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Cooperative, synergistic and antagonistic haemolytic interactions between haemolysin BL, phosphatidylcholine phospholipase C and sphingomyelinase from Bacillus cereus

机译:来自芽孢杆菌(Bacillus Cereus)的血糖素BL,磷脂酰胆碱磷脂酶C和鞘磷脂酶之间的合作,协同和拮抗血液解相互作用

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Haemolysis of erythrocytes from different species (sheep, bovine, swine and human), caused by various combinations of phosphatidylcholine (PC)-preferring phospholipase C (PC-PLC), sphingomyelinase (SMase) and the three-component, pore-forming toxin haemolysin BL (HBL) from Bacillus cereus was analysed. The lytic potency of HBL did not correlate with phospholipid (PL) content, but lysis by the individual or combined enzymes did. SMase alone lysed ruminant erythrocytes, which contain 46–53% sphingomyelin (SM). The cooperative action of PC-PLC and SMase was needed to lyse swine and human erythrocytes (22–31% PC and 28–25% SM). SMase synergistically enhanced haemolysis caused by HBL for all erythrocytes tested, which all contained 25% SM. PC-PLC enhanced HBL haemolysis only in cells containing significant amounts of PC (swine, 22% PC; human, 31% PC). Unexpectedly, PC-PLC inhibited HBL lysis of sheep erythrocytes (2% PC) and enhanced the discontinuous haemolysis pattern that is characteristic of HBL in sheep blood agar. Inhibition and pattern enhancement was abolished by washing PC-PLC-treated erythrocytes or by adding EDTA, suggesting that enzymic alteration of the membrane is not involved, but that zinc in the active site is required, perhaps to facilitate binding. These observations highlight the potential for cooperative and synergistic interactions among virulence factors in B. cereus infections and dependence of these effects on tissue composition.
机译:由不同物种(绵羊,牛,猪和人)的红细胞溶解,由磷脂酰胆碱(PC),磷脂酶C(PC-PLC),鞘氨基氨基酶(SMASE)和三组分,孔形成毒素血溶素引起的分析来自芽孢杆菌的BL(HBL)。 HBL的裂解效力与磷脂(PL)含量不相关,但是单个或组合酶的裂解表现。 Smase单独裂解反刍动物红细胞,其含有46-53 %Spingomyelin(SM)。需要PC-PLC和SMASE的合作作用,对乳酸猪和人红细胞(22-31%PC和28-25%SM)。 SMASE协同增强的溶解,由HBL造成的所有红细胞所测试的,所有含有> 25 %SM。仅PC-PLC增强了HBL SOEMOLICY,仅在含有大量PC的细胞中(SWINE,22 %PC;人,31 %PC)。意外地,PC-PLC抑制了绵羊红细胞(<2℃)的HBL裂解,增强了绵羊血琼脂中HBL的不连续溶血模式。通过洗涤PC-PLC处理的红细胞或通过添加EDTA来消除抑制和模式增强,表明不涉及膜的酶改变,但是在活性位点中的锌是必需的,也许是为了促进结合。这些观察结果突出了B.脑感染的毒力因子之间的合作和协同相互作用的可能性和这些影响对组织组合物的依赖性。

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