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Article

The Variability of Thymol and Carvacrol Contents Reveals the Level of Antibacterial Activity of the Essential Oils from Different Accessions of Oliveria decumbens

1
Department of Horticultural Science, School of Agriculture, Shiraz University, 71441-65186 Shiraz, Iran
2
Department of Agriculture, Minab Higher Education Center, University of Hormozgan, 84156-83111 Bandar Abbas, Iran
3
School of Pharmacy, University of Camerino, 62032 Camerino, Italy
*
Author to whom correspondence should be addressed.
Antibiotics 2020, 9(7), 409; https://doi.org/10.3390/antibiotics9070409
Submission received: 18 June 2020 / Revised: 10 July 2020 / Accepted: 12 July 2020 / Published: 14 July 2020
(This article belongs to the Special Issue Antibacterial Activity of Plant Extracts and Essential Oils)

Abstract

:
Oliveria decumbens (Apiaceae) is an aromatic herb traditionally employed in the Persian medicine for the treatment of infectious and gastrointestinal disorders. In the present study, we analyzed the chemical composition of essential oils obtained from different Iranian populations and evaluated their efficacy on a panel of human pathogens (Staphylococcus aureus and Escherichia coli), probiotic (Bacillus subtilis), and phytopathogens (Clavibacter michiganensis, Curtobacterium flaccumfaciens, Xanthomonas citri, and Agrobacterium tumefaciens). The gas chromatographic-mass spectrometry analysis put in evidence four main volatile constituents such as thymol (20.3–36.4%), carvacrol (18.8–33.1%), γ-terpinene (10.6–25.9%), and p-cymene (9.5–17.3%), though with significant variability from an essential oil to another. Notably, the oils from the populations sited in Nourabad Mamasani and Dehdasht showed the highest amount of the phenolic monoterpenes thymol (36.4 and 35.2%, respectively) and carvacrol (33.1 and 30.6%, respectively). The antibacterial activity of O. decumbens essential oils was assessed by the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) methods, showing high activity for the samples from Nourabad Mamasani and Dehdasht populations exhibiting high level of the above phenolics. The obtained MIC and MBC values (mg/ml) were in the ranges 0.0625–2 mg/ml and 1–16 mg/ml, respectively. Noteworthy, in some cases, the antibacterial activity of O. decumbens essential oils was higher than that of chloramphenicol used as positive control. The average MBCs displayed by the O. decumbens samples showed that C. flaccumfaciens had the highest sensitivity to the essential oils. Based on these results, our work shed light on selected O. decumbens populations deserving proper breeding and cultivation strategies in order to warrantee production of bioactive essential oils to be used at pharmaceutical and agricultural level to combat several pathogens.

1. Introduction

Oliveria decumbens Vent., belonging to the Apiaceae family, is an annual, aromatic herb, endemic to southern and western parts of Iran [1]. The aerial parts of this plant have been used to cure fever, abdominal pain, indigestion, and diarrhea [2]. Moreover, O. decumbens is exploited in Persian traditional medicine for the treatment of cancer, infections, and inflammation [3,4,5]. Oliveria decumbens is a good source of essential oil which has already been reported to exhibit notable antioxidant activity [6]. Notably, an O. decumbens emulsion exhibited strong radical scavenging effects and suppressed lipid peroxidation in both chemical assays and living cells [7]. This essential oil has also been reported to have insecticidal activity against the cabbage looper Trichoplusia ni (Hübner) [8]. Finally, the O. decumbens essential oil showed cytotoxic effects on several cancer cell lines [8,9]. Actually, essential oils are natural sources of volatile, lipophilic mixtures of several dozens of compounds which are able to interact with the cell wall, increasing its permeability, or disrupting the energy production system of the cells. In addition, they exert an important inhibition of trans-membrane and cytosol enzymes as well as anti-quorum sensing activity [10,11,12].
In this regard, the antibacterial and antifungal activities of O. decumbens essential oils have been disclosed in previous papers [8,13,14,15,16,17,18]. Staphylococcus aureus and Escherichia coli are opportunistic pathogens that cause infections in humans and the previous studies have emphasized the development of resistance in these bacteria to antibiotics [19]. Bacillus subtilis is considered as a probiotic bacterium with the beneficial effects in the animals and plants [20]. Plant pathogenic bacteria cause major constraints and losses on crop yield worldwide [21]. Clavibacter michiganensis as an economically important pathogen causes severe losses and destructive diseases in agricultural crops [22]. Also, Curtobacterium flaccumfaciens causes important emerging disease and serious problems in the legumes around the world [23]. Moreover, Xanthomonas citri is an important and serious pathogen causing citrus canker in citrus plants [24]. Agrobacterium tumefaciens is regarded as a serious and widespread plant pathogenic bacterium causing crown gall disease [25].
Considering the development of bacterial resistance to chemical antibiotics and their adverse effects on the environment and public health, there is a growing demand to replace them with plant-based derivatives or combine these green agents with antibiotics to give synergistic effects [26,27,28,29]. In this respect, plant essential oils have shown efficacy on many bacterial and fungal strains, without emergence of noteworthy resistance [28]. Thus, essential oils are promising antimicrobial sources to be employed in the years to come as an effective alternative to combat multi-drug resistant pathogens [26,27,28,29].
The chemical composition of the essential oils is affected by various factors including environment, climate, genetics, harvesting time, extraction methods, and others [30,31,32]. Previous studies revealed that the essential oil composition and content in O. decumbens collected from different regions of Iran varied significantly [2,7,30,33,34,35,36].
The main constituents and their possible synergistic interactions determine the biological activities of plant essential oils [37]. Thus, the variation in chemical composition detected among various populations may affect the level of biological properties of a plant species, compromising in some cases its use on an industrial level. A previous study showed that essential oils from five populations of O. decumbens collected in different regions showed no significant differences in antimicrobial activity [17]. With regard to possible differences in chemical composition among different O. decumbens accessions [2,7,30,33,34,35,36], it is of industrial importance to screen and select those populations characterized by the best fingerprint, in terms of bioactive compounds assuring a strong and reliable antibacterial activity. Therefore, the present study was aimed to investigate the chemical variability of essential oils in O. decumbens growing in different Iranian regions and to evaluate its effect on the antibacterial activity exerted on different bacterial strains of human pathogens and phytopathogens.

