Salipante Stephen J, Kawashima Toana, Rosenthal Christopher, Hoogestraat Daniel R, Cummings Lisa A, Sengupta Dhruba J, Harkins Timothy T, Cookson Brad T, Hoffman Noah G
Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA
Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA.
Appl Environ Microbiol. 2014 Dec;80(24):7583-91. doi: 10.1128/AEM.02206-14. Epub 2014 Sep 26.
High-throughput sequencing of the taxonomically informative 16S rRNA gene provides a powerful approach for exploring microbial diversity. Here we compare the performances of two common "benchtop" sequencing platforms, Illumina MiSeq and Ion Torrent Personal Genome Machine (PGM), for bacterial community profiling by 16S rRNA (V1-V2) amplicon sequencing. We benchmarked performance by using a 20-organism mock bacterial community and a collection of primary human specimens. We observed comparatively higher error rates with the Ion Torrent platform and report a pattern of premature sequence truncation specific to semiconductor sequencing. Read truncation was dependent on both the directionality of sequencing and the target species, resulting in organism-specific biases in community profiles. We found that these sequencing artifacts could be minimized by using bidirectional amplicon sequencing and an optimized flow order on the Ion Torrent platform. Results of bacterial community profiling performed on the mock community and a collection of 18 human-derived microbiological specimens were generally in good agreement for both platforms; however, in some cases, results differed significantly. Disparities could be attributed to the failure to generate full-length reads for particular organisms on the Ion Torrent platform, organism-dependent differences in sequence error rates affecting classification of certain species, or some combination of these factors. This study demonstrates the potential for differential bias in bacterial community profiles resulting from the choice of sequencing platform alone.
对具有分类学信息的16S rRNA基因进行高通量测序,为探索微生物多样性提供了一种强大的方法。在此,我们比较了两种常见的“台式”测序平台——Illumina MiSeq和Ion Torrent个人基因组测序仪(PGM),通过16S rRNA(V1-V2)扩增子测序对细菌群落进行分析的性能。我们使用一个包含20种微生物的模拟细菌群落和一批原发性人类标本对性能进行了基准测试。我们观察到Ion Torrent平台的错误率相对较高,并报告了一种特定于半导体测序的序列提前截断模式。序列截断取决于测序方向和目标物种,导致群落图谱中存在物种特异性偏差。我们发现,通过在Ion Torrent平台上使用双向扩增子测序和优化的流程顺序,可以将这些测序假象最小化。在模拟群落和18份人类来源的微生物标本上进行的细菌群落分析结果,在两个平台上总体上吻合良好;然而,在某些情况下,结果存在显著差异。差异可能归因于Ion Torrent平台上未能为特定生物体生成全长读数、影响某些物种分类的序列错误率的物种依赖性差异,或这些因素的某种组合。这项研究表明,仅测序平台的选择就可能导致细菌群落图谱出现差异偏差。