L. M., Poulos B. T., Lightner D. V.. The detection of white spot syndrome virus (WSSV) and yellow head virus (YHV) in imported commodity shrimp[J]. Aquaculture, 1998,160: 19-30
    [26]宋晓玲,黄捷,王崇明,等.皮下及造血组织坏死杆状病毒对中国对虾亲虾的人工感染[J].水产学报, 1996, 20(4): 374-378
    [27]包振民,胡景杰,姜明,等.杆状病毒感染越冬亲虾(Penaeus chenesis)的研究一越冬亲虾感染及其垂直传播的可能性[J].青岛海洋大学学报, 1997, 27(3): 347-351
    [28] Wang C S, Tang K F J, Kou G H etc. Light and electron microscopic evidence of white spot disease in the giant tiger shrimp, Penaeus monodon(Fabricius), and the kuruma shrimp,Penaeus japonicus(Bate), cultured in Taiwan[J]. Journal of Fish Diseases 1997,20:323-331
    [29]Chang PS, Hsiao-chao Chen, Yu-Chi. Detection of white spot syndrome associated baculovirus in experimentally infected wild shrimp, crab and lobsters by in sity hybridization[J]. Aquaculture, 1998, 164:233-242
    [30]汝少国,姜明,李永祺,等.中国对虾杆状病毒垂直传播途径的初步探讨[J].水产学报, 1998, 22(1): 49-55
    [31]朱山,郭福生,涂小林,等.用聚合酶链反应和酶联免疫吸附试验检测无包涵体对虾病毒[J].南京农业大学学报, 199, 21(2): 86-91
    [32]刘萍,孔杰,石拓,等.暴发性流行病病原对中国对虾亲虾人工感染及对子代影响的PCR检测[J].海洋与湖沼, 1999, 30(2): 139-144
    [33] Lo C F, Lightner D V, Ho C H, etc.. Specific genomic DNA fragment analysis of different geographical clinical sample of white spot syndrome [J]. Dis Aquat Org, 1999, 35:175-185
    [34]江世贵,何建国,马之明,等.白斑综合症病毒对斑节对虾幼体及仔虾的致病性[J].中山大学学报(自然科学版), 2000, 39(增): 172-176
    [35]朱建中,夏晓勤,陆承平,等.斑点杂交检测对虾白斑综合症病毒青岛株在鳌虾体内的动态分布[J].中国病毒学, 2001, 16(1): 92-95
    [36]雷质文,黄捷,杨冰,等.应用原位杂交技术检测感染中国对虾和克氏原鳌虾体内的白斑综合征病毒[J].中国预防兽医学报, 2002, 24(3): 227-230
    [37]雷质文,黄倢,梁艳,等.用核酸探针技术检测脊尾白虾体内的白斑综合症病毒[J].安徽农业大学学报, 2003, 30(1): 82-85
    [38] Yoganandhan K, Sathish S, Murugan V, et al. Screening the organs for early detection of white spot syndrome virus in Penaeus indicus by histopathology and PCR techniques[J]. Aquaculture, 2003, 215: 21-29
    [39]江世贵,翁少萍,吕玲,等.对感染白斑综合症病毒的亲虾子代的跟踪检测[J].中山大学学报(自然科学版), 2003, 42(1): 66-69
    [40]黄琪琰,宋承方.鱼病防治实用技术.农业出版社. 1990, 8-18
    [41]桃山和夫,郭文泽.海水养殖1,2期合刊. 1992:85-89
    [42] Chen,S.H.,et al.,The oceanic Institude, 1992:177-184
    [43]胡琳琳,房文红,高露娇,等.壳聚糖硫酸酯提高凡纳滨对虾抗白斑综合征病毒感染力的研究[J].海洋渔业, 2008,30(3):250-255
    [44] Kallaya Sritunyalucksanaa, Jiraporn Srisalaa, Kenneth McCollb,et al. Comparison of PCR testing methods for white spot syndrome virus (WSSV) infections in penaeid shrimp[J]. Aquaculture, 2006,255(1-4): 95-104
    [45]毕道荣,岳志芹,梁成珠等.实时定量PCR快速检测对虾白斑综合症病毒[J].山东农业大学学报(自然科学版), 2009,40(1):54-58
    [46]周优,岳志芹,梁成珠等.常规PCR、实时定量PCR检测传染性皮下及造血器官坏死病毒的效果分析[J].海洋水产研究, 2008, 29(2): 90-96
    [47]郑天伦,王国良.对虾白斑综合征病毒的诊断和检测[J].海洋湖沼通报, 2002, 3: 65-70
    [48] Lo C F, Ho C H, Peng S E, et al. White spot syndrome baculovirus(WSBV)detected in cultured and captured shrimps, crabs and other arthropods[J]. Dis Aquat Org, 1996, 27: 215-225
