CENSA National Center for Animal and Plant Health, San José de las Lajas Municipality 32700, Mayabeque, Cuba.
SIB Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland.
Toxins (Basel). 2020 Jan 2;12(1):29. doi: 10.3390/toxins12010029.
Toxin-antitoxin systems (TASs) are widely distributed in prokaryotes and encode pairs of genes involved in many bacterial biological processes and mechanisms, including pathogenesis. The TASs have not been extensively studied in (), a pathogenic bacterium of the Firmicutes phylum causing infections in animals and humans. Using our recently published TASmania database, we focused on the known and new putative TASs in 352 genomes and identified the putative core gene TASs (cgTASs) with the Pasteur BIGSdb-Lm database and, by complementarity, the putative accessory gene TAS (acTASs). We combined the cgTASs with those of an additional 227 isolates from our previous studies containing metadata information. We discovered that the differences in 14 cgTAS alleles are sufficient to separate the four main lineages of . Analyzing these differences in more details, we uncovered potentially co-evolving residues in some pairs of proteins in cgTASs, probably essential for protein-protein interactions within the TAS complex.
毒素-抗毒素系统(TASs)广泛存在于原核生物中,编码参与许多细菌生物学过程和机制的基因对,包括发病机制。在()中,TASs 并没有得到广泛研究,它是厚壁菌门的一种致病性细菌,可引起动物和人类的感染。使用我们最近发表的 TASmania 数据库,我们专注于 352 个基因组中的已知和新的假定 TASs,并使用巴斯德 BIGSdb-Lm 数据库确定了假定核心基因 TAS(cgTASs),并通过互补性确定了假定辅助基因 TAS(acTASs)。我们将 cgTASs 与我们之前研究中包含元数据信息的另外 227 个分离株中的 cgTASs 相结合。我们发现,14 个 cgTAS 等位基因的差异足以将分为四个主要谱系。通过更详细地分析这些差异,我们在 cgTASs 中的一些蛋白质对中发现了可能共同进化的残基,这些残基可能对 TAS 复合物内的蛋白质-蛋白质相互作用至关重要。