In vitro antifungal activity of hydroxychavicol isolated from Piper betle L

被引:107
作者
Ali, Intzar [1 ]
Khan, Farrah G. [3 ]
Suri, Krishan A. [2 ]
Gupta, Bishan D. [2 ]
Satti, Naresh K. [2 ]
Dutt, Prabhu [2 ]
Afrin, Farhat [4 ]
Qazi, Ghulam N. [4 ]
Khan, Inshad A. [1 ]
机构
[1] Indian Inst Integrat Med, Div Clin Microbiol, Jammu 180001, India
[2] Indian Inst Integrat Med, Nat Prod Chem Div, Jammu 180001, India
[3] Acharya Shri Chander Coll Med Sci, Dept Microbiol, Jammu 180017, India
[4] Hamdard Univ, Fac Sci, Dept Biotechnol, New Delhi 110062, India
关键词
Minimum Inhibitory Concentration; Propidium Iodide; Antifungal Activity; Candida Species; Terbinafine;
D O I
10.1186/1476-0711-9-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Hydroxychavicol, isolated from the chloroform extraction of the aqueous leaf extract of Piper betle L., (Piperaceae) was investigated for its antifungal activity against 124 strains of selected fungi. The leaves of this plant have been long in use tropical countries for the preparation of traditional herbal remedies. Methods: The minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of hydroxychavicol were determined by using broth microdilution method following CLSI guidelines. Time kill curve studies, post-antifungal effects and mutation prevention concentrations were determined against Candida species and Aspergillus species "respectively". Hydroxychavicol was also tested for its potential to inhibit and reduce the formation of Candida albicans biofilms. The membrane permeability was measured by the uptake of propidium iodide. Results: Hydroxychavicol exhibited inhibitory effect on fungal species of clinical significance, with the MICs ranging from 15.62 to 500 mu g/ml for yeasts, 125 to 500 mu g/ml for Aspergillus species, and 7.81 to 62.5 mu g/ml for dermatophytes where as the MFCs were found to be similar or two fold greater than the MICs. There was concentration-dependent killing of Candida albicans and Candida glabrata up to 8 x MIC. Hydroxychavicol also exhibited an extended post antifungal effect of 6.25 to 8.70 h at 4 x MIC for Candida species and suppressed the emergence of mutants of the fungal species tested at 2 x to 8 x MIC concentration. Furthermore, it also inhibited the growth of biofilm generated by C. albicans and reduced the preformed biofilms. There was increased uptake of propidium iodide by C. albicans cells when exposed to hydroxychavicol thus indicating that the membrane disruption could be the probable mode of action of hydroxychavicol. Conclusions: The antifungal activity exhibited by this compound warrants its use as an antifungal agent particularly for treating topical infections, as well as gargle mouthwash against oral Candida infections.
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