Affiliation:
1. Department of Pathobiology, University of Washington, Seattle, Washington 98195,1 and
2. Focus Technologies, Inc., Cypress, California 906302
Abstract
ABSTRACT
Chlamydia pneumoniae
is a common cause of respiratory infection. It has also been shown to be associated with coronary heart disease. Two proteins that have been reported to be recognized frequently during human infection are proteins having molecular masses of 43 and 53 kDa. In order to develop a useful alternative serological test to the microimmunofluorescence (micro-IF) assay, recombinant 43-kDa and 53-kDa chlamydia-specific proteins were evaluated in dot blot and/or for comparison to the standard micro-IF test. Primers for amplification were derived from genome sequence information for two
C. pneumoniae
genes (CPn0809 and CPn0980) encoding 53-kDa proteins and four
C. pneumoniae
genes (CPn0562, CPn0927, CPn0928, and Cpn0929) encoding 43-kDa proteins of unknown function, which were
Chlamydia
specific and not found in
Chlamydia trachomatis
. The 53-kDa protein product of CPn0809 or the N-terminal 18-kDa portion had better specificity than any of the 43-kDa recombinants but was much less sensitive than micro-IF. In contrast, the 53-kDa protein encoded by CPn0980 was recognized by 11 of 12 (92%) acute-phase sera, 35 of 46 (76%) chronic sera, 0 of 12 micro-IF-negative sera (
C. pneumoniae
and
C. trachomatis
negative), and 1 of 12 (8%)
C. pneumoniae
negative,
C. trachomatis
positive sera. Thus, it appears that the 53-kDa protein encoded by CPn0980 has potential use for serodiagnosis of
C. pneumoniae
infection.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Cited by
7 articles.
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