野毒株的英文

• wild parsnip
• wild strain
• ymdd

• "野"英文翻译    open country; the open
• "毒"英文翻译    poison; toxin
• "株"英文翻译    root and stem of a tree abov ...
• "街毒,狂犬簿的野毒株,街道簿" 英文翻译 :    virus de rue renforce
• "野毒" 英文翻译 :    natural virus; wild type virus
• "毒株" 英文翻译 :    ndv-f; strain
• "减毒株，无毒株" 英文翻译 :    avirulent strain
• "病毒株" 英文翻译 :    virus strain
• "放毒株" 英文翻译 :    killer strain
• "减毒株" 英文翻译 :    attenuated strain
• "街毒株" 英文翻译 :    street strain
• "强毒株" 英文翻译 :    shimen; velogen strain; virulent strain
• "弱毒株" 英文翻译 :    lentogen strain; low virulent strain
• "无毒株" 英文翻译 :    avirulent strain; avirulentstrain
• "有毒株" 英文翻译 :    virulent strain
• "中毒株" 英文翻译 :    mesogen strain
• "弗卢里毒株" 英文翻译 :    flury hep strain
• "攻击用毒株" 英文翻译 :    challenge strain
• "固定毒株" 英文翻译 :    fixed strain
• "基斯林毒株" 英文翻译 :    kissling strain
• "减毒株变种" 英文翻译 :    attenuated strain mutant
• "库班毒株" 英文翻译 :    cuban strain
• "木地毒株" 英文翻译 :    native strain
• "耐药毒株" 英文翻译 :    resistant strains of hiv
• "牛源病毒株" 英文翻译 :    original cattle strain

