From Insects to Swiss Mice: Effect of Blastocystis Species in the Intestinal Tract
Authors
School of Medical Laboratory Science, The Manila Times College of Subic (Philippines)
School of Medical Laboratory Science, The Manila Times College of Subic (Philippines)
Article Information
DOI: 10.51244/IJRSI.2026.1303000178
Subject Category: Pathology
Volume/Issue: 13/3 | Page No: 2103-2111
Publication Timeline
Submitted: 2026-03-11
Accepted: 2026-03-16
Published: 2026-04-12
Abstract
Blastocystis is a widespread enteric protozoan of zoonotic importance, frequently transmitted via contaminated food and water. This study investigated the histopathological impact of Blastocystis on the intestinal architecture of Swiss mice. Isolates were obtained from the external surfaces and digestive tracts of the American cockroach (Periplaneta americana) and the housefly (Musca domestica). Following oral inoculation, mice were sacrificed at 10 days post-infection for histopathological analysis. Findings revealed significant mucosal disruption, with moderate to severe villi erosion observed in the majority of infected subjects. Pathological hallmarks included villi blunting, apical fragmentation, thinning of the intestinal mucosa, and exposure of the lamina propria. Notably, the severity of intestinal damage was comparable between isolates sourced from both insect vectors. These results characterize Blastocystis as a significant intestinal pathogen in a murine model and underscore the critical role of synanthropic insects as mechanical vectors in its transmission cycle.
Keywords
Blastocystis, Histopathology, Intestinal villi, Swiss Mice
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References
1. Tsaousis, A. D., Nagavci, B., Carmena, D., & Stensvold, C. R. (2025). Commensal, pathogen, or passenger? Rethinking the role of Blastocystis in human health. The Lancet Microbe, 6(1), e12–e22. [Google Scholar] [Crossref]
2. Tan, K. S. (2008). New insights into Blastocystis: A neglected intestinal protozoan. Clinical Microbiology Reviews, 21(4), 639–665. [Google Scholar] [Crossref]
3. Defaye, M., et al. (2024). Multi-omics analysis of Blastocystis sp. ST4 infection in a robust rat model: Insights into chronic colonization and host interaction. PLOS Pathogens, 20(2), e1012045. [Google Scholar] [Crossref]
4. Koehler, A. V., et al. (2024). Marked genetic diversity within Blastocystis in Australian wildlife revealed using a next-generation sequencing-phylogenetic approach. International Journal for Parasitology: Parasites and Wildlife, 23, 100892. [Google Scholar] [Crossref]
5. Stensvold, C. R., Suresh, G. K., & Tan, K. S. (2007). Terminology for Blastocystis subtypes—a consensus. Trends in Parasitology, 23(3), 93–96. [Google Scholar] [Crossref]
6. Zhang, Y., Li, W., & Wang, R. (2024). Comparative genomics of Blastocystis subtypes: Insights into virulence factors and host adaptation. Parasites & Vectors, 17(1), 88–104. [Google Scholar] [Crossref]
7. Yoshikawa, H., Wu, Z., & Zenke, K. (2004). Fine structure of Blastocystis hominis cysts. Journal of Electron Microscopy, 53(2), 167–173. [Google Scholar] [Crossref]
8. Malatji, M. P., et al. (2025). Morphological plasticity and reproductive strategies of Blastocystis sp. in various host environments. Journal of Eukaryotic Microbiology, 72(2), e13045. [Google Scholar] [Crossref]
9. Zierdt, C. H. (1991). Blastocystis hominis—past and present. Clinical Microbio Reviews, 4(1), 61–79. [Google Scholar] [Crossref]
