칸디다 알비칸스에 대한 19가지 에센셜 오일과 플루코나졸의 항진균 활성 평가

Evaluation of the Antifungal Activity of 19 Essential Oils Against Candida Albicans with Fluconazole

Article information

J Korean Soc Cosmetol. 2022;28(5):991-997
Publication date (electronic) : 2022 October 27
doi : https://doi.org/10.52660/JKSC.2022.28.5.991
1Graduate Student, Department of Public Health Science, Dankook University Graduate School
2Professor, Department of Health Administration, Dankook University College of Health & Welfare
3Professor, Department of Biomedical Laboratory Science, Dankook University College of Health Sciences
최재은1,#, 장태수2,#, 김재경3,
1단국대학교 대학원 공중보건과학과, 대학원생
2단국대학교 보건복지대학 보건행정학과, 교수
3단국대학교 보건과학대학 의생명실험과학과, 교수
*Corresponding author: Jae-Kyung Kim Tel : +82-41-550-1451 E-mail : nerowolf2@dankook.ac.kr
#Co-first authors: Jae-Eun Choi and Tae-Su Jang contributed equally to this work
Received 2022 June 13; Revised 2022 August 19; Accepted 2022 September 14.

Trans Abstract

Although many plants have been investigated for their antifungal activity against candidiasis, more treatment options remain needed. This study evaluated the antifungal activity of 19 essential oils against Candida albicans. Nineteen essential oils, at concentrations of 1% and 0.5%, were added to cultures of C. albicans and incubated at 37°C for 18 h. The optical density was measured at 600 nm. The antifungal activity of the essential oils against C. albicans was dependent on concentration and the extraction site. At 0.5%, essential oils from thyme, palmarosa, and lemongrass displayed higher antifungal activities than fluconazole, suggesting that they are effective against C. albicans. The essential oils of eucalyptus, rosewood, and lavender showed the highest activity at 1% concentration and may be used as antibiotics individually. In addition, the essential oils extracted from leaves, such as thyme, were found to have higher antifungal activity than those from other sites.

I. Introduction

Candida albicans is among the most prevalent fungal species of the human microbiota that asymptomatically colonizes healthy individuals (Lohse et al., 2018). These fungal infections can develop from simple skin mucosa infections to infections that can ultimately invade any organ (Pappas et al., 2004). Although antibiotics are widely used due to their high efficiency, strains resistant to these antibiotics are being discovered one after another, and the development of antibiotics with high efficiency is required (Mukeherjee et al., 2003).

Before the introduction of antibiotics and other modern drugs, natural products have been used globally for decades as traditional medicine. According to the World Health Organization (WHO), medicinal plants are the best source of various drugs (Khan et al., 2009). Essential oils (EOs), derived from the roots, stems, leaves, and flowers of different plants, are used in folk medicine as an alternative to modern medicines. In addition, they have been widely utilized in drug discovery and development, and they are readily accessible (da Silva et al., 2016; Myszka et al., 2016; Tutar et al., 2016). Recently, EOs have attracted significant interest owing to their antibacterial and antifungal activities, which are associated with their complex composition (Ghanem & Olama, 2014; Ceylan & Ugur, 2015). Several reports demonstrated the antifungal properties of extracts from different parts of various plants (Okla et al., 2021; Mutlu-Ingok et al., 2020). Clinical candidiasis has a steadily increasing annual infection rate (Tati et al., 2016). The effective antifungal and antibiofilm activities of several EOs against Candida spp. have been demonstrated (Abu-Darwish et al., 2016; Peixoto et al., 2017). Although there have been many studies on the antibiotic susceptibility of fungi to antifungal agents, only a few have reported on the susceptibility of C. albicans to EOs. This study conducted an antibacterial test by randomly selecting 19 types of well-known oils so that essential oils can be used in various practical applications.

II. Materials and Methods

1. Materials

C. albicans (ATCC 13316) was purchased from KCTC (Korea Collection for Type Cultures). The 19 EOs were randomly selected from the products supplied by the Korean Aromatherapy Certification Society. They were classified according to the extraction site (Table 1). Fluconazole (Sigma-Aldrich, Steinheim, Germany) was used as a control, following the CLSI standard amount (8 μg/ml).

