Review Article

Bioactive Compounds from Mentha Spp. As a Potential Antifungal against Species of Candida. A Review Article

Paula Cristina Anibal, Simone Nataly Busato de Feiria, Anderson Laerte Teixeira, Jose Francisco Hofling*

Paula Cristina Anibal, Simone Nataly Busato de Feiria, Anderson Laerte Teixeira, Jose Francisco Hofling*

Faculty of Dentistry of Piracicaba- UNICAMP, 901, Av.Limeira, District Vila Areião, Piracicaba- SP, Brazil

*Address for Correspondence: Jose Francisco Hofling, Faculty of Dentistry of Piracicaba- UNICAMP, 901, Av.Limeira, District Vila Areião, Piracicaba- SP, Brazil, E-mail: hofling@fop.com.br

Dates: 16 August 2017; Approved: 21 August 2017; Published: 23 August 2017

Citation this article: Anibal PC, de Feiria SNB, Teixeira AL, Hofling JF. Bioactive Compounds from Mentha Spp. As a Potential Antifungal against Species of Candida. A Review Article. Sci J Res Dentistry. 2017;1(2): 033-037.

Copyright: © Hofling JF, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Fungi of the genus Candida, have become more frequent as agents of fungal infections, particularly associated with immunocompromised patients. It has been reported in the literature an increasing occurrence of resistance of these microorganisms to antifungal drugs available for the treatment of these pathologies, such as polyenes and azoles agents, which has led researchers in this field to seek new alternatives for drugs that have action against these organisms. Medicinal plants have long been used in the treatment of diseases through their extracts, essential oils and their bioactive components which makes them great source of new drugs research. Essential oils extracted from plants of the genus Mentha spp. have demonstrated potential of antimicrobial action, especially antifungal activity against fungi of the genus Candida.

Introduction

The use of plants as a therapeutic resource in the treatment of diseases is known millennially by many civilizations, being transmitted from generation to generation and used until today. In recent years, there has been a great scientific advance involving studies around this subject, aiming to obtain new compounds with therapeutic properties. Ethnopharmacology, an area of science that studies the interaction between plants and Human, have helped scientific advances in this area by cataloging species of plants considered medicinal by several peoples, allowing the empirical nature of the use of plants to give space for scientific reasoning, through research aimed at proving the pharmacological effect of therapeutics [1,2,3].

Studies involving the use of medicinal plants and phytotherapeutic action have already contributed to the obtaition of several drugs used in traditional medicine, among them emetin, salicylin, vincristine, among others [4,1]. In Brazil, there is great importance of studies on medicinal plants, mainly for the valorization of their use, including by the Ministry of Health, with incentive programs with the basic health units of the country. In the dental area, the recognition of phytotherapy as an integrative and complementary practice to oral health (resolution CFO-082/2008) was a great step to regulate the performance of the dentist surgeon in an area not yet explored by professionals [5]. Studies have shown that some oils and extracts obtained through some aromatic plants are efficient in antimicrobial control, including those that colonize the oral cavity [6,7].

With the increasing development of drug resistance and the appearance of undesirable effects by antifungal agents, research by new antimicrobial components has been a concern of many researchers [8]. In the last decade, interest in natural products has increased, with medicinal plants being sources of bioactive compounds. These compounds have been isolated and subjected to detailed structural analyzes, and their mode of action and target known. Many plants used in folk medicine have been studied for their antimicrobial activities, as a source of new antifungal compounds with few side effects, with a great range of action and low cost [9]. The screening of antibacterial plant extracts represents a continuous effort to find new compounds with potential to act against multiresistant bacteria [10].

The discovery of drugs involving the diversity of natural products, combined with synthetic drug methodologies and including the manipulation of biosynthetic pathways, provides a solution for the scientific community focused on the discovery and development of drugs [11]. According to the World Health Organization, at least 80% of the population in developing countries rely on “folk medicine” for the solution of health problems, and 85% of this total use medicinal plants for the treatment of various diseases. This means, according to the United Nations, that around four billion people worldwide rely on herbal remedies [12].