10. Pavanelli, M. F., Kaneshima, E. N., Uda, C. F., Colli, C. M., Falavigna-Guilherm, A. L., & Gomes, M. L. (2015). Pathogenicity of Blastocystis sp. to the gastrointestinal tract of mice: Relationship between inoculum size and period of infection. Revista do Instituto de Medicina Tropical de São Paulo, 57(6), 467–472. https://doi.org/10.1590/s0036-46652015000600002 [Google Scholar] [Crossref]
11. Adao, D. E., & Rivera, W. L. (2018). Recent advances in Blastocystis sp. research. Philippine Science Letters, 11(1), 39–60. [Google Scholar] [Crossref]
12. El-Wakil, H. S., & Hewedi, I. H. (2010). Pathogenic potential of Blastocystis hominis in experimental animals. Journal of the Egyptian Society of Parasitology, 40(1), 219–228. [Google Scholar] [Crossref]
13. Piperni, E., Nguyen, L. H., & Manghi, P. (2024). Intestinal Blastocystis is linked to healthier diets and more favorable cardiometabolic outcomes in 56,989 individuals from 32 countries. Cell, 187(17), 4554–4570. [Google Scholar] [Crossref]
14. Yason, J. A., et al. (2019). Blastocystis subtype 4 alters the gut microbiota and leads to moderate inflammation in a mouse model. Microbiome, 7(1),1–15. [Google Scholar] [Crossref]
15. Nourrisson, C., Wawrzyniak, I., & Viscogliosi, E. (2014). Blastocystis is associated with decrease in fecal microbiota diversity. PLoS ONE, 9(10), e110403. [Google Scholar] [Crossref]
16. Puthia, M. K., Sio, S. W., & Tan, K. S. (2006). Blastocystis ratti induces contact-independent apoptosis in intestinal epithelial cells. Cellular Microbiology, 8(3), 410–423. [Google Scholar] [Crossref]
17. Deng, L., et al. (2021). Blastocystis sp. subtype 4 colonizes the gut of rats and induces mucosal barrier dysfunction. Parasitology Research, 120(4), 1335–1343. [Google Scholar] [Crossref]
18. Ajjampur, S. S., & Tan, K. S. (2016). Blastocystis: Clinical and microbial features. Clinical Microbiology Reviews, 29(3), 601–635. https://doi.org/10.1128/CMR.00112-15 [Google Scholar] [Crossref]
19. Higuera, A., et al. (2021). Genetic diversity and virulence factors of Blastocystis sp. in mammalian hosts. Infection, Genetics and Evolution, 93, 104938. [Google Scholar] [Crossref]
20. Hussain, R., Kumar, S. S., & Ramachandran, V. (2012). Pathogenicity of Blastocystis hominis in Sprague-Dawley rats. Tropical Biomedicine, 29(2), 234–240. [Google Scholar] [Crossref]
21. Betts, E. L., et al. (2022). Host–parasite interactions and the gut microbiome in Blastocystis infection. Parasitology, 149(11), 1391–1405. [Google Scholar] [Crossref]
22. Clark, C. G., van der Giezen, M., Alfellani, M. A., & Stensvold, C. R. (2013). Blastocystis—Evolution, ecology, and epidemiology. Advances in Parasitology, 82, 1–30. [Google Scholar] [Crossref]
23. Stensvold, C. R., & Clark, C. G. (2020). Blastocystis: An update on epidemiology, subtype diversity, and host specificity. Clinical Microbiology Reviews, 33(3), e00002-20. [Google Scholar] [Crossref]
24. Ajjampur, S. S. R., et al. (2021). Experimental models of Blastocystis infection: A review of the histopathological and immunological findings. Current Tropical Medicine Reports, 8(3), 195–204. [Google Scholar] [Crossref]
25. Iguchi, A., Yoshikawa, H., & Yamada, M. (2007). Experimental Blastocystis infection in mice. Parasitology International, 56(3), 193–198. [Google Scholar] [Crossref]
26. Long, M., et al. (2023). Dose-dependent kinetics of Blastocystis sp. ST3 infection in a murine model. Frontiers in Microbiology, 14, 115670. [Google Scholar] [Crossref]
