Abstract
Streptococcus species release cholesterol-dependent cytolysins (CDCs), which are a main toxin, and their heat susceptibility is poorly understood. The aim of this study was to clarify the heat susceptibility of streptococcal exotoxins and CDCs. Streptococcal exotoxins were treated with heat incubation at 60 °C for 10 or 30 min. The Streptococcus suis exotoxin of serotypes 1 and 2 exhibited more than 50 % haemolytic activity, and all Streptococcus pneumoniae exotoxins exhibited more than 60 % haemolytic activity. During the thermolabile assay, the virulent streptococcal haemolytic activity remarkably decreased after being heated at 60 °C for 10 m. Then, streptococcal recombinant CDCs were produced and put through a thermolabile assay. The haemolytic activity of suilysin (SLY), pneumolysin (PLY) and streptolysin O (SLO) decreased more than 80 % after heat incubation. We also conducted a TER assay to evaluate the cell monolayer. The cell monolayer of all CDCs broke down, and the FITC–dextran translocated at 1 h post addition, while the CDCs treated with heating did not induce cell disruption. Moreover, the microscopy analysis demonstrated that CDCs treated with heating lost their activity. In conclusion, heat incubation induced the inactivation of streptococcal exotoxins and CDCs. Heat incubation plays a role in the degradation of the streptococcal exotoxin, and this result applies to the inhibition of streptococcal infection.
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References
Alouf JE (2000) Cholesterol-binding cytolytic protein toxins. Int J Med Microbiol 290:351–356
Baba H, Kawamura I, Kohda C, Nomura T, Ito Y, Kimoto T, Watanabe I, Ichiyama S, Mitsuyama M (2001) Essential role of domain 4 of pneumolysin from Streptococcus pneumoniae in cytolytic activity as determined by truncated proteins. Biochem Biophys Res Commun 281:37–44
Bayra C, Gadbois P, Cox WR, Gottschalk M, Farzan V, Bauer SA, Wilson JB (2011) Decreased mortality of weaned pigs with Streptococcus suis with the use of in-water potassium penicillin G. Can Vet J 52:272–276
Bielecki J, Youngman P, Connelly P, Portnoy DA (1990) Bacillus subtilis expressing a haemolysin gene from Listeria monocytogenes can grow in mammalian cells. Nature 345:175–176
Enache E, Mathusa EC, Elliott PH, Black DG, Chen Y, Scott VN, Schaffner DW (2011) Thermal resistance parameters for Shiga toxin-producing Escherichia coli in apple juice. J Food Prot 74:1231–1237
Farrand AJ, Lachapelle S, Hotze EM, Johnson AE, Tweten RK (2010) Only two amino acids are essential for cytolytic toxin recognition of cholesterol at the membrane surface. Proc Natl Acad Sci USA 107:4341–4346
Förtsch C, Hupp S, Ma J, Mitchell TJ, Maier E, Benz R, Iliev AI (2011) Changes in astrocyte shape induced by sublytic concentrations of the cholesterol-dependent cytolysin pneumolysin still require pore-forming capacity. Toxins 3:543–562
Fowler HN, Brown P, Rovira A, Shade B, Klammer K, Smith K, Scheftel J (2013) Streptococcus suis meningitis in swine worker, Minnesota, USA. Emerg Infect Dis 19:330–331
Hupp S, Förtsch C, Wippel C, Ma J, Mitchell TJ, Iliev AI (2013) Direct transmembrane interaction between actin and the pore-competent, cholesterol-dependent cytolysin pneumolysin. J Mol Biol 425:636–646
IIiev AI, Djannatian JR, Nau R, Mitchell TJ, Wouters FS (2007) Cholesterol-dependent actin remodeling via RhoA and Rac1 activation by the Streptococcus pneumoniae toxin pneumolysin. Proc Natl Acad Sci USA 104:2897–2902
Jacobs AA, Loeffen PL, Van den Berg AJ, Storm PK (1994) Identification, purification, and characterization of a thiol-activated hemolysin (suilysin) of Streptococcus suis. Infect Immun 62:1742–1748
Johnson MK, Boese-Marrazzo D, Pierce WA Jr (1981) Effects of pneumolysin on human polymorphonuclear leukocytes and platelets. Infect Immun 34:171–176
