PT - JOURNAL ARTICLE AU - Emma M. Briggs AU - Richard McCulloch AU - Keith R. Matthews AU - Thomas D. Otto TI - Single cell transcriptomic analysis of bloodstream form <em>Trypanosoma brucei</em> reconstructs cell cycle progression and differentiation via quorum sensing AID - 10.1101/2020.12.11.420976 DP - 2020 Jan 01 TA - bioRxiv PG - 2020.12.11.420976 4099 - http://biorxiv.org/content/early/2020/12/11/2020.12.11.420976.short 4100 - http://biorxiv.org/content/early/2020/12/11/2020.12.11.420976.full AB - The life cycles of African trypanosomes are dependent on several differentiation steps, where parasites transition between replicative and non-replicative forms specialised for infectivity and survival in mammal and tsetse fly hosts. Here, we use single cell transcriptomics (scRNA-seq) to dissect the asynchronous differentiation of replicative slender to transmissible stumpy bloodstream form Trypanosoma brucei. Using oligopeptide-induced differentiation, we accurately modelled stumpy development in vitro and captured the transcriptomes of 9,344 slender and stumpy stage parasites, as well as parasites transitioning between these extremes. Using this framework, we detail the relative order of biological events during development, profile dynamic gene expression patterns and identify putative novel regulators. Using marker genes to deduce the cell cycle phase of each parasite, we additionally map the cell cycle of proliferating parasites and position stumpy cell cycle exit at early G1, with subsequent progression to a distinct G0 state. We also explored the role of one gene, ZC3H20, with transient elevated expression at the key slender to stumpy transition point. By scRNA-seq analysis of ZC3H20 null parasites exposed to oligopeptides and mapping the resulting transcriptome to our atlas of differentiation, we identified the point of action for this key regulator. Using a developmental transition relevant for both virulence in the mammalian host and disease transmission, our data provide a paradigm for the temporal mapping of differentiation events and regulators in the trypanosome life cycle.Competing Interest StatementThe authors have declared no competing interest.