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生物膜如何逃避宿主防御。

How Biofilms Evade Host Defenses.

机构信息

Infectious Diseases Unit, 3rd Department of Pediatrics, Faculty of Medicine, Aristotle University School of Health Sciences, Hippokration Hospital, 54642 Thessaloniki, Greece.

Transplantation-Oncology Infectious Diseases Program, Weill Cornell Medical Center of Cornell University, New York, NY 14850.

出版信息

Microbiol Spectr. 2015 Jun;3(3). doi: 10.1128/microbiolspec.MB-0012-2014.

Abstract

The steps involved during the biofilm growth cycle include attachment to a substrate followed by more permanent adherence of the microorganisms, microcolony arrangement, and cell detachment required for the dissemination of single or clustered cells to other organ systems. Various methods have been developed for biofilm detection and quantitation. Biofilm-producing microorganisms can be detected in tissue culture plates, using silicone tubes and staining methods, and by visual assessment using scanning electron microscopy or confocal scanning laser microscopy. Quantitative measurement of biofilm growth is determined by using methods that include dry cell weight assays, colony-forming-unit counting, DNA quantification, or XTT 2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium hydroxide reduction assay. Upon infection, innate immune defense strategies are able to establish an immediate response through effector mechanisms mediated by immune cells, receptors, and several humoral factors. We present an overview of the life cycle of biofilms and their diversity, detection methods for biofilm development, and host immune responses to pathogens. We then focus on current concepts in bacterial and fungal biofilm immune evasion mechanisms. This appears to be of particular importance because the use of host immune responses may represent a novel therapeutic approach against biofilms.

摘要

生物膜生长周期涉及的步骤包括附着在基质上,然后是微生物更永久的附着,微菌落排列,以及单个或簇状细胞传播到其他器官系统所需的细胞脱落。已经开发了各种用于生物膜检测和定量的方法。可以在组织培养板中、使用硅酮管和染色方法、以及使用扫描电子显微镜或共聚焦扫描激光显微镜进行视觉评估来检测产生生物膜的微生物。生物膜生长的定量测量是通过使用包括干细胞重量测定、集落形成单位计数、DNA 定量或 XTT 2,3-双(2-甲氧基-4-硝基-5-磺苯基)-5-[(苯氨基)羰基]-2H-四唑鎓氢氧化物还原测定等方法来确定的。感染后,先天免疫防御策略能够通过免疫细胞、受体和几种体液因子介导的效应机制立即建立反应。我们概述了生物膜的生命周期及其多样性、生物膜发育的检测方法以及宿主对病原体的免疫反应。然后,我们专注于细菌和真菌生物膜免疫逃避机制的当前概念。这似乎尤为重要,因为利用宿主免疫反应可能代表针对生物膜的一种新的治疗方法。

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