Overexpression of Agr quorum sensing system in uropathogenic Staphylococcus aureus in response to simulated urinary metabolic conditions enhancing growth and virulence.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Overexpression of Agr quorum sensing system in uropathogenic Staphylococcus aureus in response to simulated urinary metabolic conditions enhancing growth and virulence.
Συγγραφείς: Subramaniyan Y; Division of Microbiology and Biotechnology, Yenepoya Research Centre, Yenepoya (Deemed to be University), University Road, Mangalore, 575018, India., Mujeeburahiman M; Department of Urology, Yenepoya Medical College and Hospital, Yenepoya (Deemed to be University), University Road, Mangalore, 575018, India., Khan A; Department of Urology, Yenepoya Medical College and Hospital, Yenepoya (Deemed to be University), University Road, Mangalore, 575018, India., Rekha PD; Division of Microbiology and Biotechnology, Yenepoya Research Centre, Yenepoya (Deemed to be University), University Road, Mangalore, 575018, India. rekhapd@yenepoya.edu.in.
Πηγή: Medical microbiology and immunology [Med Microbiol Immunol] 2025 Aug 05; Vol. 214 (1), pp. 35. Date of Electronic Publication: 2025 Aug 05.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0314524 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-1831 (Electronic) Linking ISSN: 03008584 NLM ISO Abbreviation: Med Microbiol Immunol Subsets: MEDLINE
Imprint Name(s): Original Publication: Berlin, New York, Springer-Verlag.
Ιατρικοί όροι (MeSH): Bacterial Proteins*/genetics , Bacterial Proteins*/metabolism , Bacterial Proteins*/biosynthesis , Staphylococcus aureus*/pathogenicity , Staphylococcus aureus*/growth & development , Staphylococcus aureus*/genetics , Staphylococcus aureus*/physiology , Urinary Tract Infections*/microbiology , Trans-Activators*/genetics , Trans-Activators*/metabolism , Trans-Activators*/biosynthesis , Urine*/chemistry , Urine*/microbiology , Quorum Sensing*, Urease/genetics ; Urease/metabolism ; Biofilms/growth & development ; Staphylococcal Infections/microbiology ; Virulence Factors/genetics ; Virulence ; Humans ; Gene Expression Regulation, Bacterial ; Hydrogen-Ion Concentration
Περίληψη: 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.
(© 2025. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
Competing Interests: Declarations. Ethical approval: All the procedures in this study involving human participants were approved by the institutional ethics committee (Protocol no. YEC-1/2021/065), Yenepoya (Deemed to be University). Prior informed consent was obtained from the participants before the collection of urine samples. Consent to publish: All the participants have consented to use the data in the scientific publication without participant identifiers. Competing interests: The authors declare no competing interests.
References: Cheung GY, Bae JS, Otto M (2021) Pathogenicity and virulence of Staphylococcus aureus. Virulence 12(1):547–569. https://doi.org/10.1080/21505594.2021.1878688. (PMID: 10.1080/21505594.2021.1878688335223957872022)
Alshomrani MK, Alharbi AA, Alshehri AA, Arshad M, Dolgum S (2023) Isolation of Staphylococcus aureus urinary tract infections at a community-based healthcare center in Riyadh. https://doi.org/10.7759/cureus.35140 . Cureus15(2).
Lafon T, Hernandez Padilla AC, Baisse A, Lavaud L, Goudelin M, Barraud O, Daix T, Francois B, Vignon P (2019) Community-acquired Staphylococcus aureus bacteriuria: a warning Microbiological marker for infective endocarditis? BMC Infect Dis 19:1–5. https://doi.org/10.1186/s12879-019-4106-0. (PMID: 10.1186/s12879-019-4106-0)
Lee AS, De Lencastre H, Garau J, Kluytmans J, Malhotra-Kumar S, Peschel A, Harbarth S (2018) Methicillin-resistant Staphylococcus aureus. Nat Rev Dis Primers 4(1):1–23. https://doi.org/10.1038/nrdp.2018.33. (PMID: 10.1038/nrdp.2018.33)
Mason CY, Sobti A, Goodman AL (2023) Staphylococcus aureus bacteriuria: implications and management. JAC-AMR 5(1):dlac123. https://doi.org/10.1093/jacamr/dlac123. (PMID: 10.1093/jacamr/dlac123366444149833284)
Subramaniyan Y, Khan A, Mujeeburahiman M, Rekha P (2024) High incidence of antibiotic resistance in the uropathogenic bacteria associated with different urological diseases and metabolic complications: A single center Cross-Sectional study. MDR 30(6). https://doi.org/10.1089/mdr.2024.0015.