2. Results and Discussion

2.1. Essential Oil Content

The essential oil content differed among the various O. decumbens populations and ranged from 3.34 to 8.52% (w/w) [33]. On the other hand, the values reported in previous reports varied from 0.1 to 8.1% [2,15,16,18,30,38,39]. The highest and lowest contents were found in Behbahan and Nourabad Mamasani populations with 8.52 and 3.34%, respectively. Moreover, Dehdasht (5.19%) and Kahnoyeh (5.32%) populations showed no significant differences. The essential oil content of Behbahan population, with 8.52%, showed a remarkable difference compared to those previously reported for several O. decumbens populations [2,15,18,30,38,39]. A number of various factors, including genetics, soil, geographic, and climatic conditions affect the essential oil content [40]. In addition, some factors like altitude have been reported to affect the essential oil content [33,40,41]. In our study, the highest content was found in the essential oil from Behbahan population growing at the lowest altitude (394 m), followed by that from Kahnoyeh and Dehdasht populations located at 758 and 971 m a.s.l., respectively. Also, the oil from Nourabad Mamasani population, growing at the highest altitude (1268 m), showed the lowest content. Based on our results, we can conclude that the highest essential oil contents were obtained at lower altitudes. This finding is in accordance with that reported in another study in which the authors showed a significant negative relationship between the O. decumbens essential oil content and the altitude [41]. Thus, fields at low cultivation altitudes should be considered to produce essential oils with high yield.

2.2. Essential Oil Composition

Our recent study showed that the number and relative percentages of essential oil compounds changed at variance with the geographic origin of O. decumbens populations [33]. A total of 18, 17, 16, and 11 compounds were identified in the populations from Nourabad Mamasani, Kahnoyeh, Behbahan, and Dehdasht, respectively [33]. The number of identified compounds in the investigated populations was partly in accordance with those reported in previous papers, that ranged from 8 to 35 [2,7,9,14,15,16,17,18,30,38].
The main essential oil constituents were thymol (20.3–36.4%), carvacrol (18.8–33.1%), γ-terpinene (10.6–25.9%), and p-cymene (9.5–17.3%). Quantitatively they showed a significant variability at variance with the geographic origin of the plant material. The highest amount of thymol was found in Nourabad Mamasani and Dehdasht populations, with 36.4 and 35.2%, respectively, whereas the lowest one (20.3%) was found in the Kahnoyeh population. Moreover, the highest percentage of carvacrol was found in the Nourabad Mamasani and Dehdasht populations, with 33.1 and 30.6%, respectively, while the lowest one was detected in the Kahnoyeh population (18.8%). γ-Terpinene, which is related to the biosynthesis of the phenolic monoterpenes [42], showed an inverse trend, with the highest percentage (25.9%) in the essential oil from the Kahnoyeh population, and the lowest one in that from Nourabad Mamasani (13%). A similar trend was observed for p-cymene, with the oil from Behbahan population containing the highest percentage (17.3%), and that from Nourabad Mamasani showing the lowest value (9.5%) [33].
The essential oil chemical profiles of O. decumbens [33] detected in this study were in agreement with those described in previous studies in which thymol, carvacrol, γ-terpinene, and p-cymene resulted the major volatile constituents [2,7,30,36,38]. The variation in the number and content of essential oil constituents may be ascribable to factors including genetics, climatic, and geographic conditions, chemotype, collection time, and extraction technique [30,31,40]. It has been shown that geographical and meteorological factors affect the content and composition of O. decumbens essential oil [33,41]. Indeed, the essential oil content in O. decumbens showed a significant positive correlation with the soil sand content and temperature, while it revealed a negative correlation with the altitude [33]. In our study, the O. decumbens populations were collected at the same stage and time (flowering stage, 1–21 June 2017), thus we can exclude the effect of the phenological cycle. Also, the extraction and analytical methods were conducted in the same way. Therefore, we assume that the climate, environmental, and geographic conditions play a major role in affecting the essential oil chemical composition.

