The Antimicrobial Activity of Essential Oil from Perovskia abrotanoides Karel and its Main Components

Indian Journal of Pharmaceutical Sciences 343 May June 2009 Results of screening of antifungal activity of Asparagus racemosus extract are summersed in Table 1. It is evident from the results, that the methanol extracts shows high anticandidal activity against all the Candida tested. The zone of inhibition ranged from 13 to 16 mm. The MIC values were between 2.5 to 0.312 mg/ml, while MFC values were between 5 to 0.625 mg/ml. The detailed chemical nature of the active principle(s) responsible for the antifungal activity is not known however, the preliminary screening has shown the presence of glycosides, steroids, saponins and flavonoids.

Results of screening of antifungal activity of Asparagus racemosus extract are summersed in Table  1. It is evident from the results, that the methanol extracts shows high anticandidal activity against all the Candida tested. The zone of inhibition ranged from 13 to 16 mm. The MIC values were between 2.5 to 0.312 mg/ml, while MFC values were between 5 to 0.625 mg/ml. The detailed chemical nature of the active principle(s) responsible for the antifungal activity is not known however, the preliminary screening has shown the presence of glycosides, steroids, saponins and flavonoids.
Perovskia genus, Labiatae family has seven species out of which three species such as P. abrotanoides, P. atriplicifolia and P. artemisoides grow in Iran [1] . P. abrotanoides with vernacular name of Brazambal, Domou, and Gevereh is a perennial herb growing wild in Iran, Afghanistan, Pakistan and Turkmenistan [2] . People customarily has been used the grinded roots of plant in water, sesame oil and wax and is used like a paste for treatment of leishmaniasis with any scientific base. Attempts have been made to explain the efficacy of this plant for treatment of leishmaniasis [2,3] . Some of the pharmacological effects of plant such as leishmanicidal, antiplasmodial and cytotoxic activity [2,3] as well as antinociceptive and antiinflammatory have been confirmed [4] . The lesions of leishmaniasis become susceptible to colonization or infection with a number of pathogenic or opportunistic fungi and bacteria that cause secondary infections. Lesion care and management of secondary infections are essential in recovery of leishmaniasis [5] . Perhaps the antimicrobial activity of P. abrotanoides could contribute to treat leishmaniasis. There was only one report about antifungal activity of essential oil from flowers of P. abrotanoides against Aspergillus niger, Aspergillus flavus, C. albicans and Trichopyhton mentagrophytes [6] . Inouye et al had documented that this oil with main constituents of 1,8-cineole and α-pinene showed no activity against C. albicans and fungi [6] . In this investigation, we have evaluated the in vitro antimicrobial activity of aerial part of P. abrotanoides essential oil and its major components against some microorganisms including Gram positive, Gram negative bacteria, yeast and fungi.
Essential oil from aerial part and its major components P. abrotanoides of known composition (α-pinene 12%, camphor 23%, 1,8-cineole 22%, β-pinene 3.1% and limonene 1.5%) was obtained from Barij Essence Pharmaceutical Company. Camphor, α-pinene, and 1, For screening of antimicrobial activity disc diffusion [7] and micro broth dilution [9] assays were used. In disc diffusion method, the cultured bacteria were suspended in normal saline but spore of fungi and yeast was inserted in RPMI 1640 (Sigma-Aldrich chemie GmbH, Steinheim, Germany) buffered with 0.165 M morpholine propane sulfonic acid (MOPS, Merck KGaA, Darmstadt, Germany) [8] . The turbidity of microorganisms was adjusted to 0.5 McFarland. The inocula were 1×10 8 , 1×10 6 CFU/ml for bacteria and fungi respectively. Inoculate was swabbed on Muller Hinton Agar (bacteria) and sabouraud dextrose Agar (fungi) by sterile cotton swab. Sterile blank discs impregnated with 3, 5, 10 µl of oil in 10 µl of dimethylsulfoxide (DMSO) were used and put on cultured plates. Disc containing DMSO and antibiotics were used as control. The plates were incubated at 37, 25 aerobically and the zone inhibition diameters was measured in millimeter (mm) after 24 and 48 h for bacteria and fungi respectively. The minimal inhibitory concentrations (MICs) were determined by micro broth dilution assay [9] . A two fold serial dilution of oil and its main components (1,8-cineole, α-pinene, and camphor) were prepared in 10% DMSO (serial dilution= 32-0.125 µl/ml). Muller Hinton broth [9] and RPMI 1640 [8] were used as a broth media for bacteria and fungi respectively. After shaking of dilutions, 100 µl of each dilution was inserted in each well and 100 µl of above microbial suspension was diluted (bacteria ca.1×10 6 , fungi ca. 0.5-1×10 5 CFU/ml) and then was added to each serial dilution and incubated. MICs were defined as the first well with no visible growth and minimal bactericidal or fungicidal concentrations (MBCs or MFCs) were as the first well that no growth on solid media after 24, 48 h for bacteria and fungi, respectively.
For viability assay of oil and main components against S. aureus, five flasks containing 5 ml of cell suspension in Cation adjusted Muller Hinton broth (approximately 5×10 6 CFU/ml) were prepared. P. abrotanoides oil and main components was added at the MIC concentration value to each flask except control. One hundred microlitres of control flask was sampled immediately, serially diluted and placed on nutrient agar to determine the cell density. After 30, 60, 120 min at room temperature, aliquots (100 µl) were removed to neutralizing buffer (0.075 M buffer phosphate pH 7.9), serially diluted and CFU/ml were determined for each components and oil and Log CFU/ml was calculated [10] .
