超强毒株+very+virulent+IBDV英语短句+例句大全这一标题涵盖了超强毒株、高毒性传染性法氏囊状病毒的相关内容。法氏囊状病毒（IBDV）是一种影响家禽的病毒，其高毒性毒株对禽类健康构成严重威胁。本标题所包含的短句和例句是对这一病毒的描述和讨论，涵盖了病毒性质、传播途径、防控措施等方面的内容，有助于扩展对这一病毒的了解。通过这些短句和例句，读者可以更全面地了解超强毒株+very+virulent+IBDV的特点和危害，同时也可以获取相关防控的建议和信息，对预防这一病毒的危害具有积极的指导意义。
超强毒株,very virulent IBDV
1)very virulent IBDV超强毒株
1.Isolation and identification ofvery virulent IBDVs from Guangxi and sequence analysis of VP2 hypervariable region广西地区传染性囊病病毒超强毒株的分离鉴定及其VP2基因高变区的序列分析
2.The result indicated that YL051 belonged tovery virulent IBDV(vvIBDV),YL052 m.结果表明:分离株YL 051属IBDV的超强毒株(vvIBDV),而YL 052株既具有强毒株的特征即七肽区(SW SA SG S)和279D,但同时也具有284T的弱毒株特征,可能属于介于强毒株与弱毒株之间的一个中间型。
3.2% nucleotide identities tovery virulent IBDV,97.初步鉴定该分离毒为鸡传染性法氏囊病病毒超强毒株。
英文短句/例句
1.Differentiation of Infectious Bursal Disease Virus between Classical and Very Virulent Strains by Real-Time RT-PCR荧光定量RT-PCR鉴别IBDV超强毒株与经典疫苗毒株
2.A Research on Atenuation of Very Virulent Infectious Busal Disease Virus of China and its Subunit Vaccine;鸡传染性法氏囊病中国超强毒株的培育致弱及亚单位疫苗的研究
3.The Establishment of RT-PCR Method for the Rapid Diagnosis of IBD and Isolation and Identification of vvIBDV in Anhui;IBD的RT-PCR快速诊断方法的建立及安徽超强毒株的分离鉴定
parison of the Pathogenicity and the Sequence of High Variable Region on VP2 Gene of the vvIBDV during the Process of Cell-Cloned Strains Were Passaged on Chickens;鸡传染性法氏囊病病毒超强毒株细胞克隆化毒在回鸡过程中致病性与VP2基因变异比较
5.Isolation and identification of very virulent IBDVs from Guangxi and sequence analysis of VP2 hypervariable region广西地区传染性囊病病毒超强毒株的分离鉴定及其VP2基因高变区的序列分析
6.Preparation of Peptide ELISA for Detecting Antibodies to Highly Virulent PRRSV and Study on Immunogenicity of the Viral Dominant EpitopesPRRSV超强毒株多肽ELISA抗体检测方法建立和主要表位多肽免疫原性研究
7.The Variation of Very Virulent Infectious Bursal Disease Virus Gx Strain;鸡传染性法氏囊病超强毒Gx株毒力变异的研究
8.Studies on the Attenuation of vvIBDV Gx Strain;鸡传染性法氏囊病超强毒Gx株的致弱研究
9.Studies on Attenuation of Cell-cloned Strains Cultivation of Very Virulent Infectious Bursal Disease Virus and Immunogenicity of Attenuated Strains;超强毒IBDV细胞克隆化毒致弱株的培育及其免疫原性的研究
10.Construction of Marek"s Disease Virus Very Virulent Strain L-ZY as a Bacterial Artificial Chromosome鸡马立克氏病病毒超强毒L-ZY株细菌人工染色体的构建
11.Genetic Characterization of the 11 Isolates of Virulent Newcastle disease virus from Chicken Flocks11株鸡新城疫病毒强毒株的分子特性
12.Studies on Pathogenicity of Very Vilulent of Infections Bursal Disease Virus in SPF Chickens at Different Ages;鸡传染性法氏囊病超强毒GX8/99株对不同日龄SPF鸡致病性研究
13.Selection and Cultivation of the Cell-cloned Virus Strains of vvIBDV and Their Influence to Immune Organs;超强毒鸡传染性法氏囊病病毒克隆化毒株选育及其对免疫器官的影响
