首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Assessing Symbiodinium diversity in scleractinian corals via next-generation sequencing-based genotyping of the ITS2 rDNA region
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Assessing Symbiodinium diversity in scleractinian corals via next-generation sequencing-based genotyping of the ITS2 rDNA region

机译:通过基于ITS2 rDNA区域的下一代测序的基因分型来评估巩膜珊瑚中的共生生物多样性

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摘要

The persistence of coral reef ecosystems relies on the symbiotic relationship between scleractinian corals and intracellular, photosynthetic dinoflagellates in the genus Symbiodinium. Genetic evidence indicates that these symbionts are biologically diverse and exhibit discrete patterns of environmental and host distribution. This makes the assessment of Symbiodinium diversity critical to understanding the symbiosis ecology of corals. Here, we applied pyrosequencing to the elucidation of Symbiodinium diversity via analysis of the internal transcribed spacer 2 (ITS2) region, a multicopy genetic marker commonly used to analyse Symbiodinium diversity. Replicated data generated from isoclonal Symbiodinium cultures showed that all genomes contained numerous, yet mostly rare, ITS2 sequence variants. Pyrosequencing data were consistent with more traditional denaturing gradient gel electrophoresis (DGGE) approaches to the screening of ITS2 PCR amplifications, where the most common sequences appeared as the most intense bands. Further, we developed an operational taxonomic unit (OTU)-based pipeline for Symbiodinium ITS2 diversity typing to provisionally resolve ecologically discrete entities from intragenomic variation. A genetic distance cut-off of 0.03 collapsed intragenomic ITS2 variants of isoclonal cultures into single OTUs. When applied to the analysis of field-collected coral samples, our analyses confirm that much of the commonly observed SymbiodiniumITS2 diversity can be attributed to intragenomic variation. We conclude that by analysing Symbiodinium populations in an OTU-based framework, we can improve objectivity, comparability and simplicity when assessing ITS2 diversity in field-based studies.
机译:珊瑚礁生态系统的持久性依赖于巩膜珊瑚与共生菌属中的细胞内光合作用鞭毛虫的共生关系。遗传证据表明,这些共生体在生物学上是多样的,并且表现出环境和宿主分布的离散模式。这使得对共生生物多样性的评估对于理解珊瑚的共生生态至关重要。在这里,我们通过内部转录间隔区2(ITS2)区域的分析,将焦磷酸测序应用于共生菌多样性的阐明,这是一种通常用于分析共生菌多样性的多拷贝遗传标记。从等速共生菌培养物中获得的重复数据表明,所有基因组均包含许多但大多数情况下很少见的ITS2序列变体。焦磷酸测序数据与更传统的变性梯度凝胶电泳(DGGE)方法用于ITS2 PCR扩增的筛选相一致,其中最常见的序列显示为最强的条带。此外,我们针对Symbiodinium ITS2多样性类型开发了基于操作分类单元(OTU)的管道,以临时解决基因组内部变异中的生态离散实体。 0.03的遗传距离临界值将等克隆培养的基因组ITS2变体折叠为单个OTU。当应用于野外采集的珊瑚样品的分析时,我们的分析证实,许多通常观察到的SymbiodiniumITS2多样性可归因于基因组内变异。我们得出结论,通过在基于OTU的框架中分析共生菌种群,我们可以在实地研究中评估ITS2多样性时提高客观性,可比性和简便性。

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