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Detection of poliovirus antigen by enzyme immunoassay.采用酶免疫测定法检测脊髓灰质炎病毒抗原。
J Clin Microbiol. 1986 Dec;24(6):954-8. doi: 10.1128/jcm.24.6.954-958.1986.
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8
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A COMPARISON OF THE REACTIVITY OF POLIOVIRUS COMPLEMENT-FIXING ANTIGENS (NATIVE, HEATED AND SUCROSE DENSITY GRADIENT C AND D) WITH HUMAN SERA.
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Observations on the complement-fixing antibody response to poliovirus in patients with certain Coxsackie and ECHO virus infections.关于某些柯萨奇病毒和埃可病毒感染患者对脊髓灰质炎病毒补体结合抗体反应的观察
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Homologous and heterologous complement fixing antibody in persons infected with ECHO; Coxsackie and poliomyelitis viruses.感染埃可病毒、柯萨奇病毒和脊髓灰质炎病毒的人群中的同源和异源补体结合抗体。
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Modification of the homotypic specificity of poliomyelitis complement-fixing antigens by heat.加热对脊髓灰质炎补体结合抗原同型特异性的改变。
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Detection of enteroviruses by spot hybridization.斑点杂交法检测肠道病毒
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Protein kinase activity in purified poliovirus particles and empty viral capsid preparations.纯化的脊髓灰质炎病毒颗粒和空病毒衣壳制剂中的蛋白激酶活性。
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Solid-phase enzyme immunoassay for rotavirus antigen: faecal protease activity as a reason for false-negative results.轮状病毒抗原的固相酶免疫测定:粪便蛋白酶活性导致假阴性结果的原因
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Detection of rotavirus in faeces by latex agglutination.通过乳胶凝集试验检测粪便中的轮状病毒。
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采用酶免疫测定法检测脊髓灰质炎病毒抗原。

Detection of poliovirus antigen by enzyme immunoassay.

作者信息

Ukkonen P, Huovilainen A, Hovi T

出版信息

J Clin Microbiol. 1986 Dec;24(6):954-8. doi: 10.1128/jcm.24.6.954-958.1986.

DOI:10.1128/jcm.24.6.954-958.1986
PMID:3023440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC269077/
Abstract

A solid-phase enzyme immunoassay (EIA) was developed for the detection of poliovirus antigen. Rabbit and guinea pig antisera for the assay were raised against purified poliovirus type 3/Fin (strain 3/Fin/K) isolated from a fecal specimen from a meningitis patient during an outbreak of poliomyelitis in Finland in 1984. The EIA was highly specific for poliovirus type 3, and it was about 30 times more sensitive for strain 3/Fin/K than for strain 3/Saukett used in the inactivated poliovirus vaccine. The sensitivity of the EIA was 2 to 5 ng of purified strain 3/Fin/K per ml, whereas disrupted viruses and soluble viral proteins were almost undetectable by the assay. Only 5 of 51 (10%) stool specimens containing poliovirus type 3/Fin detected by virus isolation were positive by the EIA. Quantitation by the EIA, using purified poliovirus 3/Fin/K as a standard, revealed that concentrations of poliovirus type 3 in undiluted fecal specimens of patients with natural poliovirus infection were only 50 ng/ml or less. In conclusion, owing to the small amount of poliovirus in feces, the EIA is not suitable for the diagnosis of poliovirus infections directly from clinical specimens, but it can be used to detect, type, and quantitate poliovirus antigen in infected cells.

摘要

开发了一种固相酶免疫测定法(EIA)用于检测脊髓灰质炎病毒抗原。该测定法所用的兔和豚鼠抗血清是针对1984年芬兰脊髓灰质炎疫情期间从一名脑膜炎患者粪便标本中分离出的纯化脊髓灰质炎3型/芬兰株(3/Fin/K株)制备的。该EIA对脊髓灰质炎3型具有高度特异性,对3/Fin/K株的敏感性比对灭活脊髓灰质炎疫苗中使用的3/Saukett株高约30倍。EIA的敏感性为每毫升2至5纳克纯化的3/Fin/K株,而裂解病毒和可溶性病毒蛋白几乎无法通过该测定法检测到。通过病毒分离检测出的51份含有脊髓灰质炎3型/芬兰株的粪便标本中,只有5份(10%)通过EIA呈阳性。以纯化的脊髓灰质炎3/Fin/K株为标准,通过EIA进行定量分析发现,自然感染脊髓灰质炎病毒患者的未稀释粪便标本中脊髓灰质炎3型的浓度仅为50纳克/毫升或更低。总之,由于粪便中脊髓灰质炎病毒含量少,EIA不适合直接从临床标本诊断脊髓灰质炎病毒感染,但可用于检测、分型和定量感染细胞中的脊髓灰质炎病毒抗原。