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宿主表面受体的暂时性上调为细菌黏附和疾病提供了一个机会窗口。

Temporal upregulation of host surface receptors provides a window of opportunity for bacterial adhesion and disease.

作者信息

Kc Rajendra, Shukla Shakti D, Walters Eugene H, O'Toole Ronan F

机构信息

School of Medicine, Faculty of Health, University of Tasmania, Hobart, TAS 7000, Australia.

School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, The University of Newcastle, Newcastle, NSW 2308, Australia.

出版信息

Microbiology (Reading). 2017 Apr;163(4):421-430. doi: 10.1099/mic.0.000434. Epub 2017 Apr 6.

Abstract

Host surface receptors provide bacteria with a foothold from which to attach, colonize and, in some cases, invade tissue and elicit human disease. In this review, we discuss several key host receptors and cognate adhesins that function in bacterial pathogenesis. In particular, we examine the elevated expression of host surface receptors such as CEACAM-1, CEACAM-6, ICAM-1 and PAFR in response to specific stimuli. We explore how upregulated receptors, in turn, expose the host to a range of bacterial infections in the respiratory tract. It is apparent that exploitation of receptor induction for bacterial adherence is not unique to one body system, but is also observed in the central nervous, gastrointestinal and urogenital systems. Prokaryotic pathogens which utilize this mechanism for their infectivity include Streptococcus pneumoniae, Haemophilus influenzae, Neisseria meningitidis and Escherichia coli. A number of approaches have been used, in both in vitro and in vivo experimental models, to inhibit bacterial attachment to temporally expressed host receptors. Some of these novel strategies may advance future targeted interventions for the prevention and treatment of bacterial disease.

摘要

宿主表面受体为细菌提供了一个附着、定植的立足点,在某些情况下,细菌还可借此侵入组织并引发人类疾病。在本综述中,我们讨论了几种在细菌致病过程中起作用的关键宿主受体和同源黏附素。特别是,我们研究了宿主表面受体如癌胚抗原相关细胞黏附分子1(CEACAM-1)、癌胚抗原相关细胞黏附分子6(CEACAM-6)、细胞间黏附分子1(ICAM-1)和血小板活化因子受体(PAFR)在特定刺激下的表达上调情况。我们探讨了上调的受体如何反过来使宿主易患一系列呼吸道细菌感染。显然,利用受体诱导进行细菌黏附并非某一个身体系统所特有,在中枢神经、胃肠和泌尿生殖系统中也有发现。利用这种机制实现感染性的原核病原体包括肺炎链球菌、流感嗜血杆菌、脑膜炎奈瑟菌和大肠杆菌。在体外和体内实验模型中,已经采用了多种方法来抑制细菌与瞬时表达的宿主受体的附着。其中一些新策略可能会推动未来预防和治疗细菌疾病的靶向干预措施的发展。

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