ArticlePLoS pathogens2025
Cryptosporidium oocyst wall proteins are true components of the oocyst wall and COWP8 is not required for parasite transmission.
Article in PLoS pathogens, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Enzymatic Degradation ofMolecules (Basel, Switzerland) · 2026Article
- Insights into the lifecycle of Cryptosporidium and compounds targeting developmental stages.Current opinion in microbiology · 2026Review
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Authors and funding
13 authors.
Funding
Abstract
Cryptosporidiosis is a significant cause of diarrhoeal disease contributing to substantial morbidity and mortality for the immunocompromised and for young children, especially those who are malnourished. There are no vaccines and no effective treatments for these patients. Cryptosporidium parasites are transmitted as an oocyst, which is composed of a hardy oocyst wall that protects parasites in the environment. Oocysts are often waterborne, and are resistant to common water treatments, including chlorination. Little is understood about how the Cryptosporidium oocyst is constructed, its composition, and the how it resists chlorination. A family of nine Cryptosporidium Oocyst Wall Proteins (COWPs) is predicted from the genome. However, due to the technical challenges of working with this parasite in the laboratory, only cowp1 has been investigated to date. Using CRISPR/Cas9, fluorescent fusions were generated for the remaining members of the family, COWPs 2-9. Microscopy confirms that all COWPs localise to the oocyst wall. Further, COWPs 2-4 appear to localise specifically to the oocyst suture, the site from which parasites emerge from the oocyst during infection. Cowp 6 and 8 were observed to be expressed by female parasites. These proteins localise to puncta consistent with organelles called wall forming bodies. These organelles store and then secrete material to form the oocyst wall. Parasites lacking cowp8 produce viable oocysts that have typical oocyst morphology. Cowp8 knockout oocysts are transmissible under laboratory settings and readily infect immunocompromised mice. Biomechanical measurements determine that COWP8 is not required for the strength of the oocyst wall. This work confirms the role of cowps in oocyst wall formation and sets a foundation for further exploration of the role of these proteins in transmission of Cryptosporidium parasites.
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