Dependence of the lethal effect of pore-forming haemolysins of Gram-positive bacteria on cytolytic activity

1 Department of Microbiology, Kyoto University Graduate School of Medicine, Yoshidakonoe-cho, Sakyo-ku, Kyoto 606-8501, Japan 2 Department of Bacteriology, Showa University School of Medicine, Tokyo 142-8555, Japan Correspondence Masao Mitsuyama mituyama{at}mb.med.kyoto-u.ac.jp Received 16 September...

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Veröffentlicht in:Journal of medical microbiology 2006-05, Vol.55 (5), p.505-510
Hauptverfasser: Watanabe, Isao, Nomura, Takamasa, Tominaga, Takanari, Yamamoto, Kazuhiro, Kohda, Chikara, Kawamura, Ikuo, Mitsuyama, Masao
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Sprache:eng
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Zusammenfassung:1 Department of Microbiology, Kyoto University Graduate School of Medicine, Yoshidakonoe-cho, Sakyo-ku, Kyoto 606-8501, Japan 2 Department of Bacteriology, Showa University School of Medicine, Tokyo 142-8555, Japan Correspondence Masao Mitsuyama mituyama{at}mb.med.kyoto-u.ac.jp Received 16 September 2005 Accepted 12 January 2006 Among bacterial haemolysins, cholesterol-dependent cytolysins (CDCs) produced by various Gram-positive bacteria are known to exhibit a lethal activity in mice. In this study, recombinant CDCs of streptolysin O, pneumolysin, ivanolysin O, listeriolysin O and several listeriolysin O mutants were constructed and the relationship between cytolytic activity and the lethal activity of each recombinant protein in mice was examined. Specific activity for cytolysis was determined by a quantitative haemolytic assay. Each protein was injected intravenously into mice and the lethal activity was evaluated by measuring the time until death of the mice. The four full-length CDC proteins exhibited lethal activity and their activities were highly proportional to their cytolytic activities. Inhibition of haemolytic activity resulted in the loss of lethal activity and non-haemolytic mutants of listeriolysin O did not exhibit any lethal activity. These data clearly indicate that the lethal effect of CDC proteins is dependent on the cytolytic activity. Abbreviations: CDC, cholesterol-dependent cytolysin; HU, haemolytic unit; ILO, ivanolysin O; LLO, listeriolysin O; PLY, pneumolysin; SLO, streptolysin O.
ISSN:0022-2615
1473-5644
DOI:10.1099/jmm.0.46333-0