Kim YS, Kim J, Cheon S, Sohn KM (2020) Higher risk for all-cause mortality of Staphylococcus aureus bacteremia in patients with non-dialysis dependent chronic kidney disease. Infect Chemother 52(1):82. https://doi.org/10.3947/ic.2020.52.1.82. (PMID: 10.3947/ic.2020.52.1.82321147227113454)
Biswas D, Pawar N, Patro SK, Krishna NS, Parida D, Bhagtana PK (2022) Clinical profile and spectrum of bacteriuria in patients with diabetes: an analytical study. J Family Med Prim Care 11(6):3190–3195. https://doi.org/10.4103/jfmpc.jfmpc&#95;1779&#95;21. (PMID: 10.4103/jfmpc.jfmpc_1779_21361191739480669)
Alemu M, Belete MA, Gebreselassie S, Belay A, Gebretsadik D (2020) Bacterial profiles and their associated factors of urinary tract infection and detection of extended spectrum beta-lactamase producing gram-negative uropathogens among patients with diabetes mellitus at Dessie referral hospital, Northeastern Ethiopia. Diabetes Metab Syndr Obes 13(2020):2935–2948. https://doi.org/10.2147/DMSO.S262760. (PMID: 10.2147/DMSO.S262760329220547450280)
Govindarajan DK, Kandaswamy K (2022) Virulence factors of uropathogens and their role in host pathogen interactions. Cell Surf 8:100075. https://doi.org/10.1016/j.tcsw.2022.100075. (PMID: 10.1016/j.tcsw.2022.100075351988428841375)
Wu X, Wang H, Xiong J, Yang GX, Hu JF, Zhu Q, Chen Z (2024) Staphylococcus aureus biofilm: formulation, regulatory, and emerging natural products-derived therapeutics. Biofilm 7:100175. https://doi.org/10.1016/j.bioflm.2023.100175. (PMID: 10.1016/j.bioflm.2023.1001753829883210827693)
Paharik AE, Horswill AR (2016) The staphylococcal biofilm: adhesins, regulation, and host response Virulence mechanisms of bacterial pathogens 22:529– 66. https://doi.org/10.1128/9781555819286.ch19.
Liu Y, Zhang J, Ji Y (2020) Environmental factors modulate biofilm formation by Staphylococcus aureus. Sci Prog 103(1):0036850419898659. https://doi.org/10.1177/0036850419898659. (PMID: 10.1177/00368504198986593190233010452756)
Ignatova N, Abidullina A, Streltsova O, Elagin V, Kamensky V (2023) Effect of pH, norepinephrine and glucose on metabolic and biofilm activity of uropathogenic microorganisms. Microorganisms 11(4):862. https://doi.org/10.3390/microorganisms11040862. (PMID: 10.3390/microorganisms110408623711028610146007)
Salari N, Karami MM, Bokaee S, Chaleshgar M, Shohaimi S, Akbari H, Mohammadi M (2022) The prevalence of urinary tract infections in type 2 diabetic patients: a systematic review and meta-analysis. Eur J Med Res 27(1):20. https://doi.org/10.1186/s40001-022-00644-9. (PMID: 10.1186/s40001-022-00644-9351235658817604)
Fernández-Grajera M, Pacha-Olivenza MA, Gallardo-Moreno AM, González-Martín ML, Pérez-Giraldo C, Fernández-Calderón MC (2022) Modification of physico-chemical surface properties and growth of Staphylococcus aureus under hyperglycemia and ketoacidosis conditions. Colloids Surf B Biointerfaces 209:112137. https://doi.org/10.1016/j.colsurfb.2021.112137. (PMID: 10.1016/j.colsurfb.2021.11213734628126)
Zhou C, Fey PD (2020) The acid response network of Staphylococcus aureus. Curr Opin Microbiol 55:67–73. https://doi.org/10.1016/j.mib.2020.03.006. (PMID: 10.1016/j.mib.2020.03.006323614057311314)
