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Updated: Jul 14, 2025

Interactions with and Membrane Permeabilization of Brain Mitochondria by Amyloid Fibrils
Published on: September 28, 2019
Staphylococcus aureus delta toxin modulates both extracellular membrane vesicle biogenesis and amyloid formation
Xiaogang Wang1, Divakara Ssm Uppu1, Seth W Dickey2,3
1Division of Infectious Diseases, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School , Boston, Massachusetts, USA.
Importance:
Extracellular membrane vesicles (MVs) produced by Staphylococcus aureus in planktonic cultures encapsulate a diverse cargo of bacterial proteins, nucleic acids, and glycopolymers that are protected from destruction by external factors. δ-toxin, a member of the phenol soluble modulin family, was shown to be critical for MV biogenesis. Amyloid fibrils co-purified with MVs generated by virulent, community-acquired S. aureus strains, and fibril formation was dependent on expression of the S. aureus δ-toxin gene (hld). Mass spectrometry data confirmed that the amyloid fibrils were comprised of δ-toxin. Although S. aureus MVs were produced in vivo in a localized murine infection model, amyloid fibrils were not observed in the in vivo setting. Our findings provide critical insights into staphylococcal factors involved in MV biogenesis and amyloid formation.
Insights
Staphylococcus aureus produces membrane vesicles (MVs) critical for biogenesis. The δ-toxin protein forms amyloid fibrils within these MVs during planktonic growth, but not in vivo.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Protein Biochemistry
Background:
- Extracellular membrane vesicles (MVs) from Staphylococcus aureus contain diverse biomolecules, protected from external degradation.
- The phenol soluble modulin family member, δ-toxin, plays a crucial role in MV biogenesis.
- Amyloid fibrils are found associated with MVs from virulent S. aureus strains.
Purpose of the Study:
- To investigate the role of δ-toxin in Staphylococcus aureus MV biogenesis and amyloid formation.
- To determine if amyloid fibrils are present in vivo during S. aureus infection.
Main Methods:
- Culturing Staphylococcus aureus in planktonic conditions.
- Co-purification of MVs and associated amyloid fibrils.
- Mass spectrometry analysis to identify fibril components.
- In vivo studies using a murine infection model.
Main Results:
- δ-toxin is essential for MV biogenesis in S. aureus.
- Amyloid fibrils composed of δ-toxin were identified in MVs from planktonic cultures.
- Amyloid fibrils were not detected in MVs produced during in vivo murine infection.
Conclusions:
- δ-toxin is a key factor in Staphylococcus aureus MV biogenesis and amyloid fibril formation.
- Amyloid fibril formation by S. aureus appears to be a condition-specific phenomenon, occurring in vitro but not in vivo.
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