Active Infection & Immunity Genetics & Molecular Biology

Cryptosporidium hatching: unzipping the suture at the perfect time

In plain English

AI plain-English summary

A microscopic parasite hides inside a shell tough enough to survive chlorine treatment, and this project aims to figure out how it unzips that shell to cause infection. Cryptosporidium causes severe diarrhoea, particularly in children in Africa and Asia, where it leads to an estimated 7.5 million cases and over 200,000 deaths each year. There is no vaccine and no effective treatment. The parasite’s oocyst—a protective shell—resists standard water treatments, making it a persistent threat to public water supplies. The moment the parasite hatches from that shell is a critical bottleneck in its life cycle, yet the biology of that process has been largely unexplored. The researchers have identified proteins at the zipper-like opening on the oocyst shell. Using genetics, biochemistry, and microscopy, they will investigate how the parasite builds both the shell and its opening, and how it times its hatching. They will also use microscopic biomechanical techniques to understand why the oocysts are so resilient. If successful, this fundamental science could reveal new ways to interrupt infection and stop transmission—potentially improving water treatment strategies or pointing toward drug targets that prevent hatching altogether.

View original technical description
Cryptosporidium is a waterborne pathogen that is transmitted inside a microscopic shell-like structure called an oocyst. This shell protects Cryptosporidium parasites from most water treatments, including chlorination. Once ingested, parasites “hatch” from the oocyst and infect the intestine, causing diarrhoeal disease. The impact of cryptosporidiosis is second only to Rotavirus. Annually there are an estimated 7.5 million cases of cryptosporidiosis in Africa and Asia, resulting in excess of 200,000 deaths and 8.2 million disability adjusted life years. There is currently no vaccine and no effective treatment for cryptosporidiosis. Hatching out of their eggshell is a critical bottleneck in parasite transmission. New tools we created allow us to investigate the biology of hatching and open this area for exploration. We recently identified proteins that are located at the zipper- like opening on the oocyst shell. We will use genetics, biochemistry, and microscopy to understand how Cryptosporidium build the protective shell and zipper opening, and hatch at the perfect time. Using microscopic biomechanical techniques will understand why oocysts are so resilient. These insights have the potential to help us understand how to interrupt infection and stop parasite transmission.

View the original record at the funder ↗

Researchers

Mattie Pawlowic (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Defining Oocyst Wall Biogenesis and Function in Cryptosporidium Transmission
Investigating the female sexual life-cycle of Cryptosporidium, a diarrhoeal pathogen of global significance
Cryptosporidium movement in water: impact of eutrophication and climate change on the zoonotic disease agent
Novel water treatments for zoonotic pathogen Cryptosporidium
Genetic manipulation of Cryptosporidium parasites

Original classification

Career Development Award

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