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新城疫病毒的神经氨酸酶在洗脱抑制反应中受到抑制。

The neuraminidase of Newcastle disease virus inhibited in the elution-inhibition reaction.

作者信息

Graves I L

机构信息

Department of Molecular Microbiology and Immunology, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, MD 21205, USA.

出版信息

Vet Res. 1996;27(1):45-54.

PMID:8620188
Abstract

The neuraminidase (NA) on strain 575 of Newcastle disease virus (NDV) was inhibited with elution-inhibition (EI) antibodies causing permanent agglutination patterns of red blood cells (RBC). Detection of EI antibody was unaffected by passage through sephadex, centrifugation or plaque purification of NDV. The haemagglutination-inhibition (HI) and EI reactions as well as the NA inhibition test all showed an increase in titre as immunization progressed. Fluorescent-stained IgG on RBC from the EI reaction appeared as foci but as a halo if NDV was disrupted with ether suggesting NDV aggregation. The haemagglutinin (HA) on "sensitized' RBC from the EI reaction was not neutralized and agglutinated newly added RBC. The NA cleaved fetuin at 49 to 88% of the maximum values while bound to RBC by EI antibody. Added NA substrates failed to block the EI reaction. The order of inactivation at 53 or 56 degrees C but not 50 degrees C was: the putative EI antibody determinant > NA > HA. The term elution inhibition is suggested for the antibody responsible for the EI reaction.

摘要

新城疫病毒(NDV)575株上的神经氨酸酶(NA)被洗脱抑制(EI)抗体抑制,导致红细胞(RBC)出现永久性凝集模式。通过葡聚糖凝胶柱层析、离心或NDV蚀斑纯化传代后,EI抗体的检测不受影响。随着免疫进程的推进,血凝抑制(HI)和EI反应以及NA抑制试验的效价均升高。EI反应中RBC上的荧光染色IgG呈现为斑点状,但如果用乙醚破坏NDV,则呈现为晕圈,提示NDV聚集。EI反应中“致敏”RBC上的血凝素(HA)未被中和,且能凝集新加入的RBC。当通过EI抗体与RBC结合时,NA对胎球蛋白的切割活性为最大值的49%至88%。添加NA底物不能阻断EI反应。在53或56℃而非50℃下的失活顺序为:推定的EI抗体决定簇>NA>HA。建议将负责EI反应的抗体称为洗脱抑制抗体。

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