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An Inactivated Vaccine from a Field Strain of Bovine Herpesvirus-1(BoHV-1) has High Antigenic Mass and Induces Strong Efficacy in a Rabbit Model 被引量:2
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作者 Julian Ruiz-Sáenz Jairo Jaime Victor Vera 《Virologica Sinica》 SCIE CAS CSCD 2013年第1期36-42,共7页
Bovine Herpesvirus-1 (BoHV-1) is a DNA virus belonging to the family Herpesviridae, subfamily Alfaherpesvirinae; it is a worldwide pathogen, causing serious economic losses in livestock. In Colombia there have been ... Bovine Herpesvirus-1 (BoHV-1) is a DNA virus belonging to the family Herpesviridae, subfamily Alfaherpesvirinae; it is a worldwide pathogen, causing serious economic losses in livestock. In Colombia there have been multiple isolates of BoHV-1 that have been subjected to molecular characterization, classifying most of the country isolates as BoHV-I.1. In the present study we developed and evaluated an ethyleneimine binary inactivated isolate from the native BoHV-1 strain (C6rdoba-2) in a rabbit model of vaccination and infection. The vaccine was evaluated in two phases, one of immunogenicity with vaccination and a booster after 21 days, and an evaluation phase of protection against challenge with a highly virulent reference strain. The results demonstrate optimum serum-conversion, with protective neutralizing antibody titers 28 days post vaccination and optimal protection against challenge with the reference strain with decreased clinical signs of infection, protection against the onset of fever and decrease of virus excretion post challenge. In conclusion, our results show the enormous potential that an immunogenic inactivated vaccine has produced from the native BoHV-I.1 strain, which produces a high antigen mass to the vaccine to induce optimal immunity and protection, and it is a strong candidate for evaluation and possible future use in different cattle populations. 展开更多
关键词 Antigenic Mass ADJUVANT Binary Ethyleneimine Bovine herpesvirus-1 VACCINE
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A Review: Interactions of Equine Herpesvirus-1 with Immune System and Equine Lymphocyte 被引量:2
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作者 Nor Dini Rusli Khairiyah Binti Mat Hasnita Che Harun 《Open Journal of Veterinary Medicine》 2014年第12期294-307,共14页
Equine herpesvirus-1 (EHV-1) remains one of the most common viral pathogens affecting horses worldwide presenting as a persistent infection which can establish latency in nerve ganglia (trigeminal ganglion), lymphoid ... Equine herpesvirus-1 (EHV-1) remains one of the most common viral pathogens affecting horses worldwide presenting as a persistent infection which can establish latency in nerve ganglia (trigeminal ganglion), lymphoid tissues of the respiratory tract and peripheral blood lymphocytes. EHV-1 infection induces both humoral and cellular immune responses in horses. Virus neutralising antibody, particularly in the nasopharynx, is to kill free virus shed from infected epithelial cells. Hence this antibody has important functions in reducing virus shedding and spreading infection to cohorts. Cellular immune responses, particularly those carried out by cytotoxic T lymphocyte (CTL), have been shown to be effective in killing virus-infected cells in vitro. This review underlines the state of knowledge regarding immunity to EHV-1 and also its interaction with equine lymphocyte. Finally, the review also includes the importance of the viral immediate early (IE) protein in the pathogenesis of EHV-1. This information can be used as the basis for future research. 展开更多
关键词 EQUINE herpesvirus-1 (EHV-1) LYMPHOCYTE CYTOTOXIC T LYMPHOCYTE (CTL) Immune Response Peripheral Blood MONONUCLEAR cell (PBMC)
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Cloning and Sequence Analysis of Glycoprotein D Gene of Bovine Herpesvirus-1 Strain Luojing
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作者 LIJi-chang TONGGuang-zhi +2 位作者 QIUHua-Ji ZHOUYan-Jun XUEQiang 《Journal of Northeast Agricultural University(English Edition)》 CAS 2003年第2期137-140,共4页
By means of PCR,the gene encoding gD of bovine herpesvirus-1 (BHV-1) strain Luojing was amplified,cloned and sequenced.The nucleotide sequence of this gD gene was (1 251 bp,)encoding 417 amino acids.Comparied with the... By means of PCR,the gene encoding gD of bovine herpesvirus-1 (BHV-1) strain Luojing was amplified,cloned and sequenced.The nucleotide sequence of this gD gene was (1 251 bp,)encoding 417 amino acids.Comparied with the published P8-2 strain,the homology of the necleotide sequence is 99.92%,and that of the deduced amino acid sequence is 100%.The results indicated that gD of BHV-1 was highly conservative. 展开更多
关键词 bovine herpesvirus-1(BHV-1) D glycoprotein gene(gD) CLONING sequence analysis.
