Antimicrobial and Antivirulence Action of Eugenia brejoensis Essential Oil in vitro and in vivo Invertebrate Models

被引:27
作者
Filho Bezerra, Clovis Macedo [1 ,2 ]
da Silva, Luis Claudio Nascimento [3 ]
da Silva, Marcia Vanusa [1 ]
Lobner-Olesen, Anders [4 ]
Struve, Carsten [5 ]
Krogfelt, Karen Angeliki [5 ,6 ]
Correia, Maria Tereza dos Santos [1 ]
Oliva, Maria Luiza [2 ]
机构
[1] Fed Pernambuco Univ, Dept Biochem, Recife, PE, Brazil
[2] Univ Fed Sao Paulo, Dept Biochem, Sao Paulo, Brazil
[3] CEUMA Univ Sao, Programa Posgrad Biol Microbiana, Sao Luis, Maranhao, Brazil
[4] Univ Copenhagen, Dept Biol, Copenhagen, Denmark
[5] Staten Serum Inst, Dept Bacteria Parasites & Fungi, Copenhagen, Denmark
[6] Roskilde Univ, Dept Sci & Environm, Roskilde, Denmark
基金
巴西圣保罗研究基金会;
关键词
Caenorhabditis elegans; Galleria melonella; infections models; multidrug resistance; natural products; Staphylococcus aureus; virulence factors; RESISTANT STAPHYLOCOCCUS-AUREUS; ANTIBACTERIAL ACTIVITY; CHEMICAL-COMPOSITION; VANCOMYCIN; VIRULENCE; DAPTOMYCIN; MYRTACEAE; LYSOZYME;
D O I
10.3389/fmicb.2020.00424
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Eugenia brejoensis L. (Myrtaceae) is an endemic plant from caatinga ecosystem (brazilian semi-arid) which have an E. brejoensis essential oil (EbEO) with reported antimicrobial activity. In this work, in vitro and in vivo models were used to characterize the inhibitory effects of EbEO in relation to Staphylococcus aureus. EbEO inhibited the growth of all tested S. aureus strains (including multidrug resistance isolates) with values ranging from 8 to 516 mu g/mL. EbEO also synergistically increased the action of ampicillim, chloramphenicol, and kanamycin. The treatment with subinhibitory concentrations (Sub-MIC) of EbEO decreased S. aureus hemolytic activity and its ability to survive in human blood. EbEO strongly reduced the levels of staphyloxanthin (STX), an effect related to increased susceptibility of S. aureus to hydrogen peroxide. The efficacy of EbEO against S. aureus was further demonstrated using Caenorhabditis elegans and Galleria mellonella. EbEO increased the lifespan of both organisms infected by S. aureus, reducing the bacterial load. In addition, EbEO reduced the severity of S. aureus infection in G. mellonella, as shown by lower levels of melanin production in those larvae. In summary, our data suggest that EbEO is a potential source of lead molecules for development of new therapeutic alternatives against S. aureus.
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页数:11
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