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Modeling ecological drivers in marine viral communities using comparative metagenomics and network analyses

机译:使用比较宏基因组学和网络分析对海洋病毒群落中的生态驱动因素进行建模

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摘要

Long-standing questions in marine viral ecology are centered on understanding how viral assemblages change along gradients in space and time. However, investigating these fundamental ecological questions has been challenging due to incomplete representation of naturally occurring viral diversity in single gene- or morphology-based studies and an inability to identify up to 90% of reads in viral metagenomes (viromes). Although protein clustering techniques provide a significant advance by helping organize this unknown metagenomic sequence space, they typically use only ∼75% of the data and rely on assembly methods not yet tuned for naturally occurring sequence variation. Here, we introduce an annotation- and assembly-free strategy for comparative metagenomics that combines shared k-mer and social network analyses (regression modeling). This robust statistical framework enables visualization of complex sample networks and determination of ecological factors driving community structure. Application to 32 viromes from the Pacific Ocean Virome dataset identified clusters of samples broadly delineated by photic zone and revealed that geographic region, depth, and proximity to shore were significant predictors of community structure. Within subsets of this dataset, depth, season, and oxygen concentration were significant drivers of viral community structure at a single open ocean station, whereas variability along onshore–offshore transects was driven by oxygen concentration in an area with an oxygen minimum zone and not depth or proximity to shore, as might be expected. Together these results demonstrate that this highly scalable approach using complete metagenomic network-based comparisons can both test and generate hypotheses for ecological investigation of viral and microbial communities in nature.
机译:海洋病毒生态学中长期存在的问题集中在理解病毒组合如何随时空梯度变化。但是,由于在基于单基因或形态学的研究中天然存在的病毒多样性的不完整表现以及无法识别病毒元基因组(病毒基因组)中多达90%的读数,因此研究这些基本的生态问题一直具有挑战性。尽管蛋白质聚类技术通过帮助组织这种未知的宏基因组序列空间提供了重大进步,但它们通常仅使用约75%的数据,并依赖尚未针对自然发生的序列变异进行调整的组装方法。在这里,我们为比较宏基因组学引入了无注释和无汇编的策略,该策略结合了共享的k-mer和社交网络分析(回归建模)。这种强大的统计框架使可视化的复杂样本网络和确定驱动社区结构的生态因素。将其应用于来自太平洋海洋基因组数据集的32种病毒学,可以识别出由光合带大致划定的样本簇,并揭示了地理区域,深度和与海岸的接近度是群落结构的重要预测因子。在此数据集的子集中,深度,季节和氧气浓度是单个开放海洋站病毒群落结构的重要驱动力,而沿陆-近海样带的变化是由氧气最小区域而不是深度的区域中的氧气浓度驱动的或接近岸边​​,这可能是预期的。这些结果加在一起表明,这种使用基于宏基因组网络的完全可比性的高度可扩展方法可以测试并生成假设,用于自然界中病毒和微生物群落的生态调查。

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