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Study of the pathogenic potential of Dientamoeba fragilis in experimentally infected mice
Eman K El-Gayar1, Amira B Mokhtar1, Wael A Hassan2
1Medical Parasitology Department, Faculty of Medicine, Suez Canal University, Egypt.
Abstract:
Dientamoebafragilis (D. fragilis) is a protozoan parasite whose pathogenic potential is still disputable. The aim of this study was to illustrate the pathogenicity of D. fragilis infection and to determine the infective dose for experimental mice infection. Three groups of mice (8/each) were orally inoculated with in vitro cultured D. fragilis. The infected groups (G1- G3) received 103, 105 and 4 × 106D. fragilis/0.5 ml culture, respectively. A control group (G4) only received parasite-free culture. Two weeks post-inoculation all mice were euthanized for histopathological examination. All mice of G3 (100%) and three mice of G2 (37.5%) were infected, and the results were confirmed by PCR and different staining methods. On the other hand, all mice from group G1 showed a completely negative result. Histopathological examination of the colon and caecum of the highly infected group G3 showed active colitis, with infiltration of mixed inflammatory cells such as eosinophils, neutrophils and lymphocytes within the lamina propria of the intestinal wall. The parasite was not invading the colonic mucosa. This study revealed that infection with D. fragilis is dose-dependent. Moreover, a dose of 105D. fragilis/mouse or higher is necessary to infect mice through the oral route. In addition, this route of infection, although non-invasive, can induce severe inflammatory changes to the colonic and caecal mucosa in experimentally infected mice.
Insights
Dientamoeba fragilis infection in mice is dose-dependent. A minimum dose of 105 D. fragilis per mouse is required for oral infection, which can cause significant colon inflammation.
Area of Science:
- Medical Parasitology
- Gastroenterology
- Immunology
Background:
- Dientamoeba fragilis is a protozoan parasite with debated pathogenicity.
- Understanding its infective dose and pathogenic potential is crucial for clinical diagnosis and treatment.
Purpose of the Study:
- To elucidate the pathogenic effects of Dientamoeba fragilis infection.
- To determine the minimum infective dose of D. fragilis in a murine model.
Main Methods:
- Oral inoculation of mice with varying doses of in vitro cultured D. fragilis (103, 105, and 4x106 parasites/mouse).
- Confirmation of infection using PCR and staining methods.
- Histopathological examination of colonic and cecal tissues.
Main Results:
- Infection was dose-dependent, with 100% infection in the highest dose group (4x106) and 37.5% in the 105 group.
- No infection was observed at the lowest dose (103).
- Histopathology revealed active colitis with inflammatory cell infiltration in the lamina propria, but no mucosal invasion.
Conclusions:
- A dose of 105 D. fragilis per mouse or higher is necessary for oral infection.
- Non-invasive oral D. fragilis infection can induce severe inflammatory changes in the colonic and cecal mucosa.
- The study confirms the dose-dependent pathogenicity of D. fragilis in an experimental setting.
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