von Hoyningen-Huene Avril J E, Bang Corinna, Rausch Philipp, Rühlemann Malte, Fokt Hanna, He Jinru, Jensen Nadin, Knop Mirjam, Petersen Carola, Schmittmann Lara, Zimmer Thorsten, Baines John F, Bosch Thomas C G, Hentschel Ute, Reusch Thorsten B H, Roeder Thomas, Franke Andre, Schulenburg Hinrich, Stukenbrock Eva, Schmitz Ruth A
Institute for General Microbiology, Kiel University, Kiel, Germany.
Institute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Front Microbiol. 2024 Feb 27;15:1347422. doi: 10.3389/fmicb.2024.1347422. eCollection 2024.
Metaorganism research contributes substantially to our understanding of the interaction between microbes and their hosts, as well as their co-evolution. Most research is currently focused on the bacterial community, while archaea often remain at the sidelines of metaorganism-related research. Here, we describe the archaeome of a total of eleven classical and emerging multicellular model organisms across the phylogenetic tree of life. To determine the microbial community composition of each host, we utilized a combination of archaea and bacteria-specific 16S rRNA gene amplicons. Members of the two prokaryotic domains were described regarding their community composition, diversity, and richness in each multicellular host. Moreover, association with specific hosts and possible interaction partners between the bacterial and archaeal communities were determined for the marine models. Our data show that the archaeome in marine hosts predominantly consists of and , which represent keystone taxa among the porifera. The presence of an archaeome in the terrestrial hosts varies substantially. With respect to abundant archaeal taxa, they harbor a higher proportion of methanoarchaea over the aquatic environment. We find that the archaeal community is much less diverse than its bacterial counterpart. Archaeal amplicon sequence variants are usually host-specific, suggesting adaptation through co-evolution with the host. While bacterial richness was higher in the aquatic than the terrestrial hosts, a significant difference in diversity and richness between these groups could not be observed in the archaeal dataset. Our data show a large proportion of unclassifiable archaeal taxa, highlighting the need for improved cultivation efforts and expanded databases.
元生物体研究极大地促进了我们对微生物与其宿主之间相互作用以及它们共同进化的理解。目前大多数研究集中在细菌群落,而古菌在元生物体相关研究中常常处于边缘地位。在这里,我们描述了生命系统发育树中总共11种经典和新兴多细胞模式生物的古菌组。为了确定每个宿主的微生物群落组成,我们利用了古菌和细菌特异性16S rRNA基因扩增子的组合。描述了这两个原核域成员在每个多细胞宿主中的群落组成、多样性和丰富度。此外,还确定了海洋模式生物中与特定宿主的关联以及细菌和古菌群落之间可能的相互作用伙伴。我们的数据表明,海洋宿主中的古菌组主要由 和 组成,它们是多孔动物门中的关键类群。陆地宿主中古菌组的存在差异很大。就丰富的古菌类群而言,它们在陆地环境中含有的甲烷古菌比例高于水生环境。我们发现古菌群落的多样性远低于细菌群落。古菌扩增子序列变体通常具有宿主特异性,这表明它们通过与宿主共同进化而适应。虽然水生宿主中的细菌丰富度高于陆地宿主,但在古菌数据集中未观察到这些组之间在多样性和丰富度上的显著差异。我们的数据显示了很大比例的无法分类的古菌类群,突出了改进培养方法和扩展数据库的必要性。