Konieczna I, Zarnowiec P, Kwinkowski M, Kolesinska B, Fraczyk J, Kaminski Z, Kaca W (2012) Bacterial urease and its role in long-lasting human diseases. Curr Protein Pept Sci 13(8):789–806. https://doi.org/10.2174/138920312804871094. (PMID: 10.2174/138920312804871094233053653816311)
Zhou C, Bhinderwala F, Lehman MK, Thomas VC, Chaudhari SS, Yamada KJ, Foster KW, Powers R, Kielian T, Fey PD (2019) Urease is an essential component of the acid response network of Staphylococcus aureus and is required for a persistent murine kidney infection. PLoS Pathog 15(1):e1007538. https://doi.org/10.1371/journal.ppat.1007538. (PMID: 10.1371/journal.ppat.1007538306089816343930)
Vandecandelaere I, Van Nieuwerburgh F, Deforce D, Coenye T (2017) Metabolic activity, urease production, antibiotic resistance and virulence in dual species biofilms of Staphylococcus epidermidis and Staphylococcus aureus. PLoS ONE 12(3):e0172700. https://doi.org/10.1371/journal.pone.0172700. (PMID: 10.1371/journal.pone.0172700282639955338783)
Oki K, Washio K, Matsui D, Kato S, Hirata Y, Morikawa M (2010) The role of urease activity on biofilm formation by Staphylococcus Sp. T-02 isolated from the toilet bowl. Biosci Biotechnol Biochem 74(3):583–589. https://doi.org/10.1271/bbb.90796. (PMID: 10.1271/bbb.9079620208338)
Novick RP, Geisinger E (2008) Quorum sensing in Staphylococci. Annu Rev Genet 42(1):541–564. https://doi.org/10.1146/annurev.genet.42.110807.091640. (PMID: 10.1146/annurev.genet.42.110807.09164018713030)
Tan L, Li SR, Jiang B, Hu XM, Li S (2018) Therapeutic targeting of the Staphylococcus aureus accessory gene regulator (agr) system. Front Microbiol 9:55. https://doi.org/10.3389/fmicb.2018.00055. (PMID: 10.3389/fmicb.2018.00055294228875789755)
Polaske TJ, West KH, Zhao K, Widner DL, York JT, Blackwell HE (2023) Chemical and biomolecular insights into the Staphylococcus aureus Agr quorum sensing system: current progress and ongoing challenges. Isr J Chem 63(5–6):e202200096. https://doi.org/10.1002/ijch.202200096. (PMID: 10.1002/ijch.2022000963876579211101167)
Williams P, Hill P, Bonev B, Chan WC (2023) Quorum-sensing, intra-and inter-species competition in the Staphylococci. Microbiol 169(8):001381. https://doi.org/10.1099/mic.0.001381. (PMID: 10.1099/mic.0.001381)
Yamazaki Y, Ito T, Tamai M, Nakagawa S, Nakamura Y (2024) The role of Staphylococcus aureus quorum sensing in cutaneous and systemic infections. Inflamm Regeneration 44(1):9. https://doi.org/10.1186/s41232-024-00323-8. (PMID: 10.1186/s41232-024-00323-8)
He Y, Xue X, Terkeltaub R, Dalbeth N, Merriman TR, Mount DB, Feng Z, Li X, Cui L, Liu Z, Xu Y (2022) Association of acidic urine pH with impaired renal function in primary gout patients: a Chinese population-based cross-sectional study. Arthritis Res Ther 24(1):32. https://doi.org/10.1186/s13075-022-02725-w. (PMID: 10.1186/s13075-022-02725-w350785138787907)
Gehrke AK, Giai C, Gómez MI (2023) Staphylococcus aureus adaptation to the skin in health and persistent/recurrent infections. Antibiotics 12(10):1520. https://doi.org/10.3390/antibiotics12101520. (PMID: 10.3390/antibiotics121015203788722010604630)
