# SARS-CoV-2 and Streptococcus pneumoniae colonization and disease: an observational study in adults

**Authors:** Sara Calvo-Silveria, Lucía Fernández-Delgado, Aida González-Díaz, Rocío España-Bonilla, Laura Calatayud, Jordi Niubó, Sara Martí, Ma Ángeles Domínguez, Jordi Càmara, Carmen Ardanuy

PMC · DOI: 10.3389/fcimb.2025.1624521 · Frontiers in Cellular and Infection Microbiology · 2025-07-18

## TL;DR

This study examines how SARS-CoV-2 and Streptococcus pneumoniae interact, showing that co-infections are rare but more severe, and that non-pharmaceutical measures impact pneumococcal dynamics.

## Contribution

The study provides new insights into the co-occurrence and clinical impact of SARS-CoV-2 and Streptococcus pneumoniae, emphasizing the role of public health measures and vaccination.

## Key findings

- IPD incidence dropped by 70% during the pandemic, rebounding after non-pharmaceutical measures were relaxed.
- Pneumococcal colonization in SARS-CoV-2 patients was low (2.8%), with slightly higher rates in severe cases and younger adults.
- Co-infected patients had more comorbidities, severe symptoms, and lower vaccination rates compared to colonized patients.

## Abstract

The COVID-19 pandemic has impacted global health and altered respiratory pathogens. While SARS-CoV-2 vaccines have mitigated COVID-19 severity, emerging variants remain challenging. Co-infection of Streptococcus pneumoniae with respiratory viruses is associated with increased disease severity, but its relationship with SARS-CoV-2 remains unclear. This study aims to analyze their co-occurrence, focusing on disease progression, colonization rates and clinical outcomes.

To this end, three approaches were used. First, a laboratory-based analysis of invasive pneumococcal disease (IPD) in adults (2019-2023). Second, a retrospective analysis of COVID-19 clinical cases with pneumococcal isolates (March,2020–December,2023), including clinical and microbiological data such as patients’ comorbidities, episode severity, serotypes and resistance genes. Third, a retrospective analysis to assess pneumococcal colonization in SARS-CoV-2 positive nasopharyngeal samples (May-October 2023; dual-target RT-PCR). WGS and bioinformatics were performed on both bacterial (serotyping and resistance analysis) and viral genomes (lineage determination). Statistical comparisons (Chi-square, Fisher’s test), with significance set at p<0.05.

First, IPD incidence declined during the COVID-19 pandemic, with cases dropping by 70% in both age groups (18–64 and >64) from 2019 to 2021 and rebounding after 2021, concomitant with the relaxation of non-pharmaceutical measures, especially among older adults. Pneumococcal serotype distribution remained stable with dominance of serotypes 3 and 8. Serotype 12F disappeared during the lockdown and re-emerged in 2023 as a multidrug-resistant sub-lineage through multi-fragment recombination, derived from the former GPSC26. Second, SARS-CoV-2 and pneumococcal co-infection occurred in 66 hospitalized patients, mainly by serotype 3 (15%), with resistance to macrolides (26.3%) and tetracycline (22.8%). Third, pneumococcal colonization in SARS-CoV-2-infected patients was low (2.8%), especially in older adults (>64 years; 1.5%), with slightly higher rates in severe cases (4.7% vs 2.5%; p=0.404; IC95% 0.13-3.05) and young adults (4.8% vs 1.5%; p=0.04; IC95% 0.92-15.21). Compared to colonized patients, those with co-infection had more comorbidities, more severe clinical presentations, higher hospitalization rates and lower vaccination rates.

This study highlights how non-pharmaceutical measures disrupt S. pneumoniae dynamics. Although pneumococcal colonization in SARS-CoV-2 patients appears to be infrequent, our data suggest an increase in disease severity. Then, vaccination programs and their monitoring remain critical in the prevention of respiratory infections.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)
- **Species:** Streptococcus pneumoniae (taxon 1313)

## Full-text entities

- **Diseases:** pneumococcal colonization (MESH:D003108), COVID-19 (MESH:D000086382), respiratory infections (MESH:D012141), Co-infection (MESH:D060085), IPD (MESH:D011008)
- **Chemicals:** tetracycline (MESH:D013752), macrolides (MESH:D018942)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Streptococcus pneumoniae (species) [taxon 1313], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12313665/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12313665/full.md

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Source: https://tomesphere.com/paper/PMC12313665