Bieke Tack, Caspar Geenen, Tessa Nieuwenhuijsen, Lize Cuypers, Kurt Beuselinck, Krzysztof Trzciński, Emmanuel André, Stefanie Desmet
Indoor air sampling captured signals of community pneumococcal circulation and serotype dynamics. With further validation, it could provide a scalable, affordable surveillance tool to support vaccine policy, monitor vaccine impact, and strengthen respiratory pathogen surveillance, particularly in LMICs.
BACKGROUND: Pneumococcal surveillance remains challenging due to limited invasive disease surveillance and logistically demanding nasopharyngeal carriage studies, particularly in low- and middle-income countries (LMICs). We evaluated indoor air sampling as a non-invasive approach for monitoring pneumococcal circulation and serotype distribution.
METHODS: Monthly indoor air samples were collected over 20 months (January 2022-September 2023) in a Belgian childcare center. Samples were analyzed by qPCR for pneumococcal detection and serotype identification.
RESULTS: Pneumococci were detected in all samples. After excluding serotypes with known specificity issues, 15 serotypes/serogroups were identified, with a mean of seven per sample. Commonly detected serotypes largely matched those reported in Belgian carriage studies and invasive disease surveillance.
CONCLUSIONS: Indoor air sampling captured signals of community pneumococcal circulation and serotype dynamics. With further validation, it could provide a scalable, affordable surveillance tool to support vaccine policy, monitor vaccine impact, and strengthen respiratory pathogen surveillance, particularly in LMICs.