Institute for Zoology and Organismic Interactions, Heinrich-Heine-University Düsseldorf, Düsseldorf, 40225, Germany.
Research Group Medical Systems Biology, Institute of Experimental Medicine, Christian-Albrechts-University Kiel, Kiel, 24105, Germany.
Microbiome. 2023 Nov 18;11(1):257. doi: 10.1186/s40168-023-01701-z.
The microbiota of multicellular organisms undergoes considerable changes during host ontogeny but the general mechanisms that control community assembly and succession are poorly understood. Here, we use bacterial recolonization experiments in Nematostella vectensis as a model to understand general mechanisms determining bacterial establishment and succession. We compared the dynamic establishment of the microbiome on the germfree host and on inert silicone tubes.
Following the dynamic reconstruction of microbial communities on both substrates, we show that the initial colonization events are strongly influenced by the host but not by the silicone tube, while the subsequent bacteria-bacteria interactions are the main driver of bacterial succession. Interestingly, the recolonization pattern on adult hosts resembles the ontogenetic colonization succession. This process occurs independently of the bacterial composition of the inoculum and can be followed at the level of individual bacteria. To identify potential metabolic traits associated with initial colonization success and potential metabolic interactions among bacteria associated with bacterial succession, we reconstructed the metabolic networks of bacterial colonizers based on their genomes. These analyses revealed that bacterial metabolic capabilities reflect the recolonization pattern, and the degradation of chitin might be a selection factor during early recolonization of the animal. Concurrently, transcriptomic analyses revealed that Nematostella possesses two chitin synthase genes, one of which is upregulated during early recolonization.
Our results show that early recolonization events are strongly controlled by the host while subsequent colonization depends on metabolic bacteria-bacteria interactions largely independent of host ontogeny. Video Abstract.
多细胞生物的微生物组在宿主个体发育过程中会发生很大变化,但控制群落组装和演替的一般机制尚不清楚。在这里,我们使用 Nematostella vectensis 的细菌再定植实验作为模型来了解决定细菌定植和演替的一般机制。我们比较了无菌宿主和惰性硅酮管上微生物组的动态建立。
在对两种基质上微生物群落的动态重建之后,我们表明初始定植事件强烈受宿主影响,但不受硅酮管影响,而随后的细菌-细菌相互作用是细菌演替的主要驱动因素。有趣的是,成年宿主上的再定植模式类似于个体发育过程中的定植演替。这个过程独立于接种物的细菌组成发生,并且可以在单个细菌的水平上进行跟踪。为了鉴定与初始定植成功相关的潜在代谢特征以及与细菌演替相关的细菌间潜在代谢相互作用,我们基于细菌的基因组重建了定植细菌的代谢网络。这些分析表明,细菌的代谢能力反映了再定植模式,并且在动物的早期再定植过程中,几丁质的降解可能是一个选择因素。同时,转录组分析表明,Nematostella 拥有两个几丁质合酶基因,其中一个在早期再定植过程中上调。
我们的结果表明,早期定植事件强烈受宿主控制,而随后的定植则取决于代谢细菌-细菌相互作用,而这些作用在很大程度上与宿主个体发育无关。