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本文引用的文献

1
Transposon mutagenesis identifies uropathogenic Escherichia coli biofilm factors.转座子突变体技术鉴定泌尿道致病性大肠杆菌生物膜形成相关因子。
J Bacteriol. 2012 Nov;194(22):6195-205. doi: 10.1128/JB.01012-12. Epub 2012 Sep 14.
2
Antibiofilm polysaccharides.抗菌黏附多糖。
Environ Microbiol. 2013 Feb;15(2):334-46. doi: 10.1111/j.1462-2920.2012.02810.x. Epub 2012 Jun 26.
3
A self-produced trigger for biofilm disassembly that targets exopolysaccharide.一种针对胞外多糖的生物膜分解自产生触发物。
Cell. 2012 Apr 27;149(3):684-92. doi: 10.1016/j.cell.2012.02.055.
4
Treatment and prevention of urinary tract infection with orally active FimH inhibitors.口服 FimH 抑制剂治疗和预防尿路感染。
Sci Transl Med. 2011 Nov 16;3(109):109ra115. doi: 10.1126/scitranslmed.3003021.
5
Escherichia coli BdcA controls biofilm dispersal in Pseudomonas aeruginosa and Rhizobium meliloti.大肠杆菌BdcA控制铜绿假单胞菌和苜蓿根瘤菌中的生物膜分散。
BMC Res Notes. 2011 Oct 26;4:447. doi: 10.1186/1756-0500-4-447.
6
The two-component QseBC signalling system regulates in vitro and in vivo virulence of Aeromonas hydrophila.双组分 QseBC 信号系统调控嗜水气单胞菌的体外和体内毒力。
Microbiology (Reading). 2012 Jan;158(Pt 1):259-271. doi: 10.1099/mic.0.051805-0. Epub 2011 Oct 13.
7
Fimbrial profiles predict virulence of uropathogenic Escherichia coli strains: contribution of ygi and yad fimbriae.菌毛图谱预测泌尿道致病性大肠杆菌菌株的毒力:ygi 和 yad 菌毛的作用。
Infect Immun. 2011 Dec;79(12):4753-63. doi: 10.1128/IAI.05621-11. Epub 2011 Sep 12.
8
Bacteriophage therapy: potential uses in the control of antibiotic-resistant pathogens.噬菌体疗法:在控制抗生素耐药性病原体中的潜在应用。
Expert Rev Anti Infect Ther. 2011 Sep;9(9):775-85. doi: 10.1586/eri.11.90.
9
The activity of a small lytic peptide PTP-7 on Staphylococcus aureus biofilms.小裂解肽 PTP-7 对金黄色葡萄球菌生物膜的活性。
J Microbiol. 2011 Aug;49(4):663-8. doi: 10.1007/s12275-011-1013-5. Epub 2011 Sep 2.
10
The whole is greater than the sum of its parts: dental plaque bacterial interactions can affect the virulence properties of cariogenic Streptococcus mutans.整体大于部分之和:牙菌斑中的细菌相互作用会影响致龋变形链球菌的毒力特性。
Am J Dent. 2011 Jun;24(3):153-4.

细菌生物膜:后抗生素时代的发展、传播和治疗策略。

Bacterial biofilms: development, dispersal, and therapeutic strategies in the dawn of the postantibiotic era.

机构信息

Department of Molecular Microbiology and Microbial Pathogenesis, Washington University in Saint Louis School of Medicine, St. Louis, MO 63110-1010, USA.

出版信息

Cold Spring Harb Perspect Med. 2013 Apr 1;3(4):a010306. doi: 10.1101/cshperspect.a010306.

DOI:10.1101/cshperspect.a010306
PMID:23545571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3683961/
Abstract

Biofilm formation constitutes an alternative lifestyle in which microorganisms adopt a multicellular behavior that facilitates and/or prolongs survival in diverse environmental niches. Biofilms form on biotic and abiotic surfaces both in the environment and in the healthcare setting. In hospital wards, the formation of biofilms on vents and medical equipment enables pathogens to persist as reservoirs that can readily spread to patients. Inside the host, biofilms allow pathogens to subvert innate immune defenses and are thus associated with long-term persistence. Here we provide a general review of the steps leading to biofilm formation on surfaces and within eukaryotic cells, highlighting several medically important pathogens, and discuss recent advances on novel strategies aimed at biofilm prevention and/or dissolution.

摘要

生物膜的形成是一种替代生活方式,其中微生物采取多细胞行为,有助于和/或延长在各种环境小生境中的生存。生物膜在环境和医疗保健环境中的生物和非生物表面上形成。在医院病房中,通风口和医疗设备上生物膜的形成使病原体能够作为储层持续存在,并且很容易传播给患者。在宿主内部,生物膜使病原体能够颠覆先天免疫防御,因此与长期存在相关。在这里,我们提供了一个关于表面和真核细胞内生物膜形成的一般综述,重点介绍了几种具有重要医学意义的病原体,并讨论了旨在预防和/或溶解生物膜的新策略的最新进展。