Retargeting from the CR3 to the LFA-1 receptor uncovers the adenylyl cyclase enzyme-translocating segment of Bordetella adenylate cyclase toxin

J Biol Chem. 2020 Jul 10;295(28):9349-9365. doi: 10.1074/jbc.RA120.013630. Epub 2020 May 11.

Abstract

The Bordetella adenylate cyclase toxin-hemolysin (CyaA) and the α-hemolysin (HlyA) of Escherichia coli belong to the family of cytolytic pore-forming Repeats in ToXin (RTX) cytotoxins. HlyA preferentially binds the αLβ2 integrin LFA-1 (CD11a/CD18) of leukocytes and can promiscuously bind and also permeabilize many other cells. CyaA bears an N-terminal adenylyl cyclase (AC) domain linked to a pore-forming RTX cytolysin (Hly) moiety, binds the complement receptor 3 (CR3, αMβ2, CD11b/CD18, or Mac-1) of myeloid phagocytes, penetrates their plasma membrane, and delivers the AC enzyme into the cytosol. We constructed a set of CyaA/HlyA chimeras and show that the CyaC-acylated segment and the CR3-binding RTX domain of CyaA can be functionally replaced by the HlyC-acylated segment and the much shorter RTX domain of HlyA. Instead of binding CR3, a CyaA1-710/HlyA411-1024 chimera bound the LFA-1 receptor and effectively delivered AC into Jurkat T cells. At high chimera concentrations (25 nm), the interaction with LFA-1 was not required for CyaA1-710/HlyA411-1024 binding to CHO cells. However, interaction with the LFA-1 receptor strongly enhanced the specific capacity of the bound CyaA1-710/HlyA411-1024 chimera to penetrate cells and deliver the AC enzyme into their cytosol. Hence, interaction of the acylated segment and/or the RTX domain of HlyA with LFA-1 promoted a productive membrane interaction of the chimera. These results help delimit residues 400-710 of CyaA as an "AC translocon" sufficient for translocation of the AC polypeptide across the plasma membrane of target cells.

Keywords: AC domain translocation; AC translocon; Bordetella pertussis; CyaA; Escherichia coli (E. coli); HlyA; RTX toxin; acylation; acyltransferase; bacterial toxin; complement receptor 3 (CR3,); fatty acid; fatty acyl; integrin; protein acylation; protein translocation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylate Cyclase Toxin / metabolism*
  • Animals
  • Bordetella*
  • CHO Cells
  • Cricetulus
  • Cytosol / metabolism*
  • Female
  • Humans
  • Jurkat Cells
  • Lymphocyte Function-Associated Antigen-1 / metabolism*
  • Macrophage-1 Antigen / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Protein Transport
  • THP-1 Cells

Substances

  • Adenylate Cyclase Toxin
  • Lymphocyte Function-Associated Antigen-1
  • Macrophage-1 Antigen