Evaluation of the Latency‐Associated Nuclear Antigen (ORF73) of Kaposi's Sarcoma–Associated Herpesvirus by Peptide Mapping and Bacterially Expressed Recombinant Western Blot Assay
Author(s) -
Sonja J. Olsen,
Ronit Sarid,
Yuan Chang,
Patrick S. Moore
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315689
Subject(s) - epitope , recombinant dna , antigen , microbiology and biotechnology , western blot , virology , immunofluorescence , biology , serology , antibody , open reading frame , immunology , peptide sequence , biochemistry , gene
Kaposi's sarcoma (KS)-associated herpesvirus open-reading frame (ORF) 73 encodes a latency-associated nuclear antigen (LANA) that is the basis for several serologic assays. Immunoreactive epitopes were searched for by peptide mapping, and 171 cleavable, biotinylated 17-mer peptides offset by 5 residues were synthesized and screened with human serum samples by ELISA. The initial screen, which used highly reactive serum diluted 1:500, identified 38 immunoreactive peptides. These were subsequently tested on additional serum samples diluted 1:40. Thirteen peptides were more reactive with serum samples from patients with KS than with control serum samples. No single epitope was recognized by most KS patient serum samples. Combined use of these peptides did not increase test sensitivity to that of current indirect immunofluorescence assays for LANA (80%-90%). For comparison, full-length ORF73 was expressed in bacteria and analyzed by Western blot. The overall sensitivity was 67% (range, 100% among US patients with classic KS to 52% among Italian patients with classic KS). These studies suggest that LANA immunoreactivity may be due to variations in patient response or conformational epitopes.
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