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用于在血清型水平高效鉴别抗肠道病毒抗体的合成肽。

Synthetic peptides for efficient discrimination of anti-enterovirus antibodies at the serotype level.

作者信息

Routsias John G, Mavrouli Maria D, Antonaki Georgia, Spanakis Nikolaos, Tsakris Athanassios

机构信息

Department of Microbiology, School of Medicine, University of Athens, 75 Mikras Asias, 11527 Athens, Greece.

Department of Microbiology, School of Medicine, University of Athens, 75 Mikras Asias, 11527 Athens, Greece.

出版信息

Peptides. 2014 Aug;58:52-9. doi: 10.1016/j.peptides.2014.04.017. Epub 2014 Jun 11.

Abstract

Enteroviruses are important human pathogens, causing a broad spectrum of diseases from minor common colds to fatal myocarditis. However, certain disease syndromes are caused by one or few serotypes. Serotype identification is difficult due to the laborious neutralization tests that lack of sensitivity, while in commercial ELISAs homotypic antibodies' activities are largely masked by the recognition of genera-specific epitopes by heterotypic antibodies. In the present study homotypic assays were developed with the ability to discriminate different enterovirus serotypes. Seventy-three children sera, positive for IgM antibodies against enterovirus genus and 49 healthy children were examined for the presence of antibodies against 14 synthetic peptides derived from a non-conserved region of the VP1 protein of coxsackieviruses B2, B3, B4, B5, A9, A16, A24, echoviruses 6, 7, 9, 11, 30, enterovirus 71 and parechovirus 1. 50% of the anti-enterovirus IgM positive sera (>150 BU) reacted with the peptides with the majority of them to preferentially recognize one of them, supporting the homotypic nature of our assay. Inhibition studies yielded homologous inhibition rates 67-95% suggesting that specific peptide recognition actually occurred. The diagnostic value of our assay was tested in blood samples drawn over a 1.5-year period from a 5-year old patient. The anti-enterovirus reactivity was clearly attributed to echovirus serotype 11. The IgM/IgG antibody ratio was reversed 4 months later and subsequently IgM antibodies dropped below the cutoff point. In this paper we demonstrate that our assay can be used to discriminate between antibodies targeting different enterovirus serotypes.

摘要

肠道病毒是重要的人类病原体,可引发从轻微普通感冒到致命心肌炎等广泛的疾病。然而,某些疾病综合征是由一种或几种血清型引起的。由于缺乏敏感性的繁琐中和试验,血清型鉴定很困难,而在商业酶联免疫吸附测定(ELISA)中,同型抗体的活性在很大程度上被异型抗体对属特异性表位的识别所掩盖。在本研究中,开发了具有区分不同肠道病毒血清型能力的同型检测方法。对73份抗肠道病毒属IgM抗体呈阳性的儿童血清和49名健康儿童进行检测,以检测针对从柯萨奇病毒B2、B3、B4、B5、A9、A16、A24、埃可病毒6、7、9、11、30、肠道病毒71和副肠道病毒1的VP1蛋白非保守区域衍生的14种合成肽的抗体。50%的抗肠道病毒IgM阳性血清(>150 BU)与这些肽发生反应,其中大多数优先识别其中一种,支持了我们检测方法的同型性质。抑制研究产生了67-95%的同源抑制率,表明确实发生了特异性肽识别。我们的检测方法的诊断价值在一名5岁患者1.5年期间采集的血样中进行了测试。抗肠道病毒反应性明确归因于埃可病毒11型。4个月后IgM/IgG抗体比值发生逆转,随后IgM抗体降至临界值以下。在本文中,我们证明了我们的检测方法可用于区分针对不同肠道病毒血清型的抗体。

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