    [49] Takahashi Y, Itami T, Maeda M, et al. Polymerase chain reaction (PCR) amplification of bacilliform virus (RV-PJ) DNA in Penaeus japonicus Bate and systemic ectodermal and mesodermal baculovirus(SEMBV) DNA in Penaeus monodon Fabricius[J]. Fish Dis, 1996, 19: 399-403
    [50] Lo C F, Ho C H, Peng S E, et al. Detection of baculovirus associated with white spot syndrome(WSBV)in penaeid shrimps using polymerase chain reaction[J]. Dis Aquat Org, 1997, 32(2): 133-141
    [51] Tang Kathy F J, Lightner D V. Quantification of white spot syndrome virus DNA through a competitive polymerase chain reaction[J]. Aquaculture, 2000, 189: 11-21
    [52]吕玲,何建国,谢数涛,等.白斑综合症杆状病毒(WSBV)PCR检测方法的改进及应用[J].热带海洋, 2000, 19(2): 90-97
    [53] Durand S V, Lightner D V. Quantitative real time PCR for the measurement of white spot syndrome virus in shrimp[J]. Fish Dis, 2002, 25: 381-389
    [54]周优,岳志芹,梁成珠,等.常规PCR、实时定量PCR检测传染性皮下及造血器官坏死病毒的效果分析[J].海洋水产研究, 2008, 29(2): 90-96
    [55]李文杰,周国勤,朱菲莉,等.检测克氏原螯虾白斑综合征病毒(WSSV)的巢式PCR方法的建立与初步应用[J].南京师大学报(自然科学版), 2009, 32(2): 98-102
    [56] Hossain M S, Otta S K, Chakraborty A, et al. Detection of WSSV in cultured shrimps, captured brooders, shrimp postlarvae and water samples in Bangladesh by PCR using different primers[J]. Aquaculture, 2004, 237: 59-71
    [57] Sritunyalucksanaa K , Srisalaa J, McColl K, et al. Comparison of PCR testing methods for white spot syndrome virus (WSSV) infections in penaeid shrimp[J]. Aquaculture, 2006, 1-4: 95-104
    [58]夏春,黄捷. PCR法检测对虾皮下和造血器官坏死杆状病毒[J].微生物学报, 1999, 39(2): 171-176
    [59]刘萍,孔杰,石拓,等.暴发性流行性病原对中国对虾亲虾人工感染及对子代影响的PCR检测[J].海洋与湖沼, 1999, 30(2): 139-144
    [60]陈信忠,任聪,龚艳清,等.实时荧光定量PCR法检测对虾白斑综合征病毒[J].检验检疫科学, 2009, 19(2): 7-11.
    [61]徐丽美,杨丰.利用定量PCR方法研究对虾白斑杆状病毒感染与发病的关系[J].高技术通讯, 2001, 11(12): 9-11
    [62] Withyachumnarnkul B. Results from black tiger shrimp Penaeus monodon culture pondsstocked with postlarvae PCR-positive or-negative for white-spot syndrome virus (WSSV)[J]. Fish Dis, 1999, 39: 21-27
    [63]Wouters R, Gomez L, Lavens P. et al. Feeding enriched Artemia biomass to Penaeus vannamei broodstocks: Its effect on reproductive performance and larval quality[J]. Shellfish Res., 1999, 18(2): 65l-656.
    [64]姚卫军,黄翔鹄,李活.不同天然饵料对凡纳滨对虾亲虾性腺发育的影响.广东海洋大学学报, 2009, 29(4):84-88.
    [65]宋晓玲,史成银,黄捷,等.用DNA斑点杂交法检测对虾及其饵料和环境生物携带白斑综合症病毒状况的调查,中国水产科学, 2001, 8(4): 36-40.
    [66] Harrison K E. The role of nutrition in maturation, reproduction and embryonic development of decapod crustaceans: Areview[J]. Shell fishRes., 1990, 9(1): 128.
    [67] Teshima S, Kanazawa A. Variation in lipid composition during the ovarian maturation of the prawn[J]. Bul1. Jap. Soc. Sci. Fish. , 1983, 49(6): 957-962.
    [68] Lytle J S, Lytle T F, Ogle J T. Poly unsaturated fatty acid profile sasa comparative tool in assessing maturation diets of Penaeus vannamei[J]. Aquculture, 1990, 89: 287-299.
