• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于合成长读长技术的全长 16S rRNA 测序进行分类学分类的效果。

The effect of taxonomic classification by full-length 16S rRNA sequencing with a synthetic long-read technology.

机构信息

Department of Nanobiomedical Science, Dankook University, Cheonan, 31116, Republic of Korea.

Microbiome Division, Theragen Bio Co., Ltd, Seongnam-si, Gyeonggi-do, 13488, Republic of Korea.

出版信息

Sci Rep. 2021 Jan 18;11(1):1727. doi: 10.1038/s41598-020-80826-9.

DOI:10.1038/s41598-020-80826-9
PMID:33462291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7814050/
Abstract

Characterizing the microbial communities inhabiting specimens is one of the primary objectives of microbiome studies. A short-read sequencing platform for reading partial regions of the 16S rRNA gene is most commonly used by reducing the cost burden of next-generation sequencing (NGS), but misclassification at the species level due to its length being too short to consider sequence similarity remains a challenge. Loop Genomics recently proposed a new 16S full-length-based synthetic long-read sequencing technology (sFL16S). We compared a 16S full-length-based synthetic long-read (sFL16S) and V3-V4 short-read (V3V4) methods using 24 human GUT microbiota samples. Our comparison analyses of sFL16S and V3V4 sequencing data showed that they were highly similar at all classification resolutions except the species level. At the species level, we confirmed that sFL16S showed better resolutions than V3V4 in analyses of alpha-diversity, relative abundance frequency and identification accuracy. Furthermore, we demonstrated that sFL16S could overcome the microbial misidentification caused by different sequence similarity in each 16S variable region through comparison the identification accuracy of Bifidobacterium, Bacteroides, and Alistipes strains classified from both methods. Therefore, this study suggests that the new sFL16S method is a suitable tool to overcome the weakness of the V3V4 method.

摘要

对栖息样本中的微生物群落进行特征描述是微生物组研究的主要目标之一。短读测序平台通过降低下一代测序 (NGS) 的成本负担,通常用于读取 16S rRNA 基因的部分区域,但由于其长度太短而无法考虑序列相似性,因此在物种水平上仍存在分类错误的问题。Loop Genomics 最近提出了一种新的基于 16S 全长的合成长读测序技术 (sFL16S)。我们使用 24 个人类肠道微生物群样本比较了基于 16S 全长的合成长读 (sFL16S) 和 V3-V4 短读 (V3V4) 方法。我们对 sFL16S 和 V3V4 测序数据的比较分析表明,除了物种水平外,它们在所有分类分辨率上都非常相似。在物种水平上,我们证实 sFL16S 在分析 alpha 多样性、相对丰度频率和鉴定准确性方面显示出比 V3V4 更好的分辨率。此外,我们通过比较两种方法分类的双歧杆菌、拟杆菌和alistipes 菌株的鉴定准确性,证明 sFL16S 可以克服每个 16S 可变区不同序列相似性引起的微生物误识别。因此,本研究表明,新的 sFL16S 方法是克服 V3V4 方法弱点的一种合适工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/d91d2227237c/41598_2020_80826_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/951971b9eddd/41598_2020_80826_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/f2222ba882b3/41598_2020_80826_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/207fb119d217/41598_2020_80826_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/034912427c71/41598_2020_80826_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/e1ce0fcd0fc7/41598_2020_80826_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/d91d2227237c/41598_2020_80826_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/951971b9eddd/41598_2020_80826_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/f2222ba882b3/41598_2020_80826_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/207fb119d217/41598_2020_80826_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/034912427c71/41598_2020_80826_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/e1ce0fcd0fc7/41598_2020_80826_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2524/7814050/d91d2227237c/41598_2020_80826_Fig6_HTML.jpg