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牡蛎疱疹病毒(OsHV-1)间接原位杂交PCR检测方法的建立与初步应用 被引量:2
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作者 李亚楠 白昌明 +6 位作者 刘金兰 辛鲁生 李晨 刘莉 黄博闻 魏智薪 王崇明 《水产学报》 CAS CSCD 北大核心 2019年第3期679-687,共9页
为建立实现牡蛎疱疹病毒(OsHV-1)在贝类宿主组织中的精确定位方法,基于原位杂交PCR (ISPCR)技术建立了OsHV-1的间接原位杂交PCR (indirect ISPCR)检测方法,并利用该方法对OsHV-1在魁蚶主要器官的分布情况进行了检测和分析。首先选择适... 为建立实现牡蛎疱疹病毒(OsHV-1)在贝类宿主组织中的精确定位方法,基于原位杂交PCR (ISPCR)技术建立了OsHV-1的间接原位杂交PCR (indirect ISPCR)检测方法,并利用该方法对OsHV-1在魁蚶主要器官的分布情况进行了检测和分析。首先选择适合原位杂交PCR的引物,在载玻片上实现对原位固定靶组织内病毒DNA的稳定、特异扩增,然后与使用相同引物制作的地高辛标记核酸探针进行原位杂交,最后通过免疫酶标技术显示样本内OsHV-1的组织分布。为了达到最佳检测效果,对间接ISPCR的扩增循环数以及组织消化的蛋白酶K浓度进行优化。结果显示,最适PCR扩增循环数为20,蛋白酶K浓度为20μg/mL。利用经优化的间接ISPCR检测方法,对OsHV-1在魁蚶外套膜、鳃、肝胰腺、斧足和闭壳肌5个样本中的组织分布情况和亲嗜性进行检测和分析。病毒阳性信号主要分布于魁蚶外套膜结缔组织中浸润的血细胞和成纤维细胞、肝胰腺和鳃浸润的血细胞、斧足和闭壳肌中坏死肌肉细胞的细胞核中。本研究建立的间接ISPCR检测方法具有灵敏、特异和精确定位的优点,通过组织切片上显示的病毒核酸阳性信号,能判别OsHV-1在不同组织部位的分布特点和受感染的细胞类型;适用于OsHV-1感染的确诊、病毒对不同组织器官的亲嗜性、病毒侵染途径和致病机理等相关研究。 展开更多
关键词 魁蚶 牡蛎疱疹病毒 间接原位杂交PCR 检测方法
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基于原位LAMP技术的牡蛎疱疹病毒(OsHV-1)易感宿主调查 被引量:3
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作者 张翔 谷莉 +5 位作者 郑玉东 李晨 白昌明 辛鲁生 王崇明 刘金兰 《渔业科学进展》 CSCD 北大核心 2023年第2期174-185,共12页
牡蛎疱疹病毒(Ostreidherpesvirus1,Os HV-1)给世界双壳贝类养殖业造成了严重的经济损失。10余种双壳贝类陆续被认定为易感宿主,仍有其他几种贝类仅有PCR核酸阳性数据,因确诊证据不足导致其易感性未得到充分评估。原位环介导等温核酸扩... 牡蛎疱疹病毒(Ostreidherpesvirus1,Os HV-1)给世界双壳贝类养殖业造成了严重的经济损失。10余种双壳贝类陆续被认定为易感宿主,仍有其他几种贝类仅有PCR核酸阳性数据,因确诊证据不足导致其易感性未得到充分评估。原位环介导等温核酸扩增(LAMP)检测技术相对传统原位杂交技术具有灵敏度高、方便快捷、可作为病原微生物感染证据的优点。为了在Os HV-1流行病学调查过程中实现病毒感染的快速检测和确诊,根据已报道的Os HV-1特异性LAMP检测引物,设计内引物,优化反应条件,建立了Os HV-1的原位LAMP检测方法。基于该方法对2019年以来采集的长牡蛎(Crassostreagigas)、福建牡蛎(Crassostrea angulata)、栉孔扇贝(Chlamysfarreri)、虾夷扇贝(Mizuhopecten yessoensis)、毛蚶(Scapharca subcrenata)和菲律宾蛤仔(Ruditapes philippinarum)样本进行检测。结果显示,毛蚶样本的Os HV-1原位LAMP检测结果呈阳性;其他几种贝类部分样本的实时定量PCR (qPCR)检测呈阳性,但原位LAMP检测呈阴性。对毛蚶样本的原位LAMP检测结果分析发现,病毒杂交信号主要分布在外套膜和肝胰腺等器官的结缔组织,推测感染的细胞为成纤维细胞和血淋巴细胞;在闭壳肌和斧足肌肉组织的肌细胞细胞核中也发现较多杂交信号。鳃丝内和周边偶现阳性信号,推测来自渗出的血淋巴细胞。基于原位LAMP技术的Os HV-1检测结果显示,毛蚶是Os HV-1的一种易感宿主,毛蚶结缔组织、肌肉组织和血淋巴细胞对该病毒有强亲嗜性。 展开更多
关键词 牡蛎疱疹病毒 原位LAMP 易感性 流行病学调查
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牡蛎疱疹病毒囊膜蛋白(ORF111)的基因克隆及表达 被引量:2
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作者 张淑敏 白昌明 +3 位作者 辛鲁生 李亚楠 李晨 王崇明 《渔业科学进展》 CSCD 北大核心 2020年第2期183-190,共8页
