Neospora caninum infection induces an isolate virulence-dependent pro-inflammatory gene expression profile in bovine monocyte-derived macrophages
Autor: | Pilar Horcajo, Luis Miguel Ortega-Mora, Laura Jiménez-Pelayo, Esther Collantes-Fernández, Marta García-Sánchez, Javier Regidor-Cerrillo |
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Rok vydání: | 2020 |
Předmět: |
Innate immune response
0301 basic medicine Chemokine Cattle Diseases Neospora caninum Phagolysosome lcsh:Infectious and parasitic diseases 03 medical and health sciences 0302 clinical medicine Immune system Animals lcsh:RC109-216 Isolate virulence Inflammation Innate immune system Virulence biology Research Macrophages Intracellular parasite Toll-Like Receptors NF-kappa B Neospora Microarray Analysis biology.organism_classification Immunity Innate Bovine macrophages Cell biology TLR2 030104 developmental biology Infectious Diseases 030220 oncology & carcinogenesis TLR3 biology.protein Cytokines Cattle Parasitology Host-parasite interactions Transcriptome |
Zdroj: | Parasites & Vectors, Vol 13, Iss 1, Pp 1-20 (2020) Parasites & Vectors |
ISSN: | 1756-3305 |
Popis: | Background Neospora caninum is an obligate intracellular parasite, and its ability to survive inside host immune cells may be a key mechanism for the establishment of infection in cattle. In vitro studies carried out by our group have shown that N. caninum is able to replicate in bovine macrophages (MØs), alter their microbicidal mechanisms and exploit their motility. Furthermore, host-cell control seems to be isolate virulence-dependent. Methods To investigate the molecular basis underlying the innate responses in MØs against N. caninum and the mechanisms of parasite manipulation of the host cell environment, the transcriptome profile of bovine monocyte-derived MØs infected with high-virulence (Nc-Spain7) or low-virulence (Nc-Spain1H) N. caninum isolates was studied. Results Functional enrichment revealed upregulation of genes involved in chemokine signalling, inflammation, cell survival, and inhibition of genes related with metabolism and phagolysosome formation. MØs activation was characterized by the induction of a predominantly M1 phenotype with expression of TLR2, TLR3 and TLR9 and activation of the NF-ƙB signalling pathway. Heat-killed N. caninum tachyzoites failed to activate NF-ƙB, and to inhibit lysosomal activity and apoptosis, which indicates active modulation by the parasite. The FoxO signalling pathway, Th1-Th2 differentiation, glycosaminoglycan degradation and apoptosis were pathways enriched only for low virulent Nc-Spain1H infection. In addition, Nc-Spain1H infection upregulated the IL12A and IL8 pro-inflammatory cytokines, whereas IL23 was downregulated by high virulent Nc-Spain7. Conclusions This study revealed mechanisms implicated in the recognition of N. caninum by bovine MØs and in the development of the subsequent immune response. NF-ƙB seems to be the main signalling pathway implicated in the pro-inflammatory bovine MØs response against this pathogen. Apoptosis and phagolysosome maturation are processes repressed by N. caninum infection, which may guarantee its intracellular survival. The results also indicate that Nc-Spain7 may be able to partially circumvent the pro-inflammatory response whereas Nc-Spain1H induces a protective response to infection, which may explain the more efficient transmission of the high-virulence Nc-Spain7 isolate observed in vivo. |
Databáze: | OpenAIRE |
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