Bartłomiej Surmacz, Daniel Stec, Monika Prus-Frankowska, Mateusz Buczek, Łukasz Michalczyk, Piotr Łukasik
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引用次数: 0
摘要
微生物群被认为在沙蜥的生物学中具有重要意义,但它们的多样性和分布在很大程度上仍未得到探索。这部分是由于研究栖息在微生物丰富环境中的小型生物的微生物群所面临的方法学挑战。在我们的研究中,我们使用 16S rRNA 扩增子测序法鉴定了 31 种培养的沙蜥的微生物群。我们采用了不同的样本制备策略和多种类型的对照,并使用合成 DNA 穗状插入物估算了样本中的微生物数量。我们还重新分析了以前的沙蜥微生物组研究数据。我们的研究结果表明,培养的沙蜥微生物群落主要由来自食物、培养基或试剂的细菌基因型组成。尽管进行了大量实验,但我们发现很难确定富集在某些沙丁鱼体内的菌株,而这些菌株可能与沙丁鱼有共生关系。推测与沙丁鱼相关的微生物在数据集中很少超过 20%,尽管有些与其他研究中发现的共生体相匹配。我们还发现了以前的沙蜥微生物组研究中存在的严重污染问题,从而对其中的一些结论产生了怀疑。我们得出的结论是,沙蜥并非普遍依赖于特化微生物。我们的工作强调了在研究微小生物的微生物群时采取严格保障措施的必要性,并为涉及微生物群丰度较低的样本的研究提供了警示。
Pinpointing the microbiota of tardigrades: What is really there?
Microbiota are considered significant in the biology of tardigrades, yet their diversity and distribution remain largely unexplored. This is partly due to the methodological challenges associated with studying the microbiota of small organisms that inhabit microbe-rich environments. In our study, we characterized the microbiota of 31 species of cultured tardigrades using 16S rRNA amplicon sequencing. We employed various sample preparation strategies and multiple types of controls and estimated the number of microbes in samples using synthetic DNA spike-ins. We also reanalysed data from previous tardigrade microbiome studies. Our findings suggest that the microbial communities of cultured tardigrades are predominantly composed of bacterial genotypes originating from food, medium, or reagents. Despite numerous experiments, we found it challenging to identify strains that were enriched in certain tardigrades, which would have indicated likely symbiotic associations. Putative tardigrade-associated microbes rarely constituted more than 20% of the datasets, although some matched symbionts identified in other studies. We also uncovered serious contamination issues in previous tardigrade microbiome studies, casting doubt on some of their conclusions. We concluded that tardigrades are not universally dependent on specialized microbes. Our work underscores the need for rigorous safeguards in studies of the microbiota of microscopic organisms and serves as a cautionary tale for studies involving samples with low microbiome abundance.
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