2.3. Antibacterial Activity

The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values (mg/ml) of the O. decumbens essential oils were in the ranges 0.0625–2 mg/ml and 1–16 mg/ml, respectively (Table 1 and Table 2). The mean of the MICs and MBCs showed that the Gram-positive bacteria had a higher sensitivity than the Gram-negative bacteria. Therefore, our findings are in accordance with previous studies showing a major impact on the Gram-positive bacteria [15,17,43]. The differences in antibacterial rate displayed by the O. decumbens essential oils may be attributed to the variation in the structure of cell wall in Gram-positive and negative bacteria as the cell wall of the latter is surrounded by an external membrane [10,14].
Moreover, the essentials oil from Nourabad Mamasani and Dehdasht populations showed the best performance in terms of MIC and MBC values, highlighting the highest inhibitory activity against both groups of bacteria. On the other hand, the essential oil from the Kahnoyeh population showed the lowest antibacterial activity with the highest MIC and MBC values. The strongest antibacterial activity of the essential oils from Nourabad Mamasani and Dehdasht populations might be attributed to the highest content of thymol (36.4 and 35.2%, respectively) and carvacrol (33.1 and 30.6%, respectively) and their possible synergism [44]. On the other hand, the oil from the Kahnoyeh population, with the lowest amount of thymol (20.3%) and carvacrol (18.8%), showed the weakest inhibitory activity. These differences in the content of thymol and carvacrol as the most important antimicrobial compounds, may explain the variability and level of the antibacterial activity among the four O. decumbens essential oils as a positive correlation exists between the content of thymol and carvacrol and the antibacterial efficacy [45]. As a matter of fact, Pearson correlation analysis was conducted to evaluate the relationship between the thymol and carvacrol contents and the antibacterial activity (MICs and MBCs). Results showed that thymol had a significant positive correlation with the carvacrol content (r = 0.996, significant at the 0.01 level), thus the thymol content increased together with that of carvacrol. Taken together, the thymol and carvacrol contents showed a significant negative correlation with MIC values (r = 0.984 and 0.979, respectively, significant at the 0.01 level) meaning that the most active essential oils were the richest in these compounds. In addition, the MBC values exhibited a non-significant positive correlation with MIC values (r = 0.729) and a non-significant negative correlation with the thymol and carvacrol contents (r = 0.833 and 0.851).
The thymol and carvacrol contents and the MIC and MBC values were selected for principal component analysis (PCA). The results of PCA based on PCI and PCII showed that Nourabad Mamasani and Dehdasht populations were placed into the same group, while Behbahan and Kahnoyeh populations belonged to two distinct groups (Figure 1). The essential oils from Nourabad Mamasani and Dehdasht populations were placed closer to the lines of thymol and carvacrol contents highlighting the greatest correlation with these components. On the other hand, the oil from Kahnoyeh population was placed close to MBC showing the lowest bactericidal activity (Figure 1).
Our results are in agreement with previous studies which documented the effectiveness of thymol and carvacrol compounds against various bacteria [46]. In addition, thymol and carvacrol were suggested as the bioactive compounds against Escherichia coli, Staphylococcus aureus, and Candida albicans [17]. Thymol and carvacrol inhibit the bacterial growth and ergosterol biosynthesis and also disrupt the bacterial membrane, resulting in ions and ATP leakage, and cell death [14,47,48]. The average MICs and MBCs displayed by the essential oils indicated that Clavibacter michiganensis and Agrobacterium tumefaciens were the most susceptible phytopathogens with the lowest MIC values (0.44 mg/ml). While, Xanthomonas citri, with the highest MIC values, showed the strongest resistance to the essential oils. In some cases, the essential oils activity was better than that of chloramphenicol used as positive control (Table 2 and Table 3). Indeed, the essential oils from Nourabad Mamasani, Dehdasht, and Behbahan populations inhibited Bacillus subtilis, with MIC values (0.0625, 0.25, and 0.5 mg/ml, respectively) lower than that of chloramphenicol. Moreover, the oil from Nourabad Mamasani showed the strongest activity against E. coli, with a MIC value (0.25 mg/ml) lower than that of chloramphenicol (Table 2). Furthermore, considering the average MBC of all essential oils assayed, Curtobacterium flaccumfaciens and S. aureus showed the highest and lowest sensitivity (2 and 8 mg/ml), respectively (Table 3). It is worth noting that the bactericidal activity of the essential oil from Nourabad Mamasani, showing the highest content of thymol and carvacrol, was higher than that of chloramphenicol against both groups of bacteria. Based on these findings, the Nourabad Mamasani population was found to be the best one, offering the conditions allowing plants to produce essential oils with high yield and high content of thymol and carvacrol. This assures a notable antibacterial activity against human pathogens and phytopathogens.

3. Materials and Methods

3.1. Plant Material

The aerial parts of O. decumbens populations were collected from Nourabad Mamasani, Kahnoyeh-Lar, Behbahan, and Dehdasht in Iran. The samples of the plants were harvested during the flowering stage in June 2017. The plant samples were identified by Prof. Ahmad Reza Khosravi and deposited at the herbarium of Biology Department, Shiraz University. The voucher specimens and geographical attributes of O. decumbens populations are shown in Table 3.

3.2. Essential Oil Isolation

The essential oils from the air-dried flowering aerial parts (50 g for each sample in three replications) were isolated by hydrodistillation using a Clevenger apparatus for 3 h. The collected essential oils were dried over anhydrous sodium sulfate. They were kept at 4 °C and under dark condition until further analysis.

