Department of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, Oklahoma, USA.
Department of Chemistry and Biochemistry, Missouri State University, Springfield, Missouri, USA.
Microbiol Spectr. 2024 Jun 4;12(6):e0423423. doi: 10.1128/spectrum.04234-23. Epub 2024 Apr 23.
Antimicrobial resistance (AMR) poses a significant worldwide public health crisis that continues to threaten our ability to successfully treat bacterial infections. With the decline in effectiveness of conventional antimicrobial therapies and the lack of new antibiotic pipelines, there is a renewed interest in exploring the potential of metal-based antimicrobial compounds. Antimony-based compounds with a long history of use in medicine have re-emerged as potential antimicrobial agents. We previously synthesized a series of novel organoantimony(V) compounds complexed with cyanoximates with a strong potential of antimicrobial activity against several AMR bacterial and fungal pathogens. Here, five selected compounds were studied for their antibacterial efficacy against three important bacterial pathogens: , , and . Among five tested compounds, SbPhACO showed antimicrobial activity against all three bacterial strains with the MIC of 50-100 µg/mL. The minimum bactericidal concentration/MIC values were less than or equal to 4 indicating that the effects of SbPhACO are bactericidal. Moreover, ultra-thin electron microscopy revealed that SbPhACO treatment caused membrane disruption in all three strains, which was further validated by increased membrane permeability. We also showed that SbPhACO acted synergistically with the antibiotics, polymyxin B and cefoxitin used to treat AMR strains of and , respectively, and that at synergistic MIC concentration 12.5 µg/mL, its cytotoxicity against the cell lines, Hela, McCoy, and A549 dropped below the threshold. Overall, the results highlight the antimicrobial potential of novel antimony-based compound, SbPhACO, and its use as a potentiator of other antibiotics against both Gram-positive and Gram-negative bacterial pathogens.
Antibiotic resistance presents a critical global public health crisis that threatens our ability to combat bacterial infections. In light of the declining efficacy of traditional antibiotics, the use of alternative solutions, such as metal-based antimicrobial compounds, has gained renewed interest. Based on the previously synthesized innovative organoantimony(V) compounds, we selected and further characterized the antibacterial efficacy of five of them against three important Gram-positive and Gram-negative bacterial pathogens. Among these compounds, SbPhACO showed broad-spectrum bactericidal activity, with membrane-disrupting effects against all three pathogens. Furthermore, we revealed the synergistic potential of SbPhACO when combined with antibiotics, such as cefoxitin, at concentrations that exert no cytotoxic effects tested on three mammalian cell lines. This study offers the first report on the mechanisms of action of novel antimony-based antimicrobial and presents the therapeutic potential of SbPhACO in combating both Gram-positive and Gram-negative bacterial pathogens while enhancing the efficacy of existing antibiotics.
抗微生物药物耐药性(AMR)是一个全球性的重大公共卫生危机,继续威胁着我们成功治疗细菌感染的能力。随着传统抗菌疗法效果的下降和新抗生素管道的缺乏,人们重新关注探索金属基抗菌化合物的潜力。具有长期医学用途的锑基化合物已重新成为有潜力的抗菌剂。我们之前合成了一系列具有潜在抗菌活性的新型有机锑(V)化合物,与氰肟酸盐配位。这里,我们研究了五种选定的化合物对三种重要的细菌病原体的抗菌功效: 、 和 。在五种测试化合物中,SbPhACO 对所有三种细菌菌株均显示出抗菌活性,MIC 为 50-100 µg/mL。最低杀菌浓度/MIC 值小于或等于 4,表明 SbPhACO 的作用是杀菌性的。此外,超薄电子显微镜显示 SbPhACO 处理导致所有三种菌株的膜破裂,这通过增加膜通透性进一步得到证实。我们还表明,SbPhACO 与抗生素多粘菌素 B 和头孢西丁协同作用,分别用于治疗 和 的 AMR 菌株,并且在协同 MIC 浓度 12.5 µg/mL 时,其对 Hela、McCoy 和 A549 细胞系的细胞毒性低于阈值。总的来说,这些结果突出了新型锑基化合物 SbPhACO 的抗菌潜力及其作为其他抗生素针对革兰氏阳性和革兰氏阴性细菌病原体的增效剂的用途。
抗生素耐药性是一个重大的全球公共卫生危机,威胁着我们对抗细菌感染的能力。鉴于传统抗生素的疗效下降,人们对替代解决方案(如金属基抗菌化合物)重新产生了兴趣。基于之前合成的创新有机锑(V)化合物,我们选择并进一步表征了其中五种化合物对三种重要的革兰氏阳性和革兰氏阴性细菌病原体的抗菌功效。在这些化合物中,SbPhACO 对所有三种病原体均表现出广谱杀菌活性,对所有三种病原体均具有破坏膜的作用。此外,我们揭示了 SbPhACO 与抗生素(如头孢西丁)联合使用时的协同潜力,在对三种哺乳动物细胞系无细胞毒性作用的浓度下发挥作用。本研究首次报道了新型锑基抗菌药物的作用机制,并提出了 SbPhACO 在对抗革兰氏阳性和革兰氏阴性细菌病原体的同时增强现有抗生素疗效方面的治疗潜力。