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D. Hvidsten, D.S. Halvorsen, B.P. Berdal, T.J. Gutteberg 

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Presentation on theme: "D. Hvidsten, D.S. Halvorsen, B.P. Berdal, T.J. Gutteberg "— Presentation transcript:

1 Chlamydophila pneumoniae diagnostics: importance of methodology in relation to timing of sampling 
D. Hvidsten, D.S. Halvorsen, B.P. Berdal, T.J. Gutteberg  Clinical Microbiology and Infection  Volume 15, Issue 1, Pages (January 2009) DOI: /j x Copyright © 2009 European Society of Clinical Infectious Diseases Terms and Conditions

2 FIG. 1 The theoretical dynamics of PCR and serology results in acute Chlamydophila pneumoniae infection. The test outcome will depend on the choice of the reference standard. If serum IgM antibody is chosen as the reference standard, a positive PCR result is taken as ‘false-positive’ during the first few weeks following onset of illness before the IgM antibody test turns positive (phase 1). Normally, PCR becomes negative after some days to months, considered as ‘false-negative’ (phase 3). If PCR is applied as the reference standard, the IgM antibody is ‘false-negative’ in phase 1 and appears ‘false-positive’ in phase 3. Only in phase 2 will the results agree. Chlamydia genus-specific IgM antibodies is first and may be present in the acute-phase serum, whereas microimmunofluorescence (specific) IgM antibodies may not appear for 3 weeks; IgG, serum IgG antibodies may not reach diagnostic titre levels for 6–8 weeks [14]. Clinical Microbiology and Infection  , 42-49DOI: ( /j x) Copyright © 2009 European Society of Clinical Infectious Diseases Terms and Conditions

3 FIG. 2 Results of PCR, IgM antibody assays and IgG seroconversion in relation to timing of sampling after onset of acute respiratory Chlamydophila pneumoniae infection. Data from 41 positive cases (date of sampling missing, n = 7). A case was defined as C. pneumoniae-positive if (i) the nasopharyngeal sample was PCR-positive and/or the serum sample was positive (ii) in ≥2 C. pneumoniae IgM antibody assays and/or (iii) with respect to IgG seroconversion. The total number of specimens for each time period is presented above the bars. Clinical Microbiology and Infection  , 42-49DOI: ( /j x) Copyright © 2009 European Society of Clinical Infectious Diseases Terms and Conditions

4 FIG. 3 Cumulative sensitivity of Chlamydophila pneumoniae PCR and IgM antibody assays in relation to timing of sampling after onset of acute respiratory C. pneumoniae infection. Data from 41 positive cases (missing data, n = 7). A case was defined as C. pneumoniae positive if (i) the nasopharyngeal sample was PCR-positive and/or the serum sample was positive (ii) in >2 C. pneumoniae IgM antibody assays and/or (iii) with respect to IgG seroconversion. The lines intersect at 5 weeks. Clinical Microbiology and Infection  , 42-49DOI: ( /j x) Copyright © 2009 European Society of Clinical Infectious Diseases Terms and Conditions


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