本研究对编码牡蛎疱疹病毒(Ostreid herpesvirus 1,OsHV-1)囊膜蛋白的orf111基因进行了生物信息学分析、克隆和表达。首先,通过特异性PCR扩增得到orf111基因全长序列,并对其编码囊膜蛋白的理化性质、高级结构、跨膜区和抗原决定簇等进... 本研究对编码牡蛎疱疹病毒(Ostreid herpesvirus 1,OsHV-1)囊膜蛋白的orf111基因进行了生物信息学分析、克隆和表达。首先,通过特异性PCR扩增得到orf111基因全长序列,并对其编码囊膜蛋白的理化性质、高级结构、跨膜区和抗原决定簇等进行生物信息学分析。结果显示,orf111编码一种稳定的疏水性蛋白,具有5个跨膜结构域和9个抗原决定簇,同时,氨基酸序列中还包含1个高度保守的精氨酰–甘氨酰–天冬氨酸(Arg-Gly-Asp,RGD)结构域。随后,构建了pET28a-orf111重组质粒,并将其转化到大肠杆菌DH5α感受态细胞中。最后,通过使用异丙基-β-D-硫代半乳糖苷(IPTG)诱导蛋白表达,表达产物分子量约为32 kDa。本研究应用原核表达得到了含RGD结构域的OsHV-1囊膜蛋白,为进一步制备ORF111蛋白单克隆抗体及开展牡蛎疱疹病毒侵染机制的研究奠定了重要基础,为将来OsHV-1的防控工作提供新的思路。 展开更多
关键词 牡蛎疱疹病毒 囊膜蛋白 原核表达 魁蚶
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福建省牡蛎疱疹病毒(OsHV-1)的检测与分析
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作者 贾圆圆 《渔业研究》 2023年第4期378-384,共7页
随着牡蛎养殖产业规模的不断扩大,牡蛎养殖病害问题日益严重。近年来,牡蛎疱疹病毒1型(Ostreid herpesvirus 1,OsHV-1)在牡蛎中的感染事件频繁发生,特别是在幼苗期,给牡蛎养殖者造成了经济损失。本文通过普通PCR和实时荧光定量PCR方法... 随着牡蛎养殖产业规模的不断扩大,牡蛎养殖病害问题日益严重。近年来,牡蛎疱疹病毒1型(Ostreid herpesvirus 1,OsHV-1)在牡蛎中的感染事件频繁发生,特别是在幼苗期,给牡蛎养殖者造成了经济损失。本文通过普通PCR和实时荧光定量PCR方法对福建省具有一定代表性的6个育苗场及3个主要牡蛎养殖海区的长牡蛎(又称太平洋牡蛎,Crassostrea gigas)和福建牡蛎(又称葡萄牙牡蛎,C.angulata)共90个样本开展OsHV-1检测。结果显示,牡蛎中OsHV-1的平均检出率约11.11%,其中幼苗样本30个,阳性检出率为23.33%,高于成贝中5%的阳性检出率。幼苗阳性样本的病毒含量明显高于成贝,其中牡蛎幼苗样本中OsHV-1最高含量达6.1×107 copies/mg。本研究可为牡蛎疱疹病毒的分子学检测及牡蛎疫病防控方面提供参考。 展开更多
关键词 牡蛎 牡蛎疱疹病毒 PCR
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牡蛎疱疹病毒结构蛋白真核表达系统构建及多聚化特性
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作者 曹书华 魏茂乐 +4 位作者 李永仁 黄博闻 辛鲁生 白昌明 王崇明 《水产学报》 CAS CSCD 北大核心 2024年第5期63-72,共10页
牡蛎疱疹病毒(OsHV-1)在全球范围内导致牡蛎、扇贝与蚶类的大规模死亡,成为双壳贝类养殖产业的重要威胁。为了解OsHV-1的结构与致病机制。本研究利用人胚胎肾细胞(HEK293t),构建OsHV-1主要核衣壳蛋白(ORF104和ORF33)的真核表达系统,并对... 牡蛎疱疹病毒(OsHV-1)在全球范围内导致牡蛎、扇贝与蚶类的大规模死亡,成为双壳贝类养殖产业的重要威胁。为了解OsHV-1的结构与致病机制。本研究利用人胚胎肾细胞(HEK293t),构建OsHV-1主要核衣壳蛋白(ORF104和ORF33)的真核表达系统,并对ORF104和ORF33潜在相互作用进行分析。实验首先通过特异性PCR扩增技术得到orf 104和orf 33的基因序列,根据其编码蛋白的理化性质、跨膜区与三维结构等生物信息学分析结果,选择pCDNA3.1(+)构建两种基因的重组表达质粒。重组质粒经大肠杆菌扩增、提取后,利用转染试剂Lipo8000™将pCDNA3.1(+)-orf 104与pCDNA3.1(+)-orf 33分别单独或共转染至HEK293t。然后,将转染后的细胞培养18 h后裂解收集蛋白。最后利用蛋白免疫印迹(Western blot,WB)与负染电镜检测两种目的蛋白的表达情况。结果显示,实验成功构建了OsHV-1衣壳蛋白ORF104和ORF33的重组表达质粒载体,通过真核细胞表达得到大小约为135与35 ku的目的蛋白。研究表明,表达质粒可在真核表达系统中实现蛋白单独转染与共转染,共转染蛋白间可能存在相互作用的趋势并形成多聚体,其中,ORF33自身即可形成分子质量不同的多聚体。本研究首次利用真核表达系统开展OsHV-1关键结构蛋白的表达,为进一步开展该病毒结构蛋白功能与互作,以及病毒入侵机制研究奠定基础。 展开更多
关键词 牡蛎疱疹病毒 核衣壳蛋白 真核表达系统 蛋白多聚化
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牡蛎疱疹病毒流行病学及其防控研究进展 被引量:2
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作者 胡宗福 任绍杰 +3 位作者 牛化欣 于建华 常杰 李树国 《水产科学》 CAS CSCD 北大核心 2018年第5期714-720,共7页
