Synergistic antibacterial effects of herbal extracts and antibiotics on methicillin-resistant Staphylococcus aureus: A computational and experimental study

被引:69
作者
Kuok, Chiu-Fai [1 ]
Hoi, Sai-On [1 ]
Hoi, Chi-Fai [1 ]
Chan, Chi-Hong [1 ]
Fong, Io-Hong [1 ]
Ngok, Cheong-Kei [1 ]
Meng, Li-Rong [1 ]
Fong, Pedro [1 ]
机构
[1] Macao Polytech Inst, Sch Hlth Sci, Macau 999078, Peoples R China
关键词
Antibiotic resistance; methicillin-resistant Staphylococcus aureus; synergistic effects; penicillin binding proteins; traditional Chinese medicines; molecular docking; IN-SILICO PREDICTION; MOLECULAR DOCKING; BETA-LACTAMASES; DRUG DISCOVERY; SURFLEX-DOCK; MRSA; DAPTOMYCIN; INHIBITORS; BACTEREMIA; VANCOMYCIN;
D O I
10.1177/1535370216689828
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Antibiotic resistance has become a serious global concern, and the discovery of antimicrobial herbal constituents may provide valuable solutions to overcome the problem. In this study, the effects of therapies combining antibiotics and four medicinal herbs on methicillin-resistant Staphylococcus aureus (MRSA) were investigated. Specifically, the synergistic effects of Magnolia officinalis, Verbena officinalis, Momordica charantia, and Daphne genkwa in combination with oxacillin or gentamicin against methicillin-resistant (ATCC43300) and methicillin-susceptible (ATCC25923) S. aureus were examined. Invitro susceptibility and synergistic testing were performed to measure the minimum inhibitory concentration and fractional inhibitory concentration (FIC) index of the antibiotics and medicinal herbs against MRSA and methicillin-susceptible S. aureus. To identify the active constituents in producing these synergistic effects, in silico molecular docking was used to investigate the binding affinities of 139 constituents of the four herbs to the two common MRSA inhibitory targets, penicillin binding proteins 2a (PBP2a) and 4 (PBP4). The physicochemical and absorption, distribution, metabolism, and excretion properties and drug safety profiles of these compounds were also analyzed. D. genkwa extract potentiated the antibacterial effects of oxacillin against MRSA, as indicated by an FIC index value of 0.375. M. officinalis and V. officinalis produced partial synergistic effects when combined with oxacillin, whereas M. charantia was found to have no beneficial effects in inhibiting MRSA. Overall, tiliroside, pinoresinol, magnatriol B, and momorcharaside B were predicted to be PBP2a or PBP4 inhibitors with good drug-like properties. This study identifies compounds that deserve further investigation with the aim of developing therapeutic agents to modulate the effect of antibiotics on MRSA. Impact statement Antibiotic resistant is a well-known threat to global health and methicillin-resistant Staphylococcus aureus is one of the most significant ones. These resistant bacteria kill thousands of people every year and therefore a new effective antimicrobial treatment is necessary. This study identified the herbs and their associated bioactive ingredients that can potential the effects of current antibiotics. These herbs have long history of human usage in China and have well-defined monograph in the Chinese Pharmacopeia. These indicate their relatively high clinical safety and may have a quicker drug development process than that of a new novel antibiotic. Based on the results of this study, the authors will perform further invitro and animal studies, aiming to accumulate significant data for the application of clinical trial.
引用
收藏
页码:731 / 743
页数:13
相关论文
共 65 条
[1]   Pharmacological synergism of bee venom and melittin with antibiotics and plant secondary metabolites against multi-drug resistant microbial pathogens [J].
Al-Ani, Issam ;
Zimmermann, Stefan ;
Reichling, Juergen ;
Wink, Michael .
PHYTOMEDICINE, 2015, 22 (02) :245-255
[2]   Antibacterial and synergy of a flavanonol rhamnoside with antibiotics against clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA) [J].
An, J. ;
Zuo, G. Y. ;
Hao, X. Y. ;
Wang, G. C. ;
Li, Z. S. .
PHYTOMEDICINE, 2011, 18 (11) :990-993
[3]  
[Anonymous], 2015, ACD PERC VERS 14 0
[4]   In-silico studies in Chinese herbal medicines' research: Evaluation of in-silico methodologies and phytochemical data sources, and a review of research to date [J].
Barlow, D. J. ;
Buriani, A. ;
Ehrman, T. ;
Bosisio, E. ;
Eberini, I. ;
Hylands, P. J. .
JOURNAL OF ETHNOPHARMACOLOGY, 2012, 140 (03) :526-534
[5]   Industrial applications of in silico ADMET [J].
Beck, Bernd ;
Geppert, Tim .
JOURNAL OF MOLECULAR MODELING, 2014, 20 (07)
[6]   Discovery of Antibiotic (E)-3-(3-CarboxyphenyI)-2-(4-cyanostyryl)quinazolin-4(3H)-one [J].
Bouley, Renee ;
Kumarasiri, Malika ;
Peng, Zhihong ;
Otero, Lisandro H. ;
Song, Wei ;
Suckow, Mark A. ;
Schroeder, Valerie A. ;
Wolter, William R. ;
Lastochkin, Elena ;
Antunes, Nuno T. ;
Pi, Hualiang ;
Vakulenko, Sergei ;
Hermoso, Juan A. ;
Chang, Mayland ;
Mobashery, Shahriar .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (05) :1738-1741
[8]   VALIDATION OF THE GENERAL-PURPOSE TRIPOS 5.2 FORCE-FIELD [J].
CLARK, M ;
CRAMER, RD ;
VANOPDENBOSCH, N .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1989, 10 (08) :982-1012
[9]   Knowledge-guided docking: accurate prospective prediction of bound configurations of novel ligands using Surflex-Dock [J].
Cleves, Ann E. ;
Jain, Ajay N. .
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 2015, 29 (06) :485-509
[10]  
Clinical and Laboratory Standards Institute, 2014, M100 CLIN LAB STAND, V34, P128