Streptococcus pyogenes EVs induce the alternative inflammasome via caspase-4/-5 in human monocytes

The sensing of Gram-negative Extracellular Vesicles (EVs) by the innate immune system has been extensively studied in the past decade. In contrast, recognition of Gram-positive EVs by innate immune cells remains poorly understood. Comparative genome-wide transcriptional analysis in human monocytes uncovered that S. pyogenes EVs induce proinflammatory signatures that are markedly distinct from those of their parental cells. Among the 209 genes exclusively upregulated by EVs, caspase-5 prompted us to study inflammasome signaling pathways in depth. We show that lipoteichoic acid (LTA), a structural component of Gram-positive bacterial membranes present on EVs from S. pyogenes and other Gram-positive species, is sensed by TLR2 which triggers the alternative inflammasome composed of NLRP3 and the inflammatory caspases-4/-5 to mount an IL-1β response without inducing cell death. For S. pyogenes, we identify TLR8 as a sensor to mediate caspase-4/-5-dependent IL-1β secretion. Notably, inflammasome activation by intact bacteria is independent of the global virulence regulator CovS in monocytes. Overall, our study highlights a new role for TLR2 and caspase-4/-5 in the recognition of Gram-positive EVs in human monocytes.

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Publication Details

Journal
EMBO Reports
Published
2025-09-08
DOI
https://doi.org/10.1038/s44319-025-00558-7
Citations
3
Primary Topic
Streptococcal Infections and Treatments
Type
article
Field-Weighted Citation Impact
5.64

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article

Streptococcus pyogenes EVs induce the alternative inflammasome via caspase-4/-5 in human monocytes

Holger Heine, Leif Erik Sander, Christian Goosmann, Kathrin Krause et al.
3 citations
EMBO Reports
Streptococcal Infections and Treatments
5.64
article

Streptococcus pyogenes EVs induce the alternative inflammasome via caspase-4/-5 in human monocytes

Holger Heine, Leif Erik Sander, Christian Goosmann, Kathrin Krause, Tonya Kueck, Kathirvel Alagesan, Ulrike Resch, Timothy J. Sullivan, Emmanuelle Charpentier, Volker Brinkmann, Matteo Ugolini, Eric J. C. Gálvez, Matthias Muenzner, Tim Vierbuchen, S. Arroyo, Christian K. Frese
article en
3 citations

Abstract

The sensing of Gram-negative Extracellular Vesicles (EVs) by the innate immune system has been extensively studied in the past decade. In contrast, recognition of Gram-positive EVs by innate immune cells remains poorly understood. Comparative genome-wide transcriptional analysis in human monocytes uncovered that S. pyogenes EVs induce proinflammatory signatures that are markedly distinct from those of their parental cells. Among the 209 genes exclusively upregulated by EVs, caspase-5 prompted us to study inflammasome signaling pathways in depth. We show that lipoteichoic acid (LTA), a structural component of Gram-positive bacterial membranes present on EVs from S. pyogenes and other Gram-positive species, is sensed by TLR2 which triggers the alternative inflammasome composed of NLRP3 and the inflammatory caspases-4/-5 to mount an IL-1β response without inducing cell death. For S. pyogenes, we identify TLR8 as a sensor to mediate caspase-4/-5-dependent IL-1β secretion. Notably, inflammasome activation by intact bacteria is independent of the global virulence regulator CovS in monocytes. Overall, our study highlights a new role for TLR2 and caspase-4/-5 in the recognition of Gram-positive EVs in human monocytes.

EMBO ReportsVol. 26(19)
Roche (Switzerland) (CH), University of Massachusetts Chan Medical School (US), Cal Poly Humboldt (US), Humboldt-Universität zu Berlin (DE), Max Planck Institute for Infection Biology (DE), Research Center Borstel - Leibniz Lung Center (DE), German Center for Lung Research (DE), Max Planck Institute for the History of Science (DE), Medical University of Vienna (AT), Charité - Universitätsmedizin Berlin (DE)
Deutsche Forschungsgemeinschaft, Louis-Jeantet Foundation, Max-Planck-Gesellschaft, Leibniz-Gemeinschaft
Openalex Percentile: Top 4%
Streptococcal Infections and Treatments
5.64
DOIOpen Access PDFOpenAlex
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