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宏基因组学和单细胞基因组学方法在探索蓝藻多样性方面面临的挑战。

Challenges of metagenomics and single-cell genomics approaches for exploring cyanobacterial diversity.

作者信息

Davison Michelle, Hall Eric, Zare Richard, Bhaya Devaki

机构信息

Department of Plant Biology, Carnegie Institution of Science, 260 Panama Street, Stanford, CA, 94305, USA.

SRI International, 333 Ravenswood Ave, Menlo Park, CA, 94025, USA.

出版信息

Photosynth Res. 2015 Oct;126(1):135-46. doi: 10.1007/s11120-014-0066-9. Epub 2014 Dec 17.

Abstract

Cyanobacteria have played a crucial role in the history of early earth and continue to be instrumental in shaping our planet, yet applications of cutting edge technology have not yet been widely used to explore cyanobacterial diversity. To provide adequate background, we briefly review current sequencing technologies and their innovative uses in genomics and metagenomics. Next, we focus on current cell capture technologies and the challenges of using them with cyanobacteria. We illustrate the utility in coupling breakthroughs in DNA amplification with cell capture platforms, with an example of microfluidic isolation and subsequent targeted amplicon sequencing from individual terrestrial thermophilic cyanobacteria. Single cells of thermophilic, unicellular Synechococcus sp. JA-2-3-B'a(2-13) (Syn OS-B') were sorted in a microfluidic device, lysed, and subjected to whole genome amplification by multiple displacement amplification. We amplified regions from specific CRISPR spacer arrays, which are known to be highly diverse, contain semi-palindromic repeats which form secondary structure, and can be difficult to amplify. Cell capture, lysis, and genome amplification on a microfluidic device have been optimized, setting a stage for further investigations of individual cyanobacterial cells isolated directly from natural populations.

摘要

蓝细菌在地球早期历史中发挥了关键作用,并在塑造我们的星球方面继续发挥重要作用,然而前沿技术的应用尚未广泛用于探索蓝细菌的多样性。为了提供充分的背景信息,我们简要回顾了当前的测序技术及其在基因组学和宏基因组学中的创新应用。接下来,我们重点关注当前的细胞捕获技术以及将其用于蓝细菌的挑战。我们通过一个微流控分离以及随后对单个陆地嗜热蓝细菌进行靶向扩增子测序的例子,阐述了将DNA扩增方面的突破与细胞捕获平台相结合的实用性。嗜热单细胞聚球藻属JA-2-3-B'a(2-13)(Syn OS-B')的单个细胞在微流控装置中进行分选、裂解,并通过多重置换扩增进行全基因组扩增。我们扩增了特定CRISPR间隔序列阵列中的区域,这些区域已知具有高度多样性,包含形成二级结构的半回文重复序列,并且可能难以扩增。微流控装置上的细胞捕获、裂解和基因组扩增已得到优化,为进一步研究直接从自然群体中分离出的单个蓝细菌细胞奠定了基础。

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