List of the essential oils used in this study and their extraction sites

2. Methods

1) C. albicans and EOs

C. albicans was plated on Blood agar (MB-N1036, Kisan Bio, Seoul, Korea), and a nutrient broth culture with 1 × 106 colony-forming units/mL was prepared using a 0.5 McFarland standard. After dispensing 100 μl of the bacterial suspension into a 96-well plate, 100 μl of essential oils (1% and 0.5% concentrations) or 100 μl of fluconazole (CLSI: Clinical and Laboratory Standards Institute standard concentration; 8 μg/ml) were added 3 each wells, and the plate was then incubated at 37°C for 24 h in an incubator. The essential oil concentrations of 1% and 0.5% were diluted using the nutrient broth (Difco, Le Pont-de-Claix, France). The essential oil diluent was homogenized by voltexing for at least 1 minute to properly mix with the medium. And pipeting was done at medium depth.

2) Detection of antifungal activity using optical density (OD)

OD was detected at 600 nm as an endpoint using the spectrophotometer absorption program of the FlexStation 3 Multi-Mode Microplate Reader (V3.4.4.2413) (Molecular Devices, California, USA). OD reading was performed in four replicates to ensure the accuracy of the results.

3) Statistical analysis

For statistics, IBM SPSS Statistics 20 (IBM Corp., NY, USA) program was used, and a one-way ANOVA test was performed to verify the statistical significance between the control group and the experimental group. And the significance test was performed at the level of *P < 0.05, **P < 0.01, ***P < 0.001; #P < 0.05, ##P < 0.01. * = Significance compared to control, # = Significance compared to fluconazole. This experiment was repeated three times.

III. Results

After reading each essential oil with a wavelength of 600 nm in a micro plate reader, the inhibition rate is shown in Table 2 and Figure 1, 2 by comparing the resulting value with the Control. First, compared to the control (100%), the inhibition rate of fluconazole was 50%. Lemon (75%), Thyme (74%), Lemongrass (72%), Cedarwood (68%), Cypress (66%), Rosemary (65%), Chamomile blue (62%), Jasmine (51%) at 0.5% Concentration showed higher antibacterial activity than fluconazole (50%) (Fig. 1). In particular, Lemon (75%), Thyme (74%) and Lemongrass (72%) showed the highest antibacterial activity. The inhibition rates observed in palmarosa respectively, showing the same inhibition rate as fluconazole (50%). However, the remaining ten essential oils had lower antibacterial activity than fluconazole. Even in the case of sandalwood, C. albicans grew even more.

Evaluation of the antifungal activity of the essential oils at 0.5 and 1.0% concentration

Fig. 1.

Antifungal effect of 19 essential oils (0.5 %) against C. albicans. The antibacterial activities of the essential oils are arranged in ascending order from left to right. * = Significance compared to control, # = Significance compared to Fluconazole *P < 0.05, **P < 0.01, ***P < 0.001; #P < 0.05, ##P < 0.01

Fig. 2.

Antifungal effect of 19 essential oils (1%) against C. albicans. The antibacterial activities of the essential oils are arranged in ascending order from left to right. * = Significance compared to control, # = Significance compared to Fluconazole *P < 0.05, **P < 0.01, ***P < 0.001; #P < 0.05, ##P < 0.01

At 1.0% concentration, Thyme (78%), Cypress (76%), Lemon (70%), Rose geranium (69%), Cedarwood atlas (66%), Palmarosa (66%), Jasmine (64%), Rosewood (64%), Lemongrass (63%), Rosemary verbenone (57%) had higher antimicrobial activity than fluconazole (72%) (Fig. 2). Thyme (78%), Cypress (76%), and Lemon (70%) had the highest antibacterial activity. Eucalyptus (50%) had similar values for fluconazole. However, the rest of the essential oils had lower antibacterial activity than fluconazole. In the case of sandalwood, the bacteria were more active.