相似文献

1
The effect of taxonomic classification by full-length 16S rRNA sequencing with a synthetic long-read technology.基于合成长读长技术的全长 16S rRNA 测序进行分类学分类的效果。
Sci Rep. 2021 Jan 18;11(1):1727. doi: 10.1038/s41598-020-80826-9.
2
Analysis of the mouse gut microbiome using full-length 16S rRNA amplicon sequencing.使用全长 16S rRNA 扩增子测序分析小鼠肠道微生物组。
Sci Rep. 2016 Jul 14;6:29681. doi: 10.1038/srep29681.
3
A multi-amplicon 16S rRNA sequencing and analysis method for improved taxonomic profiling of bacterial communities.一种用于改进细菌群落分类学分析的多扩增子16S rRNA测序及分析方法。
J Microbiol Methods. 2018 Nov;154:6-13. doi: 10.1016/j.mimet.2018.09.019. Epub 2018 Sep 29.
4
Full-length 16S rRNA gene amplicon analysis of human gut microbiota using MinION™ nanopore sequencing confers species-level resolution.使用 MinION™ 纳米孔测序对人类肠道微生物组全长 16S rRNA 基因扩增子进行分析可提供种水平分辨率。
BMC Microbiol. 2021 Jan 26;21(1):35. doi: 10.1186/s12866-021-02094-5.
5
Comparison of the full-length sequence and sub-regions of 16S rRNA gene for skin microbiome profiling.比较 16S rRNA 基因全长序列和亚区在皮肤微生物组分析中的应用。
mSystems. 2024 Jul 23;9(7):e0039924. doi: 10.1128/msystems.00399-24. Epub 2024 Jun 27.
6
Species-level bacterial community profiling of the healthy sinonasal microbiome using Pacific Biosciences sequencing of full-length 16S rRNA genes.采用 Pacific Biosciences 全长 16S rRNA 基因测序技术对健康鼻窦微生物组进行细菌群落物种水平分析。
Microbiome. 2018 Oct 23;6(1):190. doi: 10.1186/s40168-018-0569-2.
7
A comparison between full-length 16S rRNA Oxford nanopore sequencing and Illumina V3-V4 16S rRNA sequencing in head and neck cancer tissues.全长 16S rRNA 牛津纳米孔测序与 Illumina V3-V4 16S rRNA 测序在头颈部癌组织中的比较。
Arch Microbiol. 2024 May 7;206(6):248. doi: 10.1007/s00203-024-03985-7.
8
Evaluation of 16S rRNA amplicon sequencing using two next-generation sequencing technologies for phylogenetic analysis of the rumen bacterial community in steers.使用两种下一代测序技术评估16S rRNA扩增子测序用于肉牛瘤胃细菌群落的系统发育分析。
J Microbiol Methods. 2016 Aug;127:132-140. doi: 10.1016/j.mimet.2016.06.004. Epub 2016 Jun 6.
9
Characterization of Fecal Microbiota with Clinical Specimen Using Long-Read and Short-Read Sequencing Platform.使用长读长和短读短测序平台对临床标本的粪便微生物组进行特征分析。
Int J Mol Sci. 2020 Sep 26;21(19):7110. doi: 10.3390/ijms21197110.
10
Comparative analysis of gut microbiota in children with obstructive sleep apnea: assessing the efficacy of 16S rRNA gene sequencing in metabolic function prediction based on weight status.比较阻塞性睡眠呼吸暂停患儿的肠道微生物群:基于体重状况评估 16S rRNA 基因测序在代谢功能预测中的效果。
Front Endocrinol (Lausanne). 2024 Jun 14;15:1344152. doi: 10.3389/fendo.2024.1344152. eCollection 2024.

引用本文的文献

1
Potential protective role of in myopia prevention: evidence from full-length 16S rRNA sequencing and bidirectional Mendelian randomization analysis.[具体物质]在预防近视中的潜在保护作用:来自全长16S rRNA测序和双向孟德尔随机化分析的证据
Front Med (Lausanne). 2025 Aug 13;12:1634120. doi: 10.3389/fmed.2025.1634120. eCollection 2025.
2
Morpho-biochemical and molecular characterization of Bacillus subtilis and Priestia megaterium isolates from eastern Indian farmlands.从印度东部农田分离出的枯草芽孢杆菌和巨大Priestia菌的形态生化及分子特征
Mol Biol Rep. 2025 Jul 12;52(1):706. doi: 10.1007/s11033-025-10796-6.
3
Toward standardized methods in canine vaginal microbiome research: evaluation of storage, host DNA depletion, and database selection.