In this context, one of the plants better known as medicinal is Mentha spp., popularly known as Mint or mint. This plant is one of the most cited in ethnobotanical and ethno-pharmacological studies and is of great economic interest due to the production of essential oil rich in menthol [13]. Studies already carried out with Mentha spp. showed antimicrobial activities related to some species of this genus. The most cited activities of the plant are: antiviral, antibacterial and antifungal [14-16]. The activity found in literature of greater interest has been the antifungal, activity due to the innumerable cases of candidosis reported in the last decades.

In recent years, cases of fungal infections have increased. According to studies, part of this phenomena is due to the incidence of increasing cases of immunosuppressive diseases, such as AIDS (Acquired Immunodeficiency Syndrome) and cancer, diseases that cause weakness of the patient’s immune system and allows fungi of the genus Candida spp., considered as commensal, because it is in equilibrium in the organism of healthy people, becomes an opportunistic pathogen, and can lead the patient to death [17,18]. It is known that among the fungi of the genus Candida, the most common species are: C. albicans, C. krusei, C. tropicalis, C. guilliermondii, C. parapsilosis and C. glabrata [19,20].

Due to increased cases of fungal infections, many conventional antimicrobials have been used more frequently, allowing the selection of resistant microorganisms and becoming one of the major challenges in treating the disease [21-24]. Thus, one of the most promising goals involving the study of plants with medicinal potential is to find effective active principles in the discovery of new antimicrobial drugs.

Literature Review

Mentha spp.

Mentha spp., are plants belonging to the family Lamiaceaes, is an annual herb, 30 to 60 cm high [13]. The aerial parts of Mentha spp. contain structures named as glandular trichomes, which are present in the axial part of the leaf, responsible for the secretion of essential oil produced by the secondary metabolism of the plant [25].

Natural products used as phytotherapics from Mentha spp. oil, one of the most consumed essential oils, can lead to new treatment modalities, aiding in the recovery and maintenance of health. Several species of Mentha spp. have been the subject of studies on their metabolic differences, chemical compositions, antibacterial, antifungal and antiviral properties [22,26-28]. Among the antimicrobial actions, stands out the antifungal effect on the genus Candida [13,29,30], and in the biofilm of C. albicans [22,31]. Agarwal, et al. [32], tested essential oil of mint in order to evaluate the inhibitory effect against biofilm formation by C. albicans, which showed a reduction of 80.87 and 74.16% of the biofilm formation for the two oils, respectively [32].

According to Mkaddem et, al. [33], Mentha spp. is composed of approximately 89% of monoterpenes [33]. Its main chemical components are menthol, mentone, isomentone, pulegone, piperitenone, piperitenone oxide, carvone and linalol [22,34,35]. Among these compounds, menthol is the most cited target of antimicrobial studies, and according to Al-Bayati et al. (2009), menthol showed antimicrobial activity in vitro tests [36].

Mimica-Dukic et, al. [37], observed that Mentha aquatica oil was composed of 16.94% of menthofuran and 14.15% of 1,8-cineol, among other compounds; while M. piperita had 39.63% of menthol and 8.93% of mentone in its composition, among other substances [37]. They also observed that the essential oil of M. aquatica shows antimicrobial activity against Escherchia coli, Salmonella typhi, Micrococcus flavus, S. aureus, Bacillus subtillis and C albicans; while M. piperita essential oil demonstrated activity against E. coli, S. typhi, S. enteritidis, Shigella sonei, Sarcina lutea, M. flavus, S. aureus, Staphylococcus epidermidis, Bacillus subtillis and C. albicans.

Iscan et, al. [15], found antimicrobial activity in vitro Menthapiperita assays. In addition to the oil, menthol and mentone fractions were isolated from the plant, and the species of microorganisms tested showed greater sensitivity to menthol than to menthona [15]. In another study, the oil of M. piperita showed high antifungal and inhibitory action on biofilm, and the main compound identified was menthol [22]. Yigit et, al. [38], showed that Mentha piperita possesses antimicrobial activity, with antifungal activity (C. albicans) and antibacterial activity (E.coli). The author highlights that one of the main responsible for the activity presented is menthol and pulegone [38].

