中国动物传染病学报
中國動物傳染病學報
중국동물전염병학보
CHINESE JOURNAL OF VETERINARY PARASITOLOGY
2014年
3期
14-18
,共5页
吴晓刚%高旭元%余磊%李雪松%闫丽萍%滕巧泱%李国新%李泽君
吳曉剛%高旭元%餘磊%李雪鬆%閆麗萍%滕巧泱%李國新%李澤君
오효강%고욱원%여뢰%리설송%염려평%등교앙%리국신%리택군
鸭坦布苏病毒病活疫苗%毒种%保存期
鴨坦佈囌病毒病活疫苗%毒種%保存期
압탄포소병독병활역묘%독충%보존기
Duck Tembusu virus live vaccine%master seed virus%storage life
鸭坦布苏病毒病是新发的一种以蛋鸭产蛋下降为主要特征的传染病,目前仍没有疫苗可预防和控制该病。将鸭坦布苏病毒强毒(FX2010株)在鸡胚成纤维细胞(chicken embryo fibroblasts,CEFs)上连续传代培养180代,获得1株致弱毒株(FX2010-180P株),利用该弱毒株研制了鸭坦布苏病毒病活疫苗。本研究为了测定鸭坦布苏病毒病活疫苗(FX2010-180P株)毒种的保存期,将-80℃条件下保存了16个月的原始种子批和基础种子批各取3支,进行纯净性检验、鉴别检验以及病毒滴度测定。结果表明,各批次毒种在保存16个月后,病毒纯净无污染,病毒滴度没有明显下降。把基础种子在CEFs上增殖后,低剂量接种鸭子,检验毒种的免疫原性。结果显示,用毒种增殖的病毒免疫原性良好,101.5和102.5 TCID50的剂量可以为接种鸭提供90%和100%的保护。
鴨坦佈囌病毒病是新髮的一種以蛋鴨產蛋下降為主要特徵的傳染病,目前仍沒有疫苗可預防和控製該病。將鴨坦佈囌病毒彊毒(FX2010株)在鷄胚成纖維細胞(chicken embryo fibroblasts,CEFs)上連續傳代培養180代,穫得1株緻弱毒株(FX2010-180P株),利用該弱毒株研製瞭鴨坦佈囌病毒病活疫苗。本研究為瞭測定鴨坦佈囌病毒病活疫苗(FX2010-180P株)毒種的保存期,將-80℃條件下保存瞭16箇月的原始種子批和基礎種子批各取3支,進行純淨性檢驗、鑒彆檢驗以及病毒滴度測定。結果錶明,各批次毒種在保存16箇月後,病毒純淨無汙染,病毒滴度沒有明顯下降。把基礎種子在CEFs上增殖後,低劑量接種鴨子,檢驗毒種的免疫原性。結果顯示,用毒種增殖的病毒免疫原性良好,101.5和102.5 TCID50的劑量可以為接種鴨提供90%和100%的保護。
압탄포소병독병시신발적일충이단압산단하강위주요특정적전염병,목전잉몰유역묘가예방화공제해병。장압탄포소병독강독(FX2010주)재계배성섬유세포(chicken embryo fibroblasts,CEFs)상련속전대배양180대,획득1주치약독주(FX2010-180P주),이용해약독주연제료압탄포소병독병활역묘。본연구위료측정압탄포소병독병활역묘(FX2010-180P주)독충적보존기,장-80℃조건하보존료16개월적원시충자비화기출충자비각취3지,진행순정성검험、감별검험이급병독적도측정。결과표명,각비차독충재보존16개월후,병독순정무오염,병독적도몰유명현하강。파기출충자재CEFs상증식후,저제량접충압자,검험독충적면역원성。결과현시,용독충증식적병독면역원성량호,101.5화102.5 TCID50적제량가이위접충압제공90%화100%적보호。
Duck Tembusu virus (DTMUV) is a newly emerging pathogenic flavivirus causing severe decline of egg production in ducks. However, vaccine is not available for prevention of this infectious disease. An attenuated DTMUV strain FX2010-180P was developed through 180 passages of virulent FX2010 in chicken embryo fibroblasts (CEFs). To evaluate the storage life of the master seed viruses for production of live vaccine, primary seed and master seed batches were tested for purity, identity and titer after stored for 16 months at-80℃. All batches tested were free from bacteria, mycoplasma and exogenous viruses and viral titers did not decline significantly. To test the immunogenicity of seed viruses, ducks were inoculated intramuscularly with 101.5 and 102.5 TCID50 of vaccine viruses propagated in CEFs. Ducks vaccinated with 101.5 and 102.5 TCID50 of vaccine viruses gained 90%and 100%protection against FX2010 challenge.