Rosemary essential oil and its components 1,8-cineole and α-pinene induce ROS-dependent lethality and ROS-independent virulence inhibition in Candida albicans

被引:30
作者
Shahina, Zinnat [1 ]
Al Homsi, Raymond [2 ]
Price, Jared D. W. [1 ]
Whiteway, Malcolm [2 ]
Sultana, Taranum [1 ]
Dahms, Tanya E. S. [1 ]
机构
[1] Univ Regina, Dept Chem & Biochem, Regina, SK, Canada
[2] Concordia Univ, Ctr Struct & Funct Genom, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
ATOMIC-FORCE MICROSCOPY; BLOOD-STREAM INFECTIONS; PROGRAMMED CELL-DEATH; OXIDATIVE STRESS; SACCHAROMYCES-CEREVISIAE; ANTIFUNGAL ACTIVITY; AMPHOTERICIN-B; WALL INTEGRITY; GERM TUBE; YEAST;
D O I
10.1371/journal.pone.0277097
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The essential oil from Rosmarinus officinalis L., a composite mixture of plant-derived secondary metabolites, exhibits antifungal activity against virulent candidal species. Here we report the impact of rosemary oil and two of its components, the monoterpene alpha-pinene and the monoterpenoid 1,8-cineole, against Candida albicans, which induce ROS-dependent cell death at high concentrations and inhibit hyphal morphogenesis and biofilm formation at lower concentrations. The minimum inhibitory concentrations (100% inhibition) for both rosemary oil and 1,8-cineole were 4500 mu g/ml and 3125 mu g/ml for alpha-pinene, with the two components exhibiting partial synergy (FICI = 0.55 +/- 0.07). At MIC and 1/2 MIC, rosemary oil and its components induced a generalized cell wall stress response, causing damage to cellular and organelle membranes, along with elevated chitin production and increased cell surface adhesion and elasticity, leading to complete vacuolar segregation, mitochondrial depolarization, elevated reactive oxygen species, microtubule dysfunction, and cell cycle arrest mainly at the G1/S phase, consequently triggering cell death. Interestingly, the same oils at lower fractional MIC (1/8-1/4) inhibited virulence traits, including reduction of mycelium (up to 2-fold) and biofilm (up to 4-fold) formation, through a ROS-independent mechanism.
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页数:31
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共 126 条
[11]   Measuring apoptosis at the single cell level [J].
Bouchier-Hayes, Lisa ;
Munoz-Pinedo, Cristina ;
Connell, Samuel ;
Green, Douglas R. .
METHODS, 2008, 44 (03) :222-228
[12]  
Budzynska A, 2014, ACTA BIOCHIM POL, V61, P115
[13]   Calcium and reactive oxygen species in regulation of the mitochondrial permeability transition and of programmed cell death in yeast [J].
Carraro, Michela ;
Bernardi, Paolo .
CELL CALCIUM, 2016, 60 (02) :102-107
[14]  
Cavalcanti Yuri Wanderley, 2011, Rev. odonto ciênc., V26, P139
[15]   The Production of Reactive Oxygen Species Is a Universal Action Mechanism of Amphotericin B against Pathogenic Yeasts and Contributes to the Fungicidal Effect of This Drug [J].
Cecilia Mesa-Arango, Ana ;
Trevijano-Contador, Nuria ;
Roman, Elvira ;
Sanchez-Fresneda, Ruth ;
Casas, Celia ;
Herrero, Enrique ;
Carlos Argueelles, Juan ;
Pla, Jesus ;
Cuenca-Estrella, Manuel ;
Zaragoza, Oscar .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2014, 58 (11) :6627-6638
[16]   The Monoterpene Carvacrol Generates Endoplasmic Reticulum Stress in the Pathogenic Fungus Candida albicans [J].
Chaillot, Julien ;
Tebbji, Faiza ;
Remmal, Adnane ;
Boone, Charlie ;
Brown, Grant W. ;
Bellaoui, Mohammed ;
Sellam, Adnane .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (08) :4584-4592
[17]   New facets of antifungal therapy [J].
Chang, Ya-Lin ;
Yu, Shang-Jie ;
Heitman, Joseph ;
Wellington, Melanie ;
Chen, Ying-Lien .
VIRULENCE, 2017, 8 (02) :222-236
[18]   Chemogenomic Profiling of the Fungal Pathogen Candida albicans [J].
Chen, Yaolin ;
Mallick, Jaideep ;
Maqnas, Alaa ;
Sun, Yuan ;
Choudhury, Baharul I. ;
Cote, Pierre ;
Yan, Lan ;
Ni, Ting-jun-hong ;
Li, Yan ;
Zhang, Dazhi ;
Rodriguez-Ortiz, Roberto ;
Lv, Quan-zhen ;
Jiang, Yuan-ying ;
Whiteway, Malcolm .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2018, 62 (02)
[19]   Epidemiologic and molecular characterization of an outbreak of Candida parapsilosis bloodstream infections in a community hospital [J].
Clark, TA ;
Slavinski, SA ;
Morgan, J ;
Lott, T ;
Arthington-Skaggs, BA ;
Brandt, ME ;
Webb, RM ;
Currier, M ;
Flowers, RH ;
Fridkin, SK ;
Hajjeh, RA .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (10) :4468-4472
[20]  
Clinical Institute LS, 2008, REF METH BROTH DIL A