Comparative genomic and functional analysis of Akkermansia muciniphila and closely related species

被引:31
|
作者
Xing, Juyuan [2 ]
Li, Xiaobo [3 ,5 ,6 ]
Sun, Yingjiao [1 ]
Zhao, Juanjuan [1 ]
Miao, Shaohua [1 ]
Xiong, Qin [1 ]
Zhang, Yonggang [4 ]
Zhang, Guishan [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Agr Resources & Reg Planning, Key Lab Microbial Resources Collect & Preservat, Minist Agr, 12 Zhongguancun South St, Beijing 100081, Peoples R China
[2] Wuhan Univ Technol, Wuhan, Hubei, Peoples R China
[3] Univ Chinese Acad Sci, BGI Educ Ctr, Shenzhen, Peoples R China
[4] Qilu Univ Technol, Biol Inst, Shandong Acad Sci, 19 Keyuan Rd, Jinan 250014, Shandong, Peoples R China
[5] BGI Shenzhen, Shenzhen, Peoples R China
[6] BGI Shenzhen, China Natl GeneBank Shenzhen, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
Akkermansia muciniphila; Comparative genome; Phylogenetic analysis; Pan-genome; Gene clusters; SP-NOV; GEN; NOV; PHYLUM VERRUCOMICROBIA; GUT MICROBIOTA; BACTERIUM; MUCIN; ALIGNMENT; PREDICTION; PHYLOGENY; EVOLUTION;
D O I
10.1007/s13258-019-00855-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Akkermansia muciniphila is an important bacterium that resides on the mucus layer of the intestinal tract. Akkermansia muciniphila has a high abundance in human feces and plays an important role in human health. Objective In this article, 23 whole genome sequences of the Akkermansia genus were comparatively studied. Methods Phylogenetic trees were constructed with three methods: All amino acid sequences of each strain were used to construct the first phylogenetic tree using the web server of Composition Vector Tree Version 3. The matrix of Genome-to-Genome Distances which were obtained from GGDC 2.0 was used to construct the second phylogenetic tree using FastME. The concatenated single-copy core gene-based phylogenetic tree was generated through MEGA. The single-copy genes were obtained using OrthoMCL. Population structure was assessed by STRUCTURE 2.3.4 using the SNPs in core genes. PROKKA and Roary were used to do pan-genome analyses. The biosynthetic gene clusters were predicted using antiSMASH 4.0. IalandViewer 4 was used to detect the genomic islands. Results The results of comparative genomic analysis revealed that: (1) The 23 Akkermansia strains formed 4 clades in phylogenetic trees. The A. muciniphila strains isolated from different geographic regions and ecological niches, formed a closely related clade. (2) The 23 Akkermansia strains were divided into 4 species based on digital DNA-DNA hybridization (dDDH) values. (3) Pan-genome of A. muciniphila is in an open state and increases with addition of new sequenced genomes. (4) SNPs were not evenly distributed throughout the A. muciniphila genomes. The genes in regions with high SNP density are related to metabolism and cell wall/membrane envelope biogenesis. (5) The thermostable outer-membrane protein, Amuc_1100, was conserved in the Akkermansia genus, except for Akkermansia glycaniphila Pyt(T). Conclusion Overall, applying comparative genomic and pan-genomic analyses, we classified and illuminated the phylogenetic relationship of the 23 Akkermansia strains. Insights of the evolutionary, population structure, gene clusters and genome islands of Akkermansia provided more information about the possible physiological and probiotic mechanisms of the Akkermansia strains, and gave some instructions for the in-depth researches about the use of Akkermansia as a gut probiotic in the future.
引用
收藏
页码:1253 / 1264
页数:12
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