Synergistic antimicrobial effect and mechanism of enterocin Gr17 and cinnamaldehyde against Escherichia coli and Candida albicans.

IF 2.3 3区 生物学 Q3 MICROBIOLOGY
Wen-Yu Ma, Kai-Sheng Shen, Zhao Wang, Qi Liu, Xin-Jie Diao, Guo-Rong Liu
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引用次数: 0

Abstract

Bacteriocins and essential oils have potential synergistic antimicrobial effects against pathogens, but the poor understanding of their antimicrobial mechanisms, especially against Gram-negative bacteria and fungi, restricts their practical use in public health. Enterocin Gr17 (ENT) is a novel class IIa bacteriocin that exhibits synergistic effects with cinnamaldehyde essential oil (CEO) against some pathogenic Gram-negative bacteria and fungi. This study aimed to further understand the synergistic antimicrobial activity and mechanisms of ENT and CEO against pathogenic Escherichia coli and Candida albicans from the perspectives of cell wall and membrane, morphological structure, respiratory metabolism and gene expression. Results showed that the ENT-CEO combination induced sublethal damage to E. coli and C. albicans, synergistically limiting their growth in a time-dependent manner. For E. coli, ENT and CEO synergistically disrupted the cell wall structure via interfering with membrane potential and targeting cell wall components, then enhanced membrane permeability and formed non-selective pores, leading to K+ and adenosine triphosphate efflux and severe damage of morphology and intracellular organization. Furthermore, their combination also suppressed the hexose monophosphate respiratory pathway and the expression of growth and virulence-related genes, ultimately accelerating cell death. On the other hand, ENT combined with CEO minimally affected C. albicans morphology but severely disrupted its intracellular organization, indicating mechanistic differences from E. coli. Initially, ENT and CEO synergistically destabilized membrane potential and destroyed C. albicans cell wall homeostasis, facilitating their cellular internalization. They subsequently disrupted cell membrane permeability and integrity, impaired energy metabolism by inhibiting tricarboxylic acid cycle pathway, and down-regulated the growth and virulence-related gene expression, thereby leading to C. albicans cell death. This study provides theoretical support for the industrial application of bacteriocin-essential oil synergistic antimicrobial technology.

肠球菌素Gr17和肉桂醛对大肠杆菌和白色念珠菌的协同抑菌作用及机制。
细菌素和精油对病原体具有潜在的协同抗菌作用,但对它们的抗菌机制,特别是对革兰氏阴性细菌和真菌的抗菌机制了解不足,限制了它们在公共卫生中的实际应用。肠素Gr17 (Enterocin Gr17, ENT)是一种新型的IIa类细菌素,与肉桂醛精油(cinnamaldehyde精油,CEO)具有协同作用,可抑制一些致病性革兰氏阴性菌和真菌。本研究旨在从细胞壁和细胞膜、形态结构、呼吸代谢和基因表达等方面进一步了解ENT和CEO对致病性大肠杆菌和白色念珠菌的协同抑菌活性及其机制。结果表明,ENT-CEO组合对大肠杆菌和白色念珠菌产生亚致死损伤,并以时间依赖性的方式协同限制它们的生长。对于大肠杆菌,ENT和CEO通过干扰膜电位,靶向细胞壁成分,协同破坏细胞壁结构,增强细胞膜通透性,形成非选择性孔,导致K+和三磷酸腺苷外排,细胞形态和细胞内组织严重受损。此外,它们的结合还抑制了单磷酸己糖呼吸途径以及生长和毒力相关基因的表达,最终加速细胞死亡。另一方面,ENT联合CEO对白色念珠菌形态的影响最小,但严重破坏了其细胞内组织,表明与大肠杆菌的机制差异。最初,ENT和CEO协同破坏膜电位,破坏白色念珠菌细胞壁稳态,促进其细胞内化。它们随后破坏了细胞膜的通透性和完整性,通过抑制三羧酸循环途径破坏了能量代谢,下调了生长和毒力相关基因的表达,从而导致白色念珠菌细胞死亡。本研究为菌素-精油协同抗菌技术的工业应用提供了理论支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archives of Microbiology
Archives of Microbiology 生物-微生物学
CiteScore
4.90
自引率
3.60%
发文量
601
审稿时长
3 months
期刊介绍: Research papers must make a significant and original contribution to microbiology and be of interest to a broad readership. The results of any experimental approach that meets these objectives are welcome, particularly biochemical, molecular genetic, physiological, and/or physical investigations into microbial cells and their interactions with their environments, including their eukaryotic hosts. Mini-reviews in areas of special topical interest and papers on medical microbiology, ecology and systematics, including description of novel taxa, are also published. Theoretical papers and those that report on the analysis or ''mining'' of data are acceptable in principle if new information, interpretations, or hypotheses emerge.
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