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粪肠球菌中由pCF10的性信息素感应系统介导的体内毒力诱导及抗生素抗性转移

In vivo induction of virulence and antibiotic resistance transfer in Enterococcus faecalis mediated by the sex pheromone-sensing system of pCF10.

作者信息

Hirt Helmut, Schlievert Patrick M, Dunny Gary M

机构信息

Department of Microbiology, University of Minnesota, Medical School, Minneapolis, Minnesota 55455, USA.

出版信息

Infect Immun. 2002 Feb;70(2):716-23. doi: 10.1128/IAI.70.2.716-723.2002.

Abstract

Enterococcus faecalis has become one of the most notable nosocomial pathogens in the last decade. Aggregation substance (AS) on the sex pheromone plasmids of E. faecalis has been implicated as a virulence factor in several model systems. We investigated the AS-encoding plasmid pCF10 for its ability to increase virulence in a rabbit endocarditis model. Cells containing pCF10 increased the virulence in the model significantly, as assessed by an increase in aortic valve vegetation size. The results confirmed in vivo induction of the normally tightly controlled AS. In addition to the expression of AS when E. faecalis cells were in contact with plasma, plasmid transfer of the tetracycline resistance-carrying plasmid was also activated in vitro and in vivo. In vivo, plasmid transfer reached remarkable frequencies of 8 x 10(-2) to 9 x 10(-2). These values are comparable to the highest frequencies ever observed in vitro. Cells harboring pCF10 had a significant survival advantage over plasmid-free cells indicated by pCF10 present in two-thirds of the recipient population. Plasma induction was dependent on the presence of the plasmid-encoded PrgZ protein, indicating the requirement of the pheromone-sensing system in the induction process. The data suggested that the mechanism of in vivo induction may involve interference of plasma with the normal function of the pheromone peptide and its inhibitor.

摘要

粪肠球菌已成为过去十年中最显著的医院病原体之一。粪肠球菌性信息素质粒上的聚集物质(AS)在多个模型系统中被认为是一种毒力因子。我们研究了编码AS的质粒pCF10在兔心内膜炎模型中增强毒力的能力。通过主动脉瓣赘生物大小的增加评估,含有pCF10的细胞在该模型中显著增加了毒力。结果证实了体内对通常受到严格控制的AS的诱导。除了粪肠球菌细胞与血浆接触时AS的表达外,携带四环素抗性的质粒的质粒转移在体外和体内也被激活。在体内,质粒转移频率达到了8×10⁻²至9×10⁻²的显著水平。这些值与体外观察到的最高频率相当。含有pCF10的细胞比无质粒细胞具有显著的生存优势,这一点由三分之二的受体群体中存在pCF10表明。血浆诱导依赖于质粒编码的PrgZ蛋白的存在,表明在诱导过程中需要信息素传感系统。数据表明,体内诱导机制可能涉及血浆对信息素肽及其抑制剂正常功能的干扰。

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