A Technique to Develop a Parasite Infection in Intestinal Organoids via Microinjection
Transcription
Take a human intestinal organoid culture. The organoids consist of epithelial cells facing the central lumen, mimicking in vivo architecture.
Take a microinjector containing crescent-shaped sporozoites — the infective form — of Cryptosporidium parvum, a parasite.
Inject sporozoites into the organoid lumen.
Parasite lectins bind to specific carbohydrates on epithelial cells, facilitating their entry into a parasitophorous vacuole.
Internalized parasite transforms into a trophozoite — the feeding stage — which acquires nutrients and undergoes asexual reproduction to form type I meront, containing merozoites — the invasive form.
Released merozoites infect neighboring epithelial cells and develop type II meronts containing merozoites.
The merozoites enter neighboring cells and differentiate into either microgamont or macrogamont — male and female reproductive stages.
The microgamont undergoes division to form microgametes, which are released outside the vacuole.
A microgamete fertilizes the macrogamont, producing a zygote.
The zygote undergoes division, forming a sporozoite-containing oocyst. Upon release, the sporozoites repeat the infection cycle.
Harvest the organoids to assess the infection progress.
