Structure of a Rhs effector clade domain provides mechanistic insights into type VI secretion system toxin delivery

Nat Commun. 2024 Oct 8;15(1):8709. doi: 10.1038/s41467-024-52950-x.

Abstract

The type VI secretion system (T6SS) is a molecular machine utilised by many Gram-negative bacteria to deliver antibacterial toxins into adjacent cells. Here we present the structure of Tse15, a T6SS Rhs effector from the nosocomial pathogen Acinetobacter baumannii. Tse15 forms a triple layered β-cocoon Rhs domain with an N-terminal α-helical clade domain and an unfolded C-terminal toxin domain inside the Rhs cage. Tse15 is cleaved into three domains, through independent auto-cleavage events involving aspartyl protease activity for toxin self-cleavage and a nucleophilic glutamic acid for N-terminal clade cleavage. Proteomic analyses identified that significantly more peptides from the N-terminal clade and toxin domains were secreted than from the Rhs cage, suggesting toxin delivery often occurs without the cage. We propose the clade domain acts as an internal chaperone to mediate toxin tethering to the T6SS machinery. Conservation of the clade domain in other Gram-negative bacteria suggests this may be a common mechanism for delivery.

MeSH terms

  • Acinetobacter baumannii* / genetics
  • Acinetobacter baumannii* / metabolism
  • Amino Acid Sequence
  • Bacterial Proteins* / chemistry
  • Bacterial Proteins* / genetics
  • Bacterial Proteins* / metabolism
  • Bacterial Toxins* / chemistry
  • Bacterial Toxins* / genetics
  • Bacterial Toxins* / metabolism
  • Crystallography, X-Ray
  • Models, Molecular
  • Protein Domains*
  • Proteomics / methods
  • Type VI Secretion Systems* / genetics
  • Type VI Secretion Systems* / metabolism

Substances

  • Type VI Secretion Systems
  • Bacterial Toxins
  • Bacterial Proteins