Targeting biofilms using phages and their enzymes

被引:72
作者
Azeredo, Joana [1 ]
Garcia, Pilar [2 ]
Drulis-Kawa, Zuzanna [3 ]
机构
[1] Univ Minho, Ctr Engn Biol, Campus Gualtar, P-4710057 Braga, Portugal
[2] Inst Prod Lacteos Asturias IPLA CSIC, Paseo Rio Linares S-N, Villaviciosa 33300, Asturias, Spain
[3] Univ Wroclaw, Inst Genet & Microbiol, Dept Pathogen Biol & Immunol, Przybyszewskiego 63-77, PL-51148 Wroclaw, Poland
基金
欧盟地平线“2020”;
关键词
EXTRACELLULAR DNA; BACTERIAL; RESISTANCE; FORM; BACTERIOPHAGES; MECHANISMS; ENDOLYSINS; TOLERANCE; BARRIERS; THERAPY;
D O I
10.1016/j.copbio.2021.02.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The complex biofilm architecture composed of extracellular polymeric structures (EPS) provides a protective shield to physiologically diverse bacterial cells immersed in its structure. The evolutionary interplay between bacteria and their viruses (phages) forced the latter ones to develop specific strategies to overcome the biofilm defensive barriers and kill sessile cells. Phages are equipped with a wide panel of enzyme-degrading EPS macromolecules which together are powerful weapons to combat biofilms. Antibiofilm performance can be achieved by combining phages or phage-borne enzymes with other antimicrobials such as antibiotics. Nevertheless, a variety of enzymes encoded in phage genomes still need to be explored. To advance in biofilm control strategies we must deepen the understanding of the biofilm biology itself, as well as discover and better exploit the unlimited antibacterial potential of phages.
引用
收藏
页码:251 / 261
页数:11
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