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Journal of Clinical Microbiology, November 1998, p. 3155-3159, Vol. 36, No. 11
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Diagnosis of Mycoplasma pneumoniae Pneumonia in Children

Matti E. Waris,1,* Pia Toikka,2 Taina Saarinen,2 Simo Nikkari,3 Olli Meurman,4 Raija Vainionpää,1 Jussi Mertsola,2 and Olli Ruuskanen2

Department of Virology,1 Department of Pediatrics,2 and Department of Microbiology,3 University of Turku, and Turku University Hospital Central Laboratory,4 Turku, Finland

Received 5 December 1997/Returned for modification 27 April 1998/Accepted 3 August 1998

We evaluated a commercial immunoglobulin M (IgM)-capture immunoassay for the detection of Mycoplasma pneumoniae infections in 278 pediatric patients with community-acquired, radiographically defined pneumonia. Acute- and convalescent-phase serum samples were collected from all patients and were tested for M. pneumoniae-specific IgM and IgG antibodies by Platelia enzyme immunoassays (Sanofi Diagnostica Pasteur, Marnes la Coquette, France). Nasopharyngeal aspirates (NPAs) were collected at the time of admission to the hospital. A total of 227 NPAs were subjected to the detection of M. pneumoniae DNA by PCR, and 191 NPAs were cultured by using the Pneumofast kit (International Mycoplasma, Signeswere, France). Southern hybridization of PCR products and the IgM test with solid-phase antigen (Serion Immunodiagnostica, Würzburg, Germany) were used for additional confirmation of a positive result, which required agreement of at least two different methods. A total of 24 (9%) confirmed diagnoses of mycoplasma infection were made, 5 (21%) of which were in children <5 years of age. Of the positive children, 24 of 24 (sensitivity, 100%) were positive by the IgM-capture test with convalescent-phase serum, 19 of 24 (79%) were positive by the IgM-capture test with acute-phase serum, 19 of 24 (79%) were positive by IgG serology, 10 of 20 (50%) were positive by PCR, and 8 of 17 (47%) were positive by culture. An additional 5 (of 254) children were positive by the Platelia IgM test alone (specificity, 98%). When the PCR with Southern hybridization result was combined with the IgM-capture test result with the acute-phase sera, the sensitivity of rapid laboratory diagnosis increased to 95%. In conclusion, the IgM serology test was the single most valuable tool for the diagnosis of M. pneumoniae pneumonia in children of any age.


* Corresponding author. Mailing address: Department of Medical Physics and Chemistry, University of Turku, Tykistönkatu 6, FIN-20520 Turku, Finland. Phone: 358 2 333 7059. Fax: 358 2 333 7060. E-mail: matti.waris{at}utu.fi.


Journal of Clinical Microbiology, November 1998, p. 3155-3159, Vol. 36, No. 11
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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