Cottier Fabien, Srinivasan Kandhadayar Gopalan, Yurieva Marina, Liao Webber, Poidinger Michael, Zolezzi Francesca, Pavelka Norman
1Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (ASTAR), 8A Biomedical Grove, Immunos #04, Singapore, 138648 Singapore.
2Present Address: The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032 USA.
NPJ Biofilms Microbiomes. 2018 Jan 18;4:2. doi: 10.1038/s41522-017-0046-x. eCollection 2018.
Sequencing-based microbiome profiling aims at detecting and quantifying individual members of a microbial community in a culture-independent manner. While amplicon-based sequencing (ABS) of bacterial or fungal ribosomal DNA is the most widely used technology due to its low cost, it suffers from PCR amplification biases that hinder accurate representation of microbial population structures. Shotgun metagenomics (SMG) conversely allows unbiased microbiome profiling but requires high sequencing depth. Here we report the development of a meta-total RNA sequencing (MeTRS) method based on shotgun sequencing of total RNA and benchmark it on a human stool sample spiked in with known abundances of bacterial and fungal cells. MeTRS displayed the highest overall sensitivity and linearity for both bacteria and fungi, the greatest reproducibility compared to SMG and ABS, while requiring a ~20-fold lower sequencing depth than SMG. We therefore present MeTRS as a valuable alternative to existing technologies for large-scale profiling of complex microbiomes.
基于测序的微生物组分析旨在以不依赖培养的方式检测和量化微生物群落中的个体成员。虽然基于扩增子的细菌或真菌核糖体DNA测序(ABS)因其低成本而成为最广泛使用的技术,但它存在PCR扩增偏差,阻碍了微生物种群结构的准确呈现。相反,鸟枪法宏基因组学(SMG)允许进行无偏差的微生物组分析,但需要高测序深度。在此,我们报告了一种基于总RNA鸟枪法测序的元全RNA测序(MeTRS)方法的开发,并在掺入已知丰度细菌和真菌细胞的人类粪便样本上对其进行了基准测试。MeTRS对细菌和真菌均显示出最高的总体灵敏度和线性,与SMG和ABS相比具有最大的可重复性,同时所需的测序深度比SMG低约20倍。因此,我们提出MeTRS作为现有技术的一种有价值的替代方法,用于复杂微生物组的大规模分析。