High Potency of Melaleuca alternifolia Essential Oil against Multi-Drug Resistant Gram-Negative Bacteria and Methicillin-Resistant Staphylococcus aureus

被引:69
作者
Oliva, Alessandra [1 ]
Costantini, Silvia [1 ]
De Angelis, Massimiliano [1 ]
Garzoli, Stefania [2 ]
Bozovic, Mijat [3 ]
Mascellino, Maria Teresa [1 ]
Vullo, Vincenzo [1 ]
Ragno, Rino [4 ,5 ]
机构
[1] Sapienza Univ Rome, Dept Publ Hlth & Infect Dis, Viale Policlin 155, I-00161 Rome, Italy
[2] Sapienza Univ, Dept Drug Chem & Technol, Ple Aldo Moro 5, I-00185 Rome, Italy
[3] Univ Montenegro, Fac Nat Sci & Math, Dzordza Vasingtona Bb, Podgorica 81000, Montenegro
[4] Sapienza Univ, Dept Drug Chem & Technol, Rome Ctr Mol Design, Ple Aldo Moro 5, I-00185 Rome, Italy
[5] Alchem Dynam Srl, I-00125 Rome, Italy
关键词
multi-drug resistant bacteria; essential oils; Melaleuca alternifolia; methicillin-resistant Staphylococcus aureus; carbapenem-resistant microorganisms; TEA TREE OIL; DOUBLE-CARBAPENEM REGIMEN; IN-VITRO ACTIVITY; KLEBSIELLA-PNEUMONIAE; SYNERGISTIC ACTIVITY; DECOLONIZATION; INHIBITION; TOXICITY; FUNGAL; WOUNDS;
D O I
10.3390/molecules23102584
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: Herein, an extended investigation of Tea tree oil (TTO) against a number of multi-drug resistant (MDR) microorganisms in liquid and vapor phases is reported. Methods: The activity of TTO was tested against methicillin-sensitive Staphylococcus aureus (MSSA), Escherichia coli, and clinical strains of methicillin-resistant S. aureus (MRSA), extended-spectrum beta lactamases producer carbapenem-sensitive Klebsiella pneumoniae (ESBL-CS-Kp), carbapenem-resistant K. pneumoniae (CR-Kp), Acinetobacter baumannii (CR-Ab), and Pseudomonas aeruginosa (CR-Pa). Minimal inhibitory/bactericidal concentrations (MIC/MBCs) and synergistic activity between TTO and different antimicrobials were determined. In the vapor assay (VP), TTO-impregnated discs were placed on the lid of a petri dish and incubated for 24 h at 37 degrees C. Results: TTO showed a potent bactericidal activity against all the tested microorganisms. TTO in combination with each reference antimicrobial showed a high level of synergism at sub-inhibitory concentrations, particularly with oxacillin (OXA) against MRSA. The VP assay showed high activity of TTO against CR-Ab. Conclusion: Evaluation of in-vitro activity clearly indicated TTO as a potential effective antimicrobial treatment either alone or in association with known drugs against MDR. Therefore, TTO could represent the basis for a possible role in non-conventional regimens against S. aureus and Gram-negative MDR. TTO in VP might represent a promising option for local therapy of pneumonia caused by CR-Ab.
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页数:14
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