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首页> 外文期刊>Frontiers in Microbiology >RNA-Seq Reveals Enhanced Sugar Metabolism in Streptococcus mutans Co-cultured with Candida albicans within Mixed-Species Biofilms
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RNA-Seq Reveals Enhanced Sugar Metabolism in Streptococcus mutans Co-cultured with Candida albicans within Mixed-Species Biofilms

机译:RNA-Seq显示与混合物种生物膜中的白色念珠菌共培养的变形链球菌糖代谢增强。

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摘要

Early childhood caries (ECC), which can lead to rampant tooth-decay that is painful and costly to treat, is one of the most prevalent infectious diseases affecting children worldwide. Previous studies support that interactions between Streptococcus mutans and Candida albicans are associated with the pathogenesis of ECC. The presence of Candida enhances S. mutans growth, fitness and accumulation within biofilms in vitro , although the molecular basis for these behaviors is undefined. Using an established co-cultivation biofilm model and RNA-Seq, we investigated how C. albicans influences the transcriptome of S. mutans . The presence of C. albicans dramatically altered gene expression in S. mutans in the dual-species biofilm, resulting in 393 genes differentially expressed, compared to mono-species biofilms of S. mutans . By Gene Ontology analysis, the majority of up-regulated genes were related to carbohydrate transport and metabolic/catabolic processes. KEGG pathway impact analysis showed elevated pyruvate and galactose metabolism, suggesting that co-cultivation with C. albicans influences carbohydrate utilization by S. mutans . Analysis of metabolites confirmed the increases in carbohydrate metabolism, with elevated amounts of formate in the culture medium of co-cultured biofilms. Moreover, co-cultivation with C. albicans altered transcription of S. mutans signal transduction ( comC and ciaRH ) genes associated with fitness and virulence. Interestingly, the expression of genes for mutacins (bacteriocins) and CRISPR were down-regulated. Collectively, the data provide a comprehensive insight into S. mutans transcriptomic changes induced by C. albicans , and offer novel insights into how bacterial–fungal interactions may enhance the severity of dental caries.
机译:幼儿龋齿(ECC)是导致世界范围内影响儿童的最流行的传染病之一,它可能导致牙齿腐烂,治疗痛苦且费用昂贵。先前的研究支持变形链球菌和白色念珠菌之间的相互作用与ECC的发病机制有关。念珠菌的存在增强了变形链球菌在体外生物膜内的生长,适应性和积累,尽管这些行为的分子基础尚不确定。使用已建立的共培养生物膜模型和RNA-Seq,我们研究了白色念珠菌如何影响变形链球菌的转录组。白色念珠菌的存在极大地改变了双物种生物膜中变形链球菌的基因表达,与变形链球菌的单物种生物膜相比,导致393个基因差异表达。通过基因本体分析,大多数上调的基因与碳水化合物转运和代谢/分解代谢过程有关。 KEGG途径影响分析显示丙酮酸和半乳糖代谢升高,这表明与白色念珠菌的共培养会影响变形链球菌对碳水化合物的利用。代谢物分析证实,共培养生物膜的培养基中甲酸的含量增加,从而碳水化合物的代谢增加。此外,与白色念珠菌的共培养改变了变形链球菌信号转导(comC和ciaRH)与适应性和毒力相关的基因的转录。有趣的是,突变素(细菌素)和CRISPR的基因表达被下调。总体而言,这些数据提供了由白色念珠菌诱导的变形链球菌转录组变化的全面见解,并为细菌-真菌相互作用如何增加龋齿的严重程度提供了新颖的见解。

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