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Effect of four antimicrobials against an Encephalitozoon sp. (Microsporidia) in a grasshopper host
Shajahan Johny1, Douglas W Whitman,
1Department of Biological Sciences, Illinois State University, Normal, Illinois 61790-4120, USA.
Abstract:
Encephalitozoon spp. are the primary microsporidial pathogens of humans and domesticated animals. In this experiment, we test the efficacy of 4 commercial antimicrobials against an Encephalitozoon sp. infecting a grasshopper (Romalea microptera) host. Oral treatment with fumagillin or thiabendazole significantly reduced pathogen spore counts (93% and 88% respectively), whereas spore counts of grasshoppers fed quinine produced a non-significant 53% reduction in spores, and those fed streptomycin a non-significant 29% increase in spores, compared to the control. We observed a moderate dose-response effect for thiabendazole, whereby spore count decreased as drug consumption increased. No thiabendazole-treated animals died, whereas 27% of streptomycin-treated animals died, suggesting that thiabendazole was not toxic at the doses administered. The deaths among streptomycin-treated animals may have been caused by drug toxicity, parasite burden, or both. Although fumagillin and thiabendazole significantly reduced spore counts, in no individual was the pathogen totally eliminated. Our data confirm that microsporidia are difficult to control and that fumagillin and thiabendazole are partially effective antimicrobials against this group. Our study suggests that quinine and related alkaloids should be further examined for antimicrosporidial activity, and streptomycin should be examined as a possible enhancer of microsporidiosis.
Insights
Fumagillin and thiabendazole effectively reduced microsporidia spores in grasshoppers, but did not eliminate the pathogen. Quinine showed potential, while streptomycin increased spore counts and caused deaths.
Area of Science:
- Veterinary Parasitology
- Microbiology
- Entomology
Background:
- Encephalitozoon spp. are significant microsporidial pathogens affecting humans and animals.
- Microsporidia pose challenges in treatment and control due to their resilience.
Purpose of the Study:
- To evaluate the efficacy of four commercial antimicrobials against an Encephalitozoon sp. in a grasshopper model.
- To assess potential dose-response relationships and toxicity of the tested antimicrobials.
Main Methods:
- Oral administration of fumagillin, thiabendazole, quinine, and streptomycin to infected grasshoppers (Romalea microptera).
- Comparison of pathogen spore counts in treated groups versus a control group.
- Monitoring animal mortality and assessing drug toxicity.
Main Results:
- Fumagillin and thiabendazole significantly reduced Encephalitozoon spore counts by 93% and 88%, respectively.
- Quinine showed a non-significant 53% reduction, while streptomycin resulted in a non-significant 29% increase in spores.
- Thiabendazole exhibited a dose-response effect; streptomycin treatment led to 27% mortality, suggesting potential toxicity.
Conclusions:
- Fumagillin and thiabendazole are partially effective against microsporidia but do not achieve complete pathogen elimination.
- Quinine and related alkaloids warrant further investigation for antimicrosporidial properties.
- Streptomycin may potentially enhance microsporidiosis and should be studied further in this context.
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