Kart Didem, Yabanoğlu Çiftçi Samiye, Nemutlu Emirhan
Hacettepe University Faculty of Pharmacy, Department of Pharmaceutical Microbiology, Ankara, Turkey
Hacettepe University Faculty of Pharmacy, Department of Biochemistry, Ankara, Turkey
Turk J Pharm Sci. 2021 Oct 28;18(5):557-564. doi: 10.4274/tjps.galenos.2021.71235.
This study aimed to determine the effect of on the cell growth and hyphal formation of and to understand the exact mechanism of candidal inhibition by the existence of by metabolomic analysis.
Single- and dual-species biofilms of and were formed in a microtiter plate, and the metabolomic profiles of both biofilms was determined by gas chromatography-mass spectrometry. The hyphal cell growth of after treatment with both the supernatant and biofilm cells of was examined microscopically. The expression levels of Efg1 and the images of cell wall in single- and dual-species biofilms were determined by real-time quantitative polymerase chain reaction and transmission electron microscopy, respectively. The violacein levels produced by Chromobacterium violaceum were measured to determine the quorum sensing (QS) inhibitory activity of single- and dual-species biofilms.
The biofilm cell growth, Efg1 expression, and hyphal development of were inhibited by . Compared to single-species biofilms, alterations in carbohydrate, amino acid, and polyamine metabolites were observed in the dual-species biofilm for both microorganisms. Putrescine and pipecolic acid were detected at high levels in dual-species biofilm. A thicker β-glucan chitin and a denser and narrower fibrillar mannan layer of cell wall were observed in dual-species biofilm. QS inhibitory activity was higher in dual-species biofilm suspensions of and than in their single-species biofilms.
inhibited the hyphal development and biofilm formation of . Biofilm suspensions of and showed an anti-QS activity, which increased even further in the environment where the two species coexisted. Investigation of putrescine and pipecolic acid can be an important step to understand the inhibition of by bacteria.
本研究旨在确定[具体物质]对[白色念珠菌名称]细胞生长和菌丝形成的影响,并通过代谢组学分析了解[具体物质]存在时念珠菌抑制的确切机制。
在微量滴定板中形成[白色念珠菌名称]和[另一种菌名称]的单物种和双物种生物膜,通过气相色谱 - 质谱法测定两种生物膜的代谢组学谱。用[另一种菌名称]的上清液和生物膜细胞处理后,显微镜检查[白色念珠菌名称]的菌丝细胞生长情况。分别通过实时定量聚合酶链反应和透射电子显微镜测定单物种和双物种生物膜中Efg1的表达水平以及[白色念珠菌名称]细胞壁的图像。测量紫色杆菌产生的紫菌素水平,以确定单物种和双物种生物膜的群体感应(QS)抑制活性。
[具体物质]抑制了[白色念珠菌名称]的生物膜细胞生长、Efg1表达和菌丝发育。与单物种生物膜相比,在双物种生物膜中两种微生物的碳水化合物、氨基酸和多胺代谢物均有变化。在双物种生物膜中检测到高水平的腐胺和哌可酸。在双物种生物膜中观察到[白色念珠菌名称]细胞壁的β - 葡聚糖几丁质更厚,纤维甘露聚糖层更致密且更窄。[白色念珠菌名称]和[另一种菌名称]的双物种生物膜悬浮液的QS抑制活性高于其单物种生物膜。
[具体物质]抑制了[白色念珠菌名称]的菌丝发育和生物膜形成。[白色念珠菌名称]和[另一种菌名称]的生物膜悬浮液显示出抗QS活性,在两种物种共存的环境中该活性进一步增强。研究腐胺和哌可酸可能是了解细菌对[白色念珠菌名称]抑制作用的重要一步。