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用于诊断普马拉汉坦病毒感染(流行性肾病)的血清学方法评估

Evaluation of serological methods for diagnosis of Puumala hantavirus infection (nephropathia epidemica).

作者信息

Sjölander K B, Elgh F, Kallio-Kokko H, Vapalahti O, Hägglund M, Palmcrantz V, Juto P, Vaheri A, Niklasson B, Lundkvist A

机构信息

Swedish Institute for Infectious Disease Control, Stockholm.

出版信息

J Clin Microbiol. 1997 Dec;35(12):3264-8. doi: 10.1128/jcm.35.12.3264-3268.1997.

Abstract

Nephropathia epidemica (NE), Puumala (PUU) virus infection, is a febrile disease which is commonly associated with acute renal impairment. To differentiate NE from other acute febrile illnesses, a rapid and reliable serological diagnosis is important, and a number of different protocols have recently been introduced. In the present report we describe a comparative evaluation of six PUU virus immunoglobulin M (IgM) and seven IgG enzyme-linked immunosorbent assay (ELISA) protocols based on native, Escherichia coli-expressed, or baculovirus-expressed nucleocapsid protein (N). Neutralization and immunofluorescence assays were included for comparison. Equally high sensitivities and specificities were obtained with three mu-capture-based IgM ELISAs using native, baculovirus-expressed, and E. coli-expressed N antigens, respectively, and by an ELISA based on purified E. coli-expressed full-length N adsorbed to solid phase. The assays based on truncated amino-terminal N proteins, including a commercially available PUU virus IgM ELISA, all showed lower sensitivities. For detection of PUU virus-specific IgG, ELISAs based on monoclonal antibody-captured native or baculovirus-expressed N antigens showed optimal sensitivities and specificities, while the assays based on E. coli-expressed N did not detect all PUU virus IgG-positive serum samples. A commercially available PUU virus IgG ELISA based on E. coli-expressed amino-terminal N showed a significantly lower sensitivity than those of all other IgG assays.

摘要

流行性肾病(NE),即普马拉(PUU)病毒感染,是一种通常与急性肾功能损害相关的发热性疾病。为了将NE与其他急性发热性疾病区分开来,快速可靠的血清学诊断很重要,最近已引入了许多不同的检测方案。在本报告中,我们描述了基于天然、大肠杆菌表达或杆状病毒表达的核衣壳蛋白(N)的六种PUU病毒免疫球蛋白M(IgM)和七种IgG酶联免疫吸附测定(ELISA)方案的比较评估。还包括中和试验和免疫荧光试验以作比较。分别使用天然、杆状病毒表达和大肠杆菌表达的N抗原的三种基于μ捕获的IgM ELISA,以及基于吸附在固相上的纯化大肠杆菌表达的全长N的ELISA,均获得了同样高的敏感性和特异性。基于截短的氨基末端N蛋白的检测方法,包括一种市售的PUU病毒IgM ELISA,均显示出较低的敏感性。对于检测PUU病毒特异性IgG,基于单克隆抗体捕获的天然或杆状病毒表达的N抗原的ELISA显示出最佳的敏感性和特异性,而基于大肠杆菌表达的N的检测方法并未检测到所有PUU病毒IgG阳性血清样本。一种基于大肠杆菌表达的氨基末端N的市售PUU病毒IgG ELISA的敏感性明显低于所有其他IgG检测方法。

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