Targeted CRISPR screens reveal genes essential for Cryptosporidium survival in the host intestine
Lucy C. Watson,
Katarzyna A. Sala,
Netanya Bernitz,
Lotta Baumgärtel,
Mitchell A. Pallett,
N. Bishara Marzook,
Lorian Cobra Straker,
Duo Peng,
Lucy Collinson and
Adam Sateriale ()
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Lucy C. Watson: The Francis Crick Institute
Katarzyna A. Sala: The Francis Crick Institute
Netanya Bernitz: The Francis Crick Institute
Lotta Baumgärtel: The Francis Crick Institute
Mitchell A. Pallett: The Francis Crick Institute
N. Bishara Marzook: The Francis Crick Institute
Lorian Cobra Straker: The Francis Crick Institute
Duo Peng: Chan Zuckerberg Biohub
Lucy Collinson: The Francis Crick Institute
Adam Sateriale: The Francis Crick Institute
Nature Communications, 2025, vol. 16, issue 1, 1-13
Abstract:
Abstract The Cryptosporidium parasite is one of the leading causes of diarrheal morbidity and mortality in children, and adolescent infections are associated with chronic malnutrition. There are no vaccines available for protection and only one drug approved for treatment that has limited efficacy. A major barrier to developing new therapeutics is a lack of foundational knowledge of Cryptosporidium biology, including which parasite genes are essential for survival and virulence. Here, we iteratively improve the tools for genetically manipulating Cryptosporidium and develop a targeted CRISPR-based screening method to rapidly assess how the loss of individual parasite genes influence survival in vivo. Using this method, we examine the parasite’s pyrimidine salvage pathway and a set of leading Cryptosporidium vaccine candidates. From this latter group, using inducible knockout, we determined the parasite gene known as Cp23 to be essential for survival in vivo. Parasites deficient in Cp23 were able to replicate within and emerge from infected epithelial cells, yet unable to initiate gliding motility which is required for the reinfection of neighbouring cells. The targeted screening method presented here is highly versatile and will enable researchers to more rapidly expand the knowledge base for Cryptosporidium infection biology, paving the way for new therapeutics.
Date: 2025
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63012-1
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DOI: 10.1038/s41467-025-63012-1
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