Ling Meilee, Szarvas Judit, Kurmauskaitė Vaida, Kiseliovas Vaidotas, Žilionis Rapolas, Avot Baptiste, Munk Patrick, Aarestrup Frank M
Research Group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Kgs Lyngby, Denmark.
Atrandi Biosciences, Vilnius, Lithuania.
Front Microbiol. 2025 Feb 4;15:1516656. doi: 10.3389/fmicb.2024.1516656. eCollection 2024.
Single-cell sequencing may serve as a powerful complementary technique to shotgun metagenomics to study microbiomes. This emerging technology allows the separation of complex microbial communities into individual bacterial cells, enabling high-throughput sequencing of genetic material from thousands of singular bacterial cells in parallel. Here, we validated the use of microfluidics and semi-permeable capsules (SPCs) technology (Atrandi) to isolate individual bacterial cells from sewage and pig fecal samples. Our method involves extracting and amplifying single bacterial DNA within individual SPCs, followed by combinatorial split-and-pool single-amplified genome (SAG) barcoding and short-read sequencing. We tested two different sequencing approaches with different numbers of SPCs from the same sample for each sequencing run. Using a deep sequencing approach, we detected 1,796 and 1,220 SAGs, of which 576 and 599 were used for further analysis from one sewage and one fecal sample, respectively. In shallow sequencing data, we aimed for 10-times more cells and detected 12,731 and 17,909 SAGs, of which we used 2,456 and 1,599 for further analysis for sewage and fecal samples, respectively. Additionally, we identified the top 10 antimicrobial resistance genes (ARGs) in both sewage and feces samples and linked them to their individual host bacterial species.
单细胞测序可作为鸟枪法宏基因组学的一种强大补充技术,用于研究微生物群落。这项新兴技术能够将复杂的微生物群落分离成单个细菌细胞,从而实现对数千个单个细菌细胞的遗传物质进行高通量平行测序。在这里,我们验证了使用微流控和半透性胶囊(SPCs)技术(Atrandi)从污水和猪粪便样本中分离单个细菌细胞的方法。我们的方法包括在单个SPCs中提取和扩增单个细菌的DNA,随后进行组合式分割池单扩增基因组(SAG)条形码标记和短读长测序。每次测序运行时,我们用来自同一样本的不同数量的SPCs测试了两种不同的测序方法。采用深度测序方法,我们检测到1796个和1220个SAG,其中分别从一个污水样本和一个粪便样本中选取了576个和599个用于进一步分析。在浅层测序数据中,我们的目标是检测数量多10倍的细胞,检测到12731个和17909个SAG,其中分别从污水样本和粪便样本中选取了2456个和1599个用于进一步分析。此外,我们确定了污水和粪便样本中排名前十的抗菌抗性基因(ARGs),并将它们与其各自的宿主细菌物种联系起来。