Subramaniyan Y, Khan A, Fathima F, Rekha PD (2023) Differential expression of urease genes and ureolytic activity of uropathogenic Escherichia coli and Pseudomonas aeruginosa isolates in different nutritional conditions. Arch Microbiol 205(12):383. https://doi.org/10.1007/s00203-023-03722-6. (PMID: 10.1007/s00203-023-03722-637973630)
Stepanović S, Vuković D, Dakić I, Savić B, Švabić-Vlahović M (2000) A modified microtiter-plate test for quantification of Staphylococcal biofilm formation. J Microbiol Methods 40(2):175–179. https://doi.org/10.1016/S0167-7012(00)00122-6. (PMID: 10.1016/S0167-7012(00)00122-610699673)
Yoon MY, Lee KM, Park Y, Yoon SS (2011) Contribution of cell elongation to the biofilm formation of Pseudomonas aeruginosa during anaerobic respiration. PLoS ONE 6(1):e16105. https://doi.org/10.1371/journal.pone.0016105. (PMID: 10.1371/journal.pone.0016105212674553022656)
Arora NK, Verma M (2017) Modified microplate method for rapid and efficient Estimation of siderophore produced by bacteria. 3 Biotech 7(6):381. https://doi.org/10.1007/s13205-017-1008-y. (PMID: 10.1007/s13205-017-1008-y291099265658296)
Sigurdarson JJ, Svane S, Karring H (2020) Development of a M9-based Urea medium (M9U) for sensitive and real‐time monitoring of ureolytic activity of bacteria and cell‐free Urease. Microbiologyopen 9(3):e976. https://doi.org/10.1002/mbo3.976. (PMID: 10.1002/mbo3.976319439187066460)
Yuvarajan S, Hameed A, Arun AB, Saptami K, Rekha PD (2022) Urease-negative uropathogen Kalamiella piersonii YU22 metabolizes Urea by Urea carboxylase and allophanate hydrolase enzyme system. Microbiol Res 263:127142. https://doi.org/10.1016/j.micres.2022.127142. (PMID: 10.1016/j.micres.2022.12714235940107)
Dastgheyb SS, Otto M (2015) Staphylococcal adaptation to diverse physiologic niches: an overview of transcriptomic and phenotypic changes in different biological environments. Future Microbiol 10(12):1981–1995. https://doi.org/10.2217/fmb.15.116. (PMID: 10.2217/fmb.15.116265842494946774)
Orlandi PF, Fujii N, Roy J, Chen HY, Lee Hamm L, Sondheimer JH, He J, Fischer MJ, Rincon-Choles H, Krishnan G, Townsend R (2018) Hematuria as a risk factor for progression of chronic kidney disease and death: findings from the chronic renal insufficiency cohort (CRIC) study. BMC Nephrol 19:1–1. https://doi.org/10.1186/s12882-018-0951-0. (PMID: 10.1186/s12882-018-0951-0)
Shankar M, Narasimhappa S, Madhura NS (2021) Urinary tract infection in chronic kidney disease population: a clinical observational study. Cureus 13(1). https://doi.org/10.7759/cureus.12486.
Buis DT, van der Vaart TW, Mohan A, Prins JM, van der Meer JT, Bonten MJ, Jakulj L, van Werkhoven CH, Sigaloff KC (2024) Acute kidney injury in Staphylococcus aureus bacteraemia: a recurrent events analysis. Clin Microbiol Infect 30(10):1270–1275. https://doi.org/10.1016/j.cmi.2024.06.017. (PMID: 10.1016/j.cmi.2024.06.01738925460)
Scherberich JE, Fünfstück R, Naber KG (2021) Urinary tract infections in patients with renal insufficiency and dialysis–epidemiology, pathogenesis, clinical symptoms, diagnosis and treatment. GMS Infect Dis 9. https://doi.org/10.3205/id000076.
