scholarly journals Transcriptional Response of Peripheral Blood Mononuclear Cells from Cattle Infected with Mycobacterium bovis

PLoS ONE ◽  
2012 ◽  
Vol 7 (7) ◽  
pp. e41066 ◽  
Author(s):  
Federico Carlos Blanco ◽  
Marcelo Soria ◽  
María Verónica Bianco ◽  
Fabiana Bigi
PLoS ONE ◽  
2016 ◽  
Vol 11 (7) ◽  
pp. e0159779 ◽  
Author(s):  
Silvia N. Kariuki ◽  
Joseph C. Maranville ◽  
Shaneen S. Baxter ◽  
Choongwon Jeong ◽  
Shigeki Nakagome ◽  
...  

2001 ◽  
Vol 8 (6) ◽  
pp. 1204-1212 ◽  
Author(s):  
W. R. Waters ◽  
B. J. Nonnecke ◽  
T. E. Rahner ◽  
M. V. Palmer ◽  
D. L. Whipple ◽  
...  

ABSTRACT Historically, administration of vitamin D has been considered beneficial in the treatment of tuberculosis. The interaction of this vitamin {i.e., 1,25-dihdroxyvitamin D3[1,25(OH)2D3]} with the antitubercular immune response, however, is not clear. In the present study, in vitro recall responses of peripheral blood mononuclear cells (PBMC) from cattle infected with Mycobacterium bovis were used to study the immune-modulatory effects of 1,25(OH)2D3 on M. bovis-specific responses in vitro. Addition of 1 or 10 nM 1,25(OH)2D3 inhibited M. bovis-specific proliferative responses of PBMC from M. bovis-infected cattle, affecting predominately the CD4+ cell subset. In addition, 1,25(OH)2D3 inhibited M. bovis-specific gamma interferon (IFN-γ) production yet enhanced M. bovis-specific nitric oxide (NO) production. Lymphocyte apoptosis, measured by flow cytometry using annexin-V staining, was diminished by addition of 1,25(OH)2D3 to PBMC cultures. These findings support the current hypothesis that 1,25(OH)2D3enhances mycobacterial killing by increasing NO production, a potent antimicrobial mechanism of activated macrophages, and suggest that 1,25(OH)2D3 limits host damage by decreasingM. bovis-induced IFN-γ production.


2016 ◽  
Vol 42 (04) ◽  
pp. 195-201
Author(s):  
Yafen Cheng ◽  
Chung-Hsi Chou ◽  
Hsiang-Jung Tsai

Mycobacterium bovis (M. bovis) is causative agent of tuberculosis in cattle and humans populations. To understand its effects on gene expression profiles, we conducted an in vitro time-course study to identify transcriptional changes in infected bovine peripheral blood mononuclear cells (PBMCs), using quantitative RT-PCR. We discovered a likely involvement of C-type lectin domain family 4, member E (CLEC4E) in triggering a series of negative intracellular signaling via Syk/CARD9 pathway for cytokines, as early as 24 h post-infection (hpi). This is the first report confirming induction of CLEC4E and the Syk/CARD9 pathway in PBMCs in response to M. bovis infection, and these findings support the view that M. bovis inhibits signaling pathways of antimycobacterial host defense in bovine cells. In addition, M. bovis infection in PBMCs may suppress apoptosis by interfering with TNF-[Formula: see text] signaling. This study, contributes to a better understanding of M. bovis-reduced signal transduction and microbial changes in PBMCs earlier than 24 hpi.


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