| Popis: |
Macrophages clear infections by engulfing and digesting pathogens within phagolysosomes. Pathogens escape this fate by engaging in a molecular arms race; they useWxxxEmotif- containing “effector” proteins to subvert the host cells they invade and seek refuge within protective vacuoles. Here we define the host component of the molecular arms race as an evolutionarily conserved polar ‘hotspot’ on the PH-domain of ELMO1 (Engulfment and CellMotility1), which is targeted by diverseWxxxE-effectors. Using homology modeling and site- directed mutagenesis, we show that a lysine triad within the ‘patch’ directly binds allWxxxE- effectors tested: SifA (Salmonella), IpgB1 and IpgB2 (Shigella), and Map (enteropathogenicE. coli). Using an integrated SifA•host protein-protein interaction (PPI) network,in-siliconetwork perturbation, and functional studies we show that the major consequences of preventing SifA•ELMO1 interaction are reduced Rac1 activity and microbial invasion. That multiple effectors, all diverse in structure, function, and sequence bind the same hotpot on ELMO1 suggests that theWxxxE-effector(s)•ELMO1 interface is a convergence point of intrusion detection and/or host vulnerability. We conclude that the interface may represent the fault line in co-evolved molecular adaptations between pathogens and the host and its disruption may serve as a therapeutic strategy.GRAPHICAL ABSTRACTIn briefThis work defines the nature of a conserved molecular interface, assembled between diverse WxxxEmotif- containing effector proteins encoded by gut pathogens and the host innate immune sensor, ELMO1, via which pathogens exploit the host’s engulfment machinery.HIGHLIGHTSGut pathogens trick macrophages to enter and form vacuoles of refuge within the host.Diverse pathogens useWxxxEmotif-containing effectors to bind a conserved surface on ELMO1.WxxxE-effector•ELMO1 interaction activates Rac1 and promotes bacterial invasion.Disrupting theWxxxE-effector•ELMO1 interface may serve as a therapeutic strategy. |
