Shafiq Muhammad, Yao Fen, Bilal Hazrat, Rahman Sadeeq Ur, Zeng Mi, Ali Ilyas, Zeng Yuebin, Li Xin, Yuan Yumeng, Jiao Xiaoyang
Department of Cell Biology and Genetics, Shantou University Medical College, Shantou 515041, China.
Department of Pharmacology, Shantou University Medical College, Shantou 515041, China.
Antibiotics (Basel). 2022 Oct 2;11(10):1346. doi: 10.3390/antibiotics11101346.
Before the emergence of plasmid-mediated colistin resistance, colistin was once considered the last drug of choice for infections caused by carbapenem-resistant bacteria. Currently, researchers are relentlessly exploring possible alternative therapies that could efficiently curb the spread of drug resistance. In this study, we aim to investigate the synergistic antibacterial activity of tetrandrine in combination with colistin against -harboring . We examined the antibacterial activity of tetrandrine in combination with colistin in vivo and in vitro and examined the bacterial cells by fluorescence, scanning, and transmission electron microscopy (TEM) to explore their underlying mechanism of action. We further performed a computational analysis of MCR-1 protein and tetrandrine to determine the interaction interface of these two molecules. We confirmed that neither colistin nor tetrandrine could, on their own, inhibit the growth of -positive . However, in combination, tetrandrine synergistically enhanced colistin activity to inhibit the growth of both in vivo and in vitro. Similarly, molecular docking showed that tetrandrine interacted with the three crucial amino acids of the MCR-1 protein in the active site, which might inhibit MCR-1 from binding to its substrates, cause MCR-1 to lose its ability to confer resistance. This study confirmed that tetrandrine and colistin have the ability to synergistically overcome the issue of colistin resistance in -harboring .
在质粒介导的黏菌素耐药性出现之前,黏菌素曾被认为是治疗碳青霉烯类耐药菌感染的最后一道药物防线。目前,研究人员正在不懈地探索可能的替代疗法,以有效遏制耐药性的传播。在本研究中,我们旨在研究粉防己碱与黏菌素联合对携带 [具体细菌名称未给出] 的协同抗菌活性。我们在体内和体外检测了粉防己碱与黏菌素联合的抗菌活性,并通过荧光、扫描和透射电子显微镜(TEM)检查细菌细胞,以探索其潜在作用机制。我们还对MCR - 1蛋白和粉防己碱进行了计算分析,以确定这两种分子的相互作用界面。我们证实,单独使用黏菌素或粉防己碱都不能抑制 [具体细菌名称未给出] 阳性菌的生长。然而,联合使用时,粉防己碱可协同增强黏菌素的活性,在体内和体外均能抑制 [具体细菌名称未给出] 的生长。同样,分子对接显示粉防己碱与活性位点的MCR - 1蛋白的三个关键氨基酸相互作用,这可能会抑制MCR - 1与其底物结合,导致MCR - 1失去赋予耐药性的能力。本研究证实,粉防己碱和黏菌素能够协同克服携带 [具体细菌名称未给出] 的黏菌素耐药问题。