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引起侵袭性组织感染的G组链球菌菌株的细胞毒性和链球菌溶血素O活性增加。

Increased cytotoxicity and streptolysin O activity in group G streptococcal strains causing invasive tissue infections.

作者信息

Siemens Nikolai, Kittang Bård R, Chakrakodi Bhavya, Oppegaard Oddvar, Johansson Linda, Bruun Trond, Mylvaganam Haima, Svensson Mattias, Skrede Steiner, Norrby-Teglund Anna

机构信息

Center for Infectious Medicine, Karolinska Institutet, Stockholm, Sweden.

Haraldsplass Deaconess Hospital, Bergen, Norway.

出版信息

Sci Rep. 2015 Nov 25;5:16945. doi: 10.1038/srep16945.

Abstract

Streptococcus dysgalactiae subsp. equisimilis (SDSE) has emerged as an important cause of severe skin and soft tissue infections, but little is known of the pathogenic mechanisms underlying tissue pathology. Patient samples and a collection of invasive and non-invasive group G SDSE strains (n = 69) were analyzed with respect to virulence factor expression and cytotoxic or inflammatory effects on human cells and 3D skin tissue models. SDSE strains efficiently infected the 3D-skin model and severe tissue pathology, inflammatory responses and altered production of host structural framework proteins associated with epithelial barrier integrity were evident already at 8 hours post-infection. Invasive strains were significantly more cytotoxic towards keratinocytes and expressed higher Streptokinase and Streptolysin O (SLO) activities, as compared to non-invasive strains. The opposite was true for Streptolysin S (SLS). Fractionation and proteomic analysis of the cytotoxic fractions implicated SLO as a factor likely contributing to the keratinocyte cytotoxicity and tissue pathology. Analyses of patient tissue biopsies revealed massive bacterial load, high expression of slo, as well as immune cell infiltration and pro-inflammatory markers. Our findings suggest the contribution of SLO to epithelial cytotoxicity and tissue pathology in SDSE tissue infections.

摘要

马链球菌兽疫亚种(SDSE)已成为严重皮肤和软组织感染的重要病因,但对其组织病理学的致病机制了解甚少。对患者样本以及一组侵袭性和非侵袭性G群SDSE菌株(n = 69)进行了分析,以研究其毒力因子表达以及对人细胞和3D皮肤组织模型的细胞毒性或炎症作用。SDSE菌株能有效感染3D皮肤模型,感染后8小时就已出现严重的组织病理学变化、炎症反应以及与上皮屏障完整性相关的宿主结构框架蛋白产生改变。与非侵袭性菌株相比,侵袭性菌株对角质形成细胞的细胞毒性显著更高,且表达更高的链激酶和链球菌溶血素O(SLO)活性。而链球菌溶血素S(SLS)的情况则相反。对细胞毒性组分进行分级分离和蛋白质组分析表明,SLO可能是导致角质形成细胞毒性和组织病理学变化的一个因素。对患者组织活检样本的分析显示细菌载量巨大、slo表达水平高,以及免疫细胞浸润和促炎标志物。我们的研究结果表明SLO在SDSE组织感染中对上皮细胞毒性和组织病理学有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22bd/4658506/cf2739333ed8/srep16945-f1.jpg

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