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A Controlled Mouse Model for Neonatal Polymicrobial Sepsis
Published on: January 27, 2019
Effects of Kudoa septempunctata genotype ST3 isolate from Korea on ddY suckling mice
Yeounghwan Jang1, Meejung Ahn2, Hyojin Bang3
1Ocean and Fisheries Research Institute, Jeju Special Self-Governing Province, Pyoseon-myeon, Segwipo-si, Jeju 63629, Republic of Korea.
Abstract:
This study investigated the effects of Kudoa septempunctata genotype ST3 spores on ddY suckling mice. Purified Kudoa septempunctata spores were administered into the stomachs of the mice at 5 × 10(6) or 5 × 10(7) spores/mouse, with inactivated Kudoa (5 × 10(6) spores/mouse) or vehicle as controls. No abnormal clinical symptoms were observed and there were no variations in fluid accumulation ratio and cytokine gene expression in all groups. In addition, intact Kudoa spores and the 18S rDNA gene were only detected (by microscopy and quantitative PCR, respectively) in the groups administered such spores. This study thus confirms that spores from the ST3 strain of Kudoa septempunctata were excreted in the faeces without infecting the gastrointestinal tract in ddY suckling mice.
Insights
Kudoa septempunctata ST3 spores did not infect the gastrointestinal tract of ddY suckling mice. The study confirmed spores were excreted in feces without causing clinical symptoms or altering cytokine gene expression.
Area of Science:
- Parasitology
- Microbiology
- Animal Health
Background:
- Kudoa septempunctata is a myxosporean parasite found in marine fish.
- Understanding the pathogenicity of different Kudoa genotypes is crucial for food safety and aquaculture.
Purpose of the Study:
- To investigate the effects of Kudoa septempunctata genotype ST3 spores on ddY suckling mice.
- To determine if Kudoa ST3 spores can infect the gastrointestinal tract of young mice.
Main Methods:
- ddY suckling mice were orally administered purified Kudoa septempunctata ST3 spores at two different doses (5 × 10(6) or 5 × 10(7) spores/mouse).
- Control groups received inactivated Kudoa spores or vehicle.
- Mice were monitored for clinical symptoms, fluid accumulation, and cytokine gene expression.
- Microscopy and quantitative PCR were used to detect intact spores and 18S rDNA.
Main Results:
- No abnormal clinical symptoms were observed in any group.
- No significant variations in fluid accumulation ratio or cytokine gene expression were detected.
- Intact Kudoa spores and their 18S rDNA gene were only found in mice that received live spores.
- Spores were detected in the feces, indicating excretion rather than infection.
Conclusions:
- Kudoa septempunctata genotype ST3 spores are not infectious to the gastrointestinal tract of ddY suckling mice.
- The administered spores are excreted in the feces without causing pathological effects.
- This finding has implications for the safety assessment of Kudoa-infected seafood.
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