Rahmath Nishmat Abdul Kadar, Lin Shih-Yao, Young Chiu-Chung, Hameed Asif
Division of Microbiology and Biotechnology, Yenepoya Research Centre, Yenepoya (Deemed to Be University), Deralakatte, Mangalore, 575018, India.
Department of Soil & Environmental Sciences, College of Agriculture and Natural, Resources, National Chung Hsing University, Taichung, 402, Taiwan.
Sci Rep. 2025 Jul 2;15(1):23307. doi: 10.1038/s41598-025-05383-5.
Some bacteria emit dimethyl disulphide (DMDS), one of the bioactive volatile sulphurous compounds (VSCs) of environmental and ecological significance, yet unexplored in combating drug-resistant yeasts. Here, we show the anti-budding and fungicidal activity of volatile DMDS emitted from Burkholderia cepacia LS-044 on the caspofungin-resistant yeast Nakaseomyces glabratus NT2. We identified a gene encoding L-methionine-γ-lyase (mdeA) catalysing DMDS formation in LS-044 and detected volatile DMDS as one of the VSCs (12% peak area) emitted by LS-044 through solid-phase microextraction followed by gas chromatographic-mass spectrometry. Exposure to volatiles of LS-044 resulted in a significant decline in metabolism (~ 98%), media alkalinity (~ 26%), and viable cell count (52‒95%) of NT2. Confocal microscopy of carboxyfluorescein succinimidyl ester- and calcofluor white stained cells revealed significantly high mean fluorescence in NT2 exposed to the volatiles of LS-044 (~ fivefold) and standard DMDS vapour (1.7-fold), suggesting a significant thickening of the cell wall. The surface area-to-volume ratio decreased significantly in NT2 cells exposed to volatiles of LS-044 and DMDS versus unexposed NT cells (6.5‒10.2 vs. 8.3‒13.2). DMDS exhibited a minimum inhibitory concentration of 0.5% (v/v) on NT2 cells in liquid broth dilution assay, and displayed fractional inhibitory concentration index of 0.95 with commercial antifungal clotrimazole reflecting lack of synergy or antagonism during the present combination therapy. The 26S rRNA gene sequence-based phylogeny revealed a tight phylogenetic association between NT2 and N. glabratus of environmental and clinical origins. Our study provided novel mechanistic insights into DMDS-driven bacterial antagonism on drug-resistant budding yeast N. glabratus NT2 that could be exploited in the ecological engineering and therapeutics of drug-resistant fungal infection.
一些细菌会释放二甲基二硫醚(DMDS),它是具有环境和生态意义的生物活性挥发性含硫化合物(VSCs)之一,但在对抗耐药酵母方面尚未得到探索。在此,我们展示了洋葱伯克霍尔德菌LS - 044释放的挥发性DMDS对耐卡泊芬酵母光滑念珠菌NT2的抗出芽和杀菌活性。我们鉴定出一个编码L - 蛋氨酸γ - 裂解酶(mdeA)的基因,该基因在LS - 044中催化DMDS的形成,并通过固相微萃取结合气相色谱 - 质谱法检测到挥发性DMDS是LS - 044释放的VSCs之一(峰面积为12%)。暴露于LS - 044的挥发物会导致NT2的代谢显著下降(约98%)、培养基碱度显著下降(约26%)以及活细胞数量显著下降(52 - 95%)。对羧基荧光素琥珀酰亚胺酯和钙荧光白染色细胞的共聚焦显微镜观察显示,暴露于LS - 044挥发物(约五倍)和标准DMDS蒸汽(1.7倍)的NT2中平均荧光显著升高,表明细胞壁显著增厚。与未暴露的NT细胞相比,暴露于LS - 044和DMDS挥发物的NT2细胞的表面积与体积比显著降低(6.5 - 10.2对8.3 - 13.2)。在液体肉汤稀释试验中,DMDS对NT2细胞的最低抑菌浓度为0.5%(v/v),并且与商业抗真菌药克霉唑的联合使用显示出分级抑菌浓度指数为0.95,这表明在当前联合治疗中不存在协同作用或拮抗作用。基于26S rRNA基因序列的系统发育分析揭示了NT2与环境和临床来源的光滑念珠菌之间紧密的系统发育关联。我们的研究为DMDS驱动的细菌对耐药出芽酵母光滑念珠菌NT2的拮抗作用提供了新的机制见解,这可用于耐药真菌感染的生态工程和治疗。