Increased susceptibility to encephalitozoonosis associated with mixed Th1/Th2 profile and M1/M2 profile in mice
Amanda Miyuki Hidifira1, Anuska Marcelino Alvares-Saraiva1, Elizabeth Christina Perez1
1Programa de Patologia Ambiental e Experimental, Universidade Paulista (UNIP), São Paulo, Brazil.
Abstract:
Encephalitozoon cuniculi is a unicellular, spore-forming, obligate intracellular eukaryote belonging to the phylum Microsporidia. It is known to infect mainly immunocompromised and immunocompetent mammals, including humans. The parasite-host relationship has been evaluated using both in vitro cell culturing and animal models. For example, Balb/c and C57BL/6 mouse strains have been used interchangeably, although the latter has been considered more susceptible due to the higher fungal load observed after infection. In the present study, we identified the characteristics of the immune response of C57BL/6 mice treated or not with the immunosuppressant cyclophosphamide (Cy) and challenged with E. cuniculi by intraperitoneal route. After 14 days of infection, serum was collected to analyze Th1, Th2, and Th17 cytokine levels. In addition, peritoneal washes were performed, and the spleen sample was collected for immune cell phenotyping, whereas liver, spleen, kidney, lung, intestine, and central nervous system (CNS) samples were collected for histopathological analysis. Although infected mice displayed a reduced absolute number of macrophages, they showed an M1 profile, an elevated number of CD4+T, CD8+T, B-1, and B-2 lymphocytes, with a predominance of Th1 inflammatory cytokines (interferon [IFN]-γ, tumor necrosis factor [TNF]-α, and interleukin [IL]-2) and Th17. Furthermore, Cy-Infected mice showed a reduced absolute number of macrophages with an M1 profile but a reduced number of CD4+T, CD8+T, B-1, and B-2 lymphocytes, with a predominance of Th1 inflammatory cytokines (IFN-γ, TNF-α, and IL-2) and Th2 (IL-4). This group displayed a higher fungal burden as well and developed more severe encephalitozoonosis, which was associated with a reduced number of T and B lymphocytes and a mixed profile of Th1 and Th2 cytokines.
Insights
Encephalitozoon cuniculi infection in C57BL/6 mice reveals that immunosuppression exacerbates disease by altering immune cell profiles and cytokine responses. This highlights the critical role of T and B lymphocytes in controlling microsporidiosis.
Area of Science:
- Immunology
- Parasitology
- Microbiology
Background:
- Encephalitozoon cuniculi (E. cuniculi) is an opportunistic microsporidian parasite infecting mammals.
- C57BL/6 mice are a common model for studying E. cuniculi, but the impact of immunosuppression on their immune response is not fully understood.
Purpose of the Study:
- To characterize the immune response in C57BL/6 mice infected with E. cuniculi, with and without cyclophosphamide (Cy)-induced immunosuppression.
- To evaluate the influence of immunosuppression on parasite burden and disease severity.
Main Methods:
- C57BL/6 mice were infected with E. cuniculi, with or without prior treatment with cyclophosphamide.
- Immune cell phenotyping (macrophages, T cells, B cells) was performed on spleen and peritoneal washes.
- Serum cytokine levels (Th1, Th2, Th17) were analyzed.
- Histopathological analysis of multiple organs was conducted to assess parasite burden and tissue damage.
Main Results:
- E. cuniculi infection alone led to an M1 macrophage profile, increased CD4+, CD8+ T cells, B-1, and B-2 lymphocytes, and a Th1/Th17 cytokine predominance.
- Cyclophosphamide-treated infected mice exhibited reduced macrophage counts (M1 profile), fewer T and B lymphocytes, and a mixed Th1/Th2 cytokine profile.
- Immunosuppressed mice showed higher fungal burden and more severe encephalitozoonosis.
Conclusions:
- Immunosuppression significantly impairs the host immune response against E. cuniculi in C57BL/6 mice.
- The reduction in T and B lymphocytes and the shift in cytokine profiles under immunosuppression correlate with increased parasite load and disease severity.
- This study underscores the importance of a robust T and B cell-mediated immune response for controlling microsporidiosis.
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