NO donors and NO delivery methods for controlling biofilms in chronic lung infections

被引:14
|
作者
Cai, Yu-Ming [1 ]
Zhang, Ying-Dan [2 ]
Yang, Liang [2 ]
机构
[1] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
[2] Southern Univ Sci & Technol, Sch Med, Shenzhen 518000, Peoples R China
关键词
Nitric oxide; Biofilm; Chronic lung infection; Pseudomonas aeruginosa; NITRIC-OXIDE-DONOR; PRIMARY CILIARY DYSKINESIA; PSEUDOMONAS-AERUGINOSA INFECTION; CYCLIC-DI-GMP; PERSISTENT PULMONARY-HYPERTENSION; CYSTIC-FIBROSIS PATIENTS; FUROXAN DERIVATIVES; LINSIDOMINE CHLORHYDRATE; NITROGLYCERIN TOLERANCE; ALDEHYDE DEHYDROGENASE;
D O I
10.1007/s00253-021-11274-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nitric oxide (NO), the highly reactive radical gas, provides an attractive strategy in the control of microbial infections. NO not only exhibits bactericidal effect at high concentrations but also prevents bacterial attachment and disperses biofilms at low, nontoxic concentrations, rendering bacteria less tolerant to antibiotic treatment. The endogenously generated NO by airway epithelium in healthy populations significantly contributes to the eradication of invading pathogens. However, this pathway is often compromised in patients suffering from chronic lung infections where biofilms dominate. Thus, exogenous supplementation of NO is suggested to improve the therapeutic outcomes of these infectious diseases. Compared to previous reviews focusing on the mechanism of NO-mediated biofilm inhibition, this review explores the applications of NO for inhibiting biofilms in chronic lung infections. It discusses how abnormal levels of NO in the airways contribute to chronic infections in cystic fibrosis (CF), chronic obstructive pulmonary disease (COPD), and primary ciliary dyskinesia (PCD) patients and why exogenous NO can be a promising antibiofilm strategy in clinical settings, as well as current and potential in vivo NO delivery methods.
引用
收藏
页码:3931 / 3954
页数:24
相关论文
共 50 条
  • [41] New opportunities for managing acute and chronic lung infections
    William O. C. M. Cookson
    Michael J. Cox
    Miriam F. Moffatt
    Nature Reviews Microbiology, 2018, 16 : 111 - 120
  • [42] The Role of Bacterial Biofilms in Chronic Infectious Processes and the Search for Methods to Combat Them
    Ilyina, T. S.
    Romanova, Yu. M.
    MOLECULAR GENETICS MICROBIOLOGY AND VIROLOGY, 2021, 36 (02) : 68 - 78
  • [43] The Role of Bacterial Biofilms in Chronic Infectious Processes and the Search for Methods to Combat Them
    T. S. Ilyina
    Yu. M. Romanova
    Molecular Genetics, Microbiology and Virology, 2021, 36 : 68 - 78
  • [44] Chronic ethanol ingestion by donors predisposes the lung to injury in a rat model of lung transplantation.
    Mitchell, P. O.
    Guidot, D. M.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2006, 30 (06) : 224A - 224A
  • [45] An expert opinion on respiratory delivery of high dose powders for lung infections
    Adhikari, Bishal Raj
    Dummer, Jack
    Gordon, Keith C.
    Das, Shyamal C.
    EXPERT OPINION ON DRUG DELIVERY, 2022, 19 (07) : 795 - 813
  • [46] Controlling chronic Pseudomonas aeruginosa infections by strategically interfering with the sensory function of SagS
    Dingemans, Jozef
    Al-Feghali, Rebecca E.
    Lau, Gee W.
    Sauer, Karin
    MOLECULAR MICROBIOLOGY, 2019, 111 (05) : 1211 - 1228
  • [48] VIRAL AND MYCOPLASMA PNEUMONIAE INFECTIONS IN EXACERBATIONS OF CHRONIC LUNG DISEASE
    MCNAMARA, MJ
    PHILLIPS, IA
    WILLIAMS, OB
    AMERICAN REVIEW OF RESPIRATORY DISEASE, 1969, 100 (01): : 19 - &
  • [49] A LIVE BIOTHERAPEUTIC TO TREAT CHRONIC PSEUDOMONAS AERUGINOSA LUNG INFECTIONS
    Mucha, J.
    Twomey, D.
    Cann, A.
    Hardy, J.
    PEDIATRIC PULMONOLOGY, 2017, 52 : S375 - S375
  • [50] Noninvasive methods for detection of chronic lung allograft dysfunction in lung transplantation
    Tian, Dong
    Huang, Heng
    Wen, Hong-Ying
    TRANSPLANTATION REVIEWS, 2020, 34 (03)