IRSp53 links the enterohemorrhagic E. coli effectors Tir and EspFU for actin pedestal formation

• Published in: Cell host & microbe Vol. 5; no. 3; pp. 244 - 258
• Main Authors: Weiss, Stefanie M, Ladwein, Markus, Schmidt, Dorothea, Ehinger, Julia, Lommel, Silvia, Städing, Kai, Beutling, Ulrike, Disanza, Andrea, Frank, Ronald, Jänsch, Lothar, Scita, Giorgio, Gunzer, Florian, Rottner, Klemens, Stradal, Theresia E B
• Format: Journal Article
• Language: English
• Published: United States 19.03.2009
• Subjects: Actins - metabolism; Carrier Proteins - metabolism; Cell Line; Escherichia coli O157 - pathogenicity; Escherichia coli Proteins - metabolism; Host-Pathogen Interactions; Humans; Nerve Tissue Proteins - metabolism; Protein Binding; Protein Interaction Mapping; Receptors, Cell Surface - metabolism
• ISSN: 1931-3128; 1934-6069
• DOI: 10.1016/j.chom.2009.02.003

Actin pedestal formation by pathogenic E. coli requires signaling by the bacterial intimin receptor Tir, which induces host cell actin polymerization mediated by N-WASP and the Arp2/3 complex. Whereas canonical enteropathogenic E. coli (EPEC) recruit these actin regulators through tyrosine kinase signaling cascades, enterohemorrhagic E. coli (EHEC) O157:H7 employ the bacterial effector EspF(U) (TccP), a potent N-WASP activator. Here, we show that IRSp53 family members, key regulators of membrane and actin dynamics, directly interact with both Tir and EspF(U). IRSp53 colocalizes with EspF(U) and N-WASP in actin pedestals. In addition, targeting of IRSp53 is independent of EspF(U) and N-WASP but requires Tir residues 454-463, previously shown to be essential for EspF(U)-dependent actin assembly. Genetic and functional loss of IRSp53 abrogates actin assembly mediated by EHEC. Collectively, these data indentify IRSp53 family proteins as the missing host cell factors linking bacterial Tir and EspF(U) in EHEC pedestal formation.