27. Yoshikawa, H., Wu, Z., & Zenke, K. (2004). Fine structure of Blastocystis hominis cysts. Journal of Electron Microscopy, 53(2), 167–173. [Google Scholar] [Crossref]
28. Ribeiro, M., et al. (2024). Adhesion mechanisms and epithelial barrier disruption by Blastocystis sp. ST1 and ST3. Microorganisms, 12(5), 981. [Google Scholar] [Crossref]
29. Tan, K. S., Singh, M., & Yap, E. H. (2002). Blastocystis: Asexual reproduction, virulence, and chemotherapy. International Journal for Parasitology, 32(6), 659–675. [Google Scholar] [Crossref]
30. Giacomelli, A., et al. (2025). Microbiota alterations and the "gut-brain axis" in Blastocystis subtype-specific infections. Journal of Clinical Medicine, 14(2), 412. [Google Scholar] [Crossref]
31. Audebert, C., Martel, J., & Viscogliosi, E. (2016). Colonization with Blastocystis is associated with higher bacterial diversity in human gut. Scientific Reports, 6(1), 25255. [Google Scholar] [Crossref]
32. Sayegh, S., et al. (2024). The impact of Blastocystis on the gut-brain axis: Anxiety and depressive-like behaviors in a rodent model. Neuroscience & Biobehavioral Reviews, 158, 105541. [Google Scholar] [Crossref]
33. Beatty, J. K., Bhargava, A., & Buret, A. G. (2017). Blastocystis subtype 4 (ST4) is associated with irritable bowel syndrome and causes gut dysfunction in rats. Parasites & Vectors, 10(1), 1–13. [Google Scholar] [Crossref]
34. Toriano, S. B., Fabian, J. C., Matira, M. D., & Aquino, F. C. (2025). Isolation and morphologic differentiation of Blastocystis from insect vectors using staining media. International Journal of Research and Scientific Innovation,12(11), 1635–1643. https://doi.org/10.51244/IJRSI.2025.12110145 [Google Scholar] [Crossref]
35. Moe, K. T., Singh, M., Howe, J., Ho, L. C., Tan, S. W., Chen, X. Q., Ng, G. C., & Yap, E. H. (1997). Experimental Blastocystis hominis infection in mice. Parasitology Research, 83(4), 319–325. [Google Scholar] [Crossref]
36. Iguchi, A., Itoh, Y., & Itoh, K. (2007). Experimental infection of mice with Blastocystis hominis and its effect on the intestinal mucosa. Parasitology Research, 100(4), 723–727. https://doi.org/10.1007/s00436-006-0331-5 [Google Scholar] [Crossref]
37. Hussein, E. M., Ahmed, S. A., Amer, N. S., El-Hidi, M. A., & Moustafa, A. M. (2008). Blastocystis hominis isoenzyme proteins, protease activity, and intestinal mucosal changes in experimental mice. Journal of the Egyptian Society of Parasitology, 38(2), 643–656. [Google Scholar] [Crossref]
38. Barthold, S. W., Griffey, S. M., & Percy, D. H. (2016). Pathology of laboratory rodents and rabbits (4th ed.). Wiley-Blackwell. [Google Scholar] [Crossref]
39. Williams, K. J., Zachary, J. F., & McGavin, M. D. (2015). Alimentary system. In J. F. Zachary (Ed.), Pathologic basis of veterinary disease (6th ed., pp. 321–446). [Google Scholar] [Crossref]
40. Guinto, E., Slaoui, M., & Fiette, L. (2002). Artifacts in histological sections. Methods in Molecular Biology, 190, 1–30. https://doi.org/10.1385/1-59259-270-8:001 [Google Scholar] [Crossref]
41. Ajjampur, S. S., Png, C. W., Chia, W. N., Zhang, Y., & Tan, K. S. (2009). Ex vivo and in vivo mice models to study Blastocystis adhesion and host-parasite interactions. Microbial Pathogenesis, 46(6), 286–292. https://doi.org/10.1016/j.micpath.2009.04.002 [Google Scholar] [Crossref]
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