3.3. GC-MS Analysis

The EOs composition was analyzed by gas chromatography-mass spectrometry (GC-MS). GC-MS analyses of the EO samples were carried out using a GC (Model 7890A; Agilent Technologies), equipped with a flame ionization detector (FID) and an HP-5 column (30 m × 0.32 mm i.d.; film thickness 0.25 μm). The program of column thermal started at 60 °C, then increased at the rate of 3 °C/min to 210 °C. Finally, the temperature reached 240 °C at the rate of 20 °C/min and maintained at the final temperature for 8.5 min. The injector temperature was 280 °C. Nitrogen was used as the carrier gas which contained an inlet flow of 1 mL/min. Gas chromatography-mass spectrometry analysis was conducted by the same GC coupled with a mass-spectrometer (Model MS-5975C, Agilent Technologies). The column included a HP-5MS (30 m × 0.32 mm i.d.; film thickness 0.25 μm). The injector and MS detector temperature was 280 °C. The ionization energy was 70 eV. Helium was also used as the carrier gas at 1 mL/min.

3.4. Determination of Minimum Inhibitory Concentration

The antibacterial assay was assessed using Gram-positive bacteria, Bacillus subtilis, Clavibacter michiganensis, Curtobacterium flaccumfaciens, and Staphylococcus aureus and Gram-negative bacteria, Xanthomonas citri, Agrobacterium tumefaciens, and Escherichia coli. Clavibacter michiganensis, Curtobacterium flaccumfaciens, Xanthomonas citri, and Agrobacterium tumefaciens were supplied by the Department of Plant Protection, Shiraz university, and Bacillus subtilis, Staphylococcus aureus, and Escherichia coli were obtained from Institute of Biotechnology, Shiraz University. The minimum inhibitory concentration (MIC) of the essential oils was determined by nutrient broth micro-dilution assay [49]. Bacterial species were cultured at 37 °C for 18 h into a nutrient broth medium on a shaker and their density was measured at OD600 using a spectrophotometer. The EOs were dissolved in sterile nutrient broth medium containing 5% dimethyl sulfoxide and 2.5% tween 80 and the serial two-fold dilutions of essential oils were prepared within the concentration ranges of 0.0312–16 mg/ml. Chloramphenicol (0.5%, Sina Darou, Iran; ranging from 0.00625 to 5 mg/ml) was used as positive control, while 5% dimethyl sulfoxide and 2.5% tween 80 (as solvent for EOs) were considered as negative control for all the bacteria. An amount of 100 μL of the diluted essential oils was added to each well containing 20 μL fresh bacterial suspension (OD = 0.5 at 600 nm). The microplates were covered and incubated overnight at 37 °C in a shaking incubator to mix the contents of the wells and then 20 μL of 0.5% p-iodonitrotetrazolium chloride (INT, Sigma-Aldrich) solution was added and incubated for 30 min in a shaking incubator. The MIC was recorded as the first concentration of the essential oil with no bacterial growth, which prevented the color change of the medium [50]. Before adding INT to the wells, the absorbance of bacterial growth was measured at 600 nm and the results of both methods were checked to obtain the real MIC values. The experiments were repeated twice with three replicates.

3.5. Determination of Minimum Bactericidal Concentration

The minimum bactericidal concentration (MBC) of O. decumbens essential oils was determined [51]. The amount of 5 μL of MIC and higher concentrations (without INT) were spread on nutrient agar plates and incubated at 37 °C overnight. The first concentration that showed no bacterial growth on nutrient agar medium was considered as MBC. The experiments were repeated twice with three replicates.

3.6. Statistical Analysis

The significant differences of the means of experimental groups were determined using one-way ANOVA followed by Duncan’s multiple range test (P < 0.05). All data analyses were performed using SAS software version 9.4. Pearson correlation analysis was conducted by SPSS software version 21 (SPSS Inc., Chicago, IL, USA). Biplot chart was drawn by Minitab 16 statistical software. The experiment was carried out in three replicates.

4. Conclusions

The results of this work shed light on the positive relationship between thymol and carvacrol contents and the level of antibacterial activity exhibited by the O. decumbens essential oils. The present study highlighted also the remarkable variability in the essential oil composition, content, and antibacterial activity of four Iranian populations of O. decumbens. These differences might be due to a number of factors including plant genetics and environmental factors characterizing each growing area for O. decumbens populations. Notably, the essential oil from the Nourabad Mamasani population exhibited a pronounced antibacterial activity and this was correlated with the highest essential oil contents of thymol and carvacrol. Interestingly, the MBC of this essential oil revealed to be better than that of the positive control chloramphenicol. On this basis, the essential oil of Nourabad Mamasani population is a valuable thymol and carvacrol-rich source which may be considered as a promising natural alternative to conventional antibiotics to be used to combat pathogens impacting human health and agriculture. Further studies are required to determine the effect of genetics and environmental factors on the content of thymol and carvacrol in the field. These measures might be effective in improving the amount of thymol and carvacrol constituents of the plants aimed to exploit them in the agrifood and pharmaceutical industries. The findings of this study could provide effective information for the commercial cultivation and breeding of O. decumbens in order to exploit its valuable compounds.

Author Contributions

Conceptualization, A.K. and F.M.; methodology, T.K. and A.T.; discussion of results, A.K., A.T., and F.M.; writing—original draft, A.T. and T.K.; supervision, A.K. and F.M.; funding acquisition, A.K. and F.M. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported by Shiraz University.