The results showed that C. albicans and Gram positive bacteria especially S. aureus were highly susceptible to the oil. The oil showed no zone inhibition against fungi and Gram negative bacteria ( Table 1). The oil exhibited the large inhibition zone against S. aureus and the zone inhibitions were enhanced with increasing the amount of essential oil (14.4±1.4 to 29±5.8 mm). The effect of oil was larger than vancomycin.
The oil showed bactericidal effect against S. aureus with MIC and MBC values equal 8 µl/ml. The zone inhibition of S. aureus was larger than the zone inhibition of B. cereus but the MIC of oil for B. cereus was lower than MIC value of S. aureus ( Table 2). C. albicans was more sensitive than A. niger to the oil and the oil had fungicidal activity against C. albicans and its effect was comparable to amphotericin B. The MIC values of camphor was lower than that of α-pinene against all of the tested microorganisms ( Table 2). The MIC and MBC values of camphor for fungi and yeast were 2 µl/ml and were twofold of these values for Gram positive bacteria. The MIC and MBC values of camphor against Gram negative bacteria were 2, 4 µl/ ml. α-pinene showed the best antimicrobial activity against S. aureus, B. cereus and A. niger. C. albicans was more sensitive than Gram negative bacteria to α-pinene. 1,8-cineole was less effective against all of the tested microorganisms after 24 h. The oil was less active than camphor against all of the tested microorganisms like α-pinene against A. niger, S. aureus. Oil was more active than 1,8-cineole against Gram positive bacteria, yeast and fungi.
In viability assay, log CFU/ml of S. aureus for 1,8-cineole decreased more than that for α-pinene and camphor but this value was increased for α-pinene and 1,8-cineole after 60 min. The log CFU/ml of S. aureus for camphor decreased continuously. The effect of oil and camphor after 60 min on viable bacteria was increased but log CFU/ml of 1,8-cineole and α-pinene was increased and this effect is decreased ( fig.1). Finally, camphor, α-pinene and 1,8-cineole standards showed antimicrobial activity against all of the tested microorganisms, camphor being the most effective followed by α-pinene and then 1,8-cineole.
Plant products have renewed interest in their use as alternative source of antimicrobial compounds [11,12] because problems of the uncontrolled use of  MIC is minimal inhibitory concentration (µl/ml), MBC is the minimal bactericidal concentration (µl/ml) and MFC is the minimal fungicidal concentration (µl/ml) synthetic antibiotics [13] . Phytochemicals are small organic biomolecules generally hydrophobic and are designated as naturally occurring antibiotics. Cytoplasmic membrane coagulation, break down of proton motif, breakdown of electron flux and active transport unbalance are some events responsible for providing the antimicrobial property of phytochemicals [14] .
P. abrotanoides dried root has been successfully used for treatment of cutaneous leishmaniasis in Iranian traditional medicine as poultice [2,3] . In leishmaniasis, the patient may develop a secondary bacterial infection and S. aureus is the predominant species [15] . Lesion care and prevent of generation of secondary infections is important in treatment of leishmaniasis.
Probably, this plant's leishmanicidal activity has been antimicrobial activity that helps to treat the leishmaniasis.
The Gram negative bacteria were resistant to P. abrotanoides oil than Gram positive bacteria. The outer layer of Gram negative bacteria is composed of lipopolysaccharide. This layer forms a hydrophobic permeability barrier which restricts diffusion of hydrophobic compounds through its lipopolysaccharide covering [16] . Essential oils always represent a complex mixture of different chemical components. The nature and proportion of the individual constituents of the oil could influence on their antimicrobial activity. 1,8-cineole is a lipophilic compound and the lipophilic property of α-pinene is more than camphor. Generally, a more lipophilic compound had greater affinity for cell membranes and had greater toxicity. Therefore, 1,8-cineole had the best effect on viability of S. aureus and the effect of α-pinene and then camphor was lower.
After 24 h, the effect of camphor on viability of bacteria is more than that of α-pinene and 1,8-cineole. Furthermore, the lipophilic structure of components, the difference in antimicrobial activity of components is attributed to aqueous solubility of components.
Uptake of monoterpenes will be determined by both its aqueous solubility and the permeability of the outer envelope of microorganisms [10] . The aqueous solubility of camphor is larger than others and had more antimicrobial activity than other components against all of the microorganisms. 1,8-cineole are inactive probably because was unable to effectively penetrate the outer membrane for long time. Camphor and α-pinene were found in high concentration in P.
abrotanoides oil and possess antimicrobial activity.
High concentrations of α-pinene and camphor in the essential oil are probably an explanation for the antimicrobial activity possessed by P. abrotanoides against Gram positive bacteria and yeast. α-Pinene destroys the cellular integrity of Gram positive bacteria and inhibit respiratory activity in yeast mitochondria and had some antifungal activity but Gram negative bacteria were more resistant to it [17] .
It was shown that 1,8-cineole was inactive against Gram positive bacteria [18] but other study showed 1,8-cineole had some antifungal activity [19] and high insecticidal property [20] . The MIC values of oil were usually lower than those of their constituents. One reason for this result could be synergistic action of components. Therefore, the antibacterial activity of oil from P. abrotanoides can be attributed to its major components and/or trace compounds and possible synergistic and antagonistic effect of compounds in the oil. S. aureus is most sensitive organism to P. abrotanoides oil. S. aureus is an important secondary pathogenic bacterium in leishmaniasis which may play an important role in the size and shape of the lesion, as well as in scar development [5] . Treatment of secondary infection is required and elimination of parasites after treatment was followed. Therefore, P. abrotanoides can be used as antibacterial and antileishmanial agent for treatment of leishmaniasis.
Some in vivo clinical studies should be done for evaluating of this effect.