Details

Autor(en) / Beteiligte

• Dhakal, Bijaya K.
• Mulvey, Matthew A.

Titel

The UPEC Pore-Forming Toxin α-Hemolysin Triggers Proteolysis of Host Proteins to Disrupt Cell Adhesion, Inflammatory, and Survival Pathways

Ist Teil von

• Cell host & microbe, 2012-01, Vol.11 (1), p.58-69

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2012

Quelle

Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals

Beschreibungen/Notizen

• Uropathogenic Escherichia coli (UPEC), which are the leading cause of both acute and chronic urinary tract infections, often secrete a labile pore-forming toxin known as α-hemolysin (HlyA). We show that stable insertion of HlyA into epithelial cell and macrophage membranes triggers degradation of the cytoskeletal scaffolding protein paxillin and other host regulatory proteins, as well as components of the proinflammatory NFκB signaling cascade. Proteolysis of these factors requires host serine proteases, and paxillin degradation specifically involves the serine protease mesotrypsin. The induced activation of mesotrypsin by HlyA is preceded by redistribution of mesotrypsin precursors from the cytosol into foci along microtubules and within nuclei. HlyA intoxication also stimulated caspase activation, which occurred independently of effects on host serine proteases. HlyA-induced proteolysis of host proteins likely allows UPEC to not only modulate epithelial cell functions, but also disable macrophages and suppress inflammatory responses. ► HlyA, but not other pore-forming toxins, triggers proteolysis of host proteins ► Target proteins include those involved in the cytoskeleton, inflammation, and apoptosis ► Proteolysis requires stable interactions between HlyA and host membranes ► Proteolysis involves activation and redistribution of mesotrypsin precursors