Other studies have confirmed the excellent antimicrobial activity in essential oils rich in pulegone, reporting even greater susceptibility to Candida spp. To this compound specifically [35,39]. Mkaddem et, al. [33], demonstrated good antimicrobial activity of the essential oil of Mentha longifolia, whose major component was pulegone, showing strong activity against mycelial fungi and yeasts [33]. Oumzil et, al. [26], in tests performed with compounds of Mentha suaveolens, showed that all the compounds present antimicrobial activity. The highest sensitivity according to MIC (minimum inhibitory concentration) was in response to pulegone, menton, limonene and carvone respectively [26]. Carvone, a compound found in large amounts in the essential oil obtained from M. suaveolens in Egypt, appears to be involved with potent anti-candida according El-Kasshoury et, al. [40].

Through gas chromatography analyzes, Sarer et, al. [41], identified 37 compounds present in the essential oil of M. spicata, representing 95.3% of the oil, being the principal compounds the oxygenated monoterpenes (77.5%), with the presence of carvone (48.4%), and 1,8-cineol (21.3%) in greater abundance. They also found antimicrobial activity of essential oil against S. aureus, Enterococcus faecalis, Pseudomonas aeruginosa, E. coli, C. albicans and C. tropicalis [41].

Boni et, al. [42], worked with compounds isolated from Mentha (carvone, mentone, menthofuran and pulegone), finding antifungal activity at concentrations ranging from 0.5 to 8 mg / mL against strains of Candida spp., besides inhibiting adhesion, progression and formation of C. albicans MYA-2876 biofilm, and inhibition of germ tube formation [42]. Feiria et, al. [43], observed that the essential oils of M. aquatica, M. arvensis and M. piperita inhibited the formation of the mature biofilm of C. albicans MYA-2876 [43].

Candida spp. and Candidoses

Fungal infections caused by yeasts of the genus Candida spp., also called candidoses, are the most frequent infections associated with depletion of the immune system. The predisposing factors for the disease are: advanced age, hormonal diseases, nutritional deficiency, HIV incidence, frequent exposure to antimicrobials, chemotherapeutic treatments, carbohydrate-rich diets, use of prostheses and low immunity [18-20,44,45].

The yeast Candida albicans is the most frequent etiological agent in cases of fungal infections, being associated in up to 50% of cases of this type of disease [19,46]. This genus has the capacity to adapt and proliferate easily in the environment of the human body, in several places. This ability to adapt to different tissues of the human organism is related to its morphological transition capacity, called polymorphism, that presents variations of yeast growth for fungi forming hyphae [47]. According to Mayer et, al. [48], both the hyphal form and the yeast form are involved in the infection process [48], and the yeast, being smaller, is capable of spreading, whereas the hyphae invades the host tissue by penetrating the epithelium with the aspartyl proteinases and phospholipases, escaping from phagocytic cells [49-51].

The Secreted Aspartyl Proteinase (SAP) protein from the aspartic protease family consists of 10 individual members, Sap1 through Sap10, and has been described as the key to determining the virulence of C. albicans. Extensive research on Sap1 to Sap6 has demonstrated functional association of Saps with pathogenicity of C. albicans, by hydrolyzing host proteins, assisting in colonization and infection in different tissues. Sap proteins have several functions, ranging from tissue invasion to immune system evasion [52,53]. The presence of the SAP family gene is unique to pathogenic Candida species such as C. albicans [54], C. dubliniensis [55], C. tropicalis [56] e C. parapsilosis [57], but it is absent in non-pathogenic yeasts such as Saccharomyces cerevisiae, that increases the hypothesis that proteinases may be involved with virulence factors [58].

The advantage of having a family of proteinases such as Sap is that the production of several isoenzymes, each having a different optimal pH to perform its functions, can aid the colonization and infection of Candida albicans in different tissues and environments, since Sap has activity between pH 2-7, as Sap1-3 (associated with the yeast form) has pH optimum between pH 3-5, and Sap4-6 (associated with hyphae form) develops best at pH 5-7 [52].

