Aeromonas exoenzyme T of Aeromonas salmonicida is a bifunctional protein that targets the host cytoskeleton

J Biol Chem. 2007 Sep 28;282(39):28843-28852. doi: 10.1074/jbc.M704797200. Epub 2007 Jul 25.

Abstract

Type III protein secretion has been shown recently to be important in the virulence of the fish pathogen Aeromonas salmonicida. The ADP-ribosylating toxin Aeromonas exoenzyme T (AexT) is one effector protein targeted for secretion via this system. In this study, we identified muscular and nonmuscular actin as substrates of the ADP-ribosylating activity of AexT. Furthermore, we show that AexT also functions as a GTPase-activating protein (GAP), displaying GAP activity against monomeric GTPases of the Rho family, specifically Rho, Rac, and Cdc42. Transfection of fish cells with wild type AexT resulted in depolymerization of the actin cytoskeleton and cell rounding. Point mutations within either the GAP or the ADP-ribosylating active sites of AexT (Arg-143 as well as Glu-398 and Glu-401, respectively) abolished enzymatic activity, yet did not prevent actin filament depolymerization. However, inactivation of the two catalytic sites simultaneously did. These results suggest that both the GAP and ADP-ribosylating domains of AexT contribute to its biological activity. This is the first bacterial virulence factor to be described that has a specific actin ADP-ribosylation activity and GAP activity toward Rho, Rac, and Cdc42, both enzymatic activities contributing to actin filament depolymerization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP Ribose Transferases / genetics
  • ADP Ribose Transferases / metabolism*
  • Actin Cytoskeleton / genetics
  • Actin Cytoskeleton / metabolism*
  • Actins / genetics
  • Actins / metabolism*
  • Aeromonas salmonicida / enzymology*
  • Aeromonas salmonicida / genetics
  • Aeromonas salmonicida / pathogenicity
  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Bacterial Toxins / genetics
  • Bacterial Toxins / metabolism*
  • Chlorocebus aethiops
  • Cyprinidae
  • Fish Proteins / genetics
  • Fish Proteins / metabolism*
  • Point Mutation
  • Substrate Specificity
  • Vero Cells
  • cdc42 GTP-Binding Protein / genetics
  • cdc42 GTP-Binding Protein / metabolism
  • rac GTP-Binding Proteins / genetics
  • rac GTP-Binding Proteins / metabolism

Substances

  • Actins
  • Bacterial Proteins
  • Bacterial Toxins
  • Fish Proteins
  • ADP Ribose Transferases
  • cdc42 GTP-Binding Protein
  • rac GTP-Binding Proteins