AUTHOR=Espinoza Javier , Urzúa Alejandro , Sanhueza Loreto , Walter Mariana , Fincheira Paola , Muñoz Patricia , Mendoza Leonora , Wilkens Marcela 

TITLE=Essential Oil, Extracts, and Sesquiterpenes Obtained From the Heartwood of Pilgerodendron uviferum Act as Potential Inhibitors of the Staphylococcus aureus NorA Multidrug Efflux Pump

JOURNAL=Frontiers in Microbiology

VOLUME=10

YEAR=2019

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2019.00337

DOI=10.3389/fmicb.2019.00337

ISSN=1664-302X

ABSTRACT=<p><italic>Staphylococcus aureus</italic> is a serious human pathogen that is highly adaptive to environmental conditions and rapidly develops antibiotic resistance. The use of efflux pumps to reduce antibiotic concentrations at the intracellular level is one of the main mechanisms by which bacteria develop antibiotic resistance. The management of efflux pumps, specifically NorA, which is expressed by <italic>S. aureus</italic> strains, is a valuable strategy for restoring susceptibility in strains resistant to antibacterial agents. In recent years, many studies have focused on searching for natural substances that can reverse efflux pump-mediated resistance in <italic>S. aureus</italic>. Extracts and compounds obtained from plants can be efficient efflux pump inhibitors (EPIs) and represent a potentially patient-friendly strategy for controlling <italic>S. aureus</italic>. In the present study, we evaluated the ability of essential oils, petroleum ether extracts, dichloromethane extract (DCME) and six compounds isolated from the heartwood of <italic>Pilgerodendron uviferum</italic> (Cupressaceae) and two synthetic derivatives to inhibit efflux in NorA pumps in the following three <italic>S. aureus</italic> strains: K2378, which overexpressed the <italic>norA</italic> gene (<italic>norA</italic>++), K1902 (<italic>norA</italic>-deleted, Δ<italic>norA</italic>) and the parental strain, NCTC 8325-4. Efflux activity was evaluated using a fluorometric method that measured the accumulation of the universal efflux pump substrate ethidium bromide (EtBr). Only DCME and the compounds 15-copaenol and <italic>epi</italic>-cubenol inhibited EtBr efflux by K2378. Even the lowest concentration of 15-copaenol exhibited a stronger inhibitory effect than carbonyl cyanide <italic>m</italic>-chlorophenyl hydrazone on EtBr efflux by K2378. 15-copaenal only showed inhibition of EtBr efflux in K2378 cells at 125 μg/mL, but not superior to the control inhibitor and 15-copaenyl acetate exerted no intrinsic EPI activity against K2378. Fractional inhibitory concentration index (FICI) values obtained in the checkerboard assays, indicated that all combinations between DCME, <italic>epi</italic>-cubenol and 15-copaenol, and tested antibiotics showed a synergistic effect in wild type, <italic>norA</italic><sup>++</sup> and Δ<italic>norA</italic> strains. Moreover, those were not toxic for the HeLa cell line at concentrations in which the synergistic effect and inhibitory activity of efflux pumps was determined. Other extracts and compounds obtained from <italic>P. uviferum</italic> did not display EtBr efflux-inhibiting activity against the evaluated <italic>S. aureus</italic> strains.</p>