Another advantage is in the breakdown of peptides. For example, Sap1, Sap2, Sap3 and Sap6 break peptide bonds between hydrophobic chains of amino acids, with Sap1, Sap2 and Sap6 breaking phenylalanine, whereas Sap3 breaks leucine [59]. The Sap2 enzyme degrades many human proteins in the mucosa, including extracellular matrix and surface proteins, such as keratin, collagen, fibronectin, laminin and mucin [58].

Another factor associated with virulence is the ability of Candida spp. to form biofilms, promoting the cellular adhesion and formation of the extracellular matrix of the biofilm, as well as the synthesis of proteins that favor its adhesion. The biofilm formation is a relevant fact due to its ability to be more resistant to antimicrobial agents, due to the difficulty of penetration in the extracellular matrix, and the action of the immune system, besides allowing the increase of the gene expression of mechanisms of resistance to antifungals as the efflux pumps [60].

Resistance To Antimicrobials and Medicinal Plants

The resistance of organisms against antifungal drugs is rapidly becoming a major problem, especially when it comes to infections in immunocompromised patients. The major antifungal agents known to treat candidoses are polyenes (nystatin and amphotericin B) and azoles (miconazole, fluconazole, ketoconazole) [20]. Despite the range of antifungal agents available for the control of these microorganisms, Candida spp. has developed molecular strategies for the expression of resistance to existing drugs. Results evidenced by Ramesh et al. (2010) showed that strains of Candida spp., from HIV patients shows resistance to fluconazol (23.5%), itraconazole (41.1%) and nystatin (11.9%), being that other species of Candida spp. showed resistance to almost all drugs tested, which makes it difficult to treat these infections [61]. Candida species have been reported as frequent agents in hospital infections of high resistance to antifungals [62,63]. Such evidence leads to an increasing need for the development of effective new drugs [62,64].

New approaches have been reported in the literature on the control of these microorganisms, such as the combined use of antifungal agents (synergism) and development of alternative compounds such as plant extracts, essential oils and derivatives isolated from plants [65]. The development of research on antimicrobial activity of plants for the production of new drugs aimed at reducing the side effects and resistance of microorganisms is a worldwide trend [66]. Despite the great diversity of existing antimicrobials, studies with medicinal plants aim to search for new drugs capable of presenting a greater spectrum of action, lower resistance index and lower toxicity [67,63]. In addition, the use of Mentha spp. has been associated with the development of new antimicrobial compounds, which will be of great importance as a result of the numerous reported cases of resistance to some drugs [68].

