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A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability

Despite being a frequent cause of severe diarrheal disease in infants and an opportunistic infection in immunocompromised patients, Cryptosporidium research has lagged due to a lack of facile experimental methods. Here, we describe a platform for complete life cycle development and long-term growth...

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Autores principales: Wilke, Georgia, Funkhouser-Jones, Lisa J., Wang, Yi, Ravindran, Soumya, Wang, Qiuling, Beatty, Wandy L., Baldridge, Megan T., VanDussen, Kelli L., Shen, Bang, Kuhlenschmidt, Mark S., Kuhlenschmidt, Theresa B., Witola, William H., Stappenbeck, Thaddeus S., Sibley, L. David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617391/
https://www.ncbi.nlm.nih.gov/pubmed/31231046
http://dx.doi.org/10.1016/j.chom.2019.05.007
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author Wilke, Georgia
Funkhouser-Jones, Lisa J.
Wang, Yi
Ravindran, Soumya
Wang, Qiuling
Beatty, Wandy L.
Baldridge, Megan T.
VanDussen, Kelli L.
Shen, Bang
Kuhlenschmidt, Mark S.
Kuhlenschmidt, Theresa B.
Witola, William H.
Stappenbeck, Thaddeus S.
Sibley, L. David
author_facet Wilke, Georgia
Funkhouser-Jones, Lisa J.
Wang, Yi
Ravindran, Soumya
Wang, Qiuling
Beatty, Wandy L.
Baldridge, Megan T.
VanDussen, Kelli L.
Shen, Bang
Kuhlenschmidt, Mark S.
Kuhlenschmidt, Theresa B.
Witola, William H.
Stappenbeck, Thaddeus S.
Sibley, L. David
author_sort Wilke, Georgia
collection PubMed
description Despite being a frequent cause of severe diarrheal disease in infants and an opportunistic infection in immunocompromised patients, Cryptosporidium research has lagged due to a lack of facile experimental methods. Here, we describe a platform for complete life cycle development and long-term growth of C. parvum in vitro using “air-liquid interface” (ALI) cultures derived from intestinal epithelial stem cells. Transcriptomic profiling revealed that differentiating epithelial cells grown under ALI conditions undergo profound changes in metabolism and development that enable completion of the parasite life cycle in vitro. ALI cultures support parasite expansion > 100-fold and generate viable oocysts that are transmissible in vitro and to mice, causing infection and animal death. Transgenic parasite lines created using CRISPR/Cas9 were used to complete a genetic cross in vitro, demonstrating Mendelian segregation of chromosomes during meiosis. ALI culture provides an accessible model that will enable innovative studies into Cryptosporidium biology and host interactions.
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spelling pubmed-66173912019-07-22 A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability Wilke, Georgia Funkhouser-Jones, Lisa J. Wang, Yi Ravindran, Soumya Wang, Qiuling Beatty, Wandy L. Baldridge, Megan T. VanDussen, Kelli L. Shen, Bang Kuhlenschmidt, Mark S. Kuhlenschmidt, Theresa B. Witola, William H. Stappenbeck, Thaddeus S. Sibley, L. David Cell Host Microbe Article Despite being a frequent cause of severe diarrheal disease in infants and an opportunistic infection in immunocompromised patients, Cryptosporidium research has lagged due to a lack of facile experimental methods. Here, we describe a platform for complete life cycle development and long-term growth of C. parvum in vitro using “air-liquid interface” (ALI) cultures derived from intestinal epithelial stem cells. Transcriptomic profiling revealed that differentiating epithelial cells grown under ALI conditions undergo profound changes in metabolism and development that enable completion of the parasite life cycle in vitro. ALI cultures support parasite expansion > 100-fold and generate viable oocysts that are transmissible in vitro and to mice, causing infection and animal death. Transgenic parasite lines created using CRISPR/Cas9 were used to complete a genetic cross in vitro, demonstrating Mendelian segregation of chromosomes during meiosis. ALI culture provides an accessible model that will enable innovative studies into Cryptosporidium biology and host interactions. Cell Press 2019-07-10 /pmc/articles/PMC6617391/ /pubmed/31231046 http://dx.doi.org/10.1016/j.chom.2019.05.007 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wilke, Georgia
Funkhouser-Jones, Lisa J.
Wang, Yi
Ravindran, Soumya
Wang, Qiuling
Beatty, Wandy L.
Baldridge, Megan T.
VanDussen, Kelli L.
Shen, Bang
Kuhlenschmidt, Mark S.
Kuhlenschmidt, Theresa B.
Witola, William H.
Stappenbeck, Thaddeus S.
Sibley, L. David
A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability
title A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability
title_full A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability
title_fullStr A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability
title_full_unstemmed A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability
title_short A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability
title_sort stem-cell-derived platform enables complete cryptosporidium development in vitro and genetic tractability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617391/
https://www.ncbi.nlm.nih.gov/pubmed/31231046
http://dx.doi.org/10.1016/j.chom.2019.05.007
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