Chlamydia pneumoniae is a fastidious microorganism with a characterist
ic biphasic lifecycle causing a variety of human respiratory tract inf
ections. There is limited knowledge about the molecular biology of C.
pneumoniae, and only a few genes have been sequenced. The structure of
the chlamydial surface differs from that of Chlamydia trachomatis. In
order to study the surface of C. pneumoniae we generated monoclonal a
ntibodies (MAbs) against C. pneumoniae strain VR-1310 and selected 14
MAbs that reacted with the surface of C. pneumoniae. All MAbs reacted
in immunoelectron microscopy with the surface of both whole C. pneumon
iae VR-1310 elementary bodies and with purified sarcosyl extracted out
er membrane complexes. However, only 2 of the MAbs reacted in immunobl
otting with C. pneumoniae proteins and only with antigen that had not
been heat treated in SDS-sample buffer. This indicates the dominance o
f conformational epitopes at the C. pneumoniae surface.