Suppr超能文献

用于基于16S rRNA的细菌群落分析的Illumina和离子激流下一代测序平台的性能比较

Performance comparison of Illumina and ion torrent next-generation sequencing platforms for 16S rRNA-based bacterial community profiling.

作者信息

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

机构信息

Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA

Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA.

出版信息

Appl Environ Microbiol. 2014 Dec;80(24):7583-91. doi: 10.1128/AEM.02206-14. Epub 2014 Sep 26.

Abstract

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.

摘要

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。

相似文献

1
Performance comparison of Illumina and ion torrent next-generation sequencing platforms for 16S rRNA-based bacterial community profiling.
Appl Environ Microbiol. 2014 Dec;80(24):7583-91. doi: 10.1128/AEM.02206-14. Epub 2014 Sep 26.
7
A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform.
Microbiologyopen. 2018 Dec;7(6):e00611. doi: 10.1002/mbo3.611. Epub 2018 Mar 25.
8
Bioinformatic strategies to address limitations of 16rRNA short-read amplicons from different sequencing platforms.
J Microbiol Methods. 2020 Feb;169:105811. doi: 10.1016/j.mimet.2019.105811. Epub 2019 Dec 16.
9
Evaluation of PacBio sequencing for full-length bacterial 16S rRNA gene classification.
BMC Microbiol. 2016 Nov 14;16(1):274. doi: 10.1186/s12866-016-0891-4.
10
Different next generation sequencing platforms produce different microbial profiles and diversity in cystic fibrosis sputum.
J Microbiol Methods. 2016 Nov;130:95-99. doi: 10.1016/j.mimet.2016.09.002. Epub 2016 Sep 5.

引用本文的文献

1
Why Are Long-Read Sequencing Methods Revolutionizing Microbiome Analysis?
Microorganisms. 2025 Aug 9;13(8):1861. doi: 10.3390/microorganisms13081861.
2
Do we need a standardized 16S rRNA gene amplicon sequencing analysis protocol for poultry microbiota research?
Poult Sci. 2025 Jul;104(7):105242. doi: 10.1016/j.psj.2025.105242. Epub 2025 May 1.
3
Microbiota changes in lactation in the short-beaked echidna (Tachyglossus aculeatus).
FEMS Microbiol Ecol. 2025 Apr 14;101(5). doi: 10.1093/femsec/fiaf036.
5
Investigation of the marine bacterial community along the coastline of the Gulf of Thailand.
Heliyon. 2024 May 24;10(11):e31896. doi: 10.1016/j.heliyon.2024.e31896. eCollection 2024 Jun 15.
6
Forensic Microbiology: When, Where and How.
Microorganisms. 2024 May 14;12(5):988. doi: 10.3390/microorganisms12050988.
9
Effects of error, chimera, bias, and GC content on the accuracy of amplicon sequencing.
mSystems. 2023 Dec 21;8(6):e0102523. doi: 10.1128/msystems.01025-23. Epub 2023 Dec 1.
10
Integration of multi-omics data to elucidate keystone unknown taxa within microbialite-forming ecosystems.
Front Microbiol. 2023 Jul 28;14:1174685. doi: 10.3389/fmicb.2023.1174685. eCollection 2023.

本文引用的文献

1
The bias associated with amplicon sequencing does not affect the quantitative assessment of bacterial community dynamics.
PLoS One. 2014 Jun 12;9(6):e99722. doi: 10.1371/journal.pone.0099722. eCollection 2014.
2
Analysis, optimization and verification of Illumina-generated 16S rRNA gene amplicon surveys.
PLoS One. 2014 Apr 10;9(4):e94249. doi: 10.1371/journal.pone.0094249. eCollection 2014.
3
Strengths and limitations of 16S rRNA gene amplicon sequencing in revealing temporal microbial community dynamics.
PLoS One. 2014 Apr 8;9(4):e93827. doi: 10.1371/journal.pone.0093827. eCollection 2014.
4
Coinfection of Fusobacterium nucleatum and Actinomyces israelii in mastoiditis diagnosed by next-generation DNA sequencing.
J Clin Microbiol. 2014 May;52(5):1789-92. doi: 10.1128/JCM.03133-13. Epub 2014 Feb 26.
6
Metagenomic species profiling using universal phylogenetic marker genes.
Nat Methods. 2013 Dec;10(12):1196-9. doi: 10.1038/nmeth.2693. Epub 2013 Oct 20.
8
Assessing the fecal microbiota: an optimized ion torrent 16S rRNA gene-based analysis protocol.
PLoS One. 2013 Jul 15;8(7):e68739. doi: 10.1371/journal.pone.0068739. Print 2013.
10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验