    [69] Middlediteh B S, Missler S R, Hines H B, et a1. Metabolic profiles of penaeid shrimp: Dietary lipids and ovarian maruration[J]. Chromatogr. , 1980, 195: 359-368
    [70] Xu X L, Ji W L, Castell J D. Influence of dietary lipid sources on fecundity, egg hatchability and fatty acid cornposition of Chinese prawn (Penaeus chinensis) broodstock[J]. Aquculture., 1994, 119: 359-370
    [71]Cahu C L, Cuzon G, Quazuguel P. Effect of highly unsaturated fatty acids,alphatocopherol and ascorbic acid in broodstock diet on egg composition and development of Penaeus indicus[J]. Comp. Biochem. Physio1., 1995, 112: 417-424
    [72]Kulkarn G K, Nagabhushanam R. Mobilization of organic reserves during ovari and evelopment inamarine penaeid prawn, Parapenaeopsis hardwickii(Miers) (Crustacea, Decapoda, enaeidae)[J]. Aquculture, 1979, 18:373-377
    [73] Palacios E, Ibarra A M, Racotta I S. Tissue biochemical composition in relation tomultiple spawning in wild and pond reared Penaeus vannamei brookstock[J]. Aquculture, 2000, 185: 353-371
    [74]Marsden G E, McGuren J J, Handsford S W, et a1. A moist artificial diet for prawn broodstock:Its effect on the reproductive performance of wild caught Penaeus monodon[J]. Aquculture, 1997, 149: 145-156
    [75]Vidal O M, Granja C B, Aranguren F, ect. A profound effect of hyperthermia on survival of Litopenaeus vannamei juveniles infected with white spot syndrome virus[J]. J World AquacultSoc 2001, 32: 364-72
    [76]PRUDER G D.High health shrimp stocks: an advance, an opportunity but not a panacea[J]. World Aquaculture, 1994, 25(3):26-28
    [77]WYBANY J A , SWING J S, SWEENEY J N, et al. Development and commercial performance of high health shrimp using specific pathogen free(SPF) broodstock Penaeus vannamei[C]. Proceeding of the Special Session on shrimp Farming. World Aquaculture Society, Bathon Rouge, Louisiana, 1992:254-260
    [78]李健,牟乃海,孙修涛,等.无特定病原中国对虾种群选育的研究[J].海洋科学, 2001, 25(12): 30-33
    [79]潘鲁青.几种消毒剂对中国对虾受精卵和无节幼体的影响研究[J].海洋科学, 1997, 1: 7-9
    [80]林琼武,单宝堂,黄加琪.不同饵料搭配对日本对虾人工育苗存活率的影响[J].台湾海峡, 2001, 20(增刊): 44-49
    [81] Chambedain G W, Lawrence A L . Maturation, reproduction and reproduction and growth of penaeas vannamei and P.stylirostris fed natural diets[J]. J World Mariculture Sco, 1981, 12(1): 209-224
    [82]邓灯,刘萍,孔杰.卤虫在WSSV病毒病传播中的媒介作用[J].海洋水产研究, 2004, 25(5): 36-42
    [83] Canzonier W J. Accumulation and elimination of coliphage S-13 by the hard clam, Mercenaria mercenaria[J]. Applied Microbiology, 1971, 21(6):1024-1031
    [84]居华,王锋,哈益明,等.辐照控制菲律宾蛤仔中致病菌及其在贮藏期的生长情况[J],核农学报, 2009, 23 (1): 102-105
    [85] Godin D M, Carr W H, Hagino G, et al. Evaluation of a fluorescent elastomer internal tagged in juvenile and adult shrimp Penaeus vannami[J]. Aquculture, 1996, 13(9):243-248
    [86]朱丽岩,郑家声,王梅林,等.不同饵料及添加剂对中国对虾幼体的影响[研究简报].海洋科学, 2000, 24(11): 41-44
    [87]张道波,马甡,王克行,等.中国对虾蚤状及糠虾幼体的蛋白质需求量[J].中国水产科学, 1996, 6(4): 117-118
    [88]田宝军,李英文,丁茜,等.轮虫与卤虫在营养价值等方面的比较[J].河北渔业, 2007, 12: 45-47
    [89]张敏,王瑞平,王渊源.斑节对虾幼虾期对饲料不和脂肪酸的营养需求[J].厦门水产学院学报, 1996, 18(2): 22-28
    [90]荣长宽,粱素秀,岳炳宜.中国对虾对16种饲料的蛋白质和氨基酸的消化率[J].水产学报, 18(2): 131-137
    [91]张印法,耿彦生,袁志助.电离辐射灭菌研究进展[J].中国公共卫生, 1994, 10(11) :522-523.
    [92]周正宇,薛智谋.实验动物饲料60Coγ辐射灭菌剂量的研究[J].上海实验动物科学, 2001, 21(2): 100-103
    [93]袁芳,许德春,孟丽芬,等.医用一次性输液器60Coγ灭菌的研究[J].激光生物学报, 2000, 9(1): 61-64
    [94]任泽林,李爱杰,薛长湖.中国对虾对必需脂肪酸的营养需求[J].青岛海洋大学学报, 1994, 24 (1): 24-32
    [95]钟爱华,李明云.中国对虾亲虾与幼体的营养需要[研究简报],科学视野, 2004, 8(5)78-80.
