The effects of isolates and immune function on hematologic parameters of Blastocystis infection rats

Ting Deng, Juan Li, Xiaohua Li, Xiaobo Li, Yiming Yan

Article ID: 1365
Vol 5, Issue 2.1, 2021

VIEWS - 41 (Abstract) 31 (PDF)

Abstract


Objective: To define a complex of changes in hematologic parameters associated with subtypes (ST) of Blastocystis sp. infections and the status of immune function in Sprague Dawley (SD) rats, and lay the foundation for Blastocystis hominis pathogenesis research. Methods: 5 isolates of ST1, ST3 and ST7 were used, including 1 isolate of ST1 from symptomatic patient, 2 isolates of ST3 and ST7 from symptomatic patients and asymptomatic carrier separately. Immune compromise model was set up using dexamethasone (DEX) and infection models with 5 isolates of ST1, ST3 and ST7, and then examined the hematologic changes post infection 15 days using fully automatic hematology analyzer sysmex xe-2100. Results: The results showed that infections of Blastocystis STs leaded to the increase of platelet indexes including MPV and PDW except ST3 isolated from asymptomatic carrier only with PDW increase and the higher values of PLT in ST7 isolated from asymptomatic carrier compared with the controls in the immune competence status (P < 0.05). However, the infections of Blastocystis ST7 isolated from symptomatic patient gave rise to higher values of WBC, LYMP, EO, MCV and RDW-SD while lower values of NEU% compared with the controls in immune compromise status (P < 0.05). Meanwhile, higher values of WBC and LYMP and lower NEUT% values were observed in ST1 infections compared with the controls (P < 0.05); lower NEUT values in ST1 infections and controls compared with ST3 and ST7 respectively were observed (P < 0.05); the infection of ST3 isolated from symptomatic patient resulted in higher values of MCV and RDW-SD while the asymptomatic isolate of ST3 only had higher RDW-SD (P < 0.05). Conclusion: The virulence of Blastocystis sp. isolated from symptomatic patient is higher than that of the identical subtype one isolated from asymptomatic carrier. The infection of ST7 isolated from symptomatic patients may result in the most distinct hematologic changes among STs, and then followed by ST1 symptomatic isolate. And the severity of Blastocystis sp. infection may be mediated by the immune status of host.


Keywords


Blastocystis; Immune Function; Hematologic Parameters

Full Text:

PDF


References


1. Tan K. New insights on classification, identification, and clinical relevance of Blastocystis spp. Clinical Microbiology Reviews 2008; 21(4): 639–665.

2. Doğruman AF, Adisen E, Kustimur S, et al. The role of protozoan parasites in etiology of urticarial. Turkiye Parazitolojii Dergisi 2009; 33(2): 136–139.

3. Hameed DM, Hassanin OM, Zuel-Fakkar NM. Association of Blastocystis hominis genetic subtypes with urticarial. Parasitology Research 2011; 108(3): 553–560.

4. Tan K, Mirza H, Teo J, et al. Current views on the clinical relevance of Blastocystis spp. Current Infectious Disease Reports 2010; 12(1): 28–35.

5. Stensvold CR, Lewis HC, Hammerum AM, et al. Blastocystis: Unravelling potential risk factors and clinical significance of a common but neglected parasite. Epidemiol Infect 2009; 137: 1655–1663.

6. Parkar U, TraubRJ, Vitali S, et al. Molecular characterization of Blastocystis isolates from zoo animals and their animal-keepers. Veterinary Parasitology 2010; 169(1-2): 8–17.

7. Roberts T, Stark D, Harkness J, et al. Subtype distribution of Blastocystis isolates identified in a Sydney population and pathogenic potential of Blastocystis. European Journal of Clinical Microbiology & Infectious Diseases 2013; 32: 335–343.

8. Tan T, Sugnaseelan S, Sharma R, et al. Genetic diversity of caprine Blastocystis from Peninsular Malaysia. Parasitology Research 2013; 112: 85–89.

9. Domínguez-Márquez MV, Guna R, Muñoz C, et al. High prevalence of subtype 4 among isolates of Blastocystis hominis from symptomatic patients of a health district of Valencia (in Spanish). Parasitology Research 2009; 105: 949–955.

