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定量双 ELISA 试验中使用核蛋白和刺突蛋白片段 2 提高 SARS-CoV-2 的诊断。

Improved diagnosis of SARS-CoV-2 by using nucleoprotein and spike protein fragment 2 in quantitative dual ELISA tests.

机构信息

Molecular Parasitology Lab (MPL), Centre for One Health and Ryan Institute, School of Natural Science, National University of Ireland Galway, Galway, Republic of Ireland.

Department of Biology, National University of Ireland Maynooth, Maynooth, Ireland.

出版信息

Epidemiol Infect. 2021 Jun 8;149:e140. doi: 10.1017/S0950268821001308.

DOI:10.1017/S0950268821001308
PMID:34099081
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8207563/
Abstract

The novel coronavirus, severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), is the causative agent of the 2020 worldwide coronavirus pandemic. Antibody testing is useful for diagnosing historic infections of a disease in a population. These tests are also a helpful epidemiological tool for predicting how the virus spreads in a community, relating antibody levels to immunity and for assessing herd immunity. In the present study, SARS-CoV-2 viral proteins were recombinantly produced and used to analyse serum from individuals previously exposed, or not, to SARS-CoV-2. The nucleocapsid (Npro) and spike subunit 2 (S2Frag) proteins were identified as highly immunogenic, although responses to the former were generally greater. These two proteins were used to develop two quantitative enzyme-linked immunosorbent assays (ELISAs) that when used in combination resulted in a highly reliable diagnostic test. Npro and S2Frag-ELISAs could detect at least 10% more true positive coronavirus disease-2019 (COVID-19) cases than the commercially available ARCHITECT test (Abbott). Moreover, our quantitative ELISAs also show that specific antibodies to SARS-CoV-2 proteins tend to wane rapidly even in patients who had developed severe disease. As antibody tests complement COVID-19 diagnosis and determine population-level surveillance during this pandemic, the alternative diagnostic we present in this study could play a role in controlling the spread of the virus.

摘要

新型冠状病毒(SARS-CoV-2)是导致 2020 年全球冠状病毒大流行的病原体。抗体检测可用于诊断人群中既往疾病的感染情况。这些检测也是一种有用的流行病学工具,可以预测病毒在社区中的传播方式,将抗体水平与免疫相关联,并评估群体免疫。在本研究中,我们重组表达了 SARS-CoV-2 病毒蛋白,并用于分析先前接触或未接触 SARS-CoV-2 的个体的血清。核衣壳(Npro)和刺突亚单位 2(S2Frag)蛋白被鉴定为高度免疫原性,尽管前者的反应通常更大。这两种蛋白被用于开发两种定量酶联免疫吸附测定(ELISA),当它们联合使用时,可得到高度可靠的诊断测试。Npro 和 S2Frag-ELISA 比市售的 Abbott 公司的 ARCHITECT 检测方法(ARCHITECT)能检测出至少 10%更多的真正阳性 COVID-19 病例。此外,我们的定量 ELISA 还表明,即使在患有严重疾病的患者中,针对 SARS-CoV-2 蛋白的特异性抗体也会迅速消失。由于抗体检测补充了 COVID-19 的诊断,并确定了大流行期间的人群监测,因此本研究中提出的替代诊断方法可能在控制病毒传播方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/235b8ecb0ec1/S0950268821001308_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/570ecda43a9d/S0950268821001308_fig1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/a8f3f4320402/S0950268821001308_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/1eb0b26e52f4/S0950268821001308_fig5.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/235b8ecb0ec1/S0950268821001308_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/570ecda43a9d/S0950268821001308_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/5ff23058e863/S0950268821001308_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/7997f8ef536a/S0950268821001308_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/a8f3f4320402/S0950268821001308_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/1eb0b26e52f4/S0950268821001308_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/46b9f64959c0/S0950268821001308_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9835/8207563/235b8ecb0ec1/S0950268821001308_fig7.jpg

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