Affiliation:
1. Institute for Medical Microbiology, Immunology, and Hygiene, University of Cologne, 50935 Cologne, Germany
Abstract
ABSTRACT
Although
Chlamydia pneumoniae
is an important human pathogen, the antigens eliciting a specific humoral immune response remain elusive. We scrutinized several recombinant chlamydial surface proteins for species-specific recognition by a panel of human sera previously tested for the presence of anti-
C. pneumoniae
and anti-
C. trachomatis
antibodies by microimmunofluorescence and enzyme-linked immunosorbent assay. The 15-kDa cysteine-rich protein (CrpA), porin-b (PorB), 9-kDa outer membrane protein (OMP3), 60-kDa outer membrane protein (OMP2), and four fragments of the major outer membrane protein (MOMP) representing each variable domain (VD) were overexpressed in
Escherichia coli
, affinity purified, and employed for Western blot analysis. None of the sera tested contained antibodies recognizing PorB and OMP3 of
C. pneumoniae
. Sera from
C. pneumoniae
-immune patients cross-reacted with OMP2 of
C. trachomatis
, and sera from
C. trachomatis
-immune patients cross-reacted with CrpA of
C. pneumoniae
, indicating that some of chlamydial surface molecules share antigenic epitopes. In contrast, the VD2, as well as the VD3, regions of the MOMP of
C. pneumoniae
were only recognized by
C. pneumoniae
-positive sera, suggesting the existence of species-specific epitopes. The identification of such epitopes of cell surface molecules provides new insights into
C. pneumoniae
-specific immune responses and may be of value for the improvement of
C. pneumoniae
-specific diagnostic assay systems based on defined recombinant antigens.
Publisher
American Society for Microbiology
Cited by
18 articles.
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