1. Academic Validation
  2. Sub-Inhibitory Doses of Individual Constituents of Essential Oils Can Select for Staphylococcus aureus Resistant Mutants

Sub-Inhibitory Doses of Individual Constituents of Essential Oils Can Select for Staphylococcus aureus Resistant Mutants

  • Molecules. 2019 Jan 4;24(1):170. doi: 10.3390/molecules24010170.
Daniel Berdejo 1 Beatriz Chueca 2 Elisa Pagán 3 Adriana Renzoni 4 William L Kelley 5 Rafael Pagán 6 Diego Garcia-Gonzalo 7
Affiliations

Affiliations

  • 1 Tecnología de los Alimentos, Instituto Agroalimentario de Aragón-IA2 (CITA-Universidad de Zaragoza), 930 50059 Zaragoza, Spain. [email protected].
  • 2 Tecnología de los Alimentos, Instituto Agroalimentario de Aragón-IA2 (CITA-Universidad de Zaragoza), 930 50059 Zaragoza, Spain. [email protected].
  • 3 Tecnología de los Alimentos, Instituto Agroalimentario de Aragón-IA2 (CITA-Universidad de Zaragoza), 930 50059 Zaragoza, Spain. [email protected].
  • 4 Service of Infectious Diseases, Department of Medical Specialties, University Hospital of Geneva, 1205 Geneva, Switzerland. [email protected].
  • 5 Department of Microbiology and Molecular Medicine, University Hospital and Medical School of Geneva, 1205 Geneva, Switzerland. [email protected].
  • 6 Tecnología de los Alimentos, Instituto Agroalimentario de Aragón-IA2 (CITA-Universidad de Zaragoza), 930 50059 Zaragoza, Spain. [email protected].
  • 7 Tecnología de los Alimentos, Instituto Agroalimentario de Aragón-IA2 (CITA-Universidad de Zaragoza), 930 50059 Zaragoza, Spain. [email protected].
Abstract

Increased Bacterial resistance to food preservation technologies represents a risk for food safety and shelf-life. The use of natural antimicrobials, such as essential oils (EOs) and their individual constituents (ICs), has been proposed to avoid the generation of antimicrobial resistance. However, prolonged application of ICs might conceivably lead to the emergence of resistant strains. Hence, this study was aimed toward applying sub-inhibitory doses of the ICs carvacrol, citral, and (+)-limonene oxide to Staphylococcus aureus USA300, in order to evaluate the emergence of resistant strains and to identify the genetic modifications responsible for their increased resistance. Three stable-resistant strains, CAR (from cultures with carvacrol), CIT (from cultures with citral), and OXLIM (from cultures with (+)-limonene oxide) were isolated, showing an increased resistance against the ICs and a higher tolerance to lethal treatments by ICs or heat. Whole-genome Sequencing revealed in CAR a large deletion in a region that contained genes encoding transcriptional regulators and metabolic Enzymes. CIT showed a single missense mutation in aroC (N187K), which encodes for chorismate synthase; and in OXLIM a missense mutation was detected in rpoB (A862V), which encodes for RNA polymerase subunit beta. This study provides a first detailed insight into the mechanisms of action and S. aureus resistance arising from exposure to carvacrol, citral, and (+)-limonene oxide.

Keywords

(+)-limonene oxide; carvacrol; citral; genotypic resistance; whole genome sequencing.

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