Corte Laura, Tiecco Matteo, Roscini Luca, De Vincenzi Sergio, Colabella Claudia, Germani Raimondo, Tascini Carlo, Cardinali Gianluigi
Department of Pharmaceutical Sciences-Microbiology, University of Perugia, Borgo XX Giugno 74, I-06121 Perugia, Italy.
CEMIN, Centre of Excellence on Nanostructured Innovative Materials, Department of Chemistry, Biology and Biotechnology, University of Perugia, via Elce di Sotto 8, I-06123 Perugia, Italy.
PLoS One. 2015 Jan 14;10(1):e0115275. doi: 10.1371/journal.pone.0115275. eCollection 2015.
Surfactants are extremely important agents to clean and sanitize various environments. Their biocidal activity is a key factor determined by the interactions between amphiphile structure and the target microbial cells. The object of this study was to analyze the interactions between four structural variants of N-alkyltropinium bromide surfactants with the Gram negative Escherichia coli and the Gram positive Listeria innocua bacteria. Microbiological and conductometric methods with a previously described FTIR bioassay were used to assess the metabolomic damage exerted by these compounds. All surfactants tested showed more biocidal activity in L. innocua than in E. coli. N-tetradecyltropinium bromide was the most effective compound against both species, while all the other variants had a reduced efficacy as biocides, mainly against E. coli cells. In general, the most prominent metabolomic response was observed for the constituents of the cell envelope in the fatty acids (W1) and amides (W2) regions and at the wavenumbers referred to peptidoglycan (W2 and W3 regions). This response was particularly strong and negative in L. innocua, when cells were challenged by N-tetradecyltropinium bromide, and by the variant with a smaller head and a 12C tail (N-dodecylquinuclidinium bromide). Tail length was critical for microbial inhibition especially when acting against E. coli, maybe due the complex nature of Gram negative cell envelope. Statistical analysis allowed us to correlate the induced mortality with the metabolomic cell response, highlighting two different modes of action. In general, gaining insights in the interactions between fine structural properties of surfactants and the microbial diversity can allow tailoring these compounds for the various operative conditions.
表面活性剂是清洁和消毒各种环境的极为重要的制剂。它们的杀菌活性是由两亲结构与目标微生物细胞之间的相互作用所决定的关键因素。本研究的目的是分析N-烷基托品溴铵表面活性剂的四种结构变体与革兰氏阴性大肠杆菌和革兰氏阳性无害李斯特菌之间的相互作用。采用微生物学和电导法以及先前描述的傅里叶变换红外光谱生物测定法来评估这些化合物所造成的代谢组损伤。所有测试的表面活性剂对无害李斯特菌的杀菌活性均高于对大肠杆菌的杀菌活性。N-十四烷基托品溴铵是对这两种菌最有效的化合物,而所有其他变体作为杀菌剂的效力均有所降低,主要是对大肠杆菌细胞。一般来说,在脂肪酸(W1)和酰胺(W2)区域以及与肽聚糖相关的波数(W2和W3区域)观察到细胞包膜成分最显著 的代谢组反应。当细胞受到N-十四烷基托品溴铵以及头部较小且尾部含12个碳的变体(N-十二烷基喹核溴铵)攻击时,这种反应在无害李斯特菌中尤为强烈且呈阴性。尾部长度对微生物抑制至关重要,尤其是对大肠杆菌起作用时,这可能是由于革兰氏阴性菌细胞包膜的复杂性所致。统计分析使我们能够将诱导死亡率与代谢组细胞反应相关联,突出了两种不同的作用模式。一般而言,深入了解表面活性剂的精细结构特性与微生物多样性之间的相互作用可以使这些化合物适用于各种操作条件。