References

    1. Cechinel Filho V, Yunes RA. Strategies for obtaining pharmacologically active compounds from medicinal plants. Concepts about structural modification for optimization of activity. Química nova. 1998; 21: 99-105. https://goo.gl/x2mdXF
    2. Santos E B, Dantas G S, Santos H B, Diniz M F F M, Sampaio F C. Ethnobotanical study of medicinal plants for oral problems in the municipality of João Pessoa, Brazil. Brazilian Journal of Ethnopharmacognosia. 2009; 19: 321-324. https://goo.gl/4rcY11
    3. Oliveira F Q, Gobira B, Guimarães C, Batista J, Barreto M, Souza M.  Plants species indicated in odontology. Revista Brasileira de Farmacognosia. 2007; 17: 466–476. https://goo.gl/P52gzw
    4. Veiga Jr, Pinto A C, Maciel M A M. Medicinal plants: safe cure? Química Nova. 2005; 28: 519-528. https://goo.gl/EVGWAt
    5. Assis C. Medicinal plants in dentistry. Rev. bras. Odontol. 2009; 66: 72-75.
    6. Duarte M C T, Figueira G M, Pereira B, Magalhães P M, Delarmina C. Antimicrobial activity of hydroalcoholic extracts of species from the collection of medicinal plants CPQBA / UNICAMP. Rev. Bras. Farmacogn. 2004; 14: 06-08. https://goo.gl/tKiSTh
    7. Cecanho R, Koo H, Rosalen P L J A, Park Y K, Cury JÁ. Effect of the Mikania laevigata hydroethanolic extract on bacterial growth and the production of glucos by mutans streptococcus. Anais da XIV Reunião Anual da FESBE, Caxambu – MG. 1999; 14: 290.
    8. phongpaichit s, subhadhirasakul s, wattanapiromsakul c. Antifungal activities of extracts from Thai medicinal plants against opportunistic fungal pathogens associated with AIDS patients. Mycoses. 2005; 48: 333-8. https://goo.gl/khW8NX
    9. Ishida K, Mello JCP, Cortez DAG, Filho BPD, Ueda-Nakamura T, Nakamura CV. Influence of tannins from Stryphnodendron adstrngens on growth and virulence factors of Candida albicans. J Antimicrob Chemother. 2006; 58: 942-9. https://goo.gl/L1XexW
    10. Suffredini IB, Sader HS, Gonçalves AG, Reis AO, Gales AC, Varella AD, et al. Screening of antibacterial extracts from plants native to the Brazilian Amazon Rain Forest and Atlantic Forest. Braz J Med Biol Res. 2004; 37: 379-384. https://goo.gl/uWVqUi
    11. Newman DJ, Cragg GM. Natural products as source of new drugs over the last 25 years. J Nat Prod. 2007; 70: 461-77. https://goo.gl/d8qh6Q
    12. Garcia ES, Silva ACP, Gilbert B, Correa CBV, Cavalheiro MVS, Santos RR, et al. Phytotherapies In: Workshop on biodiversity: perspectives and technological opportunities, 1996.
    13. Lorenzi H, Mattos F J A. Medicinal Plants in Brazil - Native and Exotic. Ed. Plantarum, 2nd. Ed. Nova Odessa, SP, 2008. https://goo.gl/8KWWYx
    14. Dukic N M, Bozin B, Sokovic M, Mihajlovic B, Matavulj M. Antimicrobial and Antioxidant Activities of Three Mentha Species Essential Oils. Planta Medica. 2003; 69: 413–419. https://goo.gl/2Nd8BS
    15. İscan G, Kirimer N, Kurkcuoglu M, Baser K H, Demirci F. Antimicrobial Screening of Mentha piperita Essential Oils. Journal of Agricultural and Food Chemistry. 2002; 50: 3943–3946. https://goo.gl/Cs8KRT
    16. Singh R, Shushni M A M, Belkheir A. Antibacterial and antioxidant activities of Mentha piperita L. Arabian Journal of Chemistry. 2015; 8: 322-328. https://goo.gl/MCZkdt
    17. Odds F C. Pathogenic fungi in the 21st century. Trends Microbiol. 2000; 8: 200-201. https://goo.gl/BeWgxW
    18. Sant’Ana P L, Milan E P,  Martinez R, Telles F Q, Ferreira MS, Alcântara A P, Carvalho M T, Colombo A L. Multicenter Brazilian study of oral Candida species isolated from AIDS patients. Memorias do Instituto Oswaldo Cruz. 2002; 97: 253-257. https://goo.gl/QWFWeo
