A comprehensive metatranscriptome analysis pipeline and its validation using human small intestine microbiota datasets

被引:90
作者
Leimena, Milkha M. [1 ,2 ]
Ramiro-Garcia, Javier [1 ,2 ,3 ]
Davids, Mark [1 ,3 ]
van den Bogert, Bartholomeus [1 ,2 ]
Smidt, Hauke [2 ]
Smid, Eddy J. [1 ,4 ]
Boekhorst, Jos [6 ,7 ]
Zoetendal, Erwin G. [1 ,2 ]
Schaap, Peter J. [1 ,3 ]
Kleerebezem, Michiel [1 ,2 ,5 ,7 ]
机构
[1] TI Food & Nutr TIFN, NL-6700 AN Wageningen, Netherlands
[2] Microbiol Lab, NL-6703 HB Wageningen, Netherlands
[3] Wageningen Univ, Lab Syst & Synthet Biol, NL-6703 HB Wageningen, Netherlands
[4] Wageningen Univ, Lab Food Microbiol, NL-6700 EV Wageningen, Netherlands
[5] Wageningen Univ, Host Microbe Interact Grp, NL-6700 AH Wageningen, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Ctr Mol & Biomol Informat, NL-6525 ED Nijmegen, Netherlands
[7] NIZO Food Res BV, NL-6710 BA Ede, Netherlands
关键词
Metatranscriptome; Bioinformatic pipeline; Human small intestine microbiota; Illumina sequencing; Single-end reads; Paired-end reads; COG; KEGG; Metabolic pathways; RIBOSOMAL-RNA; GENE-EXPRESSION; BACTERIA; SEQ; TRANSCRIPTOMES; IDENTITIES; DIVERSITY; DATABASE; SAMPLES; NUMBER;
D O I
10.1186/1471-2164-14-530
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Next generation sequencing (NGS) technologies can be applied in complex microbial ecosystems for metatranscriptome analysis by employing direct cDNA sequencing, which is known as RNA sequencing (RNA-seq). RNA-seq generates large datasets of great complexity, the comprehensive interpretation of which requires a reliable bioinformatic pipeline. In this study, we focus on the development of such a metatranscriptome pipeline, which we validate using Illumina RNA-seq datasets derived from the small intestine microbiota of two individuals with an ileostomy. Results: The metatranscriptome pipeline developed here enabled effective removal of rRNA derived sequences, followed by confident assignment of the predicted function and taxonomic origin of the mRNA reads. Phylogenetic analysis of the small intestine metatranscriptome datasets revealed a strong similarity with the community composition profiles obtained from 16S rDNA and rRNA pyrosequencing, indicating considerable congruency between community composition (rDNA), and the taxonomic distribution of overall (rRNA) and specific (mRNA) activity among its microbial members. Reproducibility of the metatranscriptome sequencing approach was established by independent duplicate experiments. In addition, comparison of metatranscriptome analysis employing single- or paired-end sequencing methods indicated that the latter approach does not provide improved functional or phylogenetic insights. Metatranscriptome functional-mapping allowed the analysis of global, and genus specific activity of the microbiota, and illustrated the potential of these approaches to unravel syntrophic interactions in microbial ecosystems. Conclusions: A reliable pipeline for metatransciptome data analysis was developed and evaluated using RNA-seq datasets obtained for the human small intestine microbiota. The set-up of the pipeline is very generic and can be applied for (bacterial) metatranscriptome analysis in any chosen niche.
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页数:14
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