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Published on: April 4, 2019
RSV shapes serotype-specific invasive pneumococcal disease dynamics in children: an observational study
Inès Fafi1,2,3, Corinne Levy4,5,6, Emmanuelle Varon4,7
1Université Paris Cité and Université Sorbonne Paris Nord, Inserm, IAME UMR 1137, EPIC team, F-75018 Paris, France.
Insights
Respiratory syncytial virus (RSV) season significantly influences invasive pneumococcal disease (IPD) serotype distribution. RSV circulation amplifies IPD involvement of pneumococcal serotypes with lower disease potential.
Area of Science:
- Epidemiology
- Infectious Diseases
- Public Health
Background:
- Pneumococcal nasopharyngeal colonization precedes invasive pneumococcal disease (IPD).
- Respiratory syncytial virus (RSV) may increase IPD risk, especially for less virulent serotypes.
- Understanding serotype-specific IPD dynamics during RSV seasons is crucial.
Purpose of the Study:
- To analyze the distribution of pneumococcal serotypes in pediatric IPD cases in relation to RSV circulation levels.
- To investigate how RSV seasonality affects the involvement of different pneumococcal serotypes in IPD.
Main Methods:
- Utilized French surveillance data for IPD, pneumococcal carriage, and RSV infections (2008-2023).
- Assessed pneumococcal serotype proportions in IPD during RSV and non-RSV seasons.
- Correlated serotype-specific IPD likelihood with estimated disease potential during different seasons.
Main Results:
- Significant variation in pneumococcal serotype distribution was observed between RSV and non-RSV seasons among 4,574 IPD cases.
- RSV circulation was found to enhance the involvement of lower-disease-potential serotypes in IPD (Rho=0.60, p=0.0012).
Conclusions:
- The influence of RSV on triggering IPD varies considerably among pneumococcal serotypes.
- Future RSV-targeted interventions should consider these serotype-specific impacts on IPD.
Background:
Pneumococcal nasopharyngeal colonization is the first step toward invasive pneumococcal disease (IPD). Respiratory syncytial virus (RSV) may trigger IPD, particularly for serotypes with low disease potential.We aimed to analyse the distribution of pneumococcal serotypes among paediatric IPD according to RSV circulation level.
Methods:
We used data from three continuous French surveillance systems on IPD, pneumococcal carriage and RSV infections from 2008 to 2023. Based on the RSV epidemics threshold, we assessed the proportion of each serotype among IPD, depending on "RSV season" and "non-RSV season". We assessed the correlation between the likelihood of serotype-specific involvement in IPD according to non-RSV season vs RSV season and the estimated disease potential of each serotype.
Results:
Among 4,574 IPD cases, the serotype distribution strongly varied during non-RSV season vs RSV season. The lower the disease potential of serotypes, the more RSV circulation enhanced their involvement in IPD (Rho=0.60, CI95% 0.28 to 0.80, p-value = 0.0012).
Conclusions:
The role of RSV in triggering IPD strongly varies across pneumococcal serotypes. The impact of RSV-targeted interventions should be evaluated in light of these data.
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