ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026
Diagnosis of pneumococcal pneumonia using quantitative PCR targeting lytA and piaB in adult patients with community-acquired pneumonia.
Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
purposeAccurate diagnosis of pneumococcal pneumonia remains challenging due to suboptimal sensitivity of conventional microbiological methods. Molecular techniques may improve Streptococcus pneumoniae detection, but their clinical utility remains uncertain.
methodsIn this prospective observational study, we compared conventional diagnostics with qPCR-based detection of lytA and piaB genes in nasopharyngeal, oropharyngeal, saliva, and sputum samples collected from adults with community-acquired pneumonia (CAP) and three control groups without acute respiratory symptoms. Stringent sample-specific cut-offs (
resultsS. pneumoniae was detected by conventional methods in 53 (21.1%) of 251 CAP patients. Overall pneumococcal detection by qPCR was higher in CAP patients than in 564 individuals without CAP (35.9% vs. 10.3%, p < 0.001), but pneumococcal density showed substantial overlap between CAP patients and controls and across aetiological groups within the CAP cohort. Using the
conclusionsqPCR targeting lytA and piaB increased pneumococcal detection in CAP patients, but substantial overlap in pneumococcal density limited its added diagnostic value for PCAP. Using stringent lowCq criteria, qPCR identified only a small number of additional PCAP cases beyond conventional diagnostics. Our findings do not support routine use of qPCR as a stand-alone diagnostic test for PCAP. Nevertheless, sputum-based molecular detection may contribute to future surveillance studies when combined with serotype-specific analyses.
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