TY - JOUR
T1 - Modelling Cryptosporidium infection in human small intestinal and lung organoids
AU - Heo, Inha
AU - Dutta, Devanjali
AU - Schaefer, Deborah A.
AU - Iakobachvili, Nino
AU - Artegiani, Benedetta
AU - Sachs, Norman
AU - Boonekamp, Kim E.
AU - Bowden, Gregory
AU - Hendrickx, Antoni P.A.
AU - Willems, Robert J.L.
AU - Peters, Peter J.
AU - Riggs, Michael W.
AU - O'Connor, Roberta
AU - Clevers, Hans
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/7/1
Y1 - 2018/7/1
N2 - Stem-cell-derived organoids recapitulate in vivo physiology of their original tissues, representing valuable systems to model medical disorders such as infectious diseases. Cryptosporidium, a protozoan parasite, is a leading cause of diarrhoea and a major cause of child mortality worldwide. Drug development requires detailed knowledge of the pathophysiology of Cryptosporidium, but experimental approaches have been hindered by the lack of an optimal in vitro culture system. Here, we show that Cryptosporidium can infect epithelial organoids derived from human small intestine and lung. The parasite propagates within the organoids and completes its complex life cycle. Temporal analysis of the Cryptosporidium transcriptome during organoid infection reveals dynamic regulation of transcripts related to its life cycle. Our study presents organoids as a physiologically relevant in vitro model system to study Cryptosporidium infection.
AB - Stem-cell-derived organoids recapitulate in vivo physiology of their original tissues, representing valuable systems to model medical disorders such as infectious diseases. Cryptosporidium, a protozoan parasite, is a leading cause of diarrhoea and a major cause of child mortality worldwide. Drug development requires detailed knowledge of the pathophysiology of Cryptosporidium, but experimental approaches have been hindered by the lack of an optimal in vitro culture system. Here, we show that Cryptosporidium can infect epithelial organoids derived from human small intestine and lung. The parasite propagates within the organoids and completes its complex life cycle. Temporal analysis of the Cryptosporidium transcriptome during organoid infection reveals dynamic regulation of transcripts related to its life cycle. Our study presents organoids as a physiologically relevant in vitro model system to study Cryptosporidium infection.
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U2 - 10.1038/s41564-018-0177-8
DO - 10.1038/s41564-018-0177-8
M3 - Article
C2 - 29946163
AN - SCOPUS:85049315312
SN - 2058-5276
VL - 3
SP - 814
EP - 823
JO - Nature Microbiology
JF - Nature Microbiology
IS - 7
ER -