Acknowledgments

The authors would like to thank Prof. Ahmad Reza Khosravi (Department of Biology, Shiraz University) for identification and confirmation of the plant species.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Rechinger, K.H.; Hedge, I. Flora Iranica; Naturhistorisches Museum Wien: Wien, Austria, 1987. [Google Scholar]
  2. Amin, G.; Sourmaghi, M.S.; Zahedi, M.; Khanavi, M.; Samadi, N. Essential oil composition and antimicrobial activity of Oliveria decumbens. Fitoterapia 2005, 76, 704e707. [Google Scholar] [CrossRef] [PubMed]
  3. Ghahreman, A.; Okhovvat, A.R. Matching the Old Medicinal Plant Names with Scientific Terminology; University of Tehran Press: Tehran, Iran, 2010. [Google Scholar]
  4. Khorasani, M.A. Makhzanol-Advieh; Bavardaran Institute: Tehran, Iran, 2004. [Google Scholar]
  5. Tonekaboni, M.M.M. Tohfatul-Mo’menin; Nashreshahr Institute: Tehran, Iran, 2008. [Google Scholar]
  6. Saidi, M. Antioxidant activities and chemical composition of essential oils from Satureja khuzestanica, Oliveria decumbens and Thymus daenensis. J. Essent Oil. Bear. Plant 2014, 17, 513e521. [Google Scholar] [CrossRef]
  7. Karami, A.; Kavoosi, G.; Maggi, F. The emulsion made with essential oil and aromatic water from Oliveria decumbens protects murine macrophages from LPS-induced oxidation and exerts relevant radical scavenging activities. Biocatal. Agric. Biotechnol. 2019, 17, 538–544. [Google Scholar] [CrossRef]
  8. Eftekhari, M.; Ardekani, M.R.S.; Amin, M.; Attar, F.; Akbarzadeh, T.; Safavi, M.; Karimpour-razkenari, E.; Amini, M.; Isman, M.; Khanavi, M. Oliveria decumbens, a bioactive essential oil: Chemical composition and biological activities. Iran. J. Pharm. Res. 2019, 18, 412. [Google Scholar] [PubMed]
  9. Jamali, T.; Kavoosi, G.; Ardestani, S.K. In-vitro and in-vivo anti-breast cancer activity of OEO (Oliveria decumbens vent essential oil) through promoting the apoptosis and immunomodulatory effects. J. Ethnopharmacol. 2020, 248, 112313. [Google Scholar] [CrossRef] [PubMed]
  10. Hyldgaard, M.; Mygind, T.; Meyer, R.L. Essential oils in food preservation: Mode of action, synergies, and interactions with food matrix components. Front. Microbiol. 2012, 25, 3–12. [Google Scholar] [CrossRef] [Green Version]
  11. Khan, M.S.; Zahin, M.; Hasan, S.; Husain, F.M.; Ahmad, I. Inhibition of quorum sensing regulated bacterial functions by plant essential oils with special reference to clove oil. Lett. Appl. Microbiol. 2009, 49, 354–360. [Google Scholar] [CrossRef]
  12. Burt, S. Essential oils: Their antibacterial properties and potential applications in foods—a review. Int. J. Food. Microbiol. 2004, 94, 223–253. [Google Scholar] [CrossRef]
  13. Bahraminejad, S.; Seifolahpour, B.; Amiri, R. Antifungal effects of some medicinal and aromatic plant essential oils against Alternaria solani. J. Crop Prot. 2016, 5, 603–616. [Google Scholar] [CrossRef] [Green Version]
  14. Alizadeh Behbahani, B.; Tabatabaei Yazdi, F.; Vasiee, A.; Mortazavi, S.A. Oliveria decumbens essential oil: Chemical compositions and antimicrobial activity against the growth of some clinical and standard strains causing infection. Microb. Pathog. 2018, 114, 449–452. [Google Scholar] [CrossRef]
  15. Hajimehdipoor, H.; Samadi, N.; Mozaffarian, V.; Rahimifard, N.; Shoeibi, S.; Pirali, H.M. Chemical composition and antimicrobial activity of Oliveria decumbens volatile oil from west of Iran. J. Med. Plants 2010, 1, 39e44. [Google Scholar]
  16. Khajehie, N.; Golmakani, M.T.; Eblaghi, M.; Eskandari, M.H. Evaluating the Effects of Microwave-assisted hydrodistillation on antifungal and radical scavenging activities of Oliveria decumbens and Chaerophyllum macropodum essential oils. J. Food. Prot. 2017, 80, 783–791. [Google Scholar] [CrossRef]
  17. Masoum, S.; Samadi, N.; Mehrara, B.; Mahboubi, M. Potentiality of independent component regression in assessment of the peaks responsible for antimicrobial activity of Satureja hortensis L. and Oliveria decumbens Vent. Using GC-MS. J. Iran. Chem. Soc. 2018, 15, 2007–2016. [Google Scholar] [CrossRef]
  18. Vazirzadeh, A.; Jalali, S.; Farhadi, A. Antibacterial activity of Oliveria decumbens against Streptococcus iniae in Nile tilapia (Oreochromis niloticus) and its effects on serum and mucosal immunity and antioxidant status. Fish. Shellfish Immunol. 2019, 94, 407–416. [Google Scholar] [CrossRef]
  19. Bachir, R.G.; Benali, M. Antibacterial activity of the essential oils from the leaves of Eucalyptus globulus against Escherichia coli and Staphylococcus aureus. Asian. Pac. J. Trop Biomed. 2012, 2, 739–742. [Google Scholar] [CrossRef] [Green Version]
  20. Earl, A.M.; Losick, R.; Kolter, R. Ecology and genomics of Bacillus subtilis. Trends Microbiol. 2008, 16, 269–275. [Google Scholar] [CrossRef] [Green Version]
  21. Sundin, G.W.; Castiblanco, L.F.; Yuan, X.; Zeng, Q.; Yang, C.H. Bacterial disease management: Challenges, experience, innovation and future prospects: Challenges in bacterial molecular plant pathology. Mol. Plant Pathol. 2016, 17, 1506–1518. [Google Scholar] [CrossRef] [PubMed]
  22. Nandi, M.; Macdonald, J.; Liu, P.; Weselowski, B.; Yuan, Z.C. Clavibacter michiganensis ssp. michiganensis: Bacterial canker of tomato, molecular interactions and disease management. Mol. Plant Pathol. 2018, 19, 2036–2050. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Osdaghi, E.; Young, A.J.; Harveson, R.M. Bacterial wilt of dry beans caused by Curtobacterium flaccumfaciens pv. flaccumfaciens: A new threat from an old enemy. Mol. Plant Pathol. 2020, 21, 605–621. [Google Scholar] [PubMed] [Green Version]
