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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1991-10-8
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pubmed:abstractText |
The antigenic profiles of six strains of Chlamydia pneumoniae were analyzed by the microimmunofluorescence test (MIF) and immunoblotting with human serum and murine monoclonal antibody. MIF-derived antibody titers in serum samples from culture-positive patients were four- to eightfold higher against autologous isolate antigen than they were against the prototype antigen strain TW-183. Sera of patients with respiratory illness that were culture negative and complement fixation positive for Chlamydia spp. produced higher titers by MIF against a strain of C. pneumoniae isolated in the area than they did against TW-183. For two of five cases, the criteria for establishing the diagnosis of acute infection were met only with use of the antigen from the local strain; TW-183 was inadequate for this purpose. Immunoblot profiles revealed antigenic differences between strains that varied with the human serologic response; i.e., unique antigens were recognized by the sera of some individuals and not by the sera of others. Using the reactivity of a genus-specific monoclonal antibody against a major outer membrane protein, we found that strain CWL-011, isolated in Atlanta, Ga., may possess a major outer membrane protein with a molecular mass between those of C. trachomatis L2 and other C. pneumoniae strains. These data provide evidence of several new and unique serotypes of C. pneumoniae and suggest that the serologic diagnosis of C. pneumoniae infection may require the use of antigens from more than one strain of this species.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-2294060,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-2380354,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-2496986,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-2592540,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-3611029,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-4613759,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-6185424,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1885727-7228399
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0095-1137
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1312-6
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:1885727-Antibodies, Bacterial,
pubmed-meshheading:1885727-Antigenic Variation,
pubmed-meshheading:1885727-Antigens, Bacterial,
pubmed-meshheading:1885727-Chlamydia,
pubmed-meshheading:1885727-Chlamydia Infections,
pubmed-meshheading:1885727-Fluorescent Antibody Technique,
pubmed-meshheading:1885727-Humans,
pubmed-meshheading:1885727-Immunoblotting,
pubmed-meshheading:1885727-Pneumonia,
pubmed-meshheading:1885727-Serotyping
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pubmed:year |
1991
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pubmed:articleTitle |
Antigenic variation among strains of Chlamydia pneumoniae.
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pubmed:affiliation |
Center for Infectious Diseases, Centers for Disease Control, Atlanta, Georgia 30333.
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pubmed:publicationType |
Journal Article
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