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茶树油纳米乳液与抗生素对多重耐药菌的协同作用。

The synergy of tea tree oil nano-emulsion and antibiotics against multidrug-resistant bacteria.

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, PR China.

Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, PR China.

出版信息

J Appl Microbiol. 2023 Jul 4;134(7). doi: 10.1093/jambio/lxad131.

Abstract

AIMS

We determined the synergistic effects of tea tree essential oil nano-emulsion (nanoTTO) and antibiotics against multidrug-resistant (MDR) bacteria in vitro and in vivo. Then, the underlying mechanism of action of nanoTTO was investigated.

METHODS AND RESULTS

Minimum inhibitory concentrations and fractional inhibitory concentration index (FICI) were determined. The transepithelial electrical resistance (TEER) and the expression of tight junction (TJ) protein of IPEC-J2 cells were measured to determine the in vitro efficacy of nanoTTO in combination with antibiotics. A mouse intestinal infection model evaluated the in vivo synergistic efficacy. Proteome, adhesion assays, quantitative real-time PCR, and scanning electron microscopy were used to explore the underlying mechanisms. Results showed that nanoTTO was synergistic (FICI ≤ 0.5) or partial synergistic (0.5 < FICI < 1) with antibiotics against MDR Gram-positive and Gram-negative bacteria strains. Moreover, combinations increased the TEER values and the TJ protein expression of IPEC-J2 cells infected with MDR Escherichia coli. The in vivo study showed that the combination of nanoTTO and amoxicillin improved the relative weight gain and maintained the structural integrity of intestinal barriers. Proteome showed that type 1 fimbriae d-mannose specific adhesin of E. coli was downregulated by nanoTTO. Then, nanoTTO reduced bacterial adhesion and invasion and inhibited the mRNA expression of fimC, fimG, and fliC, and disrupted bacterial membranes.

摘要

目的

本研究旨在测定茶树精油纳米乳液(nanoTTO)与抗生素联合应用对多重耐药(MDR)细菌的体外和体内协同作用,并探讨 nanoTTO 的作用机制。

方法和结果

测定最低抑菌浓度和部分抑菌浓度指数(FICI)。通过测定跨上皮电阻(TEER)和紧密连接(TJ)蛋白表达来评估 nanoTTO 与抗生素联合应用的体外疗效。采用小鼠肠道感染模型评价体内协同疗效。采用蛋白质组学、黏附实验、实时定量 PCR 和扫描电子显微镜来探讨其作用机制。结果表明,nanoTTO 与抗生素联合应用对 MDR 革兰氏阳性和革兰氏阴性菌具有协同(FICI≤0.5)或部分协同(0.5<FICI<1)作用。此外,该联合应用还可增加感染 MDR 大肠杆菌的 IPEC-J2 细胞的 TEER 值和 TJ 蛋白表达。体内研究表明,nanoTTO 与阿莫西林联合应用可提高相对体重增加,并维持肠道屏障的结构完整性。蛋白质组学结果显示,nanoTTO 下调大肠杆菌的 I 型菌毛 d-甘露糖特异性黏附素。随后,nanoTTO 可减少细菌黏附和侵袭,并抑制 fimC、fimG 和 fliC 的 mRNA 表达,破坏细菌膜。

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