本文引用的文献

1
Accurate quantification of bacterial abundance in metagenomic DNAs accounting for variable DNA integrity levels.准确量化宏基因组 DNA 中细菌丰度,考虑到 DNA 完整性水平的变化。
Microb Genom. 2020 Oct;6(10). doi: 10.1099/mgen.0.000417.
2
Performance comparison of fecal preservative and stock solutions for gut microbiome storage at room temperature.室温下粪便保存剂和储存液对肠道微生物组存储的性能比较。
J Microbiol. 2020 Aug;58(8):703-710. doi: 10.1007/s12275-020-0092-6. Epub 2020 Jun 25.
3
Evolutionarily conserved transcription factors drive the oxidative stress response in .
迈向犬阴道微生物组研究的标准化方法:储存、宿主DNA去除及数据库选择的评估
Microbiol Spectr. 2025 Aug 5;13(8):e0058325. doi: 10.1128/spectrum.00583-25. Epub 2025 Jul 8.
4
Ecological management of the microbiota in patients with cancer.癌症患者微生物群的生态管理。
Nat Rev Clin Oncol. 2025 Jun 27. doi: 10.1038/s41571-025-01049-3.
5
Consistent microbial insights across sequencing methods in soil studies: the role of reference taxonomies.土壤研究中不同测序方法的一致微生物见解:参考分类法的作用
mSystems. 2025 Jul 22;10(7):e0105924. doi: 10.1128/msystems.01059-24. Epub 2025 Jun 10.
6
Tracheal and cloacal bacterial diversity of red listed Eastern Imperial Eagle ().红色名录中的东方白肩雕的气管和泄殖腔细菌多样性()。 注:括号里的内容原文缺失,所以翻译出来不太完整准确。
Front Microbiol. 2025 May 9;16:1477032. doi: 10.3389/fmicb.2025.1477032. eCollection 2025.
7
Call for caution on alleged tick-borne pathogens in blood-fed ticks from animals across nine Asian countries.呼吁对来自九个亚洲国家动物的饱血蜱中所谓的蜱传病原体保持谨慎。
Microbiol Spectr. 2025 Jul;13(7):e0050725. doi: 10.1128/spectrum.00507-25. Epub 2025 May 23.
8
Effects of dietary supplementation of nitrate on enteric methane production, performance, and rumen microbiome of Hanwoo steers.日粮添加硝酸盐对韩牛瘤胃甲烷生成、生产性能及瘤胃微生物群的影响
J Anim Sci. 2025 Jan 4;103. doi: 10.1093/jas/skaf109.
9
Backtracking identification techniques for predicting unclear bacterial taxonomy at species level: molecular diagnosis-based bacterial classification.用于预测物种水平上不明确细菌分类学的回溯识别技术:基于分子诊断的细菌分类
Genes Genomics. 2025 May;47(5):503-508. doi: 10.1007/s13258-025-01634-x. Epub 2025 Mar 20.
10
Differences in cell-associated and cell-free microbial DNA in blood.血液中细胞相关和游离微生物DNA的差异。
bioRxiv. 2025 Feb 17:2025.02.13.638214. doi: 10.1101/2025.02.13.638214.
进化保守的转录因子驱动 中的氧化应激反应。
J Exp Biol. 2020 Jul 20;223(Pt 14):jeb221622. doi: 10.1242/jeb.221622.
4
Sex-Specific Effects of Dietary Methionine Restriction on the Intestinal Microbiome.膳食蛋氨酸限制对肠道微生物组的性别特异性影响。
Nutrients. 2020 Mar 16;12(3):781. doi: 10.3390/nu12030781.
5
Evaluation of 16S rRNA gene sequencing for species and strain-level microbiome analysis.16S rRNA 基因测序在微生物组物种和菌株水平分析中的评估。
Nat Commun. 2019 Nov 6;10(1):5029. doi: 10.1038/s41467-019-13036-1.
6
Benchmarking Metagenomics Tools for Taxonomic Classification.基于元基因组工具的分类学基准测试。
Cell. 2019 Aug 8;178(4):779-794. doi: 10.1016/j.cell.2019.07.010.
7
Full-length 16S rRNA gene classification of Atlantic salmon bacteria and effects of using different 16S variable regions on community structure analysis.大西洋三文鱼细菌的全长 16S rRNA 基因分类及不同 16S 可变区对群落结构分析的影响。
Microbiologyopen. 2019 Oct;8(10):e898. doi: 10.1002/mbo3.898. Epub 2019 Jul 4.
8
High-throughput amplicon sequencing of the full-length 16S rRNA gene with single-nucleotide resolution.高通量扩增子测序全长度 16S rRNA 基因,具有单核苷酸分辨率。
Nucleic Acids Res. 2019 Oct 10;47(18):e103. doi: 10.1093/nar/gkz569.
9
induces intestinal adaptive immune responses during homeostasis.在体内平衡期间,诱导肠道适应性免疫反应。
Science. 2019 Jun 21;364(6446):1179-1184. doi: 10.1126/science.aaw7479.
10
Complete Genome Sequence of Phascolarctobacterium faecium JCM 30894, a Succinate-Utilizing Bacterium Isolated from Human Feces.屎肠球菌JCM 30894的全基因组序列,一种从人类粪便中分离出的利用琥珀酸的细菌。
Microbiol Resour Announc. 2019 Jan 17;8(3). doi: 10.1128/MRA.01487-18. eCollection 2019 Jan.