To verify the significance of the following results, one-way ANOVA analysis was performed. The part showing significance at 0.5% compared to Control was marked with *. Palmarosa and patchouli showed the highest significance, and all oils except ylang-ylang, tea tree, sandalwood, cedarwood, cypress and lemon showed significance. At 1.0%, almost all essential oils showed high significance, and lemon and bergamot showed no significance. The portion showing significance at 0.5% compared to oxacillin was marked with #. Rosewood and bergamot showed the highest significance, and all oils except rosemary, ylang-ylang, manuka, orange and cedarwood showed significance. At 1.0%, significance was shown in the remaining essential oils except for thyme, ylang-ylang, manuka, cedarwood, tea tree, and rosewood.

In general, essential oils isolated from leaves showed higher antimicrobial activity than those isolated from other plant parts.

IV. Discussion

In order to compare and analyze the antibiotic effect of essential oils on C. albicans, a cause of fungal vaginosis, with fluconazole, an antibacterial test was conducted on 19 kinds of essential oils available in Korea. Previous reports indicated that the EOs of thyme, pennyroyal, and lemon inhibited the growth of various fungi, including C. albicans (Mahdavi & Esmaeilzadeh, 2009). Patchouli oil was effective against several gram-positive and gram-negative bacteria and fungal species, including C. albicans, although the findings were contradictory (Adhavan et al., 2017; Karimi, 2014; Li et al., 2012). In this study, LG, EC, and TM showed excellent antifungal effects against C. albicans. The antifungal activity of EC was also established in earlier studies (Kim et al., 2011) and observed to be comparable to that of fluconazole in our study.

We also confirmed that the antifungal activity of EOs against C. albicans was concentration-dependent, similar to findings from a previous study. Another study confirmed the growth inhibitory effect of Manuka oil (MK) on C. albicans at a concentration of 0.01% (Kim et al., 2013). On similar lines, the present study confirmed that the antifungal effect of MK was higher at 0.5% than at 1.0%. These results show that MK exhibits higher antifungal activity at lower concentrations. In Lee et al., 2012 paper, palmarosa showed strong antibacterial activity against C. albicans compared to geranium, which is consistent with our study results.

Moreover, we concluded that the antifungal activity of EOs differed based on the extraction site. EOs extracted from the leaves, particularly TM, had the highest antifungal activity. In previous papers, it was confirmed that essential oils of Lamiaceae and Camphoraceae plants with antibacterial activity had excellent antibacterial activity. These plants contain a lot of aldehyde and alcohol compounds (Yi and Bu, 2017). According to previous studies, TM induces changes in the enzyme profile of C. albicans. These changes lead to an inability to assimilate saccharides and, consequently, may significantly impact the pathogenicity of C. albicans (Rajkowska et al., 2014). TM also disrupted C. albicans biofilms (Alves et al., 2019). The antifungal activity of Lemongrass has already been reported several times and (Heral et al., 2006; Paranagama et al., 2003) activity was citral, such as limonene, citronellal, β-myrcene, linalool and geraniol, etc. It is known to be caused by several components (Rauber et al., 2005). In particular, according to Abe et al. (2003), the main component of Lemongrass is citral It inhibits Candida mycelia growth and yeast growth. It is known that antibacterial activity against this ingredient can be expected. In this regard, the antibacterial power of citral It can be explained by the same high as this Lemongrass was presumed to be. In addition, Rosewood and Coriander et al. linalool It is an essential oil of the alcholol family with It requires further analysis and consists of dozens of different components. The essential oil has a synergistic effect between the main ingredients and trace ingredients. It is expected to have an antibiotic effect by producing or inhibiting (Deba et al., 2007). LM was the most effective among the oils extracted from fruit peels. SW, BG, and YY did not exhibit antifungal activity against C. albicans, as suggested by earlier studies (Powers et al., 2018; Bona et al., 2016; Devkatte et al., 2005).

This study has several limitations. A crucial challenge was that only limited amounts of EOs at varying concentrations were available. Therefore, further studies using several other concentrations of EOs are required. Nevertheless, our study showed the antifungal activities of 19 different EOs compared to fluconazole. Since each EO showed distinct antifungal activity based on the concentration and some were more effective in a lower concentration, they may be used independently. Overall, this study presented useful preliminary data on the utilization of EOs against C. albicans.

Notes

Conflict of Interest

The authors declare no conflict of interest.

