Department of Molecular, Cell and Systems Biology, University of California, Riverside, CA, USA.
Department of Chemistry, University of California, Riverside, CA, USA.
J Diabetes Res. 2020 Jan 27;2020:9589507. doi: 10.1155/2020/9589507. eCollection 2020.
Chronic wounds are a major global health problem with the presence of biofilm significantly contributing to wound chronicity. Current treatments are ineffective in resolving biofilm and simultaneously killing the bacteria; therefore, effective biofilm-resolving drugs are needed. We have previously shown that, together with -tocopherol, -acetyl-cysteine (NAC) significantly improves the healing of biofilm-containing chronic wounds, in a diabetic mouse model we developed, by causing disappearance of the bacteria and breakdown of the extracellular polymeric substance (EPS). We hypothesize that NAC creates a microenvironment that affects bacterial survival and EPS integrity. To test this hypothesis, we developed an biofilm system using microbiome taken directly from diabetic mouse chronic wounds. For these studies, we chose mice in which chronic wound microbiome was rich in (97%). We show that NAC at concentrations with pH < pKa causes bacterial cell death and breakdown of EPS. When used before biofilm is formed, NAC leads to bacterial cell death whereas treatment after the biofilm is established NAC causes biofilm dismantling accompanied by bacterial cell death. Mechanistically, we show that NAC can penetrate the bacterial membrane, increase oxidative stress, and halt protein synthesis. We also show that low pH is important for the actions of NAC and that bacterial death occurs independently of the presence of biofilm. In addition, we show that both the acetyl and carboxylic groups play key roles in NAC functions. The results presented here provide insight into the mechanisms by which NAC dismantles biofilm and how it could be used to treat chronic wounds after debridement (NAC applied at the start of culture) or without debridement (NAC applied when biofilm is already formed). This approach can be taken to develop biofilm from microbiome taken directly from human chronic wounds to test molecules that could be effective for the treatment of specific biofilm compositions.
慢性伤口是一个全球性的主要健康问题,生物膜的存在显著促进了伤口的慢性化。目前的治疗方法在解决生物膜和同时杀死细菌方面效果不佳;因此,需要有效的生物膜溶解药物。我们之前已经表明,-生育酚和 -乙酰半胱氨酸(NAC)一起显著改善了我们在糖尿病小鼠模型中开发的含生物膜的慢性伤口的愈合,方法是使细菌消失和细胞外聚合物质(EPS)分解。我们假设 NAC 会创造一个影响细菌存活和 EPS 完整性的微环境。为了验证这一假设,我们使用直接从糖尿病小鼠慢性伤口中提取的微生物组开发了一种生物膜系统。对于这些研究,我们选择了慢性伤口微生物组富含 (97%)的小鼠。我们表明,NAC 在 pH < pKa 的浓度下会导致细菌细胞死亡和 EPS 分解。当在生物膜形成之前使用 NAC 时,会导致细菌细胞死亡,而在生物膜形成后使用 NAC 时,会导致生物膜解体并伴有细菌细胞死亡。从机制上讲,我们表明 NAC 可以穿透细菌膜,增加氧化应激并停止蛋白质合成。我们还表明,低 pH 对 NAC 的作用很重要,并且细菌死亡与生物膜的存在无关。此外,我们表明乙酰基和羧酸基在 NAC 功能中都起着关键作用。这里呈现的结果提供了关于 NAC 如何分解生物膜的机制的见解,以及如何在清创后(在培养开始时应用 NAC)或在没有清创的情况下(当生物膜已经形成时应用 NAC)将其用于治疗慢性伤口。这种方法可以用来从直接取自人类慢性伤口的微生物组中开发生物膜,以测试可能对治疗特定生物膜组成有效的分子。