Suresh S, Naik A, Premanath R (2023) Glucose-induced enhanced virulence in strains of multidrug-resistant Pseudomonas aeruginosa isolated from diabetic patients. Curr Microbiol 80(3):100. https://doi.org/10.1007/s00284-023-03200-8. (PMID: 10.1007/s00284-023-03200-836752926)
Islam MJ, Bagale K, John PP, Kurtz Z, Kulkarni R (2022) Glycosuria alters uropathogenic Escherichia coli global gene expression and virulence. Msphere 7(3):e00004–22. https://doi.org/10.1128/msphere.00004-22. (PMID: 10.1128/msphere.00004-22354773019241551)
Nabaigwa BI, Mwambi B, Okiria J, Oyet C (2018) Common uropathogens among diabetic patients with urinary tract infection at Jinja regional referral hospital, Uganda. Afr J Lab Med 7(1):1–3. https://hdl.handle.net/10520/EJC-caee006fb. (PMID: 10.4102/ajlm.v7i1.621)
He K, Hu Y, Shi JC, Zhu YQ, Mao XM (2018) Prevalence, risk factors and microorganisms of urinary tract infections in patients with type 2 diabetes mellitus: a retrospective study in China. 403–408. Therapeutics and clinical risk management https://doi.org/10.1016/j.tcsw.2022.100075.
Vitko NP, Grosser MR, Khatri D, Lance TR, Richardson AR (2016) Expanded glucose import capability affords Staphylococcus aureus optimized glycolytic flux during infection. MBio 7(3):10–128. https://doi.org/10.1128/mbio.00296-16. (PMID: 10.1128/mbio.00296-16)
Vasiljevs S, Gupta A, Baines D (2023) Effect of glucose on growth and co-culture of Staphylococcus aureus and Pseudomonas aeruginosa in artificial sputum medium. Heliyon 9(11). https://doi.org/10.1016/j.heliyon.2023.e21469.
Pishchany G, McCoy AL, Torres VJ, Krause JC, Crowe JE, Fabry ME, Skaar EP (2010) Specificity for human hemoglobin enhances Staphylococcus aureus infection. Cell Host Microbe 8(6):544–550. https://doi.org/10.1016/j.chom.2010.11.002. (PMID: 10.1016/j.chom.2010.11.002211474683032424)
Pishchany G, Haley KP, Skaar EP (2013) Staphylococcus aureus growth using human hemoglobin as an iron source. JoVE 7(72):e50072. https://doi.org/10.3791/50072. (PMID: 10.3791/50072)
Onyango LA, Alreshidi MM (2018) Adaptive metabolism in Staphylococci: survival and persistence in environmental and clinical settings. J Pathog 2018(1):1092632. https://doi.org/10.1155/2018/1092632. (PMID: 10.1155/2018/1092632303277336171259)
Shannon MR, Zhou B, Perriman AW (2024) Leveraging the power of enzymes in engineered dead and living materials. Adv Funct Mater 2404522. https://doi.org/10.1002/adfm.202404522.
