4.8 Article

A single-cell RNA-seq atlas of Schistosoma mansoni identifies a key regulator of blood feeding

Journal

SCIENCE
Volume 369, Issue 6511, Pages 1644-+

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.abb7709

Keywords

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Funding

  1. NIH [R01 R01AI121037, R01 R01AI150715, R21 R21AI133393, F30 1F30AI131509-01A1]
  2. Welch Foundation [I-1948-20180324, I-1936-20170325]
  3. National Science Foundation [MCB1553334]
  4. Burroughs Wellcome Fund
  5. Wellcome Trust [107475/Z/15/Z]
  6. Bill and Melinda Gates Foundation [OPP1171488]
  7. Bill and Melinda Gates Foundation [OPP1171488] Funding Source: Bill and Melinda Gates Foundation

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Schistosomiasis is a neglected tropical disease that infects 240 million people. With no vaccines and only one drug available, new therapeutic targets are needed. The causative agents, schistosomes, are intravascular flatworm parasites that feed on blood and lay eggs, resulting in pathology. The function of the parasite's various tissues in successful parasitism are poorly understood, hindering identification of therapeutic targets. Using single-cell RNA sequencing (RNA-seq), we characterize 43,642 cells from the adult schistosome and identify 68 distinct cell populations, including specialized stem cells that maintain the parasite's blood-digesting gut. These stem cells express the gene hnf4, which is required for gut maintenance, blood feeding, and pathology in vivo. Together, these data provide molecular insights into the organ systems of this important pathogen and identify potential therapeutic targets.

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