作为迄今为止仅有的一种软体动物疱疹病毒,牡蜗痕瘡病毒(Ostreid herpesirus-1,OsHV-1)的分类地位及命名是由国际病毒分类委员会于2012年正式确立的,即疱疹病毒目、软体动物疱疹病毒科、痕瘆病毒属(Ostreavirus)[1].由此看来,牡蜗及其... 作为迄今为止仅有的一种软体动物疱疹病毒,牡蜗痕瘡病毒(Ostreid herpesirus-1,OsHV-1)的分类地位及命名是由国际病毒分类委员会于2012年正式确立的,即疱疹病毒目、软体动物疱疹病毒科、痕瘆病毒属(Ostreavirus)[1].由此看来,牡蜗及其他贝类的疱疹病毒皆属牡蛎疱疹病毒种类。自20世纪90年代以来,由该病毒引起的牡蛎及其他贝类疾病在以欧洲为主要发病区的世界范围内频繁爆发,感染幼虫及贝苗死亡率常常达90%以上,对产业的危害非常严重。欧盟也多次出资设立研究基金及组织团队进行科学研究和疾病的防控指导,并在2010年立法试图通过限制长牡蜗(Crassostrea gigas)的流通及介人监控程序来控制病毒的传播[3]。 展开更多
关键词 牡蛎疱疹病毒 流行 宿主 防控
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软体动物疱疹病毒及其对贝类养殖产业的危害 被引量:8
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作者 白昌明 辛鲁生 王崇明 《渔业科学进展》 CSCD 北大核心 2021年第1期214-226,共13页
中国是贝类养殖大国,30余年来,贝类养殖产量总体稳中有升,但部分贝类的养殖产业因疫病影响出现严重萎缩、甚至消失。20世纪90年代以来,中国多种双壳贝类和杂色鲍(Haliotis diversicolor supertexta)因感染疱疹病毒出现大规模死亡,成为... 中国是贝类养殖大国,30余年来,贝类养殖产量总体稳中有升,但部分贝类的养殖产业因疫病影响出现严重萎缩、甚至消失。20世纪90年代以来,中国多种双壳贝类和杂色鲍(Haliotis diversicolor supertexta)因感染疱疹病毒出现大规模死亡,成为近年来危害中国贝类养殖业的主要病原。经流行病学调查和病原鉴定,引起中国双壳贝类和杂色鲍死亡的疱疹病毒分别为牡蛎疱疹病毒(Ostreid herpesvirus 1,OsHV-1)和鲍疱疹病毒(Haliotid herpesvirus 1,HaHV-1)。贝类疱疹病毒病不仅在中国发生,同时也在全球多个国家、地区传播和暴发,引起全球贝类养殖从业者和科研人员的广泛关注。多国学者从病毒特征、流行病学、诊断技术、生态防控和抗病育种等多个角度展开研究,以期减轻此类病毒对贝类产业造成的危害。大量科研力量的投入使OsHV-1和HaHV-1成为分类地位明确,研究最深入、最全面的贝类病毒性病原。本文对近年来OsHV-1和HaHV-1研究领域取得的主要成果进行总结,重点介绍其在中国和全球范围的发生、传播过程、产业危害和防控措施等。 展开更多
关键词 贝类养殖 软体动物疱疹病毒 牡蛎疱疹病毒 鲍疱疹病毒
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基于长片段PCR扩增的牡蛎疱疹病毒基因组高通量测序 被引量:1
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作者 史杰 白昌明 +2 位作者 李晨 蔡生力 王崇明 《水产学报》 CAS CSCD 北大核心 2018年第2期216-225,共10页
为获取2001年低温冻存栉孔扇贝感染牡蛎疱疹病毒(Os HV-1)变异株(ZK2001)基因组序列,并分析ZK2001与其他Os HV-1变异株的序列差异和系统发育关系,利用基于长片段PCR的基因组DNA的扩增和富集技术,获取2001年栉孔扇贝感染Os HV-1变异株的... 为获取2001年低温冻存栉孔扇贝感染牡蛎疱疹病毒(Os HV-1)变异株(ZK2001)基因组序列,并分析ZK2001与其他Os HV-1变异株的序列差异和系统发育关系,利用基于长片段PCR的基因组DNA的扩增和富集技术,获取2001年栉孔扇贝感染Os HV-1变异株的基因组DNA;再使用Illumina Hiseq 2500 PE250高通量测序平台对其测序。最后分析ZK2001与Os HV-1其他变异株基因组的序列差异和系统发育关系。测序数据组装后获得8个Scaffold。基因组变异分析结果显示,ZK2001与参考基因组相比存在328个SNP位点,SNP和序列插入/缺失变异是导致Os HV-1基因组序列变异的主要变异类型。系统发育分析结果显示,ZK2001变异株与分离自我国的Os HV-1变异株亲缘关系最近,与分离自欧洲的Os HV-1μvar及其相关变异株的亲缘关系最远,说明中国和欧洲分布Os HV-1间存在因地理隔离导致的遗传分化。研究表明,基于长片段PCR的DNA富集技术,可以有效地扩增和富集冷冻样本中Os HV-1基因组DNA,并应用于高通量测序。Os HV-1不同变异株基因组序列数据的获取和积累,将为其基因组尺度的基因变异、株系演化和系统发育关系等研究提供重要基础。 展开更多
关键词 栉孔扇贝 高通量测序 长片段PCR 牡蛎疱疹病毒
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Importance of Viral Disease in Dairy Cow Fertility 被引量:8
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作者 D.Claire Wathes Chike F.Oguejiofor +1 位作者 Carole Thomas Zhangrui Cheng 《Engineering》 SCIE EI 2020年第1期26-33,共8页
