Agr群体感应系统在尿源性金黄色葡萄球菌中对模拟尿代谢条件的过度表达,增强其生长和毒力。

IF 3 3区 医学 Q1 IMMUNOLOGY
Yuvarajan Subramaniyan, M Mujeeburahiman, Altaf Khan, Punchappady Devasya Rekha
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引用次数: 0

摘要

金黄色葡萄球菌(S. aureus)是一种主要的机会致病菌,可引起急性和慢性感染,包括尿路感染(UTI)。金黄色葡萄球菌依靠辅助基因调控因子(Agr)、中央群体感应(QS)系统和脲酶基因ureABCEFGD调控脲酶表达及其致病性。脲酶是金黄色葡萄球菌的一个关键毒力因子,通过改变局部尿液pH值和损害不利泌尿环境中的免疫防御来调节免疫反应。QS受外界刺激调控,在泌尿系统疾病中,不同的尿代谢状况和pH值对脲酶表达和Agr-QS调控的作用尚不清楚。在本研究中,我们探索了不同模拟尿代谢和pH环境下金黄色葡萄球菌的生长、生物膜形成和脲酶活性,以研究泌尿系统疾病患者分离的金黄色葡萄球菌菌株的反应。比较QS基因和脲酶基因在不同泌尿系统(包括分离菌株的泌尿系统)中的表达水平。通过相关分析研究生长、pH变化、脲酶活性、生物膜形成与agr和ure基因表达的关系,预测它们之间的调控关系。我们的研究结果表明,在糖尿、血尿、肌酐尿和蛋白尿中,金黄色葡萄球菌菌株在生长、生物膜形成和脲酶活性方面存在显著差异
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overexpression of Agr quorum sensing system in uropathogenic Staphylococcus aureus in response to simulated urinary metabolic conditions enhancing growth and virulence.

Staphylococcus aureus (S. aureus) is a major opportunistic pathogen, causing acute and chronic infections including urinary tract infection (UTI). S. aureus relies on the Accessory gene regulator (Agr), a central quorum sensing (QS) system and the urease genes ureABCEFGD, for the regulation of urease expression and its pathogenicity. Urease is a key virulence factor for S. aureus, modulating immune responses by altering the local urinary pH and impairing immune defenses in the hostile urinary environment. QS is regulated by the external stimuli and in urological disease, the role of different urinary metabolite conditions and pH on the urease expression and Agr-QS regulation remains poorly understood. In this study, we explored the growth, biofilm formation, and urease activity under various simulated urinary metabolic and pH environments to study the response of S. aureus strains isolated from patients with urological diseases. The expression levels of QS genes and urease genes were compared in different urinary conditions that included the conditions from which the strains were isolated. A correlation analysis was used to study the associations between growth, pH changes, urease activity, biofilm formation, and the expression of agr and ure genes to predict their regulatory relationships. Our results demonstrated significant differences across glycosuria, haematuria, creatininuria, and albuminuria in growth, biofilm formation, and urease activity in S. aureus strains (p < 0.001). Significantly higher growth and urease activity were noted in glycosuria and haematuria-originated strains under the similar simulated conditions (p < 0.001). However, all the simulated conditions increased the expression levels of agr and ure genes; in the pre-adapted environment, favoring their survival highlighting niche adaptation. The simulated conditions with acidic pH significantly overexpressed the agr and ure genes compared to alkaline pH (p < 0.001). Increased expression profile of the QS system under the disease specific urine metabolic conditions, suggests its role in promoting bacterial fitness in the urinary environment and also forms the basis of managing UTI with targeted approach.

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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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