References

1. Abe S., Sato Y., Inoue S., Ishibashi H., Maruyama N., Takizawa T., Oshima H., Yamaguchi H.. 2003;Anti-Candida albicans activity of essential oils including Lemongrass (Cymbopogon citratus) oil and its component, citral. Nihon Ishinkin Gakkai Zasshi 44(4):285–291.
2. Abu-Darwish M. S., Cabral C., Gonçalves M. J., Cavaleiro C., Cruz M. T., Zulfiqar A., Khan I. A., Efferth T., Salgueiro L.. 2016;Chemical composition and biological activities of Artemisia judaica essential oil from southern desert of Jordan. J Ethnopharmacol 191:161–168. https://doi.org/10.1016/j.jep.2016.06.023.
3. Adhavan P., Kaur G., Princy A., Murugan R.. 2017;Essential oil nanoemulsions of wild patchouli attenuate multi-drug resistant gram-positive, gram-negative and Candida albicans. Ind Crops Prod 100:106–116. https://doi.org/10.1016/j.indcrop.2017.02.015.
4. Alves M., Gonçalves M. J., Zuzarte M., Alves-Silva J. M., Cavaleiro C., Cruz M. T., Salgueiro L.. 2019;Unveiling the antifungal potential of two Iberian thyme essential oils: effect on C. albicans germ tube and preformed biofilms. Front Pharmacol 10:446. https://doi.org/10.3389/fphar.2019.00446.
5. Bona E., Cantamessa S., Pavan M., Novello G., Massa N., Rocchetti A., Berta G., Gamalero E.. 2016;Sensitivity of Candida albicans to essential oils: are they an alternative to antifungal agents? J Appl Microbiol 121(6):1530–1545. https://doi.org/10.1111/jam.13282.
6. Ceylan O., Ugur A.. 2015;Chemical composition and anti-biofilm activity of Thymus sipyleus BOISS. Subsp. sipyleus BOISS. Var. davisianus RONNIGER essential oil. Arch Pharm Res 38:957–965. https://doi.org/10.1007/s12272-014-0516-0.
7. Sant'Anna Da Silva A. P., Nascimento da Silva L. C., Martins da Fonseca C. S., de Araújo J. M., dos Santos Correia M. T.. 2016;Antimicrobial activity and phytochemical analysis of organic extracts from Cleome spinosa Jaqc. Front Microbiol 7:963. https://doi.org/10.3389/fmicb.2016.00963.
8. Deba F., Xuan T. D., Yasuda M., Tawata S.. 2007;Chemical composition and antioxidant, antibacterial and antifungal activities of the essential oils from Bidens pilosa Linn. var. Radiata. Food Control 19(4):346–352.
9. Devkatte A. N., Zore G. B., Karuppayil S. M.. 2005;Potential of plant oils as inhibitors of Candida albicans growth. FEMS Yeast Res 5(9):867–873. https://doi.org/10.1016/j.femsyr.2005.02.003.
10. Ghanem S., Olama Z.. 2014;Antimicrobial potential of Lebanese cedar extract against human pathogens and food spoilage microorganisms. EJBPSP 1:13–26.
11. Heral G. A., Sarhan M. M., Abu Shahala A. N., Abou El-Khair E. K.. 2006;Effect of Cymbopogon citratus L. essential oil on growth and morphogenesis of Saccharomyces cerevisiae ML2- strain. J Basic Microbiol 46(5):375–386.
12. Karimi A.. 2014;Characterization and antimicrobial activity of patchouli essential oil extracted from Pogostemon cablin [Blanco] Benth. Adv Environ Biol 8:2301–2309.
13. Khan R., Islam B., Akram M., Shakil S., Ahmad A., Ali S. M., Siddiqui M., Khan A. U.. 2009;Antimicrobial activity of five herbal extracts against multi drug resistant (MDR) strains of bacteria and fungus of clinical origin. Molecules 14(2):586–597. https://doi.org/10.3390/molecules14020586.
14. Kim H.-S., Lee H.-Y., Lee J.-N., Joo C.-G., and Choe T.-B.. 2011;The Effects of Antimicrobial Properties of Manuka Oil and Improvement of Acne. Journal of the Korean Society of Cosmetology 17(2):245–256.
15. Kim J.-H., Kim M.-J., Choi S.-K., Bae S.-H., An S.-K., Yoon Y.-M.. 2011;Antioxidant and antimicrobial effects of lemon and eucalyptus essential oils against skin floras. J Soc Cosmet Sci Korea 37:303–308.
16. Lee E.-J., Lee S.-H., Lim M.-H.. 2012;Antimicrobial and Antioxidative Activities Essential Oil-focused on Palmarosa (Cymbopogen marini) and Geranium (Pelargonium graveolens). Journal of the Korean Society of Cosmetology 18(1):136–143.
