Potent anti-MRSA activity and synergism with aminoglycosides by flavonoid derivatives from the root barks of Morus alba, a traditional Chinese medicine

被引:0
作者
Guo-Ying Zuo
Cui-Xian Yang
Zhao-Juan Ruan
Jun Han
Gen-Chun Wang
机构
[1] Kunming General Hospital of Chengdu Military Command,Research Center for Natural Medicines
[2] Yunnan Traditional Chinese Medical College,undefined
来源
Medicinal Chemistry Research | 2019年 / 28卷
关键词
MRSA; Diels-Alder adduct; Aminoglycoside; Synergy; Resistance reversal effect;
D O I
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中图分类号
学科分类号
摘要
Infections of clinical methicillin-resistant Staphylococcus aureus (MRSA) is a very tough public health problem and a challenge of new drug development. Nearly 90 Diels-Alder adducts (DAAs) have so far been isolated from Morus plants, but only a few of them have been evaluated for their anti-MRSA activities. To study the antibacterial compounds of DAAs from the root barks’ section of Morus alba L. and their synergism with antibacterial agents against clinical MRSA strains, bioassay-guided phytochemical methods were used to screen the active components. Minimal inhibitory concentrations (MICs) and minimal bactericidal concentrations (MBCs) were assayed through broth serial microdilution. The synergism were evaluated by checker board microdilution and dynamic time-kill experiments. Three DAAs (multicaulisin (1), sanggenon G (2) and albanin G (3)) were isolated and identified from M. alba root barks. They were determined with potent effect against MRSA isolates with MICs/MBCs at 2–8/16–128 mg/L. They also showed synergy with conventional antibacterial agents, especially the aminoglycosides, with fractional inhibitory concentration indices (FICIs) ranged from 0.19 to 0.50 and the dose reduction indices (DRIs) ranged from 16 to 2. The MRSA resistance to the antibiotics could be reversed by compounds 1–3. The dose-dependent bactericidal synergism against MRSA was observed as well. The study released for the first time the anti-MRSA synergism of DAAs from M. alba root barks with antibacterial agents and the reversal of MRSA resistance to aminoglycosides. The results may be valuable for further development of new antibacterial drugs and synergists against MRSA infections.
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页码:1547 / 1556
页数:9
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  • [1] Chandrika NT(2016)A review of patents (2011-2015) towards combating resistance to and toxicity of aminoglycosides Medchemcomm 7 50-68
  • [2] Garneautsodikova S(2018)Structure-dependent activity of natural GABA (A) receptor modulators Molecules 23 1512-64
  • [3] Çiçek SS(2014)Antibiotics and bacterial resistance in the 21st century Perspec Med Chem 6 25-1011
  • [4] Fair RJ(2015)Artonin I inhibits multidrug resistance in J Appl Microb 117 996-e12
  • [5] Tor Y(2014) and potentiates the action of inactive antibiotics Lancet Glob Health 2 e11-215
  • [6] Farooq S(2000)What do we need to do to tackle antimicrobial resistance? Fitoterapia 71 213-615
  • [7] Wahab AT(1983)Multicaulisin a new Diels-Alder type adduct from Heterocycles 20 611-10
  • [8] Fozing CDA(2016)Structure of sanggenon G a new Diels-Alder adduct from the Chinese crude drug “Sang-Bai-Pi” ( Sci Rep 6 1-652
  • [9] Rahman AU(2018) root barks) Antimicrob Agents Chemother 62 639-S334
  • [10] Choudhary MI(2008)Discovery of prenylated flavonoids with dual activity against influenza virus and Phytomedicine 15 S331-125