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Mode-of-Action Studies of the Novel Bisquaternary Bisnaphthalimide MT02 against Staphylococcus aureus

机译:新型双季双萘二甲酰亚胺MT02对抗金黄色葡萄球菌的作用方式研究

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摘要

Screening of various bisquaternary bisnaphthalimides against a variety of human pathogens revealed one compound, designated MT02, with strong inhibitory effects against Gram-positive bacteria. The MICs ranged from 0.31 μg/ml against community-acquired methicillin-resistant Staphylococcus aureus (MRSA) lineage USA300 to 20 μg/ml against Streptococcus pneumoniae. Radioactive whole-cell labeling experiments indicated a strong impact of MT02 on bacterial DNA replication. DNA microarray studies generated a transcriptional signature characterized by stronger expression of genes involved in DNA metabolism, DNA replication, SOS response, and transport of positively charged compounds. Furthermore, surface plasmon resonance and gel retardation experiments demonstrated direct binding of MT02 to DNA in a concentration-dependent, reversible, and non-sequence-specific manner. The data presented suggest that the bisquaternary bisnaphthalimide MT02 exerts anti-Gram-positive activity by binding to DNA and thereby preventing appropriate DNA replication.
机译:对各种人类病原体的各种双季双萘二甲酰亚胺的筛选显示了一种名为MT02的化合物,对革兰氏阳性细菌具有很强的抑制作用。 MIC范围从针对社区获得的耐甲氧西林金黄色葡萄球菌(MRSA)美国USA300的0.31μg/ ml到针对肺炎链球菌的20μg/ ml。放射性全细胞标记实验表明MT02对细菌DNA复制有强烈影响。 DNA微阵列研究产生了一种转录特征,其特征在于与DNA代谢,DNA复制,SOS反应和带正电荷的化合物运输有关的基因表达更强。此外,表面等离振子共振和凝胶阻滞实验表明,MT02以浓度依赖性,可逆性和非序列特异性方式与DNA直接结合。所提供的数据表明,双季双萘二甲酰亚胺MT02通过与DNA结合而发挥抗革兰氏阳性活性,从而阻止了适当的DNA复制。

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