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通过直接酶免疫测定法直接检测鼻咽标本中的流感病毒抗原,并与病毒排出量定量进行比较。

Direct detection of influenza virus antigen in nasopharyngeal specimens by direct enzyme immunoassay in comparison with quantitating virus shedding.

作者信息

Döller G, Schuy W, Tjhen K Y, Stekeler B, Gerth H J

机构信息

Department of Medical Virology, Hygiene Institute, Tübingen, Germany.

出版信息

J Clin Microbiol. 1992 Apr;30(4):866-9. doi: 10.1128/jcm.30.4.866-869.1992.

Abstract

We developed a direct enzyme immunoassay [EIA; Enzygnost Influenza A(Ag) and Enzygnost Influenza B(Ag)] for the direct detection of influenza A and B virus antigens in nasopharyngeal secretion specimens (NPS). The test is performed without sonification of specimens, and results are obtained within 4 h. A direct comparison between direct EIA and quantitation of virus shedding for influenza A and B virus antigen detection was carried out. A total of 210 NPS and 98 nasopharyngeal wash specimens (NPW) were investigated. We isolated influenza A viruses from 79 (37.6%) of 210 NPS; of these 79 cell-culture-positive NPS, 70 (88.6%) were also positive by direct EIA. Of 29 (13.8%) NPS from which influenza B virus was isolated, 24 (82.8%) NPS were positive by direct EIA. Virus shedding was determined quantitatively in 48 NPS from patients with influenza A and in 24 NPS from patients with influenza B. Only a crude correlation between optical density values and virus concentrations was observed. Detection of influenza virus antigens in NPS by direct EIA showed sensitivities of 89.7% for influenza A virus and 87.9% for influenza B virus and specificities of 99.3% for influenza A virus and 100% for influenza B virus. With direct EIA, all NPW were negative for influenza A virus, although virus was isolated from 21 (21.4%) NPW. Of 15 NPW from which influenza B virus was isolated, 7 showed positive results in direct EIA. In addition, direct EIA is suitable for detecting influenza A and B viruses in cell cultures before the appearance of any cytopathic effects and can be used as a cell culture confirmation test.

摘要

我们开发了一种直接酶免疫测定法[酶免疫测定法;酶免疫诊断甲型流感(抗原)和酶免疫诊断乙型流感(抗原)],用于直接检测鼻咽分泌物标本(NPS)中的甲型和乙型流感病毒抗原。该检测无需对标本进行超声处理,4小时内即可获得结果。对直接酶免疫测定法与甲型和乙型流感病毒抗原检测中病毒脱落定量进行了直接比较。共研究了210份NPS和98份鼻咽冲洗标本(NPW)。我们从210份NPS中的79份(37.6%)中分离出甲型流感病毒;在这79份细胞培养阳性的NPS中,70份(88.6%)通过直接酶免疫测定法也呈阳性。在分离出乙型流感病毒的29份(13.8%)NPS中,24份(82.8%)NPS通过直接酶免疫测定法呈阳性。对48份甲型流感患者的NPS和24份乙型流感患者的NPS进行了病毒脱落定量测定。仅观察到光密度值与病毒浓度之间存在粗略的相关性。通过直接酶免疫测定法检测NPS中的流感病毒抗原,甲型流感病毒的敏感性为89.7%,乙型流感病毒为87.9%,甲型流感病毒的特异性为99.3%,乙型流感病毒为100%。采用直接酶免疫测定法,所有NPW的甲型流感病毒检测均为阴性,尽管从21份(21.4%)NPW中分离出了病毒。在分离出乙型流感病毒的15份NPW中,7份在直接酶免疫测定法中呈阳性结果。此外,直接酶免疫测定法适用于在细胞培养出现任何细胞病变效应之前检测细胞培养物中的甲型和乙型流感病毒,并且可作为细胞培养确认试验。

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