Many viral diseases are endemic in cattle populations worldwide. The ability of many viruses to cross the placenta and cause abortions and fetal malformations is well understood. There is also significant evidence tha... Many viral diseases are endemic in cattle populations worldwide. The ability of many viruses to cross the placenta and cause abortions and fetal malformations is well understood. There is also significant evidence that viral infections have additional actions in dairy cows, which are reflected in reduced conception rates. These effects are, however, highly dependent on the time at which an individual animal first contracts the disease and are less easy to quantify. This paper reviews the evidence relating to five viruses that can affect fertility, together with their potential mechanisms of action. Acute infection with non-cytopathic bovine viral diarrhea virus (BVDV) in mid-gestation increases abortion rates or causes the birth of persistently infected calves. BVDV infections closer to the time of breeding can have direct effects on the ovaries and uterine endometrium, which cause estrous cycle irregularities and early embryo mortality. Fertility may also be reduced by BVDV-induced immunosuppression, which increases the susceptibility to bacterial infections. Bovine herpesvirus (BHV)-1 is most common in pre-pubertal heifers, and can slow their growth, delay breeding, and increase the age at first calving. Previously infected animals subsequently show reduced fertility. Although this may be associated with lung damage, ovarian lesions have also been reported. Both BHV-1 and BHV-4 remain latent in the host following initial infection and may be reactivated later by stress, for example associated with calving and early lactation. While BHV-4 infection alone may not reduce fertility, it appears to act as a co-factor with established bacterial pathogens such as Escherichia coli and Trueperella pyogenes to promote the development of endometritis and delay uterine repair mechanisms after calving. Both Schmallenberg virus (SBV) and bluetongue virus (BTV) are transmitted by insect vectors and lead to increased abortion rates and congenital malformations.BTV-8 also impairs the development of hatched blastocysts;furthermore, infection around the time of breeding with either virus appears to reduce conception rates. Although the reductions in conception rates are often difficult to quantify, they are nevertheless sufficient to cause economic losses, which help to justify the benefits of vaccination and eradication schemes. 展开更多
