Evaluation of antibody responses against SARS coronaviral nucleocapsid or spike proteins by immunoblotting or ELISA
Journal
Journal of Medical Virology
Journal Volume
73
Journal Issue
3
Pages
338-346
Date Issued
2004
Author(s)
Huang L.-R.
Chiu C.-M.
Huang W.-H.
Yang W.-Z.
Yang J.-Y.
Su I.-J.
Abstract
Severe acute respiratory syndrome (SARS)-CoV is a newly emerging virus that causes SARS with high mortality rate in infected people. To study the humoral responses against SARS-CoV, we evaluated nucleocapsid (N) and spike (S) proteins-specific antibodies in patients' sera by Western blotting and enzyme-linked immunosorbent assay (ELISA). Recombinant N and S proteins of SARS-CoV were purified from transformed E. coli. Serum specimens from 40 SARS-CoV-infected patients in the convalescent phase were analyzed by Western blotting using the purified antigens. Serial serum specimens from 12 RT-PCR-confirmed SARS patients were assayed by ELISA using the recombinant N protein as coated antigen. By Western blotting, 97.5% of the SARS patients were positive for N protein-specific antibodies whereas only 47.5% of the samples were positive for S protein-specific antibodies. Using N protein-based ELISA, 10 out of the 12 patients were positive for N protein-specific antibodies and 6 of them showed seroconversion at mean of 16 days after onset of fever. Immunoblotting was useful for detecting the humoral immune response after SARS-CoV infection. Antibodies against SARS-CoV N protein appear at the early stage of infection, therefore, N protein-based ELISA could serve as a simple, sensitive, and specific test for diagnosing SARS-CoV infection. ? 2004 Wiley-Liss, Inc.
SDGs
Other Subjects
nucleocapsid protein; recombinant protein; virus antibody; virus antigen; virus spike protein; antibody detection; antibody response; antibody specificity; article; clinical article; diagnostic test; enzyme linked immunosorbent assay; Escherichia coli; human; humoral immunity; immunoblotting; nonhuman; nucleotide sequence; protein purification; reverse transcription polymerase chain reaction; SARS coronavirus; seroconversion; severe acute respiratory syndrome; Western blotting; SARS CoV
Type
journal article