Evidence map›Paper›PMID 41781865›Full record

ArticleBMC microbiology2026

Environmental cues shape extracellular vesicles biogenesis and function in Streptococcus pneumoniae.

Miriana Battista, Yann Bachelot, Teresa Franke, Christoph Saffer, Lioba Zimmermann, Laura Teuber, Marc Thilo Figge, Cláudia Vilhena

Abstract read
In one paragraph

Article in BMC 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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Miriana BattistaDepartment of Biology, Bacterial Interface Dynamics lab, Chair of Pharmaceutical Biology, Friedrich-Alexander University Erlangen Nürnberg, Staudtstraße 5, Erlangen, 91058, Germany.
Yann BachelotDepartment of Applied Systems Biology, HKI-Center for Systems Biology of Infection, Leibniz-Institute for Natural Product Research and Infection Biology, Jena, Germany.
Teresa FrankeDepartment of Biology, Bacterial Interface Dynamics lab, Chair of Pharmaceutical Biology, Friedrich-Alexander University Erlangen Nürnberg, Staudtstraße 5, Erlangen, 91058, Germany.
Christoph SafferDepartment of Applied Systems Biology, HKI-Center for Systems Biology of Infection, Leibniz-Institute for Natural Product Research and Infection Biology, Jena, Germany.
Lioba ZimmermannDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, Jena, Germany.
Laura TeuberDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, Jena, Germany.
Marc Thilo FiggeDepartment of Applied Systems Biology, HKI-Center for Systems Biology of Infection, Leibniz-Institute for Natural Product Research and Infection Biology, Jena, Germany.ORCID 0000-0002-4044-9166
Cláudia VilhenaDepartment of Biology, Bacterial Interface Dynamics lab, Chair of Pharmaceutical Biology, Friedrich-Alexander University Erlangen Nürnberg, Staudtstraße 5, Erlangen, 91058, Germany. claudia.vilhena@fau.de.ORCID 0000-0003-2884-8970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Gram-positive human pathogen Streptococcus pneumoniae adapts its metabolism to the environment during colonization and host invasion. Extracellular vesicles (EVs) are produced by S. pneumoniae in the process of infection but the exact interplay between metabolic adaptation and vesicle formation remains elusive. This study investigates the role of environmental cues in modulating pneumococcal EVs biogenesis and function.

resultsHere, we demonstrate that exposure to normal human serum induced rearrangement of the pneumococcal cell wall and considerably increased Sp-EVs production. Temperature and pH were critical factors for Sp-EVs formation: 37 °C supported optimal EV production, while bacterial exposure to either basic or acidic environments slowed down pneumococcal EV biogenesis and led to a heterogeneous subpopulation profile. Proteomic analysis revealed that Sp-EVs are enriched in carbon metabolism-related proteins, specifically those associated with glycolysis (e.g. Eno, GapA, GapN, GpmA, PfkA, PykF, and Tpi). Moderate glucose availability enhanced Sp-EVs production and intracellular ATP level, underlying a relation between metabolic status and EV biogenesis. Functionally, Sp-EVs promoted biofilm formation in both S. pneumoniae and Streptococcus pyogenes. Sp-EVs isolated under glucose-rich conditions enhanced S. pneumoniae biofilms, whereas Sp-EVs from glucose-poor conditions strongly stimulated S. pyogenes biofilm formation.

conclusionsThese findings underscore the role of host and environmental cues in shaping pneumococcal EV production, composition, and function, highlighting their potential involvement in metabolic adaptation and interspecies interactions.

Indexed as

Extracellular VesiclesStreptococcus pneumoniaeBacterial ProteinsBiofilmsCell WallGlucoseGlycolysisHumansHydrogen-Ion ConcentrationProteomicsStreptococcus pyogenesTemperatureBacterial ProteinsGlucoseBiofilmBiogenesisCarbon sourceIntercellular communicationMetabolismVesicles

Identifiers

PMID41781865
PMCPMC13064100

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.