A nanoscale visual exploration of the pathogenic effects of bacterial extracellular vesicles on host cells

J Nanobiotechnology. 2024 Sep 6;22(1):548. doi: 10.1186/s12951-024-02817-6.

Abstract

Background: Bacterial extracellular vesicles (EVs) are pivotal mediators of intercellular communication and influence host cell biology, thereby contributing to the pathogenesis of infections. Despite their significance, the precise effects of bacterial EVs on the host cells remain poorly understood. This study aimed to elucidate ultrastructural changes in host cells upon infection with EVs derived from a pathogenic bacterium, Staphylococcus aureus (S. aureus).

Results: Using super-resolution fluorescence microscopy and high-voltage electron microscopy, we investigated the nanoscale alterations in mitochondria, endoplasmic reticulum (ER), Golgi apparatus, lysosomes, and microtubules of skin cells infected with bacterial EVs. Our results revealed significant mitochondrial fission, loss of cristae, transformation of the ER from tubular to sheet-like structures, and fragmentation of the Golgi apparatus in cells infected with S. aureus EVs, in contrast to the negligible effects observed following S. epidermidis EV infection, probably due to the pathogenic factors in S. aureus EV, including protein A and enterotoxin. These findings indicate that bacterial EVs, particularly those from pathogenic strains, induce profound ultrastructural changes of host cells that can disrupt cellular homeostasis and contribute to infection pathogenesis.

Conclusions: This study advances the understanding of bacterial EV-host cell interactions and contributes to the development of new diagnostic and therapeutic strategies for bacterial infections.

Keywords: Bacterial EV; Cristae loss; Extracellular vesicle; Super-resolution fluorescence microscopy.

MeSH terms

  • Endoplasmic Reticulum / metabolism
  • Extracellular Vesicles* / metabolism
  • Golgi Apparatus / metabolism
  • Host-Pathogen Interactions
  • Humans
  • Lysosomes / metabolism
  • Lysosomes / microbiology
  • Microscopy, Fluorescence
  • Microtubules / metabolism
  • Mitochondria / metabolism
  • Staphylococcal Infections / microbiology
  • Staphylococcus aureus*
  • Staphylococcus epidermidis / physiology