17. Li Y. C., Liang H. C., Chen H. M., Tan L. R., Yi Y. Y., Qin Z., Zhang W.-M., Wu D.-W., Li C.-W., Lin R.-F., Su Z.-R., Lai X.-P.. 2012;Anti-Candida albicans activity and pharmacokinetics of pogostone isolated from Pogostemonis Herba. Phytomedicine 20(1):77–83. https://doi.org/10.1016/j.phymed.2012.08.008.
18. Lohse M. B., Gulati M., Johnson A. D., Nobile C. J.. 2018;Development and regulation of single- and multi-species Candida albicans biofilms. Nat Rev Microbiol 16:19–31. https://doi.org/10.1038/nrmicro.2017.107.
19. Mahdavi O. S., Esmaeilzadeh S.. 2009;Comparison of anti-candida activity of thyme, pennyroyal, and lemon essential oils versus antifungal drugs against candida species. Jundishapur J Microbiol 2:53–60.
20. Mukherjee P. K., Chandra J., Kuhn D. M., Ghannoum M. A.. 2003;Mechanism of Fluconazole Resistance in Candida albicans Biofilms: Phase-Specific Role of Efflux Pumps and Membrane Sterols. Infect Immun 71(8):4333–4343.
21. Mutlu-Ingok A., Devecioglu D., Dikmetas D. N., Karbancioglu-Guler F., Capanoglu E.. 2020;Antibacterial, antifungal, antimycotoxigenic, and antioxidant activities of essential oils: an updated review. Molecules 25(20):4711. https://doi.org/10.3390/molecules25204711.
22. Myszka K., Schmidt M. T., Majcher M., Juzwa W., Olkowicz M., Czaczyk K.. 2016;Inhibition of quorum sensing-related biofilm of Pseudomonas fluorescens KM121 by Thymus vulgare essential oil and its major bioactive compounds. Int Biodeterior Biodegrad 114:252–259. https://doi.org/10.1016/j.ibiod.2016.07.006.
23. Okla M. K., Alatar A. A., Al-Amri S. S., Soufan W. H., Ahmad A., Abdel-Maksoud M. A.. 2021;Antibacterial and antifungal activity of the extracts of different parts of Avicennia marina (Forssk.) Vierh. Plants (Basel) 10(2):252. https://doi.org/10.3390/plants10020252.
24. Pappas P. G., Rex J. H., Sobel J. D., Filler S. G., Dismukes W. E., Walsh T. J., Edwards J. E.. 2004;Guidelines for Treatment of Candidiasis. Clin Infect Dis 38(2):161–189.
25. Paranagama P. A., Abeysekera K. H. T., Abeywickrama K., Nugaliyadde L.. 2003;Fungicidal and anti-aflatoxigenic effects of the essential oil of Cymbopogon citratus (DC.) Stapf. (lemongrass) against Aspergillus flavus Link. isolated from stored rice. Lett Appl Microbiol 37(1):86–90.
26. Peixoto L. R., Rosalen P. L., Ferreira G. L., Freires I. A., de Carvalho F. G., Castellano L. R., Castro R. D.. 2017;Antifungal activity, mode of action and anti-biofilm effects of Laurus nobilis Linnaeus essential oil against Candida spp. Arch Oral Biol 73:179–185.
27. Powers C. N., Osier J. L., McFeeters R. L., Brazell C. B., Olsen E. L., Moriarity D. M., Satyal P., Setzer W. N.. 2018;Antifungal and cytotoxic activities of sixty commercially available essential oils. Molecules 23(7):1549.
28. Rajkowska K., Kunicka-Styczyńska A., Maroszyńska M., Dąbrowska M.. 2014;The effect of thyme and tea tree oils on morphology and metabolism of Candida albicans. Acta Biochim Pol 61(2):305–310. https://doi.org/10.18388/abp.2014_1900.
29. Rauber C da S., Guterres S. S., Schapoval E. E.. 2005;LC determination of citral in Cymbopogon citratus volatile oil. J Pharm Biomed Anal 37(3):597–601.
30. Silva Cde B., Guterres S. S., Weisheimer V., Schapoval E. E.. 2008;Antifungal activity of the lemongrass oil and citral against Candida spp. Braz J Infect Dis 12(1):63–66.
31. Tati S., Davidow P., McCall A., Hwang-Wong E., Rojas I. G., Cormack B., Edgerton M.. 2016;Candida glabrata binding to Candida albicans hyphae enables its development in oropharyngeal candidiasis. PLOS Pathog 12e1005522.
32. Tutar U., Çelik C., Karaman İ., Ataş M., Hepokur C.. 2016;Anti-biofilm and antimicrobial activity of Mentha pulegium L. essential oil against multidrug-resistant Acinetobacter baumannii. Trop J Pharm Res 15(5):1039–1046.
33. Yi M.-R., Bu H.-J.. 2017;Antioxidant, Antimicrobial and Melanogenesis Inhibition Effects of 35 species Essential Oil. Journal of the Korean Society of Cosmetology 23(4):677–687.