14.Isolation and Identification of a Virulent Strain of Canine Adenovirus Type 1一株犬1型腺病毒强毒株的分离与鉴定
15.Analysis of TK gene of a virulent duck plague virus CY07 strain鸭瘟病毒CY07强毒株TK基因的序列分析
16.Difference of the vaccine strain M5 and the virulent strain 16M of Brucella species布鲁氏菌强毒株16M和疫苗株M5差异探索
17.Isolation and Identification of a Virulent Strain of Mycoplasma hyopneumoniae一株猪肺炎支原体强毒株的分离和鉴定
18.Molecular Identification of Mild and Severe Isolates of Citrus Tristeza Virus from Pummelos;柚类柑橘衰退病毒（CTV）强、弱毒分离株的分子鉴定
相关短句/例句
vvIBDV超强毒株
1.The Establishment of RT-PCR Method for the Rapid Diagnosis of IBD and Isolation and Identification ofvvIBDV in Anhui;IBD的RT-PCR快速诊断方法的建立及安徽超强毒株的分离鉴定
2.By RT PCR,a single DNA fragment of about 1 5 kb was obtained from GZ strain ofvvIBDV.序列分析和聚类分析表明 ,GZ株与欧洲超强毒株 UK6 6 1非常相似 ,而与经典强毒株、弱毒株和变异株相差较
3)very virulent strain超强毒株
1.An isolated strain HN01 of Infectious Bursal Disease Virus (IBDV),a suspectedvery virulent strain,was purified and inoculated into SPF chickens,which were proved infected 36 h later with lethal rate more than 70% and incidence rate 100%.经血清学试验、毒力试验、鸡胚接种试验、分子生物学和电镜形态学观察均证明该分离物为超强毒株,从而证明河南省鸡群中存在不同于IBDV一般强毒株、经典株和变异株的超强毒株。
4)very virulent IBDV(vvIBDV)超强毒株(vvIBDV)
5)Virulent strain强毒株
1.After 10 passages through 1 day old SPF chicks with IBV D971,a virulent strain IBV D971J was developed.用腺胃病变型鸡传染性支气管炎病毒分离株 IBV-D971株接种 1日龄 SPF鸡 ,连续传 1 0代后 ,培育出了腺胃病变型鸡传染性支气管炎强毒株 IBV-D971 J株。
6)high virulent strain强毒株
1.At 0,5,11,18,30,40 and 50 d post-inoculation,the sera and leucocytes were separated aseptically,and the tissues were collected from the died piglets infectedhigh virulent strain or the anatomical piglets infected low virulent strain at 50 d post-inoculation.20日龄猪繁殖与呼吸综合征(PRRS)阴性健康仔猪滴鼻感染猪繁殖与呼吸综合征病毒(PRRSV)Hn-1/06强毒株和BJ-4弱毒株,于接种后0、5、11、18、30、405、0 d无菌采血,制备血清和分离白细胞,并在感染猪发病死亡或第50天后分别剖杀取各器官组织。
延伸阅读
强-5单座双发超音速攻击机Image:11737017117438283.jpg 强-5单座双发超音速攻击机
强-5单座双发超音速攻击机，国内称“强击机”，由南昌飞机制造公司研制的。其主要任务是近距空中支援和对地攻击，也可进行对空自卫作战。强-5的研制过程动荡曲折，堪称我国自研军用飞机中颇有曲折性和戏剧性的一幕。五十年代初解放军在攻占一江山岛等两栖作战中，对苏制伊尔-10强击机的近距对地支援能力深有感触，为此正式向科研部门下达了超音速近距支援强击机的任务。于是58年8月强-5飞机正式在南昌飞机制造公司上马，陆孝彭任总设计师(图)。60年5月所有理论、图纸设计完毕，试制工作展开。随着国内局势动荡、经济条件恶化，为确保两弹一星等重点计划，强-5的研制工作被搁置，科研人员被抽调岛重点计划中。此时陆孝彭提出个人及未被抽调的科研人员愿以最少的力量坚持研制工作，经上级批准后，陆总师带领剩下的14名下属继续进行研制，首先完成了一架静力试验机体。期间身为总设计师的陆孝彭还兼任试制车间主任，经常亲自扛着零件，候在机床旁插空加工。至64年1月，强-5试制工作全面恢复，决定先生产两架原型机。第一架原型机在静力试验中，加载至98%负载时彻底毁坏，事后查明工作人员自以为是的用两条8mm钢缆代替一条16mm钢缆。1964年6月30日，空军领导联名给中央写报告，要求继续研制强-5型飞机以增强空军对地攻击能力，强-5型飞机研制才得以“复活”。
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