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黏菌素联合PFK-158对耐黏菌素革兰氏阴性菌的协同活性及生物膜形成作用

Synergistic Activity and Biofilm Formation Effect of Colistin Combined with PFK-158 Against Colistin-Resistant Gram-Negative Bacteria.

作者信息

Chen Liqiong, Yu Kaihang, Chen Lijiang, Zheng Xiangkuo, Huang Na, Lin Yishuai, Jia Huaiyu, Liao Wenli, Cao Jianming, Zhou Tieli

机构信息

Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province, People's Republic of China.

Department of Medical Laboratory Science, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, Zhejiang Province, People's Republic of China.

出版信息

Infect Drug Resist. 2021 Jun 9;14:2143-2154. doi: 10.2147/IDR.S309912. eCollection 2021.

Abstract

PURPOSE

The emergence of colistin resistance among Gram-negative bacteria (GNB) poses a serious public health threat. Therefore, it is necessary to enhance the antibacterial activity of colistin through the combination with other drugs. In this study, we demonstrated the synergistic activity and the possible synergy mechanism of colistin with PFK-158 against colistin-resistant GNB, including non-fermenting bacteria and Enterobacteriaceae.

PATIENTS AND METHODS

Thirty-one colistin-resistant GNB, including (n = 9), (n = 5), (n = 8) and (n = 9), were collected as the experimental strains and the minimum inhibitory concentrations (MICs) of colistin, other routine antimicrobial agents and PFK-158 against all strains were determined by the broth microdilution method. The synergistic activity of colistin with PFK-158 was assessed by the checkerboard assay and time-kill assay. The biofilm formation assay and scanning electron microscopy were used to demonstrate the biofilm formation effect of colistin with PFK-158 against colistin-resistant GNB.

RESULTS

The results of the checkerboard assay showed that when colistin was used in combination with PFK-158, synergistic activity was observed against the 31 colistin-resistant GNB. The time-kill assay presented a significant killing activity of colistin with PFK-158 against the 9 colistin-resistant GNB selected randomly, including (n = 6), (n = 1), (n = 1), and (n = 1). The biofilm formation assay and scanning electron microscopjihy showed that colistin with PFK-158 can effectively suppress the formation of biofilm and reduce the cell arrangement density of biofilm against most experimental strains.

CONCLUSION

The results of the performed experiments suggest that the combination of colistin and PFK-158 may be a potential new choice as a new antibiofilm group for the treatment of infections caused by the colistin-resistant GNB.

摘要

目的

革兰氏阴性菌(GNB)中耐黏菌素菌株的出现对公共卫生构成了严重威胁。因此,有必要通过与其他药物联合使用来增强黏菌素的抗菌活性。在本研究中,我们证明了黏菌素与PFK - 158联合使用对耐黏菌素GNB(包括非发酵菌和肠杆菌科细菌)的协同活性及可能的协同作用机制。

患者与方法

收集31株耐黏菌素GNB作为实验菌株,其中包括(n = 9)、(n = 5)、(n = 8)和(n = 9),采用肉汤微量稀释法测定黏菌素、其他常规抗菌药物及PFK - 158对所有菌株的最低抑菌浓度(MIC)。通过棋盘法和时间杀菌试验评估黏菌素与PFK - 158的协同活性。采用生物膜形成试验和扫描电子显微镜观察黏菌素与PFK - 158对耐黏菌素GNB生物膜形成的影响。

结果

棋盘法结果显示,黏菌素与PFK - 158联合使用时,对31株耐黏菌素GNB具有协同活性。时间杀菌试验表明,黏菌素与PFK - 158对随机选取的9株耐黏菌素GNB具有显著的杀菌活性,其中包括(n = 6)、(n = 1)、(n = 1)和(n = 1)。生物膜形成试验和扫描电子显微镜观察结果表明,黏菌素与PFK - 158能有效抑制大多数实验菌株生物膜的形成,并降低生物膜中细胞排列密度。

结论

所进行的实验结果表明,黏菌素与PFK - 158联合使用可能是治疗耐黏菌素GNB引起感染的新型抗生物膜组合的潜在新选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce1e/8200155/8eaa55ce19a2/IDR-14-2143-g0001.jpg

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