    19. Montero J G, Martin A D, Piappon M R P, Cabrera E G.  Invasive fungal infection in patients admitted to critical areas. Enferm Infecc Microbiol Clin. 2012; 30: 338-343. https://goo.gl/ekSsQ5
    20. Marsh, P, Martin, M.V. Oral microbiology. Ed. Santos, 4a. Ed. Sao Paulo-SP, 2005.
    21. YangYL, ChenHT, Lin CC, Chu WL, Lo H J. Speciesdistribution and drug susceptibilities of  Candida isolates in TSARY 2010.Diagnostic microbiology and infectious disease. 2013; 76: 182-186. https://goo.gl/yH2Rix
    22. Saharkhiz M J, Motamedi M, Zomorodian K, Pakshir K, Miri R, Hemyari K. Chemical Composition, Antifungal and Antibiofilm Activities of the Essential Oil of Mentha piperita L. ISRN Pharmaceutics. 2012; 2012: 1-6. https://goo.gl/ZJhhHr
    23. Kunamoto C A. Candida Biofilms. Current Opinion in Microbiology. 2002; 5: 608-611. https://goo.gl/fWkFf2
    24. Jewtuchowicz V M, Brusca M I, Mujica M T, Gliosca L A, Finquelievich J L, Lovannitti C A, Rosa A C. Subgingival distribution of yeast and their antifungal susceptibility in immunocompetent subjects with and without dental devices. Acta Odontol Latinoam. 2007; 20: 17-22. https://goo.gl/e5Fshm
    25. Morais LAS Influence of abiotic factors on the chemical composition of essential oils. Brazilian Horticulture. 2009; 27: 4050- 4063.
    26. Oumzil H, Ghoulami S, Rhajaouni M, Ilidrissi A, Tetouani SF, Faid M, Benjouad A. Antibacterial and antifungal activity of essential oils of Mentha suaveolens. Phytotherapy research. 2002; 16: 727-731. https://goo.gl/kicfiJ
    27. McKay D L, Bumberg J B. A review of the bioactivity and potential health benefits of peppermint tea (Mentha piperita L.). Phytoterapy Research. 2006; 20: 619-633. https://goo.gl/6nfhyd
    28. Peixoto I T A, Furletti V F, Anibal P C, Duarte M C T, Hofling J F. Potential pharmacological and toxicological basis of the essential oil from Menthaspp. Rev Cienc Farm Básica Apl. 2009; 30: 235-239. https://goo.gl/dfZABP
    29. Duarte M C T, Figueira G M, Sartoratto A, Rehder V L G, Delarmelina C. Anti-candida activity of Brazilian medicinal plants. Journal of ethnopharmacology. 2005; 97: 305-311. https://goo.gl/AxXBxg
    30. Höfling J F, Anibal P C, Pereda G A O, Peixoto I A T, Furletti V F, Foglio M A, Goncalves R B. Antimicrobial potential of some plant extracts against Candida species. Brazilian journal of biology. 2010; 70: 1065-1068. https://goo.gl/tfaz31
    31. Tyagi A K, Malik A. Antimicrobial potential and chemical composition of Mentha piperita oil in liquid and vapour phase against food spoiling microorganisms. Food Control. 2011; 22: 1707–1714. https://goo.gl/WiqLNw
    32. Agarwal V, Lal P, Pruthi V. Prevention of Candida albicans biofilm by plant oils. Mycopathologia. 2008; 165: 13-19. https://goo.gl/pLuiNt
    33. Mkaddem M, Bouajila J, Ennajar M, Lebrihi A, Mathieu F, Romdhane M. Chemical composition and antimicrobial and a antioxidant activities of  Mentha (longifolia L. and viridis) essential oils. Journal of food science. 2009; 74: 358-63. https://goo.gl/gUVc6G
    34. Yadegarinia D, Gachkar L, Rezaei M B, Taghizadeh M, Astaneh S A, Rasooli I. Biochemical activities of Iranian Mentha piperita L. and Myrtus communis L. essential oils. Phytochemistry. 2006; 67: 1249-1255. https://goo.gl/F5DVkp   
    35. Duru M E, Ozturk M, Ugur A, Ceylan O. The constituents of essential oil and in vitro antimicrobial activity of Micromeria cilicica from Turkey. J Ethnopharmacol. 2004; 94: 43-48. https://goo.gl/bQQvR9
