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4
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Trop Anim Health Prod. 1997 Feb;29(1):25-8. doi: 10.1007/BF02632342.
5
Precipitation reactions with Newcastle disease virus.
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本文引用的文献

1
Optimizing the enzyme-linked immunosorbent assay for evaluating immunity of chickens to Newcastle disease.优化用于评估鸡新城疫免疫力的酶联免疫吸附测定法。
Avian Dis. 1983 Oct-Dec;27(4):1112-25.
2
Rapid serological profiling by enzyme-linked immunosorbent assay. I. Measurement of antibody activity titer against Newcastle disease virus in a single serum dilution.通过酶联免疫吸附测定进行快速血清学分析。I. 在单一血清稀释度下测量针对新城疫病毒的抗体活性滴度。
Avian Dis. 1983 Jan-Mar;27(1):161-70.
3
Evaluation in swine of a subunit vaccine against pseudorabies.针对伪狂犬病的亚单位疫苗在猪身上的评估。
Am J Vet Res. 1983 Jan;44(1):123-5.
4
Preparation and efficacy of an inactivated subunit vaccine against Aujeszky's disease virus infection.
Res Vet Sci. 1981 Sep;31(2):261-3.
5
Evaluation of experimental subunit vaccines for infectious bovine rhinotracheitis.牛传染性鼻气管炎实验性亚单位疫苗的评估
Am J Vet Res. 1980 Mar;41(3):383-90.
6
Demonstration of type-specific influenza antibody in mammalian and avian sera by immunodiffusion.通过免疫扩散法检测哺乳动物和鸟类血清中特定类型流感抗体
Bull World Health Organ. 1970;42(5):779-85.
7
Reactions of Newcastle disease virus with infectious mononucleosis sera in agar gel.新城疫病毒与传染性单核细胞增多症血清在琼脂凝胶中的反应
J Immunol. 1967 Oct;99(4):778-84.
8
The binding of deoxycholate and Triton X-100 to proteins.脱氧胆酸盐和曲拉通X-100与蛋白质的结合。
J Biol Chem. 1973 Jul 25;248(14):4926-32.
9
Isolation and purification of the envelope proteins of Newcastle disease virus.新城疫病毒包膜蛋白的分离与纯化。
J Virol. 1973 Feb;11(2):263-71. doi: 10.1128/JVI.11.2.263-271.1973.
10
Immunodiffusion reaction to avian infectious bursal virus.针对禽传染性法氏囊病病毒的免疫扩散反应
Avian Dis. 1972 Jul-Sep;16(4):961-4.

经去污剂处理的新城疫病毒作为琼脂凝胶沉淀试验抗原。

Detergent-treated Newcastle disease virus as an agar gel precipitin test antigen.

作者信息

Gelb J, Cianci C G

出版信息

Poult Sci. 1987 May;66(5):845-53. doi: 10.3382/ps.0660845.

DOI:10.3382/ps.0660845
PMID:3628165
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7107192/
Abstract

A soluble Newcastle disease virus (NDV) agar gel precipitin (AGP) antigen was prepared by treating 100-fold concentrated NDV with a nonionic detergent. Virus concentration prior to detergent treatment was best accomplished by ultracentrifugation or by a simple, less expensive, and more practical method involving acid (HCl) precipitation of NDV. Virus concentrated by polyethylene glycol precipitation was found to have a low antigen titer and was not considered suitable as an AGP antigen. Antigens derived from the LaSota, Roakin, and Texas GB strains formed at least two lines of identity in the AGP test as early as 24 hr after inoculation of the agar gels. Virus used for AGP antigen production could be grown in chicken embryos from an NDV-immune as well as susceptible breeder flock. The NDV AGP antigen was found to be stable after 20 consecutive freezing and thawing cycles and storage at -20 C or 4 C for at least 6 months. Detergent-treated NDV was used as an AGP test antigen to determine serum antibody responses of chickens following infection and vaccination. Hemagglutination-inhibition, virus neutralization, and enzyme-linked immunosorbent assay antibody production was also evaluated for comparative purposes. The AGP test was found to be useful as an aid in diagnosing field infections and assessing inactivated virus vaccination responses. These purposes were achieved by demonstrating an increase in the number of AGP positive chickens between preinfection and postinfection or vaccination bleedings. The ease of performance and low cost of the AGP test favors its use for screening large numbers of serum samples, perhaps in conjunction with a quantitative serological test.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过用非离子去污剂处理100倍浓缩的新城疫病毒(NDV)制备了一种可溶性新城疫病毒琼脂凝胶沉淀(AGP)抗原。去污剂处理前的病毒浓缩最好通过超速离心或一种简单、成本较低且更实用的方法来完成,该方法涉及用酸(盐酸)沉淀NDV。发现通过聚乙二醇沉淀浓缩的病毒抗原效价较低,不适合用作AGP抗原。源自LaSota、Roakin和Texas GB毒株的抗原在接种琼脂凝胶后最早24小时就在AGP试验中形成了至少两条同一线。用于生产AGP抗原的病毒可以在来自NDV免疫以及易感种鸡群的鸡胚中培养。发现NDV AGP抗原在连续20次冻融循环以及在-20℃或4℃储存至少6个月后仍稳定。经去污剂处理的NDV用作AGP试验抗原来确定鸡在感染和接种疫苗后的血清抗体反应。还为了比较目的评估了血凝抑制、病毒中和以及酶联免疫吸附测定抗体产生情况。发现AGP试验有助于诊断田间感染和评估灭活病毒疫苗接种反应。这些目的是通过证明在感染前和感染后或接种疫苗后采血之间AGP阳性鸡的数量增加来实现的。AGP试验操作简便且成本低,有利于用于筛查大量血清样本,可能与定量血清学试验联合使用。(摘要截短至250字)