N-acetylcysteine prevents catheter occlusion and inflammation in catheter associated-urinary tract infections by suppressing urease activity

被引:5
作者
Manoharan, Arthika [1 ,2 ]
Farrell, Jessica [1 ,3 ]
Aldilla, Vina R. [4 ]
Whiteley, Greg [1 ,3 ,5 ]
Kriel, Erik [3 ]
Glasbey, Trevor [3 ]
Kumar, Naresh [4 ]
Moore, Kate H. [6 ]
Manos, Jim [1 ,2 ]
Das, Theerthankar [1 ,2 ,7 ]
机构
[1] Univ Sydney, Charles Perkins Ctr, Sch Med Sci, Infect Immun & Inflammat Theme, Sydney, NSW, Australia
[2] Univ Sydney, Sydney Inst Infect Dis, Sydney, NSW, Australia
[3] Whiteley Corp, Tomago, NSW, Australia
[4] Univ New South Wales, Sch Chem, Sydney, NSW, Australia
[5] Western Sydney Univ, Sch Med, Sydney, NSW, Australia
[6] Univ New South Wales, St George Hosp, Dept Urogynaecol, Sydney, NSW, Australia
[7] Western Sydney Univ, Ingham Inst, Sch Med, Microbiol & Infect Dis, Sydney, NSW, Australia
来源
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY | 2023年 / 13卷
关键词
Proteus mirabilis; UTI; catheter-associated urinary tract infections (CA-UTI); N-acetyl cysteine (NAC); urease; biofilms; PROTEUS-MIRABILIS UREASE; BACTERIAL ADHERENCE; BIOFILMS; CYSTEINE; INDIVIDUALS; BACTEREMIA;
D O I
10.3389/fcimb.2023.1216798
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Proteus mirabilis is a key pathobiont in catheter-associated urinary tract infections (CA-UTIs), which is well known to form crystalline biofilms that occlude catheters. Urease activity alkylates urine through the release of ammonia, consequentially resulting in higher levels of Mg2+ and Ca2+ and formation of crystals. In this study, we showed that N-acetyl cysteine (NAC), a thiol antioxidant, is a potent urease inhibitor that prevents crystalline biofilm formation.Methods: To quantify urease activity, Berthelot's method was done on bacterial extracts treated with NAC. We also used an in vitro catheterised glass bladder model to study the effect of NAC treatment on catheter occlusion and biofilm encrustation in P. mirabilis infections. Inductively-coupled plasma mass spectrometry (ICP-MS) was performed on catheter samples to decipher elemental profiles.Results: NAC inhibits urease activity of clinical P. mirabilis isolates at concentrations as low as 1 mM, independent of bacterial killing. The study also showed that NAC is bacteriostatic on P. mirabilis, and inhibited biofilm formation and catheter occlusion in an in vitro. A significant 4-8(log10) reduction in viable bacteria was observed in catheters infected in this model. Additionally, biofilms in NAC treated catheters displayed a depletion of calcium, magnesium, or phosphates (>10 fold reduction), thus confirming the absence of any urease activity in the presence of NAC. Interestingly, we also showed that not only is NAC anti-inflammatory in bladder epithelial cells (BECs), but that it mutes its inflammatory response to urease and P. mirabilis infection by reducing the production of IL-6, IL-8 and IL-1b.Discussion: Using biochemical, microbiological and immunological techniques, this study displays the functionality of NAC in preventing catheter occlusion by inhibiting urease activity. The study also highlights NAC as a strong anti-inflammatory antibiofilm agent that can target both bacterial and host factors in the treatment of CA-UTIs.
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页数:19
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共 60 条
  • [1] Inhibition of Urease Enzyme Production and some Other Virulence Factors Expression in Proteus mirabilis by N-Acetyl Cysteine and Dipropyl Disulphide
    Abdel-Baky, Rehab Mahmoud
    Ali, Mohamed Abdullah
    Abuo-Rahma, Gamal El-Din Ali A.
    AbdelAziz, Neveen
    [J]. ADVANCES IN MICROBIOLOGY, INFECTIOUS DISEASES AND PUBLIC HEALTH, VOL 7, 2017, 973 : 99 - 113
  • [2] Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance
    Aiyer, Aditi
    Visser, Simone K.
    Bye, Peter
    Britton, Warwick J.
    Whiteley, Gregory S.
    Glasbey, Trevor
    Kriel, Frederik H.
    Farrell, Jessica
    Das, Theerthankar
    Manos, Jim
    [J]. ANTIBIOTICS-BASEL, 2021, 10 (10):
  • [3] THE ROLE OF SWARM CELL-DIFFERENTIATION AND MULTICELLULAR MIGRATION IN THE UROPATHOGENICITY OF PROTEUS-MIRABILIS
    ALLISON, C
    EMODY, L
    COLEMAN, N
    HUGHES, C
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (05) : 1155 - 1158
  • [4] Armbruster CE., 2018, ECOSAL PLUS, V8, DOI DOI 10.1128/ECOSALPLUS.ESP-0009-2017
  • [5] The Pathogenic Potential of Proteus mirabilis Is Enhanced by Other Uropathogens during Polymicrobial Urinary Tract Infection
    Armbruster, Chelsie E.
    Smith, Sara N.
    Johnson, Alexandra O.
    DeOrnellas, Valerie
    Eaton, Kathryn A.
    Yep, Alejandra
    Mody, Lona
    Wu, Weisheng
    Mobley, Harry L. T.
    [J]. INFECTION AND IMMUNITY, 2017, 85 (02)
  • [6] Increased Incidence of Urolithiasis and Bacteremia During Proteus mirabilis and Providencia stuartii Coinfection Due to Synergistic Induction of Urease Activity
    Armbruster, Chelsie E.
    Smith, Sara N.
    Yep, Alejandra
    Mobley, Harry L. T.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2014, 209 (10) : 1524 - 1532
  • [7] The effect of N-acetylcysteine on biofilms: Implications for the treatment of respiratory tract infections
    Blasi, Francesco
    Page, Clive
    Rossolini, Gian Maria
    Pallecchi, Lucia
    Matera, Maria Gabriella
    Rogliani, Paola
    Cazzola, Mario
    [J]. RESPIRATORY MEDICINE, 2016, 117 : 190 - 197
  • [8] A simple artificial urine for the growth of urinary pathogens
    Brooks, T
    Keevil, CW
    [J]. LETTERS IN APPLIED MICROBIOLOGY, 1997, 24 (03) : 203 - 206
  • [9] Immunomodulation therapy offers new molecular strategies to treat UTI
    Butler, Daniel
    Ambite, Ines
    Wan, Murphy Lam Yim
    Tran, Thi Hien
    Wullt, Bjorn
    Svanborg, Catharina
    [J]. NATURE REVIEWS UROLOGY, 2022, 19 (07) : 419 - 437
  • [10] BRENDA, the ELIXIR core data resource in 2021: new developments and updates
    Chang, Antje
    Jeske, Lisa
    Ulbrich, Sandra
    Hofmann, Julia
    Koblitz, Julia
    Schomburg, Ida
    Neumann-Schaal, Meina
    Jahn, Dieter
    Schomburg, Dietmar
    [J]. NUCLEIC ACIDS RESEARCH, 2021, 49 (D1) : D498 - D508