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家蚕蛹表达的重组Vp28疫苗对克氏原螯虾的抗病毒保护效应
引用本文:魏克强,许梓荣.家蚕蛹表达的重组Vp28疫苗对克氏原螯虾的抗病毒保护效应[J].分子细胞生物学报,2005,38(3):190-198.
作者姓名:魏克强  许梓荣
作者单位:浙江大学饲料科学研究所教育部动物分子营养学重点实验室,浙江大学饲料科学研究所教育部动物分子营养学重点实验室 杭州 310029,杭州 310029
摘    要:对虾白斑综合症病毒(WSSV)的致病性强、危害性大、地域分布和宿主范围广泛,目前还不能有效地控制疫情。将含有WSSV囊膜蛋白Vp28基因的重组杆状病毒HyNPV-Vp28感染家蚕(Bombyx mori)蛹,对发病蚕血淋巴进行SDS-PAGE和Western blotting分析,结果表明Vp28在家蚕体内得到了表达。将重组病毒囊膜蛋白rVp28疫苗配制成药饵,持续口服免疫75天,对克氏原螯虾进行预防WSSV,实验虾分为2%重组Vp28疫苗、2%普通蚕蛹组织匀浆(阳性对照)和普通饵料(阴性对照)3个处理组。免疫35天后进行口服攻毒,20天内rVp28疫苗组的累积存活率为63.33%,与阳性和阴性对照比差异显著(P<0.05),PRP分别达54.16%和59.26%;注射攻毒后20 天内rVp28疫苗组的累积存活率与阳性和阴性对照组比差异不显著(P>0.05),PRP分别为46.12% 和49.99%。第55天对存活虾再口服攻毒,20天内rVp28疫苗组与阳性和阴性对照组比累积存活率差异显著(P<0.05),PRP分别为55.80%和63.16%;二次注射攻毒后,rVp28疫苗组的PRP均为31.25%。对vVp28疫苗组存活虾的胃、肠和肝胰腺组织进行病毒的原位杂交检测均呈阴性反应,而对照组死亡虾组织都呈阳性反应。本研究表明,口服免疫家蚕蛹表达的病毒囊膜蛋白Vp28能诱导螯虾产生抗病毒保护作用,对应用疫苗预防对虾的病毒性疾病具有重要意义。

关 键 词:白斑综合症病毒  家蚕  囊膜蛋白Vp28  克氏原螯虾
修稿时间:2004年9月22日

EFFECT OF WHITE SPOT SYNDROME VIRUS ENVELOPE PROTEIN Vp28 EXPRESSED IN SILKWORM (BOMBYX MORI) PUPAE ON DISEASE RESISTENCE IN PROCAMBARUS CLARKII
WEI Ke Qiang,XU Zi Rong The key laboratory of Molecular Animal Nutrition Ministry of Education.EFFECT OF WHITE SPOT SYNDROME VIRUS ENVELOPE PROTEIN Vp28 EXPRESSED IN SILKWORM (BOMBYX MORI) PUPAE ON DISEASE RESISTENCE IN PROCAMBARUS CLARKII[J].Journal of Molecular Cell Biology,2005,38(3):190-198.
Authors:WEI Ke Qiang  XU Zi Rong The key laboratory of Molecular Animal Nutrition Ministry of Education
Institution:WEI Ke Qiang,XU Zi Rong The key laboratory of Molecular Animal Nutrition Ministry of Education,Institute of Feed Science,Zhejiang University,Hangzhou,310029
Abstract:The vaccine made of recombinant envelope protein (rVp28) of white spot syndrome virus (WSSV) expressed in silkworm (Bombyx mori) pupae using a baculovirus vector was used to investigate the efficacy of oral administration on WSSV disease resistance of Procambarus clarkii. Vaccine was mixed with diet at a ratio of 2% (w/w), and Procambarus clarkii were orally admin- istered throughout 75 days. Vaccination with rVP28 showed the significantly higher cumulative survival compared with positive and negative control (P<0.05) following an oral challenge on the 35th day post-vaccination (dpv), with PRP values 54.16% and 59.26%, respectively. rVP28 in- duced higher resistance via IM (intramuscular) injection challenge with WSSV stock, with PRP value of 46.12% and 49.99%, respectively. The survivors were subsequently re-challenged on the 55th dpv. rVP28 induced the significantly higher resistance to oral re-challenge (P<0.05), with both PRP values 55.80% and 63.16%, respectively. rVP28 induced higher resistance to IM injec- tion re-challenge, with both PRP values 31.25%. A DIG labeled WSSV DNA probe was used to detect WSSV by in situ hybridization. The positive cells were observed in epithelial cells of stom- ach, hepatopancreas and gut of the infected control crayfish, while negative reaction were observed in the tissues of survivors-vaccinated. These results indicated that vaccination of crayfish with re- combinant protein had significant effect on oral infection, and had higher resistance against intra- muscular injection challenge. This suggested the protection against WSSV could be induced in crayfish by recombinant protein rVp28 expressed in silkworm pupae.
Keywords:White spot syndrome viruse  Silkworm (Bombyx mori)  Envelope protein Vp28  Procambarus clarkii
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