Milani Christian, Alessandri Giulia, Mangifesta Marta, Mancabelli Leonardo, Lugli Gabriele Andrea, Fontana Federico, Longhi Giulia, Anzalone Rosaria, Viappiani Alice, Duranti Sabrina, Turroni Francesca, Costi Renato, Annicchiarico Alfredo, Morini Andrea, Sarli Leopoldo, Ossiprandi Maria Cristina, van Sinderen Douwe, Ventura Marco
Laboratory of Probiogenomics, Department of Chemistry, Life Sciences, and Environmental Sustainability, University of Parma, Parma, Italy.
Microbiome Research Hub, University of Parma, Parma, Italy.
mSystems. 2020 Jul 28;5(4):e00404-20. doi: 10.1128/mSystems.00404-20.
16S small-subunit (SSU) rRNA gene-based bacterial profiling is the gold standard for cost-effective taxonomic reconstruction of complex bacterial populations down to the genus level. However, it has been proven ineffective in clinical and research settings requiring higher taxonomic resolution. We therefore developed a bacterial profiling method based on the internal transcribed spacer (ITS) region employing optimized primers and a comprehensive ITS database for accurate cataloguing of bacterial communities at (sub)species resolution. Performance of the microbial ITS profiling pipeline was tested through analysis of host-associated, food, and environmental matrices, while its efficacy in clinical settings was assessed through analysis of mucosal biopsy specimens of colorectal cancer, leading to the identification of putative novel biomarkers. The data collected indicate that the proposed pipeline represents a major step forward in cost-effective identification and screening of microbial biomarkers at (sub)species level, with relevant impact in research, industrial, and clinical settings. We developed a novel method for accurate cataloguing of bacterial communities at (sub)species level involving amplification of the internal transcribed spacer (ITS) region through optimized primers, followed by next-generation sequencing and taxonomic classification of amplicons by means of a comprehensive database of bacterial ITS sequences. Host-associated, food, and environmental matrices were employed to test the performance of the microbial ITS profiling pipeline. Moreover, mucosal biopsy samples from colorectal cancer patients were analyzed to demonstrate the scientific relevance of this profiling approach in a clinical setting through identification of putative novel biomarkers. The results indicate that the ITS-based profiling pipeline proposed here represents a key metagenomic tool with major relevance for research, industrial, and clinical settings.
基于16S小亚基(SSU)rRNA基因的细菌谱分析是对复杂细菌群体进行经济高效的分类重建直至属水平的金标准。然而,在需要更高分类分辨率的临床和研究环境中,它已被证明是无效的。因此,我们开发了一种基于内转录间隔区(ITS)区域的细菌谱分析方法,该方法采用优化的引物和一个全面的ITS数据库,用于以(亚)种分辨率准确编目细菌群落。通过对宿主相关、食物和环境基质的分析测试了微生物ITS谱分析流程的性能,同时通过对结直肠癌黏膜活检标本的分析评估了其在临床环境中的功效,从而鉴定出了假定的新型生物标志物。收集到的数据表明,所提出的流程在以(亚)种水平经济高效地鉴定和筛选微生物生物标志物方面向前迈出了重要一步,在研究、工业和临床环境中具有相关影响。我们开发了一种在(亚)种水平准确编目细菌群落的新方法,该方法包括通过优化的引物扩增内转录间隔区(ITS)区域,然后进行下一代测序,并借助细菌ITS序列的综合数据库对扩增子进行分类。利用宿主相关、食物和环境基质来测试微生物ITS谱分析流程的性能。此外,对结直肠癌患者的黏膜活检样本进行了分析,以通过鉴定假定的新型生物标志物来证明这种谱分析方法在临床环境中的科学相关性。结果表明,这里提出的基于ITS的谱分析流程代表了一种关键的宏基因组学工具,在研究、工业和临床环境中具有重要意义。