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High-throughput single-cell transcriptomics of bacteria using combinatorial barcoding.
Gaisser, Karl D; Skloss, Sophie N; Brettner, Leandra M; Paleologu, Luana; Roco, Charles M; Rosenberg, Alexander B; Hirano, Matthew; DePaolo, R William; Seelig, Georg; Kuchina, Anna.
Afiliação
  • Gaisser KD; Institute for Systems Biology, Seattle, WA, USA.
  • Skloss SN; Institute for Systems Biology, Seattle, WA, USA.
  • Brettner LM; Biodesign Institute Center for Mechanisms of Evolution, Arizona State University, Tempe, AZ, USA.
  • Paleologu L; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Roco CM; Parse Biosciences, Seattle, WA, USA.
  • Rosenberg AB; Parse Biosciences, Seattle, WA, USA.
  • Hirano M; Department of Electrical and Computer Engineering, University of Washington, Seattle, WA, USA.
  • DePaolo RW; Center for Microbiome Sciences and Therapeutics, School of Medicine, University of Washington, Seattle, WA, USA.
  • Seelig G; Department of Medicine, Division of Gastroenterology, School of Medicine, University of Washington, Seattle, WA, USA.
  • Kuchina A; Department of Electrical and Computer Engineering, University of Washington, Seattle, WA, USA.
Nat Protoc ; 2024 Jun 17.
Article em En | MEDLINE | ID: mdl-38886529
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Protoc Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Protoc Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos