Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvum

Cryptosporidium research has been hampered by the lack of in vitro models that can recapitulate the life cycle of the parasite, thus relying on repeated animal infections. Traditional in vitro systems, employing cancerous cell lines, have been unable to support sexual reproduction, but have been wid...

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Main Authors: Mathilde S. Varegg, Ian D. Woolsey, Lucy J. Robertson, Alejandro Jiménez-Meléndez
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Current Research in Parasitology and Vector-Borne Diseases
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Online Access:http://www.sciencedirect.com/science/article/pii/S2667114X25000299
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author Mathilde S. Varegg
Ian D. Woolsey
Lucy J. Robertson
Alejandro Jiménez-Meléndez
author_facet Mathilde S. Varegg
Ian D. Woolsey
Lucy J. Robertson
Alejandro Jiménez-Meléndez
author_sort Mathilde S. Varegg
collection DOAJ
description Cryptosporidium research has been hampered by the lack of in vitro models that can recapitulate the life cycle of the parasite, thus relying on repeated animal infections. Traditional in vitro systems, employing cancerous cell lines, have been unable to support sexual reproduction, but have been widely employed for drug screening assays and allowed transcriptome mapping of the parasite, but extrapolation of those results to in vivo infections is limited. In recent years, intestinal organoids (enteroids), grown as 3D structures, have come to be recognized as more physiologically relevant, complex systems, since they more accurately reproduce the cell populations present in the small intestine. A key advantage of these systems is their ability to fulfil the life cycle of the parasite. However, studies employing bovine organoids, the target species of the major zoonotic species Cryptosporidium parvum, are lacking. Future research should emphasize bioengineered systems, with heterogeneous populations of intestinal epithelial and mesenchymal cells, to advance the in vitro field closer to in vivo infection models. The present review summarizes the history of cell line use in Cryptosporidium research and the most recent advances in organoids, bio-engineered and organ-on-a-chip platforms, including methodological approaches used to facilitate exposure of the apical side of the target cells to the parasite, and the influence of mechanical forces and microenvironment.
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spelling doaj-art-ff9db621622d4e29b4f0057e8724f5262025-08-20T03:21:52ZengElsevierCurrent Research in Parasitology and Vector-Borne Diseases2667-114X2025-01-01710026910.1016/j.crpvbd.2025.100269Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvumMathilde S. Varegg0Ian D. Woolsey1Lucy J. Robertson2Alejandro Jiménez-Meléndez3Corresponding author.; Department of Paraclinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Elizabeth Stephansens vei 15, 1433, Aas, NorwayDepartment of Paraclinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Elizabeth Stephansens vei 15, 1433, Aas, NorwayDepartment of Paraclinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Elizabeth Stephansens vei 15, 1433, Aas, NorwayDepartment of Paraclinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Elizabeth Stephansens vei 15, 1433, Aas, NorwayCryptosporidium research has been hampered by the lack of in vitro models that can recapitulate the life cycle of the parasite, thus relying on repeated animal infections. Traditional in vitro systems, employing cancerous cell lines, have been unable to support sexual reproduction, but have been widely employed for drug screening assays and allowed transcriptome mapping of the parasite, but extrapolation of those results to in vivo infections is limited. In recent years, intestinal organoids (enteroids), grown as 3D structures, have come to be recognized as more physiologically relevant, complex systems, since they more accurately reproduce the cell populations present in the small intestine. A key advantage of these systems is their ability to fulfil the life cycle of the parasite. However, studies employing bovine organoids, the target species of the major zoonotic species Cryptosporidium parvum, are lacking. Future research should emphasize bioengineered systems, with heterogeneous populations of intestinal epithelial and mesenchymal cells, to advance the in vitro field closer to in vivo infection models. The present review summarizes the history of cell line use in Cryptosporidium research and the most recent advances in organoids, bio-engineered and organ-on-a-chip platforms, including methodological approaches used to facilitate exposure of the apical side of the target cells to the parasite, and the influence of mechanical forces and microenvironment.http://www.sciencedirect.com/science/article/pii/S2667114X25000299Bio-engineered systemCell cultureEnteroidOrganoidOrgan-on-a-chip
spellingShingle Mathilde S. Varegg
Ian D. Woolsey
Lucy J. Robertson
Alejandro Jiménez-Meléndez
Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvum
Current Research in Parasitology and Vector-Borne Diseases
Bio-engineered system
Cell culture
Enteroid
Organoid
Organ-on-a-chip
title Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvum
title_full Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvum
title_fullStr Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvum
title_full_unstemmed Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvum
title_short Rapid review: Recent advances in in vitro models for the study of Cryptosporidium parvum
title_sort rapid review recent advances in in vitro models for the study of cryptosporidium parvum
topic Bio-engineered system
Cell culture
Enteroid
Organoid
Organ-on-a-chip
url http://www.sciencedirect.com/science/article/pii/S2667114X25000299
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