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鼻咽部细菌生物膜形成过程中宿主-病原体相互作用的未来展望。

Future perspective on host-pathogen interactions during bacterial biofilm formation within the nasopharynx.

机构信息

The University of Texas Health Science Center at San Antonio, Department of Microbiology & Immunology, 7703 Floyd Curl Drive, MC7758, San Antonio, TX 78229-3900, USA.

出版信息

Future Microbiol. 2012 Feb;7(2):227-39. doi: 10.2217/fmb.11.160.

DOI:10.2217/fmb.11.160
PMID:22324992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3286033/
Abstract

Nasopharyngeal colonization provides bacteria with a place of residence, a platform for person-to-person transmission and for many opportunistic pathogens it is a prerequisite event towards the development of invasive disease. Therefore, how host factors within the nasopharynx contribute to, inhibit or otherwise shape biofilm formation, the primary mode of existence for colonizing bacteria, and how biofilm bacteria subvert the acute inflammatory response that facilitates clearance, are important topics for future microbiological research. This review proposes the examination of host components as bridging molecules for bacterial interactions during biofilm formation, altered virulence determinant production and cell wall modification as a mechanism for immunoquiescence, and the role of host factors as signals and co-opted mechanisms for bacterial dissemination, together providing an opportunity for disease.

摘要

鼻咽定植为细菌提供了一个居住场所、一个人际传播的平台,对于许多机会性病原体而言,它是发展为侵袭性疾病的先决条件事件。因此,鼻咽内的宿主因素如何促进、抑制或以其他方式影响生物膜的形成(定植细菌的主要生存方式),以及生物膜细菌如何颠覆促进清除的急性炎症反应,是未来微生物学研究的重要课题。本综述提出了将宿主成分作为生物膜形成过程中细菌相互作用、改变毒力决定因素产生和细胞壁修饰的桥接分子进行研究,将免疫静止机制作为宿主因素作为信号和细菌传播的被劫持机制的作用,共同为疾病提供机会。

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本文引用的文献

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Streptococcus pneumoniae in biofilms are unable to cause invasive disease due to altered virulence determinant production.生物膜中的肺炎链球菌由于毒力决定因素的产生发生改变而无法引起侵袭性疾病。
PLoS One. 2011;6(12):e28738. doi: 10.1371/journal.pone.0028738. Epub 2011 Dec 8.
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Minimization of bacterial size allows for complement evasion and is overcome by the agglutinating effect of antibody.细菌体积越小,越能逃避补体作用,而抗体的凝集作用则能克服这一点。
Cell Host Microbe. 2011 Nov 17;10(5):486-96. doi: 10.1016/j.chom.2011.09.009.
3
Biofilm and planktonic pneumococci demonstrate disparate immunoreactivity to human convalescent sera.生物膜和浮游状态肺炎球菌与人恢复期血清的免疫反应不同。
BMC Microbiol. 2011 Nov 2;11:245. doi: 10.1186/1471-2180-11-245.
4
Characterisation of regulatory T cells in nasal associated lymphoid tissue in children: relationships with pneumococcal colonization.儿童鼻腔相关淋巴组织中调节性 T 细胞的特征:与肺炎球菌定植的关系。
PLoS Pathog. 2011 Aug;7(8):e1002175. doi: 10.1371/journal.ppat.1002175. Epub 2011 Aug 11.
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The LuxS-dependent quorum-sensing system regulates early biofilm formation by Streptococcus pneumoniae strain D39.LuxS 依赖性群体感应系统调控肺炎链球菌 D39 早期生物膜形成。
Infect Immun. 2011 Oct;79(10):4050-60. doi: 10.1128/IAI.05186-11. Epub 2011 Aug 8.
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A structural model for binding of the serine-rich repeat adhesin GspB to host carbohydrate receptors.富含丝氨酸的重复黏附素 GspB 与宿主碳水化合物受体结合的结构模型。
PLoS Pathog. 2011 Jul;7(7):e1002112. doi: 10.1371/journal.ppat.1002112. Epub 2011 Jul 7.
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Cellular senescence increases expression of bacterial ligands in the lungs and is positively correlated with increased susceptibility to pneumococcal pneumonia.细胞衰老会增加肺部细菌配体的表达,并与对肺炎球菌性肺炎易感性的增加呈正相关。
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