Tytgat Bjorn, Verleyen Elie, Obbels Dagmar, Peeters Karolien, De Wever Aaike, D'hondt Sofie, De Meyer Tim, Van Criekinge Wim, Vyverman Wim, Willems Anne
Laboratory for Microbiology, Department of Biochemistry and Microbiology, Ghent University, Ghent, Belgium.
Laboratory of Protistology and Aquatic Ecology, Department of Biology, Ghent University, Ghent, Belgium.
PLoS One. 2014 Jun 2;9(6):e97564. doi: 10.1371/journal.pone.0097564. eCollection 2014.
The application of high-throughput sequencing of the 16S rRNA gene has increased the size of microbial diversity datasets by several orders of magnitude, providing improved access to the rare biosphere compared with cultivation-based approaches and more established cultivation-independent techniques. By contrast, cultivation-based approaches allow the retrieval of both common and uncommon bacteria that can grow in the conditions used and provide access to strains for biotechnological applications. We performed bidirectional pyrosequencing of the bacterial 16S rRNA gene diversity in two terrestrial and seven aquatic Antarctic microbial mat samples previously studied by heterotrophic cultivation. While, not unexpectedly, 77.5% of genera recovered by pyrosequencing were not among the isolates, 25.6% of the genera picked up by cultivation were not detected by pyrosequencing. To allow comparison between both techniques, we focused on the five phyla (Proteobacteria, Actinobacteria, Bacteroidetes, Firmicutes and Deinococcus-Thermus) recovered by heterotrophic cultivation. Four of these phyla were among the most abundantly recovered by pyrosequencing. Strikingly, there was relatively little overlap between cultivation and the forward and reverse pyrosequencing-based datasets at the genus (17.1-22.2%) and OTU (3.5-3.6%) level (defined on a 97% similarity cut-off level). Comparison of the V1-V2 and V3-V2 datasets of the 16S rRNA gene revealed remarkable differences in number of OTUs and genera recovered. The forward dataset missed 33% of the genera from the reverse dataset despite comprising 50% more OTUs, while the reverse dataset did not contain 40% of the genera of the forward dataset. Similar observations were evident when comparing the forward and reverse cultivation datasets. Our results indicate that the region under consideration can have a large impact on perceived diversity, and should be considered when comparing different datasets. Finally, a high number of OTUs could not be classified using the RDP reference database, suggesting the presence of a large amount of novel diversity.
16S rRNA基因高通量测序的应用使微生物多样性数据集的规模增加了几个数量级,与基于培养的方法以及更成熟的非培养技术相比,能更好地获取稀有生物圈的信息。相比之下,基于培养的方法能够分离出在所用条件下可生长的常见和不常见细菌,并获得用于生物技术应用的菌株。我们对之前通过异养培养研究过的两个陆地和七个水生南极微生物垫样本中的细菌16S rRNA基因多样性进行了双向焦磷酸测序。不出所料,通过焦磷酸测序回收的属中有77.5%不在分离株中,而通过培养获得的属中有25.6%未被焦磷酸测序检测到。为了便于两种技术之间的比较,我们重点关注通过异养培养回收的五个门(变形菌门、放线菌门、拟杆菌门、厚壁菌门和嗜热栖热菌门)。其中四个门是通过焦磷酸测序回收量最多的门。令人惊讶的是,在属(17.1 - 22.2%)和OTU(3.5 - 3.6%)水平上(基于97%相似性截止水平定义),培养与基于正向和反向焦磷酸测序的数据集之间的重叠相对较少。16S rRNA基因的V1 - V2和V3 - V2数据集的比较显示,回收的OTU和属的数量存在显著差异。正向数据集尽管OTU数量多50%,但仍遗漏了反向数据集中33%的属,而反向数据集不包含正向数据集中40%的属。比较正向和反向培养数据集时也有类似的观察结果。我们的结果表明所考虑的区域可能对感知到的多样性有很大影响,在比较不同数据集时应予以考虑。最后,大量的OTU无法使用RDP参考数据库进行分类,这表明存在大量新的多样性。