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Updated: Feb 1, 2026

Embryo Microinjection and Electroporation in the Chordate Ciona intestinalis
Published on: October 16, 2016
[Evaluation of the reproductive potential of Encephalitozoon intestinalis in four different cell line]
Ülfet Çetinkaya1, Arzuv Charyyeva2, Esra Gürbüz3
1Erciyes University Halil Bayraktar Vocational School of Health Services, Kayseri, Turkey.
Abstract:
Microsporidia are parasites that can cause infections in many vertebrate and invertebrate organisms and produce small spores resistant to environmental conditions. As they are obligate intracellular parasites, axenic cultures cannot be performed. The aim of this study was to investigate the reproductive potential of the parasite in human colon epidermal adenocarcinoma (Caco-2), human monocytic (U937), African green monkey renal epithelial (VERO) and human kidney epithelial (HEK-293) cell lines of tissue and organs where the parasite is located by following the culture of the parasites and the amount of spores for six weeks. RPMI-1640 medium was used for the cultivation of U937 cells, while DMEM was used for other cell lines and the immature U937 cells were stimulated with Phorbol-12-Myristate-13-Acetate before infection. All of the host cell groups were infected with freshly collected Encephalitozoon intestinalis spores in ratio 1:30 and free spores in the culture media were removed after overnight incubation at 37°C under 5% CO2 condition for parasite invasion. The first release of the spores from the infected cells was observed and recorded by following for six weeks. Furthermore, the spore density released from each cell groups was evaluated by measuring the parasite load by Thoma cell counting chamber and quantified by real-time PCR. As a result of the study, it was observed that four cell lines could be infected by E.intestinalis and the spore production can be maintained for six weeks. It was observed that the monolayer macrophages and CaCo-2 cells, started to be detached from the culture flasks in few days following the parasite invasion, thus decreasing the number of host cells. After 1-2 weeks, HEK-293 cells were also detached from the surface, thus negatively affected the pure spore production by contaminating the media with dead host cell suspension. Spores started to appear in VERO cell media at the end of the second week after initial infection, while it took longer time for other cells to start releasing spores. Over the course of six weeks, the VERO cell line had the highest spore-producing potential among the other cell lines. In conclusion, this study compared the potential for reproduction of E.intestinalis in three human cell lines and monkey originated VERO cell line. This study demonstrated that cells derived from the tissues or organs where Microsporidia species causes disseminated infections could be infected by the parasitic spores in vitro. Additionally, the parasite can survive and propagate longer than six weeks. The authors believe that the results of this study will contribute to the further studies related to the parasite in the area of genetics, pharmacology, biochemistry, immunology and eradication studies.
Insights
This study investigated Encephalitozoon intestinalis reproduction in human and monkey cell lines. VERO cells showed the highest spore production over six weeks, indicating potential for future parasite research.
Area of Science:
- Parasitology
- Cell Biology
- Infectious Diseases
Background:
- Microsporidia are obligate intracellular parasites causing infections in diverse hosts.
- Axenic culture of Microsporidia is not possible, necessitating host cell line studies.
- Understanding parasite-host interactions is crucial for developing control strategies.
Purpose of the Study:
- To investigate the reproductive potential of Encephalitozoon intestinalis in various cell lines.
- To compare spore production and propagation in human (Caco-2, U937, HEK-293) and monkey (VERO) cell lines over six weeks.
Main Methods:
- Infection of Caco-2, U937, VERO, and HEK-293 cell lines with E. intestinalis spores.
- Cultivation of infected cells for six weeks, monitoring spore release and density.
- Quantification of parasite load using Thoma cell counting chamber and real-time PCR.
Main Results:
- All four cell lines supported E. intestinalis infection and spore production for six weeks.
- VERO cells exhibited the highest spore-producing potential compared to human cell lines.
- Caco-2, U937, and HEK-293 cells showed detachment, negatively impacting pure spore production.
Conclusions:
- VERO cells are a suitable model for studying E. intestinalis reproduction in vitro.
- E. intestinalis can survive and propagate in relevant host cell lines for extended periods.
- Findings support further research in genetics, pharmacology, and immunology of Microsporidia.
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