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Clinical Chemistry 51: 1382-1396, 2005. First published June 23, 2005; 10.1373/clinchem.2005.051045
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(Clinical Chemistry. 2005;51:1382-1396.)
© 2005 American Association for Clinical Chemistry, Inc.


Molecular Diagnostics and Genetics

Comprehensive Antibody Epitope Mapping of the Nucleocapsid Protein of Severe Acute Respiratory Syndrome (SARS) Coronavirus: Insight into the Humoral Immunity of SARS

Yunfei Liang1, Ying Wan1, Li-wen Qiu2, Jingran Zhou1, Bing Ni1, Bo Guo1, Qiang Zou1, Liyun Zou1, Wei Zhou1, Zhengcai Jia1, Xiao-yan Che2,a and Yuzhang Wu1,a

1 The Institute of Immunology, PLA, The Third Military Medical University, Shapingba District, Chongqing, China.
2 Central Laboratory, Zhujiang Hospital, The Southern Medical University, Guangzhou, China.

aAddress correspondence to Yuzhang Wu at: The Institute of Immunology, PLA, The Third Military Medical University, Shapingba District, Chongqing 400038, People’s Republic of China; fax 086-023-68752789; e-mail wuyuzhang{at}gmail.com; or Xiao-yan Che at: Central Laboratory, Zhujiang Hospital, The Southern Medical University, Guangzhou 510282, People’s Republic of China; fax 086-020-61643592; e-mail linche{at}pub.guangzhou.gd.cn.

Background: The epidemic outbreak of severe acute respiratory syndrome (SARS) posed a worldwide threat to public health and economic stability. Although the pandemic has been contained, concerns over its recurrence remain. It is essential to identify specific diagnostic agents and antiviral vaccine candidates to fight this highly contagious disease.

Methods: We generated 14 monoclonal antibodies (mAbs) specific to the SARS coronavirus (SARS-CoV) nucleocapsid (N) protein and used these to thoroughly map the N protein antigenic determinants. We identified the immunodominant antigenic sites responsible for the antibodies in sera from SARS patients and antisera from small animals and differentiated the linear from the conformational antibody-combining sites comprising the natural epitopes by use of yeast surface display.

Results: We identified 5 conformational and 3 linear epitopes within the entire N protein; 3 conformational and 3 linear epitopes were immunodominant. The antibody responses to the N protein fragments in mammalian sera revealed that 3 regions of the N protein are strong antigenic domains. We expanded the specificity of the N protein epitope and identified 4 novel conformational epitopes (amino acids 1–69, 68–213, 212–341, and 337–422).

Conclusion: The antigenic structures identified for the SARS-CoV N protein, the epitope-specific mAbs, and the serum antibody profile in SARS patients have potential use in the clinical diagnosis and understanding of the protective immunity to SARS-CoV.




The following articles in journals at HighWire Press have cited this article:


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J. Clin. Microbiol.Home page
K. Fujimoto, K.-H. Chan, K. Takeda, K.-F. Lo, R. H. K. Leung, and T. Okamoto
Sensitive and Specific Enzyme-Linked Immunosorbent Assay Using Chemiluminescence for Detection of Severe Acute Respiratory Syndrome Viral Infection
J. Clin. Microbiol., January 1, 2008; 46(1): 302 - 310.
[Abstract] [Full Text] [PDF]




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