Enterococcal cytolysin: A novel two component peptide system that serves as a bacterial defense against eukaryotic and prokaryotic cells

被引:115
作者
Cox, CR
Coburn, PS
Gilmore, MS
机构
[1] Schepens Eye Res Inst, Boston, MA 02114 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Oklahoma Ctr Neurosci, Oklahoma City, OK USA
[3] Univ Oklahoma, Hlth Sci Ctr, Coll Pharm, Dept Pharmaceut Sci, Oklahoma City, OK 73117 USA
关键词
cytolysin; toxin; bacteriocin; hemolysin; enterococcal pathogenesis;
D O I
10.2174/1389203053027557
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cytolysin is a novel, two-peptide lytic toxin produced by some strains of Enterococcus faecalis. It is toxic in animal models of enterococcal infection, and associated with acutely terminal outcome in human infection. The cytolysin exerts activity against a broad spectrum of cell types including a wide range of gram positive bacteria, eukaryotic cells such as human, bovine and horse erythrocytes, retinal cells, polymorphonuclear leukocytes, and human intestinal epithelial cells. The cytolysin likely originated as a bacteriocin involved with niche control in the complex microbial ecologies associated with eukaryotic hosts. However, additional anti-eukaryotic activities may have been selected for as enterococci adapted to eukaryotic cell predation in water or soil ecologies. Cytolytic activity requires two unique peptides that possess modifications characteristic of the lantibiotic bacteriocins, and these peptides are broadly similar in size to most cationic eukaryotic defensins. Expression of the cytolysin is tightly controlled by a novel mode of gene regulation in which the smaller peptide signals high-level expression of the cytolysin gene cluster. This complex regulation of cytolysin expression may have evolved to balance defense against eukaryotic predators with stealth.
引用
收藏
页码:77 / 84
页数:8
相关论文
共 65 条
[1]  
Aarestrup FM, 2002, ENTEROCOCCI: PATHOGENESIS, MOLECULAR BIOLOGY, AND ANTIBIOTIC RESISTANCE, P55
[2]   ROLES OF ANTIBODIES AND COMPLEMENT IN PHAGOCYTIC KILLING OF ENTEROCOCCI [J].
ARDUINO, RC ;
MURRAY, BE ;
RAKITA, RM .
INFECTION AND IMMUNITY, 1994, 62 (03) :987-993
[3]   BACTERIOCIN (HEMOLYSIN) OF STREPTOCOCCUS ZYMOGENES [J].
BASINGER, SF ;
JACKSON, RW .
JOURNAL OF BACTERIOLOGY, 1968, 96 (06) :1895-&
[4]   Structural analysis and proteolytic activation of Enterococcus faecalis cytolysin, a novel lantibiotic [J].
Booth, MC ;
Bogie, CP ;
Sahl, HG ;
Siezen, RJ ;
Hatter, KL ;
Gilmore, MS .
MOLECULAR MICROBIOLOGY, 1996, 21 (06) :1175-1184
[5]   PROBABLE IDENTITY OF A GROUP D HEMOLYSIN WITH A BACTERIOCINE [J].
BROCK, TD ;
DAVIE, JM .
JOURNAL OF BACTERIOLOGY, 1963, 86 (04) :708-&
[6]   SURVEY OF BACTERIOCINES OF ENTEROCOCCI [J].
BROCK, TD ;
PEACHER, B ;
PIERSON, D .
JOURNAL OF BACTERIOLOGY, 1963, 86 (04) :702-&
[7]   Role of lipid-bound peptidoglycan precursors in the formation of pores by nisin, epidermin and other lantibiotics [J].
Brötz, H ;
Josten, M ;
Wiedemann, I ;
Schneider, U ;
Götz, F ;
Bierbaum, G ;
Sahl, HG .
MOLECULAR MICROBIOLOGY, 1998, 30 (02) :317-327
[8]   PLASMID-ASSOCIATED HEMOLYSIN AND AGGREGATION SUBSTANCE PRODUCTION CONTRIBUTE TO VIRULENCE IN EXPERIMENTAL ENTEROCOCCAL ENDOCARDITIS [J].
CHOW, JW ;
THAL, LA ;
PERRI, MB ;
VAZQUEZ, JA ;
DONABEDIAN, SM ;
CLEWELL, DB ;
ZERVOS, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (11) :2474-2477
[9]   A novel means of self-protection, unrelated to toxin activation, confers immunity to the bactericidal effects of the Enterococcus faecalis cytolysin [J].
Coburn, PS ;
Hancock, LE ;
Booth, MC ;
Gilmore, MS .
INFECTION AND IMMUNITY, 1999, 67 (07) :3339-3347
[10]   The Enterococcus faecalis cytolysin:: a novel toxin active against eukaryotic and prokaryotic cells [J].
Coburn, PS ;
Gilmore, MS .
CELLULAR MICROBIOLOGY, 2003, 5 (10) :661-669