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Published on: February 15, 2013
Pneumolysin PCR-based diagnosis of invasive pneumococcal infection in children
P Toikka1, S Nikkari, O Ruuskanen
1Department of Pediatrics, Turku University Hospital, Turku, Finland. pia@toikka@utu.fi
Insights
Diagnosing pneumococcal infection in children requires multiple tests. Pneumolysin PCR is sensitive but needs multiple blood samples for optimal Streptococcus pneumoniae detection.
Area of Science:
- Microbiology
- Infectious Diseases
- Molecular Diagnostics
Background:
- Streptococcus pneumoniae causes significant childhood infections.
- Accurate and rapid diagnosis of pneumococcal infections is crucial for effective treatment.
- Current diagnostic methods have limitations in sensitivity and specificity.
Purpose of the Study:
- To evaluate the diagnostic performance of blood-based pneumolysin PCR.
- To compare pneumolysin PCR with other diagnostic assays for pneumococcal infection.
- To assess the utility of multiple blood fractions in PCR-based diagnosis.
Main Methods:
- Compared pneumolysin PCR in plasma, serum, and leukocytes against blood culture and immune complex detection.
- Analyzed antibody responses to pneumolysin and C polysaccharide.
- Included 75 febrile children with suspected invasive pneumococcal infection and 15 healthy controls.
Main Results:
- Pneumolysin PCR was the most sensitive assay (44% positive in diagnosed cases).
- Antibody increases and immune complexes were detected in 30-39% and 16-30% of patients, respectively.
- Blood culture yielded positive results in 20% of patients; PCR was specific in healthy controls.
Conclusions:
- Diagnosing Streptococcus pneumoniae infection necessitates a combination of diagnostic assays.
- Pneumolysin PCR shows promise as a sensitive diagnostic tool but requires analysis of multiple blood fractions.
- Further optimization is needed to enhance the clinical utility of pneumolysin PCR for pneumococcal infections.
Abstract:
Blood-based pneumolysin PCR was compared to blood culture and detection of pneumolysin immune complexes, as well as to detection of antibodies to pneumolysin and to C polysaccharide, in the diagnosis of pneumococcal infection in 75 febrile children. Invasive pneumococcal infection was suspected on clinical grounds in 67 of the febrile children, and viral infection was suspected on clinical grounds in 8 of the febrile children. In addition, 15 healthy persons were examined to test the specificity of the PCR assay. Plasma, serum, and leukocyte fractions were analyzed by PCR. The combination of all test results led to the diagnosis of pneumococcal infection in 25 patients. Pneumolysin PCR was positive in 44% of these children, an increase occurred in the pneumolysin antibodies in 39% and in the C polysaccharide antibodies in 30% of the patients; pneumolysin immune complexes were found in convalescent serum in 30%, pneumolysin immune complexes occurred in acute-phase serum samples in 16%, and a positive blood culture was found in 20% of the patients. None of the healthy controls had positive results by PCR. The results suggest that the diagnosis of Streptococcus pneumoniae infection from blood samples necessitates the use of several different assays. Pneumolysin PCR was the most sensitive assay, but its clinical value is reduced by the fact that three blood fractions are needed.
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