Genome-Wide Analysis of the First Sequenced Mycoplasma capricolum subsp capripneumoniae Strain M1601

文献类型： 外文期刊

第一作者： Chen, Shengli

作者： Chen, Shengli;Hao, Huafang;Zhao, Ping;He, Ying;Gao, Pengcheng;Guo, Han;Ji, Wenheng;Wang, Zhanhui;Lu, Zhongxin;Chu, Yuefeng;Liu, Yongsheng;Thiaucourt, Francois;Thiaucourt, Francois

作者机构：

关键词： Mycoplasma capricolum subsp capripneumoniae;genome;virulence factor;comparative analysis;phylogenetic analysis;Genome Report

期刊名称：G3-GENES GENOMES GENETICS （ 影响因子：3.154； 五年影响因子：3.369 ）

ISSN： 2160-1836

年卷期： 2017 年 7 卷 9 期

页码：

收录情况： SCI

摘要： Mycoplasma capricolum subsp. capripneumoniae (Mccp) is a common pathogen of goats that causes contagious caprine pleuropneumonia. We closed the gap and corrected rRNA operons in the draft genome of Mccp M1601: a strain isolated from an infected goat in a farm in Gansu, China. The genome size of M1601 is 1,016,707 bp with a GC content of 23.67%. We identified 915 genes (occupying 90.27% of the genome), of which 713 are protein-coding genes (excluding 163 pseudogenes). No genomic islands and complete insertion sequences were found in the genome. Putative determinants associated with the organism's virulence were analyzed, and 26 genes (including one adhesion protein gene, two capsule synthesis gene clusters, two lipoproteins, hemolysin A, ClpB, and proteins involved in pyruvate metabolism and cation transport) were potential virulence factors. In addition, two transporter systems (ATP-binding cassette [ABC] transporters and phosphotransferase) and two secretion systems (Sec and signal recognition particle [SRP] pathways) were observed in the Mccp genome. Genome synteny analysis reveals a good collinear relationship between M1601 and Mccp type strain F38. Phylogenetic analysis based on 11 single-copy core genes of 31 Mycoplasma strains revealed good collinearity between M1601 and Mycoplasma capricolum subsp. capricolum (Mcc) and close relationship among Mycoplasma mycoides cluster strains. Our genome-wide analysis of Mccp M1601 provides helpful information on the pathogenic mechanisms and genetics of Mccp.

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