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Actinomyces spp. gene expression in root caries lesions

机译:放线菌属基因在龋齿病变中的表达

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BackgroundThe studies of the distribution of Actinomyces spp. on carious and non-carious root surfaces have not been able to confirm the association of these bacteria with root caries, although they were extensively implicated as a prime suspect in root caries.ObjectiveThe aim of this study was to observe the gene expression of Actinomyces spp. in the microbiota of root surfaces with and without caries.DesignThe oral biofilms from exposed sound root surface (SRS; n=10) and active root caries (RC; n=30) samples were collected. The total bacterial RNA was extracted, and the mRNA was isolated. Samples with low RNA concentration were pooled, yielding a final sample size of SRS=10 and RC=9. Complementary DNA (cDNA) libraries were prepared and sequenced on an Illumina? HiSeq 2500 system. Sequence reads were mapped to eight Actinomyces genomes. Count data were normalized using DESeq2 to analyse differential gene expression applying the Benjamini-Hochberg correction (false discovery rate [FDR]0.001).ResultsActin...
机译:背景技术放线菌属的分布研究。龋齿和非龋齿的根表面上的细菌,尽管被广泛认为是龋齿的主要嫌疑人,但仍无法证实这些细菌与龋齿的关联。目的本研究的目的是观察放线菌属的基因表达。设计从暴露的有声根表面(SRS; n = 10)和活动根龋(RC; n = 30)样本中收集口腔生物膜。提取细菌总RNA,并分离mRNA。合并具有低RNA浓度的样品,最终样品大小为SRS = 10和RC = 9。制备互补DNA(cDNA)文库并在Illumina?上测序。 HiSeq 2500系统。序列读取被定位到八个放线菌基因组。使用DESeq2对计数数据进行归一化,以应用Benjamini-Hochberg校正法分析差异基因表达(错误发现率[FDR] <0.001)。

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