Institute for Systems Biology, Seattle, WA, USA.
Biodesign Institute Center for Mechanisms of Evolution, Arizona State University, Tempe, AZ, USA.
Nat Protoc. 2024 Oct;19(10):3048-3084. doi: 10.1038/s41596-024-01007-w. Epub 2024 Jun 17.
Microbial split-pool ligation transcriptomics (microSPLiT) is a high-throughput single-cell RNA sequencing method for bacteria. With four combinatorial barcoding rounds, microSPLiT can profile transcriptional states in hundreds of thousands of Gram-negative and Gram-positive bacteria in a single experiment without specialized equipment. As bacterial samples are fixed and permeabilized before barcoding, they can be collected and stored ahead of time. During the first barcoding round, the fixed and permeabilized bacteria are distributed into a 96-well plate, where their transcripts are reverse transcribed into cDNA and labeled with the first well-specific barcode inside the cells. The cells are mixed and redistributed two more times into new 96-well plates, where the second and third barcodes are appended to the cDNA via in-cell ligation reactions. Finally, the cells are mixed and divided into aliquot sub-libraries, which can be stored until future use or prepared for sequencing with the addition of a fourth barcode. It takes 4 days to generate sequencing-ready libraries, including 1 day for collection and overnight fixation of samples. The standard plate setup enables single-cell transcriptional profiling of up to 1 million bacterial cells and up to 96 samples in a single barcoding experiment, with the possibility of expansion by adding barcoding rounds. The protocol requires experience in basic molecular biology techniques, handling of bacterial samples and preparation of DNA libraries for next-generation sequencing. It can be performed by experienced undergraduate or graduate students. Data analysis requires access to computing resources, familiarity with Unix command line and basic experience with Python or R.
微生物分裂池连接转录组学(microSPLiT)是一种高通量的细菌单细胞 RNA 测序方法。通过四轮组合条形码实验,microSPLiT 可以在单个实验中对数十万革兰氏阴性和革兰氏阳性细菌的转录状态进行分析,而无需专门的设备。由于在条形码实验之前细菌样本需要被固定和通透化,因此它们可以提前收集和储存。在第一轮条形码实验中,固定和通透化的细菌被分配到 96 孔板中,在细胞内将其转录物反转录成 cDNA,并标记上第一个孔特异性的条形码。然后将细胞混合并重新分配到另外两个新的 96 孔板中,通过细胞内连接反应将第二和第三个条形码附加到 cDNA 上。最后,将细胞混合并分成等分的子文库,可以储存起来以备将来使用,或者在添加第四个条形码后准备进行测序。生成测序就绪的文库需要 4 天的时间,包括 1 天的样本收集和过夜固定。标准板设置允许在单个条形码实验中对多达 100 万个细菌细胞和多达 96 个样本进行单细胞转录组分析,并且可以通过添加条形码实验轮次来进行扩展。该方案需要具备基本分子生物学技术、细菌样本处理和下一代测序 DNA 文库制备方面的经验。有经验的本科生或研究生可以完成该方案。数据分析需要具备计算资源、熟悉 Unix 命令行以及 Python 或 R 的基本经验。