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肠道微生物组的甲基组:肠道拟杆菌中不同的 Dam 甲基化模式。

The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei.

机构信息

Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida Gainesville, FL, USA.

Department of Clinical Microbiology, University of Eastern Finland Kuopio, Finland ; Immunogenetics Laboratory, University of Turku Turku, Finland.

出版信息

Front Microbiol. 2014 Jul 17;5:361. doi: 10.3389/fmicb.2014.00361. eCollection 2014.

Abstract

Despite the large interest in the human microbiome in recent years, there are no reports of bacterial DNA methylation in the microbiome. Here metagenomic sequencing using the Pacific Biosciences platform allowed for rapid identification of bacterial GATC methylation status of a bacterial species in human stool samples. For this work, two stool samples were chosen that were dominated by a single species, Bacteroides dorei. Based on 16S rRNA analysis, this species represented over 45% of the bacteria present in these two samples. The B. dorei genome sequence from these samples was determined and the GATC methylation sites mapped. The Bacteroides dorei genome from one subject lacked any GATC methylation and lacked the DNA adenine methyltransferase genes. In contrast, B. dorei from another subject contained 20,551 methylated GATC sites. Of the 4970 open reading frames identified in the GATC methylated B. dorei genome, 3184 genes were methylated as well as 1735 GATC methylations in intergenic regions. These results suggest that DNA methylation patterns are important to consider in multi-omic analyses of microbiome samples seeking to discover the diversity of bacterial functions and may differ between disease states.

摘要

尽管近年来人们对人类微生物组产生了浓厚的兴趣,但目前尚未有关于微生物组中细菌 DNA 甲基化的报道。本文使用 Pacific Biosciences 平台进行宏基因组测序,能够快速鉴定人类粪便样本中细菌的 GATC 甲基化状态。为此,选择了两个以单一物种 Bacteroides dorei 为主导的粪便样本。基于 16S rRNA 分析,该物种在这两个样本中代表了超过 45%的细菌。从这些样本中确定了 B. dorei 的基因组序列,并对 GATC 甲基化位点进行了映射。这两个样本中,一个样本的 Bacteroides dorei 基因组没有任何 GATC 甲基化,也缺乏 DNA 腺嘌呤甲基转移酶基因。相比之下,另一个样本的 B. dorei 含有 20,551 个甲基化的 GATC 位点。在所鉴定的 4970 个开放阅读框中,3184 个基因被甲基化,271 个基因在基因间区域被甲基化。这些结果表明,在对微生物组样本进行多组学分析以发现细菌功能多样性时,DNA 甲基化模式是一个需要考虑的重要因素,并且可能因疾病状态而异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f9/4101878/173632b3f32a/fmicb-05-00361-g0001.jpg

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