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致病性链球菌的体外和体内生物膜形成

In Vitro and In Vivo Biofilm Formation by Pathogenic Streptococci.

作者信息

Chao Yashuan, Bergenfelz Caroline, Håkansson Anders P

机构信息

Division of Experimental Infection Medicine, Department of Translational Medicine, Wallenberg Laboratory, Lund University, 53 Inga Marie Nilsson Street, 20502, Malmö, Sweden.

出版信息

Methods Mol Biol. 2017;1535:285-299. doi: 10.1007/978-1-4939-6673-8_19.

Abstract

This manuscript presents novel approaches to grow and evaluate Streptococcal biofilm formation using the human respiratory pathogen Streptococcus pneumoniae (the pneumococcus) as the main model organism on biological surfaces in vitro and in vivo. Most biofilm models are based on growth on abiotic surfaces, which is relevant for many pathogens whose growth on surfaces or medical devices is a major cause of disease transmission and infections, especially in hospital environments. However, most infections with commensal organisms require biofilm formation on biological surfaces in the host at the site of colonization or infection. In vitro model systems incorporating biological components from the host and taking into account the host environment of the infectious site are not well described.In a series of publications, we have shown that S. pneumoniae form complex biofilms in the nasopharynx of mice and have devised methodology to evaluate the biofilm structure and function in this environment. We have also been able to recapitulate this biofilm phenotype in vitro by incorporating crucial factors associated with the host environment. Although the protocols presented in this manuscript are focused on S. pneumoniae, the same methodology can and has been used for other Streptococcal species that form biofilms on mucosal surfaces.

摘要

本手稿介绍了以人类呼吸道病原体肺炎链球菌(肺炎球菌)作为主要模式生物,在体外和体内生物表面上培养和评估链球菌生物膜形成的新方法。大多数生物膜模型基于在非生物表面上的生长,这对于许多病原体来说是相关的,其在表面或医疗设备上的生长是疾病传播和感染的主要原因,尤其是在医院环境中。然而,大多数共生生物感染需要在宿主定植或感染部位的生物表面上形成生物膜。包含宿主生物成分并考虑感染部位宿主环境的体外模型系统尚未得到充分描述。在一系列出版物中,我们已经表明肺炎链球菌在小鼠鼻咽部形成复杂的生物膜,并设计了评估该环境中生物膜结构和功能的方法。我们还能够通过纳入与宿主环境相关的关键因素在体外重现这种生物膜表型。尽管本手稿中介绍的方案侧重于肺炎链球菌,但相同的方法可以并且已经用于在粘膜表面形成生物膜的其他链球菌物种。

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