Researchers have established a culture system for the cultivation of Cryptosporidium parvum derived from mouse and bovine cholangiocyte organoids (Chol-orgs).

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Source: EPA/H.D.A. Lindquist

Immunofluorescence image of Cryptosporidium parvum oocysts, purified from murine fecal material.

The study, published in hLife, is led by Prof. Feng (College of Veterinary Medicine, South China Agricultural University) and Prof. Xiao (College of Veterinary Medicine, South China Agricultural University). 

Cryptosporidium parvum is a protozoan parasite that causes gastrointestinal disease in humans and animals worldwide. Infection is usually self-limited in immunocompetent individuals, but is a major problem in immunocompromised hosts and a serious health risk in AIDS patients. C. parvum can infect the epithelial cells lining the gallbladder and bile ducts, resulting in sclerosing cholangitis. However, studies of the mechanisms and host-pathogen interactions are severely limited by the lack of accessible cultures and models of biliary cryptosporidiosis.

Simple procedures

This team described simple procedures for the generation of mouse and bovine Chol-orgs, and the establishment of an in vitro model of biliary cryptosporidiosis. Chol-orgs expressing stem and biliary cell markers could be maintained for more than three months and stored in liquid nitrogen for more than a year. The Chol-orgs allow the complete development of C. parvum in vitro, producing oocysts that are infectious to mice. In RNA-seq analysis, C. parvum upregulates host immune and inflammatory responses, and downregulates metabolic and signaling pathways involved in cell growth and proliferation.

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Source: Yaoyu Feng, South China Agricultural University

Image depicts the generation of mouse and cattle cholangiocyte organoids, and the complete development of Cryptosporidium parvum in vitro.

The results of this study provide a convenient method to study Cryptosporidium-host interactions and biliary cryptosporidiosis. The cholangiocyte organoid culture system will greatly facilitate further studies on the pathogenesis and effective therapies for AIDS cholangiopathy and other liver infections.