  24. Bansal, K.; Midha, S.; Kumar, S.; Patil, P.B. Ecological and evolutionary insights into Xanthomonas citri pathovar diversity. Appl. Environ. Microbiol. 2017, 83, e02993-16. [Google Scholar] [CrossRef] [Green Version]
  25. Escobar, M.A.; Dandekar, A.M. Agrobacterium tumefaciens as an agent of disease. Trends. Plant Sci. 2003, 8, 380–386. [Google Scholar] [CrossRef]
  26. Altundag, S.; Aslim, B. Effect of some endemic plants essential oils on bacterial spot of tomato. J. Plant Pathol. 2011, 93, 37–41. [Google Scholar]
  27. Wińska, K.; Mączka, W.; Łyczko, J.; Grabarczyk, M.; Czubaszek, A.; Szumny, A. Essential oils as antimicrobial agents–myth or real alternative? Molecules 2019, 24, 2130. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Aghraz, A.; Benameur, Q.; Gervasi, T.; Ait Dra, L.; Ben-Mahdi, M.H.; Larhsini, M.; Markouk, M.; Cicero, N. Antibacterial activity of Cladanthus arabicus and Bubonium imbricatum essential oils alone and in combination with conventional antibiotics against Enterobacteriaceae isolates. Lett. Appl. Microbiol. 2018, 67, 175–182. [Google Scholar] [CrossRef] [PubMed]
  29. Benameur, Q.; Gervasi, T.; Pellizzeri, V.; Pľuchtová, M.; Tali-Maama, H.; Assaous, F.; Guettou, B.; Rahal, K.; Gruľová, D.; Dugo, G.; et al. Antibacterial activity of Thymus vulgaris essential oil alone and in combination with cefotaxime against bla ESBL producing multidrug resistant Enterobacteriaceae isolates. Nat. Prod. Res. 2019, 33, 2647–2654. [Google Scholar] [CrossRef]
  30. Esmaeili, H.; Karami, A.; Maggi, F. Essential oil composition, total phenolic and flavonoids contents, and antioxidant activity of Oliveria decumbens Vent. (Apiaceae) at different phenological stages. J. Clean. Prod. 2018, 198, 91–95. [Google Scholar] [CrossRef]
  31. Tahmasebi, A.; Hosseini, S.M.; Karami, A.; Afsharifar, A.; Sharifi Olounabadi, A.R. Variation in essential oil composition of Rydingia michauxii at the three developmental stages. Nat. Prod. Res. 2019, 33, 1–4. [Google Scholar] [CrossRef] [PubMed]
  32. Eyres, G.; Dufour, J.P.; Hallifax, G.; Sotheeswaran, S.; Marriott, P.J. Identification of character-impact odorants in coriander and wild coriander leaves using gas chromatography-olfactometry (GCO) and comprehensive two-dimensional gas chromatographyetime-of-flight mass spectrometry (GC_ GCeTOFMS). J. Sep. Sci. 2005, 28, 1061e1074. [Google Scholar] [CrossRef]
  33. Karami, A.; Khoushbakht, T.; Esmaeili, H.; Maggi, F. Essential oil chemical variability in Oliveria decumbens (Apiaceae) from different regions of Iran and its relationship with environmental factors. Plants 2020, 9, 680. [Google Scholar] [CrossRef] [PubMed]
  34. Jamali, T.; Kavoosi, G.; Safavi, M.; Ardestani, S.K. In-vitro evaluation of apoptotic effect of OEO and thymol in 2D and 3D cell cultures and the study of their interaction mode with DNA. Sci. Rep. 2018, 8, 1–19. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Mahboubi, M.; Taghizadeh, M.; Khamechian, T.; Tamtaji, O.R.; Mokhtari, R.; Talaei, S.A. The wound healing effects of herbal cream containing Oliveria decumbens and Pelargonium graveolens essential oils in diabetic foot ulcer model. World. J. Plast. Surg. 2018, 7, 45–50. [Google Scholar]
  36. Sajjadi, S.E.; Hoseini, S.A. Essential oil constituents of Oliveria decumbens Vent. J. Essent. Oil. Res. 2002, 14, 220–221. [Google Scholar] [CrossRef]
  37. Chorianopoulos, N.; Kalpoutzakis, E.; Aligiannis, N.; Mitaku, S.; Nychas, G.J.; Haroutounian, S.A. Essential oils of Satureja, Origanum, and Thymus species: Chemical composition and antibacterial activities against foodborne pathogens. J. Agric. Food Chem. 2004, 52, 8261e8267. [Google Scholar] [CrossRef]
  38. Sereshti, H.; Izadmanesh, Y.; Samadi, S. Optimized ultrasonic assisted extraction–dispersive liquid–liquid microextraction coupled with gas chromatography for determination of essential oil of Oliveria decumbens Vent. J. Chromatogr. A 2011, 1218, 4593–4598. [Google Scholar] [CrossRef] [PubMed]
  39. Najafpour Navaei, M.; Mirza, M. Essential oil of Oliveria decumbens Vent. Iran. J. Med. Aromat Plant. 2003, 15, 23–31. [Google Scholar]
  40. Zouari, S.; Ayadi, I.; Fakhfakh, N.; Jdir, H.; Aloui, L.; Kossentini, M.; Rebai, A.; Zouari, N. Essential oil variation in wild populations of Artemisia saharae (Asteraceae) from Tunisia: Chemical composition, antibacterial and antioxidant properties. Bot. Stud. 2014, 55, 76. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Nejad, S.; Badi, H.N.; Mehrafarin, A.; Abdossi, V.; Khalighi-Sigaroodi, F. The impact of macro environmental factors on essential oils of Oliveria decumbens Vent. from different regions of Iran. Jundishapur. J. Nat. Pharm. Prod. 2019, 14, e59456. [Google Scholar]
  42. Morshedloo, M.R.; Craker, L.E.; Salami, A.; Nazeri, V.; Sang, H.; Maggi, F. Effect of prolonged water stress on essential oil content, compositions and gene expression patterns of mono-and sesquiterpene synthesis in two oregano (Origanum vulgare L.) subspecies. Plant. Physiol. Biochem. 2017, 111, 119–128. [Google Scholar] [CrossRef]
  43. Mahboubi, M.; Feizabadi, M.M.; Haghi, G.; Hosseini, H. Antimicrobial activity and chemical composition of essential oil from Oliveria decumbens Vent. Iran. J. Med. Aromat. Plants. 2008, 24, 56–65. [Google Scholar]
