Virulence factors of gram-negative bacteria in sepsis with a focus on Neisseria meningitidis.

Contributions to microbiology Pub Date : 2011-01-01 Epub Date: 2011-06-09 DOI:10.1159/000324008
Daniel J Livorsi, Edward Stenehjem, David S Stephens
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引用次数: 29

Abstract

Gram-negative bacterial pathogens of humans have evolved a range of virulence factors to promote motility, attach to epithelial or endothelial cell surfaces, avoid host immune responses, activate or inactivate host cellular pathways and ultimately cause clinical disease. Gram-negative sepsis is a life-threatening complication of these events. This review discusses the virulence factors of common Gram-negative bacteria causing human sepsis with a focus on Neisseria meningitidis. Adherence, motility, colonization and cell entry involve bacterial pili, flagella and outer membrane proteins. Endotoxin (lipopoly-or lipo-oligosaccharide), other membrane components or exotoxins can be potent inducers of the host inflammatory cascade via innate receptor pathways. Capsular polysaccharides and outer membrane proteins can help the bacterium evade immune defenses. The role in pathogenesis of iron acquisition, bacterial secretion systems, quorum sensing, and biofilm formation is also reviewed. Through multiple genetic mechanisms leading to phase variation, Gram-negative bacteria can adapt to changing host and environmental conditions and selective pressures. Further, the antimicrobial resistance of Gram-negative bacteria driven by antibiotic use will continue to influence the clinical outcomes of Gram-negative sepsis in the coming years.

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革兰氏阴性菌在败血症中的毒力因子,重点是脑膜炎奈瑟菌。
人类革兰氏阴性细菌病原体已进化出一系列毒力因子,以促进运动,附着于上皮或内皮细胞表面,避免宿主免疫反应,激活或灭活宿主细胞通路并最终引起临床疾病。革兰氏阴性败血症是这些事件的危及生命的并发症。本文综述了引起人类败血症的常见革兰氏阴性菌的毒力因素,重点讨论了脑膜炎奈瑟菌。粘附、运动、定植和细胞进入涉及细菌毛、鞭毛和外膜蛋白。内毒素(脂聚或脂寡糖),其他膜成分或外毒素可以通过先天受体途径诱导宿主炎症级联反应。荚膜多糖和外膜蛋白可以帮助细菌逃避免疫防御。在铁获取,细菌分泌系统,群体感应和生物膜形成的发病机制中的作用也进行了综述。革兰氏阴性菌通过多种遗传机制导致相变化,能够适应不断变化的宿主和环境条件以及选择压力。此外,由于抗生素的使用,革兰氏阴性菌的耐药性将在未来几年继续影响革兰氏阴性败血症的临床结果。
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Clinical aspects of sepsis. Virulence factors of gram-negative bacteria in sepsis with a focus on Neisseria meningitidis. Molecular mechanisms of sepsis. Pro-inflammatory mechanisms in sepsis. Anti-inflammatory mechanisms of sepsis.
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