Amino terminus of the SARS coronavirus protein 3a elicits strong, potentially protective humoral responses in infected patients
Author(s) -
Xiaofen Zhong,
Zufeng Guo,
Huanghao Yang,
Lisheng Peng,
Yong Xie,
Tin-Yau Wong,
Sik-To Lai,
Zhihong Guo
Publication year - 2006
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/vir.0.81078-0
Subject(s) - ectodomain , biology , immunogen , antibody , virology , coronavirus , immune system , humoral immunity , severe acute respiratory syndrome coronavirus , immunology , extracellular , receptor , covid-19 , microbiology and biotechnology , medicine , infectious disease (medical specialty) , biochemistry , monoclonal antibody , disease , pathology
The 3a protein of severe acute respiratory syndrome (SARS)-associated coronavirus is expressed and transported to the plasma membrane in tissue cells of infected patients. Its short N-terminal ectodomain was found to elicit strong humoral responses in half of the patients who had recovered from SARS. The ectodomain-specific antibodies from the convalescent-phase plasma readily recognized and induced destruction of 3a-expressing cells in the presence of the human complement system, demonstrating their potential ability to provide immune protection by recognizing and eliminating SARS coronavirus-infected cells that express the target protein. In addition, when coupled to a carrier protein, the ectodomain peptide elicited 3a-specific antibodies in mice and rabbit at high titres. These results showed that the N terminus of the 3a protein is highly immunogenic and elicits potentially protective humoral responses in infected patients. Therefore, the short extracellular domain may be a valuable immunogen in the development of a vaccine for infectious SARS.
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