Zhao Xiaoou, Zhang Mengna, Zhang Zhendu, Wang Lei, Wang Yu, Liu Lizai, Wang Duojia, Zhang Xin, Zhao Luobing, Zhao Yunhui, Jin Xiangshu, Liu Xiaoxiao, Ma Hongxia
College of Animal Science and Technology, Jilin Agricultural University, Xincheng Street No. 2888, Changchun 130118, China.
Institute of Animal Husbandry and Veterinary Medicine, Jilin Academy of Agricultural Science, Kemao Street No. 186, Gongzhuling 136100, China.
Antibiotics (Basel). 2024 Oct 15;13(10):973. doi: 10.3390/antibiotics13100973.
The worrying issue of antibiotic resistance in pathogenic bacteria is aggravated by the scarcity of novel therapeutic agents. Antibiotic adjuvants offer a promising solution due to their cost-effectiveness and high efficacy in addressing this issue, such as the β-lactamase inhibitor sulbactam (a β-lactam adjuvant) and the dihydrofolate reductase inhibitor trimethoprim (a sulfonamide adjuvant). This study aimed to discover potential adjuvants for tetracyclines from a list of previously approved drugs to restore susceptibility to carrying the gene. We have screened guanethidine, a compound from the Chinese pharmacopoeia, which effectively potentiates the activity of tetracyclines by reversing resistance in -positive , enhancing its antibacterial potency, and retarding the development of resistance. Guanethidine functions via the inhibition of the TetA efflux pump, thereby increasing the intracellular concentration of tetracyclines. Our findings suggest that guanethidine holds promise as an antibiotic adjuvant.
病原菌中令人担忧的抗生素耐药性问题因新型治疗药物的稀缺而加剧。抗生素佐剂因其成本效益高且在解决这一问题方面疗效显著而提供了一个有前景的解决方案,例如β-内酰胺酶抑制剂舒巴坦(一种β-内酰胺佐剂)和二氢叶酸还原酶抑制剂甲氧苄啶(一种磺胺类佐剂)。本研究旨在从一系列先前批准的药物中发现四环素的潜在佐剂,以恢复携带该基因的菌株的敏感性。我们筛选了来自中国药典的化合物胍乙啶,它通过逆转阳性菌株中的耐药性、增强其抗菌效力以及延缓耐药性的发展,有效地增强了四环素的活性。胍乙啶通过抑制TetA外排泵发挥作用,从而增加四环素的细胞内浓度。我们的研究结果表明胍乙啶有望成为一种抗生素佐剂。