关键词 Bovine viral diarrhea virus Bovine herpesvirus-1 Bovine herpesvirus-4 Schmallenberg virus Bluetongue virus IMMUNOSUPPRESSION Embryo mortality
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Infectious laryngotracheitis virus in chickens 被引量:7
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作者 Shan-Chia Ou Joseph J Giambrone 《World Journal of Virology》 2012年第5期142-149,共8页
Infectious laryngotracheitis(ILT) is an important respiratory disease of chickens and annually causes significant economic losses in the poultry industry worldwide. ILT virus(ILTV) belongs to alphaherpesvirinae and th... Infectious laryngotracheitis(ILT) is an important respiratory disease of chickens and annually causes significant economic losses in the poultry industry worldwide. ILT virus(ILTV) belongs to alphaherpesvirinae and the Gallid herpesvirus 1 species. The transmission of ILTV is via respiratory and ocular routes. Clinical and post-mortem signs of ILT can be separated into two forms according to its virulence. The characteristic of the severe form is bloody mucus in the trachea with high mortality. The mild form causes nasal discharge, conjunctivitis, and reduced weight gain and egg production. Conventional polymerase chain reaction(PCR), nested PCR, real-time PCR, and loop-mediated isothermal amplification were developed to detect ILTV samples from natural or experimentally infected birds. The PCR combined with restriction fragment length polymorphism(RFLP) can separate ILTVs into several genetic groups. These groups can separate vaccine from wild type field viruses. Vaccination is a common method to prevent ILT. However, field isolates and vaccine viruses can establish latent infected carriers. According to PCR-RFLP results, virulent field ILTVs can be derived from modified-live vaccines. Therefore, modified-live vaccine reversion provides a source for ILT outbreaks on chicken farms. Two recently licensed commercial recombinant ILT vaccines are also in use. Other recombinant and gene-deficient vaccine candidates are in the developmental stages. They offer additional hope for the control of this disease. However, in ILT endemic regions, improved biosecurity and management practices are critical for improved ILT control. 展开更多
关键词 INFECTIOUS laryngotracheitis virus INFECTIOUS laryngotracheitis Gallid herpesvirus-1 POLYMERASE chain reaction combined with RESTRICTION FRAGMENT length polymorphism RECOMBINANT laryngotracheitis vaccines
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