[HTML][HTML] Cytolysin-mediated translocation (CMT): a functional equivalent of type III secretion in gram-positive bacteria

JC Madden, N Ruiz, M Caparon - Cell, 2001 - cell.com
JC Madden, N Ruiz, M Caparon
Cell, 2001cell.com
Type III secretion for injection of effector proteins into host cells has not been described for
Gram-positive bacteria despite their importance in disease. Here, we describe an injection
pathway for the Gram-positive pathogen Streptococcus pyogenes that utilizes streptolysin O
(SLO), a cholesterol-dependent cytolysin. The data support a model in which an effector is
translocated through the SLO pore by a polarized process. The effector, SPN (S. p yogenes
N AD-glycohydrolase), is capable of producing the potent second messenger cyclic ADP …
Abstract
Type III secretion for injection of effector proteins into host cells has not been described for Gram-positive bacteria despite their importance in disease. Here, we describe an injection pathway for the Gram-positive pathogen Streptococcus pyogenes that utilizes streptolysin O (SLO), a cholesterol-dependent cytolysin. The data support a model in which an effector is translocated through the SLO pore by a polarized process. The effector, SPN (S . p yogenes N AD-glycohydrolase), is capable of producing the potent second messenger cyclic ADP-ribose, and SLO and SPN act synergistically to trigger cytotoxicity. These data provide a novel paradigm for the function of the cholesterol-dependent cytolysin family and its wide distribution suggests that cytolysin-mediated translocation (CMT) may be the equivalent of type III secretion for Gram-positive pathogens.
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