    36. Al-Bayati F A. Isolation and identification of antimicrobial compound from Mentha longifolia L. leaves grown wild in Iraq. Annals of clinical microbiolgy and antimicrobials. 2009; 12: 8-20. https://goo.gl/HXmNRm
    37. Mimica-Dukic N, Bozin B, Sokovic M, Mihajlovic B, Matavulj M. Antimicrobial and antioxidant activities of three Mentha species essential oils. Planta Med. 2003; 69: 413-419. https://goo.gl/guDdV1
    38. Yigit D, Yigit N, ozgen U. An investigation on the anticandidal activity of some traditional medicinal plants in Turkey.  Mycoses. 2008; 52: 135-140. https://goo.gl/gdvBE7
    39. Kasrati A, Jamali C A, Bekkouche K, Lahcen H, Markouk M, Wohlmuth H, Leach D, Abbad A. Essential oil composition and antimicrobial activity of wild and cultivated mint timija (Mentha suaveolens subsp. timija (Briq.) Harley), an endemic and threatened medicinal species in Morocco. Nat Prod Res. 2012; 27: 1119-1122. https://goo.gl/MQUxPW
    40. El-Kashoury el-S A, El-Askary H I, Kandii Z A, Salem M A, Slemm A A. Chemical composition and biological activities of the essential oil of Mentha suaveolens Ehrh. Z Naturforsch C. 2012; 67: 571-571. https://goo.gl/yRg87j
    41. Sarer E, Toprak S Y, Otlu B, Durmaz R. Composition and antimicrobial activity of essential oil from Mentha spicata L. subsp. spicata. J Essential Oil Res. 2011; 23: 105-108.  https://goo.gl/oCqSMi
    42. Boni G C, Feiria S N B, Santana P L, Anibal P C, Boriollo M F G, Buso-Ramos M M, et, al. Antifungal and cytotoxic activity of purified biocompounds as carvone, menthone, menthofuran and pulegon from Menthaspp. African Journal of Plant Science. 2016; 10: 203-210. https://goo.gl/zFoLf8
    43. Feiria S N B, Santana P L, Boni G C, Anibal P C, Boriollo M F G, Figueira G M, Sousa I M O, Pereira B, Foglio M A, Höfling J F. Essential oil composition of Mentha spp. extracted seasonally and their effects agaisnt Candida yeast growth and biofilm formation. Advancement in Medicinal Plant Research. 2016; 4: 106-115. https://goo.gl/b43GZU
    44. Asmundsdottir L R, Erlendsdottir H, Agnarsson B A, Gottfredsson. The importance of strain variation in virulence of Candida dubliniensis and Candida albicans: results of a blinded histopathological study of invasive candidiasis. Clinical microbiology and infection: the official publication of the European Society of Clinical Microbiology and Infectious Diseases. 2009; 15: 576–585. https://goo.gl/y5Ly5K
    45. Samaranayake L P. Fungi of relevance to dentistry. Essential microbiology for dentistry. 2002; 2: 142-147. https://goo.gl/ijypPM
    46. Pemán J, Zaragoza R. Towards the early diagnosis of invasive candidiasis in the patient. See Iberoam Micol. 2012; 29: 71-75. https://goo.gl/2KnYDL
    47. Tsang P W K, Bandara H M H N, Fong W P. Purpurin suppresses Candida albicans biofilm formation and hyphal development. PloS one. 2012; 7: 50866. https://goo.gl/4DU1fm
    48. Mayer F L, Wilson D, Hube B. Candida albicans pathogenicity mechanisms. Virulence. 2013; 4: 119-128. https://goo.gl/YJYcYG
    49. Raju S B, Rajappa S. Isolation and Identification of Candida from the oral cavity. International Scholarly research network. 2011; 2011: 1-7. https://goo.gl/4bmwsP
    50. Luo S, Skerk, C, Kurzai O, Zipfel P F. Complement and innate immune evasion strategies of the human pathogenic fungus Candida albicans. Molecular Immunology. 2013; 56: 161-169. https://goo.gl/NAaAh5
    51. Coutinho H D M. Factors influencing the virulence of Candida spp. West Indian Medical Journal. 2009; 58: 160–163. https://goo.gl/GGMDJ8