  44. Gavaric, N.; Mozina, S.S.; Kladar, N.; Bozin, B. Chemical profile, antioxidant and antibacterial activity of thyme and oregano essential oils, thymol and carvacrol and their possible synergism. J. Essent Oil. Bear. Plant 2015, 18, 1013–1021. [Google Scholar] [CrossRef]
  45. Pirbalouti, A.; Rahimmalek, M.; Malekpoor, F.; Karimi, A. Variation in antibacterial activity, thymol and carvacrol contents of wild populations of’ Thymus daenensis subsp. daenensis’ Celak. Plant Omics. 2011, 4, 209–214. [Google Scholar]
  46. Zakaria Nabti, L.; Sahli, F.; Laouar, H.; Olowo-okere, A.; Wandjou, N.; Guileine, J.; Maggi, F. Chemical composition and antibacterial activity of essential oils from the Algerian endemic Origanum glandulosum Desf. Against Multidrug-Resistant Uropathogenic E. coli isolates. Antibiotics 2020, 9, 29. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Memar, M.Y.; Raei, P.; Alizadeh, N.; Aghdam, M.A.; Kafil, H.S. Carvacrol and thymol: Strong antimicrobial agents against resistant isolates. Rev. Med. Microbiol. 2017, 28, 63–68. [Google Scholar] [CrossRef]
  48. Lambert, R.; Skandamis, P.N.; Coote, P.J.; Nychas, G.J. A study of the minimum inhibitory concentration and mode of action of oregano essential oil, thymol and carvacrol. J. Appl. Microbiol. 2001, 91, 453–462. [Google Scholar] [CrossRef] [Green Version]
  49. Eloff, J.N. A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria. Planta Med. 1998, 64, 711–713. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Valgas, C.; Souza, S.M.D.; Smânia, E.F.; Smânia, J.A. Screening methods to determine antibacterial activity of natural products. Braz. J. Microbiol. 2007, 38, 369–380. [Google Scholar] [CrossRef] [Green Version]
  51. Ghasemi Pirbalouti, A.; Nourafcan, H.; Solyamani-Babadi, E. Variation in chemical composition and antibacterial activity of essential oils from Bakhtiari Savory (Satureja bachtiarica Bunge.). J. Essent Oil. Bear. Plant 2017, 20, 474–484. [Google Scholar] [CrossRef]
Figure 1. Biplot of the first two principal components (PCs) for the thymol and carvacrol contents and the MIC and MBC values of Oliveria decumbens populations.
Figure 1. Biplot of the first two principal components (PCs) for the thymol and carvacrol contents and the MIC and MBC values of Oliveria decumbens populations.
Antibiotics 09 00409 g001
Table 1. Antibacterial activity (expressed as minimum inhibitory concentration, MIC (mg/ml)) of different essential oils from Oliveria decumbens populations against Gram-positive and Gram-negative bacteria.
Table 1. Antibacterial activity (expressed as minimum inhibitory concentration, MIC (mg/ml)) of different essential oils from Oliveria decumbens populations against Gram-positive and Gram-negative bacteria.
BacteriaMeanEssential OilsChloramphenicol (mg/ml)
Nourabad MamasaniDehdashtBehbahanKahnoyeh
Gram-positive S. aureus0.63 ± 0.25 a*0.50.510.50.2
B. subtilis0.45 ± 0.41 a0.06250.250.510.8
C. michiganensis0.44 ± 0.13 a0.50.250.50.50.025
C. flaccumfaciens0.47 ± 0.39 a0.1250.250.510.025
Average MIC against Gram-positive bacteria0.490.30 ± 0.24 a0.31 ± 0.13 a0.63 ± 0.25 ab0.75 ± 0.29 b0.26 ± 0.37 a
Gram-negativeX. citri1.25 ± 0.5 b11210.4
A. tumefaciens0.44 ± 0.38 a0.250.250.2510.025
E. coli0.69 ± 0.38 ab0.250.5110.4
Average MIC against Gram-negative bacteria0.780.5 ± 0.43 a0.58 ± 0.38 a1.08 ± 0.88 a1 ± 0 a0.28 ± 0.22 a
Average MIC against both groups of bacteria0.610.38 ± 0.32 a0.43 ± 0.28 ab0.82 ± 0.59 bc0.86 ± 0.24 c0.27 ± 0.29 a
* Means followed by the same letters (a, b, c) are not significantly different according to Duncan’s multiple range test at the significance level P < 0.05. The results of significant differences are means ± standard deviations of the populations and bacteria.
Table 2. Antibacterial activity (expressed as minimum bactericidal concentration, MBC (mg/ml)) of different essential oils from Oliveria decumbens populations against Gram-positive and Gram-negative bacteria.
Table 2. Antibacterial activity (expressed as minimum bactericidal concentration, MBC (mg/ml)) of different essential oils from Oliveria decumbens populations against Gram-positive and Gram-negative bacteria.
BacteriaMeanEssential OilsChloramphenicol (mg/ml)
Nourabad Mamasani DehdashtBehbahanKahnoyeh
Gram-positiveS. aureus8 ± 5.66 b*484165
B.subtilis7 ± 2 ab48881.6
C. michiganensis4.25 ± 2.87 ab14481.6
C. flaccumfaciens2 ± 1.41 a11243.2
Average MBC against Gram-positive bacteria5.312.5 ± 1.73 a5.25 ± 3.4 ab4.5 ± 2.52 ab9 ± 5.03 b2.85 ± 1.62 a
Gram-negativeX. citri4.5 ± 2.52 a24485
A. tumefaciens6 ± 6.73 a224160.1
E. coli6 ± 6.73 a224165
Average MBC against Gram-negative bacteria5.52 ± 0 a2.67 ± 1.15 a4 ± 0 a13.33 ± 4.62 b3.37 ± 2.83 a
Average MBC against both groups of bacteria5.392.29 ± 1.25 a4.14 ± 2.85 a4.29 ± 1.8 a10.86 ± 5.01 b3.07 ± 2.01 a
* Means followed by the same letters (a, b) are not significantly different according to Duncan’s multiple range test at the significance level P < 0.05. The results of significant differences are means ± standard deviations of the populations and bacteria.
Table 3. Geographical characteristics and voucher specimens of Oliveria decumbens populations from which essential oils were obtained.
Table 3. Geographical characteristics and voucher specimens of Oliveria decumbens populations from which essential oils were obtained.
No.PopulationProvinceLatitude (N)Longitude (E)Altitude (m)Voucher Specimen
1Nourabad MamasaniFars30°08′21.6”51°33′16.3”126855079
2Kahnoyeh, LarFars27°57′59.6”53°24′11.8”75855076
3BehbahanKhuzestan30°32′09.2”50°23′36.5”39455075
4DehdashtKohgiluyeh and Boyer-Ahmad30°51′07.3”50°35′14.5”97155080

