Standardized 16S Meta-Analysis Reveals Consistent Host-Associated Patterns in Laminariales Epiphytic Microbiomes

IF 3.6 3区 生物学 Q2 MICROBIOLOGY
J. Z. Florez, A. Zárate, P. Bruna, B. Leyton-Carcaman, V. Molina, M. B. Hengst, C. Camus, M. Abanto, L. Barrientos, A. H. Buschmann
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引用次数: 0

Abstract

Macroalgae and their associated microbes form tightly integrated holobionts, yet cross-study comparisons of epiphytic microbiomes remain constrained by heterogeneous sampling designs, primer selection, and analytical pipelines. We performed a harmonized meta-analysis of publicly available 16S rRNA gene datasets to examine diversity, community structure, and inferred functional profiles within a common analytical framework. A structured search identified 16 studies, totaling 763 samples, from macroalgae and adjacent seawater across four oceanic regions. All datasets were reprocessed using a standardized workflow to ensure cross-study comparability. The compiled dataset was strongly skewed towards brown macroalgae (Phaeophyceae) and the V4 region of the 16S gene, highlighting both the prominence of Laminariales in current research and the need for methodological harmonization. Within this framework, alpha diversity differed among macroalgal orders, with Fucales hosting the richest epiphytic assemblages, Desmarestiales intermediate diversity, and Laminariales the lowest, while seawater exhibited intermediate values. Community composition was structured by host taxonomic identity and sample type. Within Laminariales, thalli supported assemblages distinct from seawater, sharing a limited taxonomic core and displaying reproducible genus-level signatures. Trait-based functional annotation indicated enrichment of aerobic chemoheterotrophy and polysaccharide-associated metabolisms in Laminariales communities, whereas seawater showed greater representation of nitrogen- and sulfur-related processes. These findings demonstrate that cross-study reprocessing resolves consistent host-associated patterns and establishes a quantitative framework for future multi-omics and experimental investigations.

标准化16S荟萃分析揭示了层压藻附生微生物组中与宿主相关的一致模式
大型藻类及其相关微生物形成了紧密结合的整体生物,但附生微生物组的交叉研究比较仍然受到异质采样设计、引物选择和分析管道的限制。我们对公开可用的16S rRNA基因数据集进行了统一的荟萃分析,以在一个共同的分析框架内检查多样性、群落结构和推断的功能概况。一项结构化搜索确定了16项研究,总共763个样本,来自四个海洋区域的大型藻类和邻近的海水。使用标准化工作流程对所有数据集进行重新处理,以确保交叉研究的可比性。收集的数据严重偏向于褐藻(Phaeophyceae)和16S基因的V4区,这既表明了层藻在当前研究中的重要性,也表明了方法协调的必要性。在此框架内,α多样性在各大藻目之间存在差异,岩藻目的附生组合最丰富,desmarestiale的多样性居中,层压藻目的多样性最低,而海水则处于中等水平。群落组成根据寄主分类特征和样本类型划分。在层层体中,菌体支持的组合与海水不同,共享有限的分类核心,并显示可复制的属水平特征。基于性状的功能注释表明,在层带藻群落中,有氧化学异养和多糖相关代谢富集,而海水中则更多地代表了氮和硫相关过程。这些发现表明,交叉研究再处理解决了一致的宿主相关模式,并为未来的多组学和实验研究建立了定量框架。
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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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