Klichko VI, Miller J, Wu A, Popov SG, Alibek K (2003) Anaerobic induction of Bacillus anthracis hemolytic activity. Biochem Biophys Res Commun 303:855–862
Lun S, Perez-Casal J, Connor W, Willson PJ (2003) Role of suilysin in pathogenesis of Streptococcus suis capsular serotype 2. Microb Pathog 34:27–37
Nakayama T, Nomura N, Matsumura M (2006) Study on the relationship of protease production and luminescence in Vibrio harveyi. J Appl Microbiol 101:200–205
Nakayama T, Lu H, Nomura N (2009) Inhibitory effects of Bacillus probionts on growth and toxin production of Vibrio harveyi pathogens of shrimp. Lett Appl Microbiol 49:679–684
Nakayama T, Takeuchi D, Akeda Y, Oishi K (2010) Streptococcus suis infection induces bacterial accumulation in the kidney. Microb Pathog 50:87–93
Nakayama T, Takeuchi D, Matsumura T, Akeda Y, Fujinaga Y, Oishi K (2013) Alcohol consumption promotes the intestinal translocation of Streptococcus suis infections. Microb Pathog 65:14–20
O’Brien DK, Melville SB (2004) Effects of Clostridium perfringens alpha-toxin (PLC) and perfringolysin O (PFO) on cytotoxicity to macrophages, on escape from the phagosomes of macrophages, and on persistence of C. perfringens in host tissues. Infect Immun 72:5204–5215
Paton JC, Rowan-Kelly B, Ferrante A (1984) Activation of human complement by the pneumococcal toxin pneumolysin. Infect Immun 43:1085–1087
Segers RP, Kenter T, de Haan LA, Jacobs AA (1998) Characterization of the gene encoding suilysin from Streptococcus suis and expression in field strains. FEMS Microbiol Lett 167:255–261
Segura M, Gottschalk M (2002) Streptococcus suis interactions with the murine macrophage cell line J774: adhesion and cytotoxicity. Infect Immun 70:4312–4322
Shannon JG, Ross CL, Koehler TM, Rest RF (2003) Characterization of anthrolysin O, the Bacillus anthracis cholesterol-dependent cytolysin. Infect Immun 71:3183–3189
Sierig G, Cywes C, Wessels MR, Ashbaugh CD (2003) Cytotoxic effects of streptolysin o and streptolysin s enhance the virulence of poorly encapsulated group a streptococci. Infect Immun 71:446–455
Srivastava A, Henneke P, Visintin A, Morse SC, Martin V, Watkins C, Paton JC, Wessels MR, Golenbock DT, Malley R (2005) The apoptotic response to pneumolysin is toll-like receptor 4 dependent and protects against pneumococcal disease. Infect Immun 73:6479–6487
Sumitomo T, Nakata M, Higashino M, Jin Y, Terao Y, Fujinaga Y, Kawabata S (2011) Streptolysin S contributes to group A streptococcal translocation across an epithelial barrier. J Biol Chem 286:2750–2761
Taniguchi H, Ohta H, Ogawa M, Mizuguchi Y (1985) Cloning and expression in Escherichia coli of Vibrio parahaemolyticus thermostable direct hemolysin and thermolabile hemolysin genes. J Bacteriol 162:510–515
Walker JA, Allen RL, Falmagne P, Johnson MK, Boulnois GJ (1987) Molecular cloning, characterization, and complete nucleotide sequence of the gene for pneumolysin, the sulfhydryl-activated toxin of Streptococcus pneumoniae. Infect Immun 55:1184–1189
Xu L, Huang B, Du H, Zhang XC, Xu J, Li X, Rao Z (2010) Crystal structure of cytotoxin protein suilysin from Streptococcus suis. Protein Cell 1:96–105
Acknowledgments
We thanks research staffs in laboratory of infection cell biology and laboratory of clinical research on infectious disease, RIMD, Osaka University who helped us to use the operating microscope and produce recombinant proteins. This work was supported by research grants from the Grants-in Aid for Young Scientist B (24791022) and by the Ministry of Education, Science and Culture of Japan.
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Nakayama, T., Ezoe, K. Heat Incubation Inactivates Streptococcal Exotoxins and Recombinant Cholesterol-Dependent Cytolysins: Suilysin, Pneumolysin and Streptolysin O. Curr Microbiol 69, 690–698 (2014). https://doi.org/10.1007/s00284-014-0639-z
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DOI: https://doi.org/10.1007/s00284-014-0639-z