首页> 外文期刊>Clinical and vaccine immunology: CVI >Differentiation between human coronaviruses NL63 and 229E using a novel double-antibody sandwich enzyme-linked immunosorbent assay based on specific monoclonal antibodies.
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Differentiation between human coronaviruses NL63 and 229E using a novel double-antibody sandwich enzyme-linked immunosorbent assay based on specific monoclonal antibodies.

机译:区分人类冠状病毒NL63使用小说和229 e double-antibody三明治酶联免疫吸附试验的基础上特定的单克隆抗体。

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Human coronaviruses (HCoVs) are responsible for respiratory tract infections ranging from common colds to severe acute respiratory syndrome. HCoV-NL63 and HCoV-229E are two of the four HCoVs that circulate worldwide and are close phylogenetic relatives. HCoV infections can lead to hospitalization of children, elderly individuals, and immunocompromised patients. Globally, approximately 5% of all upper and lower respiratory tract infections in hospitalized children are caused by HCoV-229E and HCoV-NL63. The latter virus has recently been associated with the childhood disease croup. Thus, differentiation between the two viruses is relevant for epidemiology studies. The aim of this study was to develop a double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) as a potential tool for identification and differentiation between HCoV-NL63 and HCoV-229E. The nucleocapsid (N) proteins of HCoV-NL63 and HCoV-229E were expressed in an Escherichia coli system and used to immunize mice in order to obtain monoclonal antibodies (MAbs) specific for each virus. Three specific MAbs to HCoV-NL63, one MAb specific to HCoV-229E, and four MAbs that recognized both viruses were obtained. After their characterization, three MAbs were selected in order to develop a differential DAS-ELISA. The described assay could detect up to 3 ng/ml of N protein and 50 50% tissue culture infective doses/ml of virus stock. No cross-reactivity with other human coronaviruses or closely related animal coronaviruses was found. The newly developed DAS-ELISA was species specific, and therefore, it could be considered a potential tool for detection and differentiation of HCoV-NL63 and HCoV-229E infections.
机译:人类冠状病毒(HCoVs)负责呼吸道感染常见不等感冒严重急性呼吸系统综合症。HCoV-NL63和hcov - 229 e两个四HCoVs,在世界范围内流通,是接近系统发育的亲戚。住院的儿童,老人个人,免疫力低下的患者。在全球范围内,大约5%的上部和下部呼吸道感染住院孩子们由hcov - 229 e和HCoV-NL63引起的。后者病毒最近联系在一起儿童疾病的臀部。区分两种病毒相关的流行病学研究。本研究旨在开发一个double-antibody夹心酶联免疫吸附试验(DAS-ELISA)作为一个潜在的工具识别和区分HCoV-NL63和hcov - 229 e。蛋白质的HCoV-NL63和hcov - 229 e在大肠杆菌表达系统和使用为了获得单克隆免疫小鼠为每个病毒抗体(mab)具体。具体马伯HCoV-NL63,马伯特有的hcov - 229 e,和四个马伯承认病毒了。描述,三个马伯被选中为了开发一个微分DAS-ELISA。描述分析可以检测3 ng / ml的N蛋白质和组织培养感染性50 50%病毒剂量/毫升的股票。其他人类冠状病毒或密切相关动物冠状病毒被发现。开发DAS-ELISA种特异性的,因此,它可以被视为一个潜在的检测和分化的工具HCoV-NL63和hcov - 229 e感染。

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