BGI-Shenzhen, Shenzhen 518083, China.
Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, 2100 Copenhagen, Denmark.
Cell Rep Methods. 2023 Mar 27;3(3):100437. doi: 10.1016/j.crmeth.2023.100437.
Sequencing of hypervariable regions as well as internal transcribed spacer regions of ribosomal RNA genes (rDNA) is broadly used to identify bacteria and fungi, but taxonomic and phylogenetic resolution is hampered by insufficient sequencing length using high throughput, cost-efficient second-generation sequencing. We developed a method to obtain nearly full-length rDNA by assembling single DNA molecules combining DNA co-barcoding with single-tube long fragment read technology and second-generation sequencing. Benchmarking was performed using mock bacterial and fungal communities as well as two forest soil samples. All mock species rDNA were successfully recovered with identities above 99.5% compared to the reference sequences. From the soil samples we obtained good coverage with identification of more than 20,000 unknown species, as well as high abundance correlation between replicates. This approach provides a cost-effective method for obtaining extensive and accurate information on complex environmental microbial communities.
对核糖体 RNA 基因(rDNA)的高变区和内部转录间隔区进行测序被广泛用于鉴定细菌和真菌,但由于使用高通量、经济高效的第二代测序时测序长度不足,限制了分类和系统发育分辨率。我们开发了一种通过将单个 DNA 分子与 DNA 共条形码和单管长片段读取技术相结合来组装几乎全长 rDNA 的方法,并结合第二代测序。使用模拟细菌和真菌群落以及两个森林土壤样本进行了基准测试。与参考序列相比,所有模拟物种 rDNA 的身份识别率均超过 99.5%,成功回收。从土壤样本中,我们获得了良好的覆盖率,鉴定出了超过 20,000 个未知物种,并且重复之间的丰度相关性很高。这种方法为获取复杂环境微生物群落的广泛而准确的信息提供了一种具有成本效益的方法。