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Spatial structure in the Plastisphere: Molecular resources for imaging microscopic communities on plastic marine debris

机译:塑料圈中的空间结构:在塑料海洋垃圾上对微观群落成像的分子资源

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摘要

Plastic marine debris (PMD) affects spatial scales of life from microbes to whales. However, understanding interactions between plastic and microbes in the “Plastisphere”—the thin layer of life on the surface of PMD—has been technology‐limited. Research into microbe–microbe and microbe–substrate interactions requires knowledge of community phylogenetic composition but also tools to visualize spatial distributions of intact microbial biofilm communities. We developed a CLASI‐FISH (combinatorial labelling and spectral imaging – fluorescence hybridization) method using confocal microscopy to study Plastisphere communities. We created a probe set consisting of three existing phylogenetic probes (targeting all Bacteria, ‐, and ) and four newly designed probes (targeting , , and ) labelled with a total of seven fluorophores and validated this probe set using pure cultures. Our nested probe set strategy increases confidence in taxonomic identification because targets are confirmed with two or more probes, reducing false positives. We simultaneously identified and visualized these taxa and their spatial distribution within the microbial biofilms on polyethylene samples in colonization time series experiments in coastal environments from three different biogeographical regions. Comparing the relative abundance of 16S rRNA gene amplicon sequencing data with cell‐count abundance data retrieved from the microscope images of the same samples showed a good agreement in bacterial composition. Microbial communities were heterogeneous, with direct spatial relationships between bacteria, cyanobacteria and eukaryotes such as diatoms but also micro‐metazoa. Our research provides a valuable resource to investigate biofilm development, succession and associations between specific microscopic taxa at micrometre scales.
机译:塑料海洋垃圾(PMD)影响从微生物到鲸鱼的生活空间尺度。然而,了解“塑料层”中塑料与微生物之间的相互作用(PMD表面生命的薄层)受到技术限制。对微生物-微生物和微生物-底物相互作用的研究不仅需要了解群落的系统发育组成,还需要可视化完整的微生物生物膜群落的空间分布的工具。我们使用共聚焦显微镜开发了一种CLASI-FISH(组合标记和光谱成像-荧光杂交)方法来研究原生质球群落。我们创建了一个探针组,该探针组由三个现有的系统发育探针(针对所有细菌,-和)以及四个新设计的探针(targeting和-)组成,总共标记了七个荧光团,并使用纯培养物验证了该探针组。我们的嵌套探针集策略可提高对分类学鉴定的信心,因为可通过两个或多个探针确认目标,从而减少了假阳性。我们在三个不同生物地理区域的沿海环境中,在殖民化时间序列实验中同时识别并可视化了这些分类单元及其在聚乙烯样品上的微生物生物膜内的空间分布。将16S rRNA基因扩增子测序数据的相对丰度与从相同样品的显微镜图像中检索到的细胞计数丰度数据进行比较,表明细菌组成方面有很好的一致性。微生物群落是异质的,在细菌,蓝细菌和真核生物(如硅藻)之间还有空间上的直接关系,但也包括微量金属甲硝唑。我们的研究提供了宝贵的资源,可以在微米尺度上研究生物膜的发育,演替以及特定显微分类群之间的关联。

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