Laboratory of Systems and Synthetic Biology, Department of Agrotechnology and Food Sciences, Wageningen University and ResearchWageningen, Netherlands; Bioprocess Technology and Support, MSD Animal HealthBoxmeer, Netherlands.
Laboratory of Systems and Synthetic Biology, Department of Agrotechnology and Food Sciences, Wageningen University and Research Wageningen, Netherlands.
Front Cell Infect Microbiol. 2017 Feb 7;7:31. doi: 10.3389/fcimb.2017.00031. eCollection 2017.
Mycoplasmas are the smallest self-replicating organisms and obligate parasites of a specific vertebrate host. An in-depth analysis of the functional capabilities of mycoplasma species is fundamental to understand how some of simplest forms of life on Earth succeeded in subverting complex hosts with highly sophisticated immune systems. In this study we present a genome-scale comparison, focused on identification of functional protein domains, of 80 publically available mycoplasma genomes which were consistently re-annotated using a standardized annotation pipeline embedded in a semantic framework to keep track of the data provenance. We examined the pan- and core-domainome and studied predicted functional capability in relation to host specificity and phylogenetic distance. We show that the pan- and core-domainome of mycoplasma species is closed. A comparison with the proteome of the "minimal" synthetic bacterium JCVI-Syn3.0 allowed us to classify domains and proteins essential for minimal life. Many of those essential protein domains, essential Domains of Unknown Function (DUFs) and essential hypothetical proteins are not persistent across mycoplasma genomes suggesting that mycoplasma species support alternative domain configurations that bypass their essentiality. Based on the protein domain composition, we could separate mycoplasma species infecting blood and tissue. For selected genomes of tissue infecting mycoplasmas, we could also predict whether the host is ruminant, pig or human. Functionally closely related mycoplasma species, which have a highly similar protein domain repertoire, but different hosts could not be separated. This study provides a concise overview of the functional capabilities of mycoplasma species, which can be used as a basis to further understand host-pathogen interaction or to design synthetic minimal life.
支原体是最小的自我复制生物,是特定脊椎动物宿主的专性寄生虫。深入分析支原体物种的功能能力对于理解地球上一些最简单的生命形式如何成功地颠覆具有高度复杂免疫系统的复杂宿主至关重要。在这项研究中,我们对 80 个公开可用的支原体基因组进行了基于功能的全基因组比较,重点是识别功能蛋白结构域,这些基因组使用标准化注释管道进行了一致的重新注释,该管道嵌入在语义框架中,以跟踪数据来源。我们检查了泛和核心结构域组,并研究了预测的功能能力与宿主特异性和系统发育距离的关系。我们表明,支原体物种的泛和核心结构域组是封闭的。与“最小”合成细菌 JCVI-Syn3.0 的蛋白质组进行比较使我们能够对最小生命所必需的结构域和蛋白质进行分类。其中许多必需的蛋白质结构域、功能未知的必需结构域(DUFs)和必需的假设蛋白在支原体基因组中并不持久,这表明支原体物种支持替代的结构域配置,从而避免了它们的必需性。基于蛋白质结构域组成,我们可以将感染血液和组织的支原体物种分开。对于选定的组织感染支原体基因组,我们还可以预测宿主是反刍动物、猪还是人。具有高度相似蛋白质结构域库的功能上密切相关的支原体物种,由于不同的宿主而无法区分。本研究提供了支原体物种功能能力的简明概述,可作为进一步了解宿主-病原体相互作用或设计合成最小生命的基础。