    [96]程安玮,杜方岭,徐同成,等.辐照对食品中营养成分的影响[J].山东农业科学, 2009, 11:57-60
    [97]杜少波,胡超群,沈琪.亲虾营养需求研究进展[J].热带海洋学报, 2002, 21(4): 80-91.
    [98]罗莉,周初霞.中国对虾的营养需求[J].水产饲料, 2004, 119/120(5/6): 22-25.
    [99]胡鹏,蔡荣宝,王文亮,等.辐照肉及肉制品中“辐照味”的产生机理及预防措施[J].中国食物与营养, 2009, 4: 28-31.
    [100]Gjoen, H. M, Gjerde, B. Comparing breeding schemes using individual phenotypic values and BLUP breeding values as selection triteria. Proceedings of the 6th World Congress on Genetics Applied to Livestock Production, University of New L;England, Armidale, New SouthWales, Australia, 1998, 27:111-114
    [101] Argue, B., Arce, S., M .Lotz,J. et al. Selective breeding of Pacific white shrimp (Litopenaeusvannamei) for growth and resistance to taura Syndrome Virus[J]. Aquculture, 2002, 204:447-460
    [102]Gitterle et al., T. Gitterle, R. Salte. et al. Genetic (co)variation in resistance to white spot syndrome virus (WSSV) and harvest weight in Penaeus (Litopenaeus) vannamei[J]. Aquaculture, 2005, 246: 139–149.
    [103]杨翠华.中国对虾与抗性相关性状的遗传学参数分析[D]. 2007.见:中国海洋大学博士学位论义.
    [104]栾生,孔杰,张天时.等.基于表型值和育种值的中国对虾生长、抗逆性状相关分析[J].海洋水产研究, 2008, 29(3): 15-21.
    [105]刘莉,宋晓玲,黄捷.等. 60Coγ辐照对对虾白斑综合征病毒( WSSV)的灭活效果[J].海洋水产研究. 2004, 25(1): 28-33.
    [106]Withyachumnarnkul, Kanokporn Chayaburakul, Supak Lao-Aroon. ect.cn. Low impact of infectious hypodermal and hematopoietic necrosis virus (IHHNV) on growth and reproductive performance of Penaeus monodon. Boonsirm[J]. DISEASES OF AQUATIC ORGANISMS. 2006, 69: 129-136
    [107]李战军,孔杰,孟宪红.等.三种DNA提取方法对WSSV检测结果的影响[J].渔业科学进展,2011, 32(待刊)
    [108] In-Kwon Jang, Xian-Hong Meng, Hyung-Chul,et al. A TaqMan real-time PCR assay for quantifying white spot syndrome virus (WSSV) infections in wild broodstock and hatchery-reared postlarvae of ?eshy shrimp[J], Fenneropenaeus chinensis. Aquaculture, 2009, 287: 40-45
    [109] Xian-Hong Meng, In-Kwon Jang, Hyung-Chul Seo. et al. White spot syndrome virus quantification in blue crab Portunus trituberculatus hatchery-produced larvae and wild populations by TaqMan real-time PCR, with an emphasis on the relationship between viral infection and crab health[J]. Aquaculture, 2009 , 291: 18-22
    [110] Peinado-Guevara, L.I., López-Meyer, M., Detailed monitoring of white spot syndrome virus (WSSV) in shrimp commercial ponds in Sinaloa, Mexico by nested PCR[J]. Aquaculture . 2006, 251:33-45
    [111] O.M. Vidal, C.B. Granja, L.F. Aranguren, J.A. et al. A profound effect of hyperthermia on survival of Litopenaeus vannamei juveniles infected with White Spot Syndrome Virus[J]. J. World Aquac. Soc. 2001, 32: 364-372
    [112]Lo, C.F., Chang, Y.S., et al. PCR monitoring of cultured shrimp for white spot syndrome virus (WSSV) infection in growout ponds. In: Flegel, T.W.(Ed.), Advances in Shrimp Biotechnology. National Center for Genetic Engineering and Biotechnology, Bangkok, 1998, 281-286
    [113]孟宪红,孔杰,刘萍.等.中国明对虾抗白斑综合症病毒分子标记的筛选.中国水产科学2005, 12(1)14-19
    [114] James Cock , Thomas Gitterle ,Marcela Salazar. et al. Breeding for disease resistance of Penaeid shrimps[J]. Aquaculture, 2009, 286: 1-11