Yuvarajan Subramaniyan, M Mujeeburahiman, Altaf Khan, Punchappady Devasya Rekha
{"title":"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。","authors":"Yuvarajan Subramaniyan, M Mujeeburahiman, Altaf Khan, Punchappady Devasya Rekha","doi":"10.1007/s00430-025-00830-6","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18369,"journal":{"name":"Medical Microbiology and Immunology","volume":"214 1","pages":"35"},"PeriodicalIF":3.0000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Overexpression of Agr quorum sensing system in uropathogenic Staphylococcus aureus in response to simulated urinary metabolic conditions enhancing growth and virulence.\",\"authors\":\"Yuvarajan Subramaniyan, M Mujeeburahiman, Altaf Khan, Punchappady Devasya Rekha\",\"doi\":\"10.1007/s00430-025-00830-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":18369,\"journal\":{\"name\":\"Medical Microbiology and Immunology\",\"volume\":\"214 1\",\"pages\":\"35\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical Microbiology and Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s00430-025-00830-6\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Microbiology and Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00430-025-00830-6","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
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.
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.