Article information Continued

Fig. 1.

Antifungal effect of 19 essential oils (0.5 %) against C. albicans. The antibacterial activities of the essential oils are arranged in ascending order from left to right. * = Significance compared to control, # = Significance compared to Fluconazole *P < 0.05, **P < 0.01, ***P < 0.001; #P < 0.05, ##P < 0.01

Fig. 2.

Antifungal effect of 19 essential oils (1%) against C. albicans. The antibacterial activities of the essential oils are arranged in ascending order from left to right. * = Significance compared to control, # = Significance compared to Fluconazole *P < 0.05, **P < 0.01, ***P < 0.001; #P < 0.05, ##P < 0.01

Table 1.

List of the essential oils used in this study and their extraction sites

Extraction part Oils name Botanical name Origin Abbreviation
Blossom Lavender Bulgarian Lavandula vera Bulgaria LV
Ylang Ylang Cananga odorata Madagascar YY
Jasmine Jasminum sambac India JM
Chamomile Blue Tanacetum annum Morocco CB
Leaf Cypress Cupressus sempervirens Austria CP
Eucalyptus radiata Eucalyptus radiata Australia EC
Lemongrass Cymbopogon schoenathus Guatemala LG
Manuka Leptospermum scoparium New Zealand MK
Palmarosa Andropogon martini India PR
Rose Geranium Pelargonium roseum China RG
Rosemary verbenone Rosmarinus officinalis France RM
Tea Tree Melaleuca alternifolia Australia TT
Thyme white Thymus vulgaris Spain TM
Peel Bergamot Citrus bergamia Italy BG
Lemon Citrus lemon Argentina LM
Orange Sweet Citrus sinensis Argentine OR
Wood Cedarwood Atlas Cedrus atlantica Morocco CW
Rosewood Aniba rosaeodora Brazil RW
Sandalwood Santalum album India SW

Table 2.

Evaluation of the antifungal activity of the essential oils at 0.5 and 1.0% concentration

Name Abbreviation Inhibition rate (%) 0.5% Inhibition rate (%) 1.0%
Chamomile blue CB 38 55
Cypress CP 34 24
Cedarwood atlas CW 32 34
Eucalyptus radiata EC 53 50
Lemon LM 25 30
Lemongrass LG 28 37
Jasmine JM 49 36
Palmarosa PR 50 34
Rosemary verbenone RM 35 43
Rose geranium RG 51 31
Rosewood RW 63 36
Thyme TM 26 22
Bergamot BG 83 63
Lavender Bulgarian LV 73 65
Manuka MK 66 70
Orange sweet OR 70 69
Tea tree TT 60 56
Sandal wood SW 110 101
Ylang Ylang YY 73 84
Fluconazole 50
C. albicans 100