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补体对革兰氏阴性菌的杀伤作用。补体C5b-9沉积于明尼苏达沙门氏菌Re595表面后细胞膜的分级分离。

Killing of gram-negative bacteria by complement. Fractionation of cell membranes after complement C5b-9 deposition on to the surface of Salmonella minnesota Re595.

作者信息

Tomlinson S, Taylor P W, Morgan B P, Luzio J P

机构信息

Department of Clinical Biochemistry, University of Cambridge, Addenbrooke's Hospital, U.K.

出版信息

Biochem J. 1989 Oct 15;263(2):505-11. doi: 10.1042/bj2630505.

DOI:10.1042/bj2630505
PMID:2597121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1133457/
Abstract

The effect of C5b-9 deposition on the envelope of target Gram-negative bacteria was studied. In order to understand the changes occurring after complement deposition on the bacterial surface, the preparation of Gram-negative bacterial membranes by different methods involving the osmotic lysis of spheroplasts was investigated. Subsequent fractionation of the outer membrane (OM) and cytoplasmic membrane (CM) by sucrose-density-gradient centrifugation showed differences in the membrane profiles obtained. The results indicate that optimum separation of OM and CM components requires effective digestion of DNA in the total membrane preparation before density-gradient fractionation. Salmonella minnesota Re595 carrying the intermediate complement complex C5b-7 (BC1-7) or C5b-8 (BC1-8) were efficiently killed upon incubation with purified C8 + C9 or C9 respectively. Human-alpha-thrombin-cleaved C9 (C9n), which is unable to form tubular poly(C9), was shown to be more effective at killing than native C9. By using an optimized system for the separation of OM and CM, it was found that, subsequent to lethal complement attack, the CM could not be recovered when C9 was used as the terminal complement component, but was recovered with reduced yield when C9n replaced C9. The results show that inability to recover the CM on sucrose density gradients after complement attack may not be a consequence of an essential membrane damage event required for complement-mediated killing of Gram-negative bacteria.

摘要

研究了C5b - 9沉积对革兰氏阴性靶细菌包膜的影响。为了了解补体沉积在细菌表面后发生的变化,研究了通过不同方法(包括原生质球的渗透裂解)制备革兰氏阴性细菌膜的情况。随后通过蔗糖密度梯度离心对外膜(OM)和细胞质膜(CM)进行分级分离,结果显示所获得的膜图谱存在差异。结果表明,在进行密度梯度分级分离之前,要实现OM和CM成分的最佳分离,需要有效消化总膜制剂中的DNA。携带中间补体复合物C5b - 7(BC1 - 7)或C5b - 8(BC1 - 8)的明尼苏达沙门氏菌Re595分别与纯化的C8 + C9或C9孵育后被有效杀死。人α - 凝血酶裂解的C9(C9n)不能形成管状多聚C9,但已证明其杀菌效果比天然C9更有效。通过使用优化的OM和CM分离系统发现,在致死性补体攻击后,当使用C9作为末端补体成分时,无法回收CM,但当C9n替代C9时,CM回收产量降低。结果表明,补体攻击后无法在蔗糖密度梯度上回收CM可能不是补体介导的革兰氏阴性细菌杀伤所需的基本膜损伤事件的结果。

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Killing of gram-negative bacteria by complement. Fractionation of cell membranes after complement C5b-9 deposition on to the surface of Salmonella minnesota Re595.补体对革兰氏阴性菌的杀伤作用。补体C5b-9沉积于明尼苏达沙门氏菌Re595表面后细胞膜的分级分离。
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本文引用的文献

1
The complement-dependent bacteriolytic activity of normal human serum. I. The effect of pH and ionic strength and the role of lysozyme.正常人血清的补体依赖性溶菌活性。I. pH值和离子强度的影响以及溶菌酶的作用。
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Studies on the mechanism of bacterial resistance to complement-mediated killing. I. Terminal complement components are deposited and released from Salmonella minnesota S218 without causing bacterial death.细菌对补体介导杀伤作用的抗性机制研究。I. 末端补体成分沉积于明尼苏达沙门氏菌S218并从该菌释放,但未导致细菌死亡。
J Exp Med. 1982 Mar 1;155(3):797-808. doi: 10.1084/jem.155.3.797.
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Stable insertion of C5b-9 complement complexes into the outer membrane of serum treated, susceptible Escherichia coli cells as a prerequisite for killing.C5b-9补体复合物稳定插入经血清处理的易感大肠杆菌细胞外膜是杀菌的前提条件。
Zentralbl Bakteriol Mikrobiol Hyg A. 1984 Dec;258(2-3):316-26. doi: 10.1016/s0176-6724(84)80050-4.
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Interaction of human complement proteins with serum-sensitive and serum-resistant strains of Escherichia coli.人补体蛋白与大肠杆菌血清敏感株和血清耐受株的相互作用。
Mol Immunol. 1984 Jul;21(7):609-20. doi: 10.1016/0161-5890(84)90046-4.
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Membrane changes induced by exposure of Escherichia coli to human serum.大肠杆菌暴露于人体血清所诱导的膜变化。
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Molecular architecture and functioning of the outer membrane of Escherichia coli and other gram-negative bacteria.大肠杆菌及其他革兰氏阴性菌外膜的分子结构与功能
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How complement kills E. coli. I. Location of the lethal lesion.补体如何杀死大肠杆菌。I. 致死损伤的位置。
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Immunoaffinity purification of human complement component C9 using monoclonal antibodies.使用单克隆抗体对人补体成分C9进行免疫亲和纯化。
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Killing of an encapsulated strain of Escherichia coli by human serum.人血清对一种包膜化大肠杆菌菌株的杀伤作用。
Infect Immun. 1983 Jan;39(1):122-31. doi: 10.1128/iai.39.1.122-131.1983.
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Molecular organization of C9 within the membrane attack complex of complement. Induction of circular C9 polymerization by the C5b-8 assembly.补体膜攻击复合物中C9的分子组织。C5b-8组装诱导C9环状聚合。
J Exp Med. 1982 Jul 1;156(1):268-82. doi: 10.1084/jem.156.1.268.