Segura Audrey, Auffret Pauline, Klopp Christophe, Bertin Yolande, Forano Evelyne
Université Clermont Auvergne, INRA, MEDIS, F-63000 Clermont-Ferrand, France.
Plateforme Bioinformatique Toulouse, Midi-Pyrénées UBIA, INRA, Auzeville Castanet-Tolosan, France.
Stand Genomic Sci. 2017 Oct 10;12:61. doi: 10.1186/s40793-017-0272-0. eCollection 2017.
is the most abundant facultative anaerobic bacteria in the gastro-intestinal tract of mammals but can be responsible for intestinal infection due to acquisition of virulence factors. Genomes of pathogenic strains are widely described whereas those of bovine commensal strains are very scarce. Here, we report the genome sequence, annotation, and features of the commensal BG1 isolated from the gastro-intestinal tract of cattle. Whole genome sequencing analysis showed that BG1 has a chromosome of 4,782,107 bp coding for 4465 proteins and 97 RNAs. BG1 belonged to the serotype O159:H21, was classified in the phylogroup B1 and possessed the genetic information encoding "virulence factors" such as adherence systems, iron acquisition and flagella synthesis. A total of 12 adherence systems were detected reflecting the potential ability of BG1 to colonize different segments of the bovine gastro-intestinal tract. BG1 is unable to assimilate ethanolamine that confers a nutritional advantage to some pathogenic in the bovine gastro-intestinal tract. Genome analysis revealed the presence of i) 34 amino acids change due to non-synonymous SNPs among the genes encoding ethanolamine transport and assimilation, and ii) an additional predicted alpha helix inserted in cobalamin adenosyltransferase, a key enzyme required for ethanolamine assimilation. These modifications could explain the incapacity of BG1 to use ethanolamine. The BG1 genome can now be used as a reference (control strain) for subsequent evolution and comparative studies.
[细菌名称]是哺乳动物胃肠道中最丰富的兼性厌氧菌,但由于获得毒力因子,可导致肠道感染。致病性菌株的基因组已有广泛描述,而牛共生菌株的基因组却非常稀少。在此,我们报告了从牛胃肠道分离出的共生菌株BG1的基因组序列、注释及特征。全基因组测序分析表明,BG1有一条4,782,107 bp的染色体,编码4465种蛋白质和97种RNA。BG1属于O159:H21血清型,归类于B1系统发育群,拥有编码“毒力因子”的遗传信息,如黏附系统、铁摄取和鞭毛合成。共检测到12种黏附系统,反映出BG1在牛胃肠道不同部位定殖的潜在能力。BG1不能同化乙醇胺,这赋予了牛胃肠道中一些致病菌营养优势。基因组分析显示:i) 在编码乙醇胺转运和同化的基因中,由于非同义单核苷酸多态性导致34个氨基酸发生变化;ii) 在钴胺腺苷转移酶(乙醇胺同化所需的关键酶)中额外插入了一个预测的α螺旋。这些修饰可能解释了BG1无法利用乙醇胺的原因。BG1基因组现在可作为后续进化和比较研究的参考(对照菌株)。