    52. Naglik J, Albrecht A, Bader O, Hube B. Candida albicans proteinases and host/pathogen interactions. Cell Microbiol. 2004; 6: 915-26. https://goo.gl/jfDL7c
    53. Wu T, Wright K, Hurst S F, Morrison C J. Enhanced Extracellular Production of Aspartyl Proteinase, a Virulence Factor, by Candida albicans Isolates following Growth in Subinhibitory Concentrations of Fluconazole. Antimicrobial Agents and Chemotherapy. 2000; 44: 1200–1208. https://goo.gl/C99b2c
    54. Magee B B, Hube B, Wright R J, Sullivan P J, Magee P T. The genes encoding the secreted aspartyl proteinases of Candida albicans constitute a family with at least three members. Infect Immun. 1993; 618: 3240-3. https://goo.gl/HCjSgg
    55. Gilfillan GD, Sullivan DJ, Haynes K, Parkinson T, Coleman DC, Gow NA. Candida dubliniensis: phylogeny and putative virulence factors. Microbiology. 1998; 144: 829-38. https://goo.gl/pfMiTV
    56. Zaugg C, Borg-Von Zepelin M, Reichard U, Sanglard D, Monod M. Secreted aspartic proteinase family of Candida tropicalis. Infect Immun.2001; 69: 405-12. https://goo.gl/t3ydya
    57. Monod M, Togni G, Hube B, Sanglard D. Multiplicity of genes encoding secreted aspartic proteinases in Candida species. Mol Microbiology.1994; 13: 357-68. https://goo.gl/xVtXqk
    58. Hube B, Naglik J. Candida albicans proteinases: resolving the mystery of a gene family. Microbiology. 2001; 147: 1997-2005. https://goo.gl/bXMJdV   
    59. Koelsch G, Tang J, Loy J A, Monod M, Jackson K, Founding S I, Lin X. Enzymic chacteristics of secreted aspartic proteases of Candida albicans. Biochim Biophys Acta. 2000; 1480: 117-131. https://goo.gl/nmXAWU
    60. Santana D P, Ribeiro E L, Menezes ACS, Naves PLF. New approaches on the virulence factors of Candida albicans. Journal of Medical and Biological Sciences. 2013; 12 (2): 229-233.
    61. Ramesh N, Priyadharsini M, Sumathi C S, Balasubramanian V, Hemapriya J, Kannan R. Virulence Factors and Anti-Fungal Sensitivity Pattern of Candida sp. Isolated from HIV and TB Patients. Indian journal of microbiology. 2011; 51: 273–278.   https://goo.gl/mbpHUK
    62. Jabra-Rizk M A, Falkler W A, Meiller T F. Fungal biofilms and drug resistance. Emerging Infectious Diseases. 2004; 10: 14-19. https://goo.gl/UZht2W
    63. Sardi J C, Scorzoni L, Bernardi T, Fusco-Almeida AM, Mendes Giannini M J. Candida species: current epidemiology, pathogenicity, biofilm formation, natural antifungal products and new therapeutic options. J Med Microbiol. 2012; 62: 10-24. https://goo.gl/NESxHm
    64. Wynn R L, Jabra-Rizk M A, Meiller T F. Antifungal drugs and fungal resistance: the need for a new generation of drugs. Gen Dent. 1999; 47: 352-5. https://goo.gl/Zt82u8
    65. Rodrigues ME, Silva S, Azeredo J, Henriques M. Novel strategies to fight Candida species infection. Crit Rev Microbiol. 2014; 10; 1-13. https://goo.gl/nw73p1
    66. Al-Mariri A, Safi M. The antibacterial activity of selected Labiatae (Lamiaceae) essential oil against Brucella melitensis. Iran J Med Sci. 2013; 38: 44-50. https://goo.gl/jgBZrN
    67. Alvarenga A L, Schwan R F, Dias D R, Schwan-Estrada K R F, Bravo-Martins C E C. Antimicrobial activity of plant extracts on human pathogenic bacteria. Rev. bras. pl. med. 2007; 9: 86-91. https://goo.gl/F7MZhU
    68. Sartoratto A, Machado A L M, Delarmelina C, Figueira G M, Duarte M C T, Rehder V L G. Composition and antimicrobial activity of essential oils from aromatic plants used in Brazil. Brazilian Journal of Microbiology. 2004; 35: 275-280. https://goo.gl/p2hxpG
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