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PMID: 11163247 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Cell ·Vol. 104 ·No. 1 ·2001-01-12 ·Pages 143-52

Madden JC, Ruiz N, Caparon M

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. pyogenes NAD-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.

MeSH Terms
Adenosine Diphosphate Ribose/analogs & derivatives,metabolism Bacterial Adhesion/physiology Bacterial Proteins Biological Transport/physiology Cell Line Cell Membrane/metabolism Cyclic ADP-Ribose Cytoplasm/enzymology Cytotoxins/metabolism Humans Keratinocytes/cytology,microbiology NAD+ Nucleosidase/metabolism Protein Sorting Signals/physiology Second Messenger Systems/physiology Streptococcus pyogenes/metabolism,pathogenicity Streptolysins/metabolism Virulence
Chemicals
Bacterial Proteins Cytotoxins Protein Sorting Signals Streptolysins streptolysin O Cyclic ADP-Ribose Adenosine Diphosphate Ribose NAD+ Nucleosidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Madden J C
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Ruiz N
Caparon M
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
2001-01-12
Pages
143-52
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIAID NIH HHS · AI38273 · United States
NIAMS NIH HHS · AR45254 · United States
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