Sharma Garima, Rao Saloni, Bansal Ankiti, Dang Shweta, Gupta Sanjay, Gabrani Reema
Department of Biotechnology, Jaypee Institute of Information Technology, A-10, Sector-62, Noida 201307, India.
Department of Biotechnology, Jaypee Institute of Information Technology, A-10, Sector-62, Noida 201307, India.
Biologicals. 2014 Jan;42(1):1-7. doi: 10.1016/j.biologicals.2013.11.001. Epub 2013 Dec 3.
Pseudomonas aeruginosa is a gram-negative pathogen that has become an important cause of infection, especially in patients with compromised host defense mechanisms. It is frequently related to nosocomial infections such as pneumonia, urinary tract infections (UTIs) and bacteremia. The biofilm formed by the bacteria allows it to adhere to any surface, living or non-living and thus Pseudomonal infections can involve any part of the body. Further, the adaptive and genetic changes of the micro-organisms within the biofilm make them resistant to all known antimicrobial agents making the Pseudomonal infections complicated and life threatening. Pel, Psl and Alg operons present in P. aeruginosa are responsible for the biosynthesis of extracellular polysaccharide which plays an important role in cell-cell and cell-surface interactions during biofilm formation. Understanding the bacterial virulence which depends on a large number of cell-associated and extracellular factors is essential to know the potential drug targets for future studies. Current novel methods like small molecule based inhibitors, phytochemicals, bacteriophage therapy, photodynamic therapy, antimicrobial peptides, monoclonal antibodies and nanoparticles to curtail the biofilm formed by P. aeruginosa are being discussed in this review.
铜绿假单胞菌是一种革兰氏阴性病原体,已成为感染的重要原因,尤其是在宿主防御机制受损的患者中。它经常与医院感染有关,如肺炎、尿路感染(UTIs)和菌血症。细菌形成的生物膜使其能够粘附在任何表面,无论是有生命的还是无生命的,因此铜绿假单胞菌感染可累及身体的任何部位。此外,生物膜内微生物的适应性和基因变化使其对所有已知抗菌药物产生耐药性,从而使铜绿假单胞菌感染变得复杂且危及生命。铜绿假单胞菌中存在的Pel、Psl和Alg操纵子负责细胞外多糖的生物合成,这在生物膜形成过程中的细胞间和细胞表面相互作用中起着重要作用。了解依赖于大量细胞相关和细胞外因素的细菌毒力对于确定未来研究的潜在药物靶点至关重要。本文综述了目前用于抑制铜绿假单胞菌形成生物膜的新方法,如基于小分子的抑制剂、植物化学物质、噬菌体疗法、光动力疗法、抗菌肽、单克隆抗体和纳米颗粒。