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沿海海域细菌多样性的捕获方法比较。

Comparative approach to capture bacterial diversity of coastal waters.

机构信息

Center for Geomicrobiology, University of Aarhus, Ny Munkegade, Bld. 1535, 8000, Århus C, Denmark.

出版信息

J Microbiol. 2011 Oct;49(5):729-40. doi: 10.1007/s12275-011-1205-z. Epub 2011 Nov 9.

DOI:10.1007/s12275-011-1205-z
PMID:22068488
Abstract

Despite the revolutionary advancements in DNA sequencing technology and cultivation techniques, few studies have been done to directly compare these methods. In this study, a 16S rRNA gene-based, integrative approach combining culture-independent techniques with culture-dependent methods was taken to investigate the bacterial community structure of coastal seawater collected from the Yellow Sea, Korea. For culture-independent studies, we used the latest model pyrosequencer, Roche/454 Genome Sequencer FLX Titanium. Pyrosequencing captured a total of 52 phyla including 27 candidate divisions from the water column, whereas the traditional cloning approach captured only 15 phyla including 2 candidate divisions. In addition, of 878 genera retrieved, 92.1 % of the sequences were unique to pyrosequencing. For culture-dependent analysis, plate culturing, plate washing, enrichment, and high-throughput culturing (HTC) methods were applied. Phylogenetic analysis showed that the plate-washing clones formed a cluster devoid of any previously cultured representatives within the family Rhodobacteraceae. One HTC isolate (SF293) fell into the OM182 clade, which was not recovered by other culturing methods described here. By directly comparing the sequences obtained from cultures with those from culture-independent work, we found that only 33% of the culture sequences were identical to those from clone libraries and pyrosequences. This study presents a detailed comparison of common molecular and cultivation techniques available in microbial ecology. As different methods yielded different coverage, we suggest choosing the approach after carefully examining the scientific questions being asked.

摘要

尽管在 DNA 测序技术和培养技术方面取得了革命性的进步,但很少有研究直接比较这些方法。在这项研究中,采用了一种基于 16S rRNA 基因的综合方法,将非培养技术与培养方法相结合,来研究从韩国黄海采集的海水的细菌群落结构。在非培养研究中,我们使用了最新的模型焦磷酸测序仪,罗氏/454 基因组测序仪 FLX Titanium。焦磷酸测序总共捕获了 52 个门,包括 27 个候选门,而传统的克隆方法仅捕获了 15 个门,包括 2 个候选门。此外,在 878 个属中,92.1%的序列是焦磷酸测序特有的。对于培养分析,应用了平板培养、平板洗涤、富集和高通量培养(HTC)方法。系统发育分析表明,平板洗涤克隆形成了一个集群,在 Rhodobacteraceae 科内没有任何以前培养的代表。一个 HTC 分离株(SF293)属于 OM182 分支,其他培养方法没有分离到这个分支。通过直接比较从培养物中获得的序列与非培养工作获得的序列,我们发现只有 33%的培养序列与克隆文库和焦磷酸测序的序列相同。本研究对微生物生态学中常用的分子和培养技术进行了详细比较。由于不同的方法产生的覆盖范围不同,我们建议在仔细检查所提出的科学问题后选择方法。

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