Zhao JingChao, Yang Wen, Deng Hui, Li Dong, Wang QianYong, Yi LingXian, Kuang QiHong, Xu Rui, Li Di, Li RuoNan, Yu DaoJin, Yang Bo
University Key Laboratory for Integrated Chinese Traditional and Western Veterinary Medicine and Animal Healthcare in Fujian Province, Fujian Agriculture and Forestry University, Fuzhou, Fujian Province, China.
Fujian Key Laboratory of Traditional Chinese Veterinary Medicine and Animal Health, Fujian Agriculture and Forestry University, Fuzhou, Fujian Province, China.
Front Microbiol. 2024 Mar 15;15:1364339. doi: 10.3389/fmicb.2024.1364339. eCollection 2024.
Matrine (MT) is a potential resistance reversal agent. However, it remains unclear whether MT can reverse the resistance of () to β-lactams, and, if so, by what mechanism MT works.
We screened one cefaclor (CEC)-resistant strain (clinical strain C7) from eight clinical () strains and determined the underlying resistance mechanism. Then, we investigated the reversal effect of MTon the resistance of this strain to CEC.
The production of β-lactamase, overexpression of AcrAB-TolC system, and formation of biofilm might not be responsible for the resistance of clinical strain C7 to CEC. Fourteen mutation sites were found in four PBP genes (, and ) of clinical strain C7, among which the mutation sites located in (YD and LR) and (AV) genes triggered the resistance to CEC. The minimum inhibitory concentration (MIC) of CEC against clinical strain C7 was reduced by two to eight folds after MT treatment, accompanied by the significant down-regulated expression of mutated and genes. Based on such results, we believed that MT could reverse the resistance of to CEC by inhibiting the mutations in and genes. Our research would provide useful information for restoring the antimicrobial activity of β-lactams and improving the therapeutic efficacy of Glässer's disease.
苦参碱(MT)是一种潜在的耐药逆转剂。然而,MT是否能逆转()对β-内酰胺类抗生素的耐药性,以及如果可以,MT的作用机制仍不清楚。
我们从8株临床()菌株中筛选出1株耐头孢克洛(CEC)菌株(临床菌株C7),并确定其潜在的耐药机制。然后,我们研究了MT对该菌株对CEC耐药性的逆转作用。
β-内酰胺酶的产生、AcrAB-TolC系统的过表达以及生物膜的形成可能不是临床菌株C7对CEC耐药的原因。在临床菌株C7的4个PBP基因(、和)中发现了14个突变位点,其中位于(YD和LR)和(AV)基因中的突变位点引发了对CEC的耐药性。MT处理后,CEC对临床菌株C7的最低抑菌浓度(MIC)降低了2至8倍,同时突变的和基因的表达显著下调。基于这些结果,我们认为MT可以通过抑制和基因的突变来逆转()对CEC的耐药性。我们的研究将为恢复β-内酰胺类抗生素的抗菌活性和提高猪传染性胸膜肺炎的治疗效果提供有用的信息。