10. Jimenez-Gonzalez DE, Martinez-Flores WA, Reyes-Gordillo J, et al. Blastocystis infection is associated with irritable bowel syndrome in a Mexican patient population. Parasitology Research 2012; 110(3): 1269–1275.

11. Souppart L, Moussa H, Cian A, et al. Subtype analysis of Blastocystis isolates from symptomatic patients in Egypt. Parasitology Research 2010; 106(2): 505–511.

12. Yan Y, Su S, Lai R, et al. Genetic variability of Blastocystis hominis isolates in China. Parasitology Research 2006; 99(5): 597–601.

13. Forsell J, Granlund M, Stensvold CR, et al. Subtype analysis of Blastocystis isolates in Swedish patients. European Journal of Clinical Microbiology & Infectious Diseases Official Publication of the Europe 2012; 31: 1689–1696.

14. Fortun J, Sanz MA, Madero L, et al. Update on bacteraemia in oncology and hematology. Enfermedades Infecciosas Y Microbiología Clínica 2011; 29: 48–53.

15. Burciaga-Robles LO, Step DL, Krehbiel CR, et al. Effects of exposure to calves persistently infected with bovine viral diarrhea virus type 1b and subsequent infection with Mannheima haemolytica on clinical signs and immune variables: Model for bovine respiratory disease via viral and bacterial interaction. Journal of Animal Science 2010; 88(6): 2166–2178.

16. Carreras E, Vazquez L, Rodriguez Tudela JL, et al. Update on fungemia in oncology and hematology. Enfermedades Infecciosas Y Microbiología Clínica 2011; 29(Suppl 4): 42–47.

17. Cheng H, Guo Y, Shin JW. Hematological effects of Blastocystis hominis infection in male foreign workers in Taiwan. Parasitology Research 2003; 90(1): 48–51.

18. Blanar CA, Curtis MA, Chan HM. Growth, nutritional composition, and hematology of Arctic charr (Salvelinus alpinus) exposed to toxaphene and tapeworm (Diphyllobothrium dendriticum) larvae. Archives of Environmental Contamination and Toxicology 2005; 48(3): 397–404.

19. Ruiz-Saez A, Sifontes LN, Feijoo R, et al. Platelet dysfunction-eosinophilia syndrome in parasitized Venezuelan children. American Journal of Tropical Medicine & Hygiene 2005; 73(2): 381–385.

20. Yasini S, Khaki Z, Rahbari S, et al. Hematologic and clinical aspects of experimental ovine anaplasmosis caused by Anaplasma ovis in Iran. Iranian Journal of Parasitology 2012; 7(4): 91–98.

21. Li X, Bai S, Zhou L, et al. Comparison of the immunosuppressive functions induced by cyclophosphamide and dexamethasone in intestinal mucosa in mice. Chinese Journal of Immunology 2013; 29(1): 39–44.

22. Malatyali E, Ozcelik S. Isolation of Blastocystis spp. from human hosts and in vitro determination of different morphological forms. Turkiye Parazitolojii Dergisi 2011; 35: 19–22.

23. Nagel R, Cuttell L, Stensvold CR, et al. Blastocystis subtypes in symptomatic and asymptomatic family members and pets and response to therapy. Internal Medicine Journal 2012; 42(11): 1187–1195.

24. Meloni D, Poirier P, Mantini C, et al. Mixed human intra- and inter-subtype infections with the parasite Blastocystis sp. Parasitology International 2012; 61(4): 719–722.

25. El Deeb HK, Salah-Eldin H, Khodeer S. Blastocystis hominis as a contributing risk factor for development of iron deficiency anemia in pregnant women. Parasitology Research 2012; 110: 2167–2174.




DOI: https://doi.org/10.24294/ti.v5.i2.1.1365

Refbacks

  • There are currently no refbacks.


Copyright (c) 2021 Ting Deng, Juan Li, Xiaohua Li, Xiaobo Li, Yiming Yan

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

This site is licensed under a Creative Commons Attribution 4.0 International License.