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Overcoming Polymyxin Resistance in Klebsiella pneumoniae with Ocotea Essential Oils: Insights from In Vitro and In Vivo Analyses

Year: 2025

Type: article

Abstract: High Resolution Image Download MS PowerPoint Slide Antimicrobial resistance, particularly in carbapenem-polymyxin-resistant Klebsiella pneumoniae (CPR- Kp ), is a major challenge associated with severe infections. In this study, we assessed the chemical composition and antimicrobial properties of essential oils (EOs) from Ocotea diospyrifolia (OdEO) and Ocotea velloziana (OvEO) against CPR- Kp . The EOs were extracted from the leaves via hydrodistillation and analyzed using gas chromatography–mass spectrometry. The antimicrobial activities of the EOs, alone and along with polymyxin B (OdEO-PMB and OvEO-PMB), were assessed through checkerboard assays, survival curves, and biofilm inhibition. Cell membrane permeability, reactive oxygen species levels, and scanning electron microscopy (SEM) were used to investigate antimicrobial mechanisms. Safety was evaluated by conducting hemolysis and toxicity tests in Caenorhabditis elegans . An in vivo infection model was constructed using C. elegans larvae to assess survival rates. OdEO and OvEO exhibited distinct chemical compositions, with α-bisabolol and viridiflorene as the major components, respectively. In silico analyses revealed that OdEO components can modulate the porin OmpK36, suggesting their ability to serve as antibiotic adjuvants. OdEO-PMB and OvEO-PMB reduced the PMB concentration required to inhibit CPR- Kp growth by 32-fold. Both combinations inhibited biofilm formation and caused bacterial death. The OdEO-PMB combination induced oxidative stress and increased protein leakage. Both treatments were nontoxic and nonhemolytic in the assay performed. In the infection models, OdEO-PMB and OvEO-PMB improved C. elegans survival rates to 72.4% and 50.9%, respectively. These results indicated that the Ocotea essential oils investigated are effective adjuvants for PMB, suggesting that they can be used to develop novel therapeutic strategies against CPR- Kp strains.

Source: ACS Omega

DOI: 10.1021/acsomega.5c07706