Journal
PATHOGENS
Volume 9, Issue 9, Pages -Publisher
MDPI
DOI: 10.3390/pathogens9090710
Keywords
Neospora caninum; host-pathogen interaction; blood-brain barrier; infrared spectroscopy; Synchrotron-based XRF mapping; differential gene expression
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Funding
- Ministry of Higher Education of Saudi Arabia
- University of Nottingham
- School of Veterinary Medicine and Science, University of Nottingham
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In this work, the effects of the protozoanNeospora caninumon the bioenergetics, chemical composition, and elemental content of human brain microvascular endothelial cells (hBMECs) were investigated. We showed thatN. caninumcan impair cell mitochondrial (Mt) function and causes an arrest in host cell cycling at S and G2 phases. These adverse effects were also associated with altered expression of genes involved in Mt energy metabolism, suggesting Mt dysfunction caused byN. caninuminfection. Fourier Transform Infrared (FTIR) spectroscopy analysis of hBMECs revealed alterations in the FTIR bands as a function of infection, where infected cells showed alterations in the absorption bands of lipid (2924 cm(-1)), amide I protein (1649 cm(-1)), amide II protein (1537 cm(-1)), nucleic acids and carbohydrates (1092 cm(-1), 1047 cm(-1), and 939 cm(-1)). By using quantitative synchrotron radiation X-ray fluorescence (mu SR-XRF) imaging and quantification of the trace elements Zn, Cu and Fe, we detected an increase in the levels of Zn and Cu from 3 to 24 h post infection (hpi) in infected cells compared to control cells, but there were no changes in the level of Fe. We also used Affymetrix array technology to investigate the global alteration in gene expression of hBMECs and rat brain microvascular endothelial cells (rBMVECs) in response toN. caninuminfection at 24 hpi. The result of transcriptome profiling identified differentially expressed genes involved mainly in immune response, lipid metabolism and apoptosis. These data further our understanding of the molecular events that shape the interaction betweenN. caninumand blood-brain-barrier endothelial cells.
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