Kozień Łucja, Gallienne Estelle, Martin Olivier, Front Sophie, Strus Magdalena, Heczko Piotr
Department of Bacteriology, Microbial Ecology and Parasitology, Chair of Microbiology, Jagiellonian University Medical College, 31-121 Cracow, Poland.
Institut de Chimie Organique et Analytique (ICOA), UMR 7311, Université d'Orléans & CNRS, rue de Chartres, BP 6759, CEDEX 2, 45067 Orléans, France.
Microorganisms. 2022 Jun 15;10(6):1222. doi: 10.3390/microorganisms10061222.
Many difficult-to-treat human infections related to catheters and other indwelling devices are caused by bacteria residing in biofilms. One of the key properties of microorganisms residing in a biofilm is decreased susceptibility towards antimicrobial agents. Therefore, many different approaches have been researched to destroy or inhibit biofilm production by bacteria. Different iminosugars (IS) were reported to inhibit biofilm formation in , and . The aim of this study was to look for a spectrum of the activity in one of these IS. The iminosugar PDIA beta-1-C-propyl-1,4-dideoxy-1,4-imino-L-arabinitol was tested in vitro at the same concentration against 30 different strains of the most important Gram-negative and Gram-positive human pathogens looking for their biofilm production and viability at different time intervals. It appeared that PDIA inhibited biofilm production of spp., , spp. and in 8 h, and spp., spp. and in 24 h. PDIA caused no growth inhibition of the tested bacteria at a concentration of 0.9 mM. Our results indicate a broad-spectrum biofilm inhibitory activity of PDIA. which may be the basis for future application studies that will help in control of the associated device and biofilm-related infections caused by a wide spectrum of the causative agents.
许多与导管及其他植入性器械相关的难以治疗的人类感染是由生物膜中的细菌引起的。存在于生物膜中的微生物的一个关键特性是对抗菌剂的敏感性降低。因此,人们研究了许多不同的方法来破坏或抑制细菌产生生物膜。据报道,不同的亚氨基糖(IS)在[具体文献1]、[具体文献2]和[具体文献3]中可抑制生物膜形成。本研究的目的是探寻其中一种亚氨基糖的活性谱。亚氨基糖PDIAβ-1-C-丙基-1,4-二脱氧-1,4-亚氨基-L-阿拉伯糖醇在体外以相同浓度针对30种不同的革兰氏阴性和革兰氏阳性人类重要病原体菌株进行测试,以寻找它们在不同时间间隔的生物膜产生情况和生存能力。结果显示,PDIA在8小时内可抑制[具体菌株1]、[具体菌株2]、[具体菌株3]和[具体菌株4]的生物膜产生,在24小时内可抑制[具体菌株5]、[具体菌株6]和[具体菌株7]的生物膜产生。在浓度为0.9 mM时,PDIA对受试细菌没有生长抑制作用。我们的结果表明PDIA具有广谱生物膜抑制活性,这可能为未来的应用研究奠定基础,有助于控制由多种病原体引起的相关器械及生物膜相关感染。