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具核梭杆菌无细胞废弃培养液对白色念珠菌和变形链球菌共物种生物膜生长的影响。

Effect of cell-free spent media prepared from Aggregatibacter actinomycetemcomitans on the growth of Candida albicans and Streptococcus mutans in co-species biofilms.

机构信息

Department of Oral Biology and Oral Science Research Center, Faculty of Dentistry, Universitas Indonesia, Jakarta, Indonesia.

出版信息

Eur J Oral Sci. 2020 Oct;128(5):395-404. doi: 10.1111/eos.12725. Epub 2020 Aug 18.

Abstract

This study explored the influence of cell-free spent media prepared from Aggregatibacter actinomycetemcomitans LuxS mutant (Aa-LuxS), its wild type strain (Aa-WT), and the laboratory strain (Aa-Y4), on the interaction between Candida albicans and Streptococcus mutans while growing in co-species biofilm for 48 h. By analyzing the results of crystal violet staining, [3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide] (MTT) assays, and quantitative real-time polymerase chain reaction (qPCR), we found that the presence of Aa-LuxS in treated biofilms did not affect biofilm development, while added Aa-WT or Aa-Y4 resulted in a significant decrease in both biofilm mass and the number of cells. The inhibitory effect of Aa-WT or Aa-Y4 was not dependent on the protein concentration in the spent media tested (1 and 10%). Gene transcription analyses indicated that Aa-WT/Aa-Y4 exhibits comparable inhibitory effects on the expression of hyphal-associated genes (ALS3 and HWP1), but not on the expression of YWP1, which encodes a yeast form of C. albicans. In contrast, except for gtfD, the expression of S. mutans gtfB/C genes encoding glucosyltransferase was not affected in Aa-WT and Aa-Y4 treated biofilms compared to the levels found in Aa-LuxS treated biofilms. Our results indicate that AI-2-containing spent media derived from Aa can reduce biofilm biomass without significantly inhibiting the survival rate of S. mutans.

摘要

本研究探讨了源自伴放线放线杆菌 LuxS 突变体(Aa-LuxS)、其野生型菌株(Aa-WT)和实验室菌株(Aa-Y4)的无细胞废弃培养基对白色念珠菌和变形链球菌在共物种生物膜中生长 48 小时的相互作用的影响。通过结晶紫染色、[3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2H-四唑溴盐](MTT)测定和实时定量聚合酶链反应(qPCR)分析,我们发现处理生物膜中存在 Aa-LuxS 不会影响生物膜的发展,而添加 Aa-WT 或 Aa-Y4 则导致生物膜质量和细胞数量显著减少。Aa-WT 或 Aa-Y4 的抑制作用不依赖于测试的废弃培养基中的蛋白浓度(1%和 10%)。基因转录分析表明,Aa-WT/Aa-Y4 对菌丝相关基因(ALS3 和 HWP1)的表达表现出相似的抑制作用,但对编码白色念珠菌酵母形式的 YWP1 基因的表达没有抑制作用。相比之下,除了 gtfD 外,与 Aa-LuxS 处理的生物膜相比,在 Aa-WT 和 Aa-Y4 处理的生物膜中,编码葡糖基转移酶的 S. mutans gtfB/C 基因的表达不受影响。我们的研究结果表明,源自 Aa 的含有 AI-2 的废弃培养基可以减少生物膜生物量,而不会显著抑制变形链球菌的存活率。

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