Antifungal Activity and Type of Interaction of Melissa officinalis Essential Oil with Antimycotics against Biofilms of Multidrug-Resistant Candida Isolates from Vulvovaginal Mucosa

(1) Background: Vulvovaginal candidosis (VVC) is a major therapy issue due to its high resistance rate and virulence factors such as the ability to form biofilms. The possibility of combining commonly used antifungals with natural products might greatly improve therapeutic success. (2) Methods: A to...

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Published in:Journal of fungi (Basel) 2023-11, Vol.9 (11), p.1080
Main Authors: Ranđelović, Marina, Dimitrijević, Marina, Otašević, Suzana, Stanojević, Ljiljana, Išljamović, Milica, Ignjatović, Aleksandra, Arsić-Arsenijević, Valentina, Stojanović-Radić, Zorica
Format: Article
Language:English
Subjects:
Antifungal activity
Antimicrobial agents
biofilm
Biofilms
Chromatography
Essential oils
Fluconazole
Infections
Mass spectrometry
Melissa officinalis
Multidrug resistance
Natural products
Nystatin
Oils & fats
Scientific imaging
Temperature
Virulence
Virulence factors
vulvovaginal candidosis
Yeast
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Summary:(1) Background: Vulvovaginal candidosis (VVC) is a major therapy issue due to its high resistance rate and virulence factors such as the ability to form biofilms. The possibility of combining commonly used antifungals with natural products might greatly improve therapeutic success. (2) Methods: A total of 49 vulvovaginal isolates, causative agents of recurrent VVC, were tested for their susceptibility to fluconazole, nystatin, and Melissa officinalis essential oil (MOEO). This examination included testing the antibiofilm potential of antifungals and MOEO and the determination of their types of interaction with mature biofilms. (3) Results: Antimicrobial testing showed that 94.4% of the Candida albicans isolates and all the Candida krusei isolates were resistant to fluconazole, while all strains showed resistance to nystatin. The same strains were susceptible to MOEO in 0.156–2.5 mg/mL concentrations. Additionally, the results revealed very limited action of fluconazole, while nystatin and MOEO reduced the amount of biofilm formed by as much as 17.7% and 4.6%, respectively. Testing of the combined effect showed strain-specific synergistic action. Furthermore, the lower concentrations exhibited antagonistic effects even in cases where synergism was detected. (4) Conclusions: This study showed that MOEO had a very good antibiofilm effect. However, combining MOEO with antimycotics demonstrated that the type of action depended on the choice of antifungal drugs as well as the applied concentration.
ISSN:2309-608X
2309-608X
DOI:10.3390/jof9111080