Department of Veterinary Biosciences, University of Helsinki, PO Box 66, FI-00014, Helsinki, Finland.
Laboratory of Microbiology, Wageningen University, Dreijenplein 10, 6703 HB Wageningen, The Netherlands.
J Med Microbiol. 2014 Feb;63(Pt 2):293-308. doi: 10.1099/jmm.0.064220-0. Epub 2013 Nov 19.
Toll-like receptor (TLR) signalling plays an important role in epithelial and immune cells of the intestine. TLR9 recognizes unmethylated CpG motifs in bacterial DNA, and TLR9 signalling maintains the gut epithelial homeostasis. Here, we carried out a bioinformatic analysis of the frequency of CpG motifs in the genomes of gut commensal bacteria across major bacterial phyla. The frequency of potentially immunostimulatory CpG motifs (all CpG hexamers) or purine-purine-CG-pyrimidine-pyrimidine hexamers was linearly dependent on the genomic G+C content. We found that species belonging to Proteobacteria, Bacteroidetes and Actinobacteria (including bifidobacteria) carried high counts of GTCGTT, the optimal motif stimulating human TLR9. We also found that Enterococcus faecalis, Lactobacillus casei, Lactobacillus plantarum and Lactobacillus rhamnosus, whose strains have been marketed as probiotics, had high counts of GTCGTT motifs. As gut bacterial species differ significantly in their genomic content of CpG motifs, the overall load of CpG motifs in the intestine depends on the species assembly of microbiota and their cell numbers. The optimal CpG motif content of microbiota may depend on the host's physiological status and, consequently, on an adequate level of TLR9 signalling. We speculate that microbiota with increased numbers of microbes with CpG motif-rich DNA could better support mucosal functions in healthy individuals and improve the T-helper 1 (Th1)/Th2 imbalance in allergic diseases. In autoimmune disorders, CpG motif-rich DNA could, however, further increase the Th1-type immune responsiveness. Estimation of the load of microbe-associated molecular patterns, including CpG motifs, in gut microbiota could shed new light on host-microbe interactions across a range of diseases.
Toll 样受体 (TLR) 信号在肠道的上皮细胞和免疫细胞中发挥着重要作用。TLR9 识别细菌 DNA 中未甲基化的 CpG 基序,TLR9 信号维持肠道上皮细胞的稳态。在这里,我们对主要细菌门的肠道共生菌基因组中的 CpG 基序频率进行了生物信息学分析。潜在免疫刺激性 CpG 基序(所有 CpG 六聚体)或嘌呤-嘌呤-CG-嘧啶-嘧啶六聚体的频率与基因组 G+C 含量呈线性相关。我们发现,属于变形菌门、拟杆菌门和放线菌门(包括双歧杆菌)的物种携带大量 GTCGTT,这是刺激人 TLR9 的最佳基序。我们还发现,已作为益生菌上市的屎肠球菌、干酪乳杆菌、植物乳杆菌和鼠李糖乳杆菌携带大量 GTCGTT 基序。由于肠道细菌在 CpG 基序的基因组含量上存在显著差异,肠道中 CpG 基序的总负荷取决于微生物群的物种组成及其细胞数量。微生物群的最佳 CpG 基序含量可能取决于宿主的生理状态,进而取决于 TLR9 信号的适当水平。我们推测,具有富含 CpG 基序 DNA 的微生物数量增加的微生物群可以更好地支持健康个体的黏膜功能,并改善过敏疾病中的 T 辅助 1(Th1)/Th2 失衡。然而,在自身免疫性疾病中,富含 CpG 基序的 DNA 可能会进一步增加 Th1 型免疫反应性。估计肠道微生物群中微生物相关分子模式(包括 CpG 基序)的负荷可以为宿主-微生物相互作用在一系列疾病中的作用提供新的视角。