• Chickens at 4 weeks of age were the most sensitive
  结果表明，这些野毒株的毒力差异甚大。
• Immunity of live attenuated japanese encephalitis vaccine to differentwild je virus strains
  流行性乙型脑炎减毒活疫苗国内外不同野毒株的免疫性
• In this study three wild strains of rabies virus were isolated from nanning , longan and bama of guangxi and were designated as 119 , gxla and gxbm respectively
  本试验从广西南宁、隆安和巴马分离到三株狂犬病毒野毒株，分别编号为119 、 gxla和gxbm 。
• Relatively , the new wibdv strains gx8 / 99 had less homology to wibdv reference strain hk46 and other 3 field strains as 96 . 8 % - 97 . 2 % at dna or aa levels , than the homology among hk46 and 3 strains , strains gx8 / 99 more than 98 . 4 % - 98 . 6 % at dna or aa levels
  为研究病毒的核酸分子结构与其致病性的关系，本研究选取了在致死率上不同的4个ibdv野毒株，比较了它们的vpz基因高变区共494个碱基序列。
• The amplified e2 fragments of two hcv strains were all 1280bp in length by 2 % agrose gel electrophoresis . expected size of 1280bp of 2 fragments and their specificity were confirmed by restriction endonuclease digestion and then they were cloned respectively into pmd - 18t vector
  以此病毒rna为模板，利用rt - pcr技术，扩增出了猪瘟野毒株hcv - jn 、 hcv - yc完整的e2基因，用pmd - 18t载体克隆，经电泳检测、酶切分析及pcr鉴定初步证实了所扩增片段的特异性。
• These results showed that the three isolates were infectious bursal disease virus . the full - length cdna of the genomic segment a of two viruses , one virulent field strain ibdv zj2000 and one attenuated strains ibdv jd1 , were amplified in a single step procedure by long - accurate reverse - transcription polymerase chain reaction ( la - pcr ) , cloned into pgem - t easy vector , and sequenced
  分别以传染性法氏囊病病毒zj2000株(野毒株)和jd1株(弱毒株)基因组dsrna为模板，采用long - accuratert - pcr ( la - pcr )一步法扩增并克隆了两株病毒的基因组a节段全长cdna 。
• The result shows that the high degree of homology of e2 sequences and 426 residues amino acid sequences existed in the strain hclv , hcv - jn , hcv - yc , fc and the epitopes between the four strains are not variable obviously by analysising the variation of some main amino acid residues substitutions of e2 major antigenic domains , confirming initially immunization with hcv vaccine strain can resist challenging of field strains
  结果发现， hclv与fc间核苷酸及氨基酸序列的同源性分别为98 . 3 、 99 . 2 ；两个野毒株与hclv和fc株之间的同源性也分别在98以上，与alfort株的同源性最低，分别在83 、 89左右。据此，可推测hclv 、猪瘟野毒株和c株之间的e2基因序列及氨基酸序列无明显差异。
• G gene of rabies virus m , the of two main regions ( about 1000nt ) , ranging from 3161nt to 4162nt and ranging from 4012nt to 4863nt of glycoprotein gene of rabies virus strain m , isolated from mouse in he nan , china were amplified by reverse transcriptase - polynerase chain reaction ( rt - pcr ) in order to complete glycoprotein gene of strain m . these regions were sequenced by the produce of pcr directly . comparison and analysis of nucleotide sequence and amino acid sequence deduced with that of other strains published was performed by computer with dnasisv 2 . 5demo software
  本研究对我国河南某地野鼠体内分离的狂犬病野毒株mrv基因的3161位? 4162位( 1001个碱基)和4012位? 4863位( 851个碱基)片段进行了反转录pcr扩增和序列测定，得到mrv的糖蛋白基因全序列，用dnasisv2 . 5demo分析软件，与已发表的代表性毒株g基因全序列进行核苷酸和氨基酸序列的比较分析，结果表明在同一基因型中， mrv和国际标准攻毒株cvs的同源性最高( 96 . 5 ) ，和中国减毒株ctn的同源性最低( 79 . 8 ) 。
• After transfection , we also testified the co - expression of pp38 and pp24 by ifa and by western - blotting with anti - gst - pp24 sera . we cloned and sequenced the pp38 and pp24 gene amplified from 814 , cvi988 ( mmdv ) , ga ( vmdv ) , md5 ( vvmdv ) , md11 ( vvmdv ) , rblb ( vvmdv ) , 648a ( vv + mdv ) , and other 7 isolated strains from china . sequence analysis shows pp24 and pp38 gene are very conservative
  对包括型mdv疫苗毒、强毒、超强毒、特超强毒共7个国际参考株与7个中国分离野毒株的pp24基因和pp38基因分别进行了克隆测序，序列分析结果表明，型mdv的pp24基因和pp38基因均非常保守，比较的15个毒株的pp24基因的核苷酸和氨基酸之间的同源性分别高于98 . 9和98 . 1 ，同时比较的14个毒株的pp38基因的核苷酸和氨基酸之间的同源性分别高于99 . 4和99 . 0 。
• The comparison of meq gene sequences of different pathotypes of marek ' s disease virus meq genes of different pathotypes of marek ' s disease virus ( mdv ) were amplified , in the whole opening reading frame ( orf ) by polymerase chain reaction ( pcr ) technique , sequenced and compared with the published sequence of ga strain ( representing vmdv ) . cvi988 / rispens and 814 , commercial vaccine strains popularly used worldwide and in china respectively ; 648a , representing very virulent plus ( vv + mdv ) and 6 field isolates , originated from guangxi commercial chickens with visceral lymphomas and vaccine breaks , representing high pathogenic ( hpmdv ) and two of them ( g2 and n ) were proved to be vvmdv , were used
  本研究通过三个方面进行了研究，取得了如下主要实验结果： 1mdv不同致病型( pathotypes )毒株meq基因序列的比较研究应用pcr技术扩增了不同致病型mdvs ，即国际通用型疫苗毒cv1988 rispens株和中国特有的疫苗毒814株、特超强毒648a株( vv + mdv )以及6个广西分离到的野毒株共9个毒株的meq基因，进行核苷酸序列的测定并与标准强毒ga株( vmdv )进行核苷酸和氨基酸序列的比较。