Tomusiak-Plebanek Anna, Kozień Łucja, Gallienne Estelle, Florczyk Maciej, Ciesielski Sławomir, Heczko Piotr, Strus Magdalena
Chair of Microbiology, Department of Bacteriology and Parasitology, Jagiellonian University Medical College, 31-121 Krakow, Poland.
Institut de Chimie Organique et Analytique (ICOA), UMR 7311, Université d'Orléans & CNRS, 45067 Orleans, France.
Antibiotics (Basel). 2025 Jul 1;14(7):668. doi: 10.3390/antibiotics14070668.
Iminosugars are natural or synthetic sugar analogues with a very broad spectrum of activities, including those against the most prominent bacterial pathogens, like or In a series of studies, we have demonstrated that one of the synthetic iminosugars, PDIA (beta-1-C-propyl-1,4-dideoxy-1,4-imino-L-arabinitol), possesses the ability to suppress biofilm production by different pathogenic bacteria without inhibiting their growth. Thereby, PDIA is able to influence experimental skin infection caused by . To elucidate molecular mechanisms by which PDIA impedes biofilm formation by , a transcriptomic study was performed in which a biofilm-producing strain was grown in the presence of PDIA for 24 and 48 h in comparison to a control without the iminosugar. The RNA was then isolated, converted into cDNA, sequenced, and data analysis was performed. It appeared that PDIA caused the down-regulation of many bacteriophage genes responsible for the processes of bacterial cell lysis, and some genes responsible for cell wall degradation were also down-regulated. Among the 25 most upregulated genes were those representing the phosphotransferase system (PTS), which is required for carbohydrate uptake and control of carbon metabolism. The ranking of the most significant down-regulated genes after 24 h exposure to PDIA shows that they predominantly coded for both the synthesis and lysis of the peptidoglycan. We have shown here that the influence of PDIA on the expression of genes is broad and affects many genes encoding metabolism and ribosomes.
亚氨基糖是天然或合成的糖类似物,具有非常广泛的活性,包括对最主要的细菌病原体的活性,如 或 。在一系列研究中,我们已经证明,一种合成亚氨基糖PDIA(β-1-C-丙基-1,4-二脱氧-1,4-亚氨基-L-阿拉伯糖醇)具有抑制不同病原菌生物膜形成的能力,而不抑制其生长。因此,PDIA能够影响由 引起的实验性皮肤感染。为了阐明PDIA阻碍 生物膜形成的分子机制,进行了一项转录组学研究,其中将产生生物膜的 菌株在有PDIA的情况下培养24小时和48小时,并与没有亚氨基糖的对照进行比较。然后分离RNA,转化为cDNA,进行测序并进行数据分析。结果表明,PDIA导致许多负责细菌细胞裂解过程的噬菌体基因下调,一些负责细胞壁降解的基因也下调。在25个上调最显著的基因中,有代表磷酸转移酶系统(PTS)的基因,碳水化合物摄取和碳代谢控制需要该系统。暴露于PDIA 24小时后下调最显著的基因排名表明,它们主要编码肽聚糖的合成和裂解。我们在此表明,PDIA对 基因表达的影响广泛,影响许多编码代谢和核糖体的基因。