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Studying Cryptosporidium Infection in 3D Tissue-derived Human Organoid Culture Systems by Microinjection
Published on: September 14, 2019
Studying Cryptosporidium Infection in 3D Tissue-derived Human Organoid Culture Systems by Microinjection
Devanjali Dutta1, Inha Heo2, Roberta O'Connor3
1Hubrecht Institute, Oncode Institute, Royal Netherlands Academy of Arts and Sciences (KNAW), UMC Utrecht; d.dutta@hubrecht.eu.
Abstract:
Cryptosporidium parvum is one of the major causes of human diarrheal disease. To understand the pathology of the parasite and develop efficient drugs, an in vitro culture system that recapitulates the conditions in the host is needed. Organoids, which closely resemble the tissues of their origin, are ideal for studying host-parasite interactions. Organoids are three-dimensional (3D) tissue-derived structures which are derived from adult stem cells and grow in culture for extended periods of time without undergoing any genetic aberration or transformation. They have well defined polarity with both apical and basolateral surfaces. Organoids have various applications in drug testing, bio banking, and disease modeling and host-microbe interaction studies. Here we present a step-by-step protocol of how to prepare the oocysts and sporozoites of Cryptosporidium for infecting human intestinal and airway organoids. We then demonstrate how microinjection can be used to inject the microbes into the organoid lumen. There are three major methods by which organoids can be used for host-microbe interaction studies-microinjection, mechanical shearing and plating, and by making monolayers. Microinjection enables maintenance of the 3D structure and allows for precise control of parasite volumes and direct apical side contact for the microbes. We provide details for optimal growth of organoids for either imaging or oocyst production. Finally, we also demonstrate how the newly generated oocysts can be isolated from the organoid for further downstream processing and analysis.
Insights
This study presents a novel method for culturing Cryptosporidium parvum within human organoids, enabling detailed study of host-parasite interactions and facilitating the development of new treatments for cryptosporidiosis.
Area of Science:
- Parasitology
- Cell Biology
- Infectious Diseases
Background:
- Cryptosporidium parvum is a significant cause of human diarrheal illness.
- Effective drug development requires in vitro models that mimic host conditions.
- Organoids offer a promising 3D model for studying host-pathogen interactions.
Purpose of the Study:
- To establish a protocol for infecting human intestinal and airway organoids with Cryptosporidium parvum.
- To detail the microinjection technique for introducing Cryptosporidium into organoids.
- To provide a method for isolating newly generated Cryptosporidium oocysts from organoids.
Main Methods:
- Preparation of Cryptosporidium parvum oocysts and sporozoites.
- Infection of human intestinal and airway organoids using microinjection.
- Isolation of oocysts from infected organoids for downstream analysis.
Main Results:
- A step-by-step protocol for preparing and infecting organoids with Cryptosporidium was successfully demonstrated.
- Microinjection allows precise control and direct apical contact for parasite infection within the 3D organoid structure.
- Newly generated oocysts can be effectively isolated from organoids for further study.
Conclusions:
- Human organoids provide a valuable in vitro system for studying Cryptosporidium parvum pathogenesis.
- The described microinjection technique facilitates controlled host-parasite interaction studies.
- This protocol supports the development of new therapeutic strategies against cryptosporidiosis.
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