比较基因组学确定了海绵相关微生物共生体的关键适应性状。

IF 4.3 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2024-09-03 DOI:10.1111/1462-2920.16690
Paul A. O'Brien, Steven J. Robbins, Shangjin Tan, Laura Rix, David J. Miller, Nicole S. Webster, Guojie Zhang, David G. Bourne
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引用次数: 0

摘要

海绵微生物群通常具有高度多样性,因此很难确定哪些菌系对维持宿主的健康和平衡非常重要。鉴定与共生相关的基因组特征可以提高我们对哪些品系适应了宿主以及它们可能提供哪些功能的认识。在这里,我们研究了与海绵相关的五个微生物科,包括内生单胞菌科(Endozoicomonadaceae)、亚硝基单胞菌科(Nitrosopumilaceae)、螺旋藻科(Spirochaetaceae)、微丝胞菌科(Microtrichaceae)和Thermoanaerobaculaceae,以更好地了解它们共生背后的机制。我们将海绵相关基因组与其他环境中发现的基因组进行了比较,发现海绵特异性支系富含编码许多已知共生体生存机制的基因,如避免吞噬和抵御外来遗传因子。我们扩展了以往的知识,发现糖基水解酶与硫酸酯酶和硫酸转移酶可能形成多酶降解途径,以分解和重塑硫酸化多糖,并发现超氧化物歧化酶的富集可能防止宿主产生的自由氧自由基造成的损害。最后,我们发现了海绵相关共生体的新特征,例如螺旋藻科的尿素代谢,而此前的研究表明这种代谢在螺旋藻门中十分罕见。这些结果确定了共生体适应与海绵共生的可能机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Comparative genomics identifies key adaptive traits of sponge-associated microbial symbionts

Sponge microbiomes are often highly diverse making it difficult to determine which lineages are important for maintaining host health and homeostasis. Characterising genomic traits associated with symbiosis can improve our knowledge of which lineages have adapted to their host and what functions they might provide. Here we examined five microbial families associated with sponges that have previously shown evidence of cophylogeny, including Endozoicomonadaceae, Nitrosopumilaceae, Spirochaetaceae, Microtrichaceae and Thermoanaerobaculaceae, to better understand the mechanisms behind their symbiosis. We compared sponge-associated genomes to genomes found in other environments and found that sponge-specific clades were enriched in genes encoding many known mechanisms for symbiont survival, such as avoiding phagocytosis and defence against foreign genetic elements. We expand on previous knowledge to show that glycosyl hydrolases with sulfatases and sulfotransferases likely form multienzyme degradation pathways to break and remodel sulfated polysaccharides and reveal an enrichment in superoxide dismutase that may prevent damage from free oxygen radicals produced by the host. Finally, we identified novel traits in sponge-associated symbionts, such as urea metabolism in Spirochaetaceae which was previously shown to be rare in the phylum Spirochaetota. These results identify putative mechanisms by which symbionts have adapted to living in association with sponges.

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来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
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