O’Connor MJ, Bartler AV, Ho KC, Zhang K, Casas Fuentes RJ, Melnick BA, Huffman KN, Hong SJ, Galiano RD (2024) Understanding Staphylococcus aureus in hyperglycaemia: A review of virulence factor and metabolic adaptations. Wound Repair Regeneration 32(5):661–670. https://doi.org/10.1111/wrr.13192. (PMID: 10.1111/wrr.1319238853489)
Duran Ramirez JM, Gomez J, Obernuefemann CL, Gualberto NC, Walker JN (2022) Semi-quantitative assay to measure urease activity by urinary catheter-associated uropathogens. Front Cell Infect Microbiol 12:859093. https://doi.org/10.3389/fcimb.2022.859093. (PMID: 10.3389/fcimb.2022.859093353926118980526)
Lade H, Park JH, Chung SH, Kim IH, Kim JM, Joo HS, Kim JS (2019) Biofilm formation by Staphylococcus aureus clinical isolates is differentially affected by glucose and sodium chloride supplemented culture media. J Clin Med 8(11):1853. https://doi.org/10.3390/jcm8111853. (PMID: 10.3390/jcm8111853316841016912320)
Xu K, Wang Y, Jian Y, Chen T, Liu Q, Wang H, Li M, He L (2023) Staphylococcus aureus ST1 promotes persistent urinary tract infection by highly expressing the urease. Front Microbiol 14:1101754. https://doi.org/10.3389/fmicb.2023.1101754. (PMID: 10.3389/fmicb.2023.1101754369102159992547)
Paudel S, Bagale K, Patel S, Kooyers NJ, Kulkarni R (2021) Human urine alters methicillin-resistant Staphylococcus aureus virulence and transcriptome. Appl Environ Microbiol 87(16):e00744–e00721. https://doi.org/10.1128/AEM.00744-21. (PMID: 10.1128/AEM.00744-21341059878315183)
Bore E, Langsrud S, Langsrud Ø, Rode TM, Holck A (2007) Acid-shock responses in Staphylococcus aureus investigated by global gene expression analysis. Microbiology 153(7):2289–2303. https://doi.org/10.1099/mic.0.2007/005942-0. (PMID: 10.1099/mic.0.2007/005942-017600073)
Chen YY, Burne RA (1996) Analysis of Streptococcus salivarius urease expression using continuous Chemostat culture. FEMS Microbiol Lett 135(2–3):223–229. https://doi.org/10.1111/j.1574-6968.1996.tb07993.x. (PMID: 10.1111/j.1574-6968.1996.tb07993.x8595861)
Bury-Moné S, Skouloubris S, Labigne A, De Reuse H (2001) The Helicobacter pylori UreI protein: role in adaptation to acidity and identification of residues essential for its activity and for acid activation. Mol Microbiol 42(4):1021–1034. https://doi.org/10.1046/j.1365-2958.2001.02689.x. (PMID: 10.1046/j.1365-2958.2001.02689.x11737644)
Sharndama HC, Mba IE (2022) Helicobacter pylori: an up-to-date overview on the virulence and pathogenesis mechanisms. Braz J Microbiol 53(1):33–50. https://doi.org/10.1007/s42770-021-00675-0. (PMID: 10.1007/s42770-021-00675-0349889378731681)
Righetto RD, Anton L, Adaixo R, Jakob RP, Zivanov J, Mahi MA, Ringler P, Schwede T, Maier T, Stahlberg H (2020) High-resolution cryo-EM structure of urease from the pathogen Yersinia Enterocolitica. Nat Commun 11(1):5101. https://doi.org/10.1038/s41467-020-18870-2. (PMID: 10.1038/s41467-020-18870-2330372087547064)
Coker C, Poore CA, Li X, Mobley HL (2000) Pathogenesis of proteus mirabilisurinary tract infection. Microbes Infect 2(12):1497–1505. https://doi.org/10.1016/S1286-4579(00)01304-6. (PMID: 10.1016/S1286-4579(00)01304-611099936)
Aust AC, Weigel M, Herrmann JP, Shevchuk O, Engel DR, Dobrindt U, Hain T, Wagenlehner F (2024) Influence of kidney environment parameters on antibiotic efficacy against uropathogenic Escherichia coli. Eur Urol Focus 10(5):742–750. https://doi.org/10.1016/j.euf.2024.07.007. (PMID: 10.1016/j.euf.2024.07.00739089966)
Substance Nomenclature: 0 (Bacterial Proteins)
EC 3.5.1.5 (Urease)
0 (Agr protein, Staphylococcus aureus)
0 (Trans-Activators)
0 (Virulence Factors)
Entry Date(s): Date Created: 20250805 Date Completed: 20250805 Latest Revision: 20251230
Update Code: 20260130
DOI: 10.1007/s00430-025-00830-6
PMID: 40762857
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1432-1831
DOI:10.1007/s00430-025-00830-6