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Khoshbakht, T.; Karami, A.; Tahmasebi, A.; Maggi, F. The Variability of Thymol and Carvacrol Contents Reveals the Level of Antibacterial Activity of the Essential Oils from Different Accessions of Oliveria decumbens. Antibiotics 2020, 9, 409. https://doi.org/10.3390/antibiotics9070409

AMA Style

Khoshbakht T, Karami A, Tahmasebi A, Maggi F. The Variability of Thymol and Carvacrol Contents Reveals the Level of Antibacterial Activity of the Essential Oils from Different Accessions of Oliveria decumbens. Antibiotics. 2020; 9(7):409. https://doi.org/10.3390/antibiotics9070409

Chicago/Turabian Style

Khoshbakht, Tahereh, Akbar Karami, Aminallah Tahmasebi, and Filippo Maggi. 2020. "The Variability of Thymol and Carvacrol Contents Reveals the Level of Antibacterial Activity of the Essential Oils from Different Accessions of Oliveria decumbens" Antibiotics 9, no. 7: 409. https://doi.org/10.3390/antibiotics9070409

APA Style

Khoshbakht, T., Karami, A., Tahmasebi, A., & Maggi, F. (2020). The Variability of Thymol and Carvacrol Contents Reveals the Level of Antibacterial Activity of the Essential Oils from Different Accessions of Oliveria decumbens. Antibiotics, 9(7), 409. https://doi.org/10.3390/antibiotics9070409

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