TY - JOUR
T1 - Single-cell atlas of the first intra-mammalian developmental stage of the human parasite Schistosoma mansoni
AU - Diaz Soria, Carmen Lidia
AU - Lee, Jayhun
AU - Chong, Tracy
AU - Coghlan, Avril
AU - Tracey, Alan
AU - Young, Matthew D.
AU - Andrews, Tallulah
AU - Hall, Christopher
AU - Ng, Bee Ling
AU - Rawlinson, Kate
AU - Doyle, Stephen R.
AU - Leonard, Steven
AU - Lu, Zhigang
AU - Bennett, Hayley M.
AU - Rinaldi, Gabriel
AU - Newmark, Phillip A.
AU - Berriman, Matthew
N1 - Funding Information:
Wellcome provided core-funding support to the Wellcome Sanger Institute (Sanger), award number 206194. The work was supported by the Wellcome Strategic Award number 107475/Z/15/Z. P.A.N. is an investigator of the Howard Hughes Medical Institute. B. glabrata snails used in the United States were provided by the NIAID Schistosomiasis Resource Center of the Biomedical Research Institute (Rockville, MD) through NIH-NIAID Contract HHSN272201700014I for distribution through BEI Resources. We thank the following individuals at Sanger: Gal Horesh for initial technical assistance optimising dissociation conditions; Catherine McCarthy and Simon Clare for assistance and technical support with animal infections and maintenance of the Schistosoma mansoni life cycle; David Goulding and Claire Cormie at the Electron and Advanced Light Microscopy facility; Jennie Graham and Sam Thompson at the Cytometry Core Facility; Nancy Holroyd, Mandy Sanders, Elizabeth Cook and Nathalie Smerdon for facilitating the submission of 10X samples; Matthew Jones for 10X training and library preparations; Cellular Genetics Informatics, especially Martin Prete and Vladimir Kiselev, for creation of a data visualisation website. We thank Dr. Shristi Pandey for sharing the random forest code used in this work and Dr. Mireya Plass for sharing the planaria dataset. Finally, we thank the single cell online community for enthusiastically sharing their work online.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/18
Y1 - 2020/12/18
N2 - Over 250 million people suffer from schistosomiasis, a tropical disease caused by parasitic flatworms known as schistosomes. Humans become infected by free-swimming, water-borne larvae, which penetrate the skin. The earliest intra-mammalian stage, called the schistosomulum, undergoes a series of developmental transitions. These changes are critical for the parasite to adapt to its new environment as it navigates through host tissues to reach its niche, where it will grow to reproductive maturity. Unravelling the mechanisms that drive intra-mammalian development requires knowledge of the spatial organisation and transcriptional dynamics of different cell types that comprise the schistomulum body. To fill these important knowledge gaps, we perform single-cell RNA sequencing on two-day old schistosomula of Schistosoma mansoni. We identify likely gene expression profiles for muscle, nervous system, tegument, oesophageal gland, parenchymal/primordial gut cells, and stem cells. In addition, we validate cell markers for all these clusters by in situ hybridisation in schistosomula and adult parasites. Taken together, this study provides a comprehensive cell-type atlas for the early intra-mammalian stage of this devastating metazoan parasite.
AB - Over 250 million people suffer from schistosomiasis, a tropical disease caused by parasitic flatworms known as schistosomes. Humans become infected by free-swimming, water-borne larvae, which penetrate the skin. The earliest intra-mammalian stage, called the schistosomulum, undergoes a series of developmental transitions. These changes are critical for the parasite to adapt to its new environment as it navigates through host tissues to reach its niche, where it will grow to reproductive maturity. Unravelling the mechanisms that drive intra-mammalian development requires knowledge of the spatial organisation and transcriptional dynamics of different cell types that comprise the schistomulum body. To fill these important knowledge gaps, we perform single-cell RNA sequencing on two-day old schistosomula of Schistosoma mansoni. We identify likely gene expression profiles for muscle, nervous system, tegument, oesophageal gland, parenchymal/primordial gut cells, and stem cells. In addition, we validate cell markers for all these clusters by in situ hybridisation in schistosomula and adult parasites. Taken together, this study provides a comprehensive cell-type atlas for the early intra-mammalian stage of this devastating metazoan parasite.
KW - Animals
KW - Esophagus/metabolism
KW - Exons/genetics
KW - Gene Expression Regulation
KW - Humans
KW - Mammals/parasitology
KW - Muscle Cells/metabolism
KW - Nervous System/cytology
KW - Neurons/cytology
KW - Parasites/cytology
KW - Schistosoma mansoni/cytology
KW - Single-Cell Analysis
KW - Stem Cells/cytology
KW - Transcription, Genetic
UR - http://www.scopus.com/inward/record.url?scp=85097764418&partnerID=8YFLogxK
U2 - 10.1038/s41467-020-20092-5
DO - 10.1038/s41467-020-20092-5
M3 - Article
C2 - 33339816
AN - SCOPUS:85097764418
SN - 2041-1723
VL - 11
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6411
ER -