Biofilm formation mechanisms and targets for developing antibiofilm agents

被引:47
作者
Rabin, Nira [1 ]
Zheng, Yue [1 ]
Opoku-Temeng, Clement [1 ]
Du, Yixuan [1 ]
Bonsu, Eric [2 ]
Sintim, Herman O. [1 ]
机构
[1] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[2] Bowie State Univ, Dept Nat Sci, Bowie, MD 20715 USA
基金
美国国家科学基金会;
关键词
C-DI-GMP; ANTIMICROBIAL PEPTIDE RESISTANCE; INITIAL DENTAL BIOFILM; PSEUDOMONAS-AERUGINOSA; CYSTIC-FIBROSIS; STAPHYLOCOCCUS-EPIDERMIDIS; ESCHERICHIA-COLI; CYCLIC DIGUANYLATE; CELLULOSE SYNTHESIS; BACTERIAL BIOFILMS;
D O I
10.4155/FMC.15.6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Biofilms are communities of microorganisms that are attached to a surface and play a significant role in the persistence of bacterial infections. Bacteria within a biofilm are several orders of magnitude more resistant to antibiotics, compared with planktonic bacteria. Thus far, no drugs are in clinical use that specifically target bacterial biofilms. This is probably because until recently the molecular details of biofilm formation were poorly understood. Bacteria integrate information from the environment, such as quorum-sensing autoinducers and nutrients, into appropriate biofilm-related gene expression, and the identity of the key players, such as cyclic dinucleotide second messengers and regulatory RNAs are beginning to be uncovered. Herein, we highlight the current understanding of the processes that lead to biofilm formation in many bacteria.
引用
收藏
页码:493 / 512
页数:20
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