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Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) <t>CD11b</t> + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.
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Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) <t>CD11b</t> + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.
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Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) <t>CD11b</t> + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.
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Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) <t>CD11b</t> + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.
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Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) <t>CD11b</t> + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.
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Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) <t>CD11b</t> + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.
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Image Search Results


Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) CD11b + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.

Journal: Frontiers in Cellular and Infection Microbiology

Article Title: Human HLA prolongs the host inflammatory response in Streptococcus suis serotype 2 infection compared to mouse H2 molecules

doi: 10.3389/fcimb.2023.1285055

Figure Lengend Snippet: Influence of HLA-A11/DR1 on macrophage mitochondrial ROS-associated bacterial clearance. BMDM cells from WT and HLA-A11/DR1 mice were subjected to infection with S. suis at a MOI of 10. Subsequently, gentamicin treatment was applied 60 minutes post-infection to eliminate extracellular bacteria. The quantification of live bacteria was accomplished by plating on THY agar supplemented with ampicillin at (A) 1 h or (B) 6 h post-infection. Mitochondrial ROS production was assessed under the following conditions: (C) BMDM cells exposed to S. suis at MOI 20 at the specified time points in vitro , and (D) CD11b + cells collected from WT and HLA-A11/DR1 mice during S. suis infection. Data are represented as mean ± SEM. * P < 0.05; ** P < 0.01.

Article Snippet: To selectively characterize monocytes/macrophages, an acutely isolated monocytes/macrophages fraction was obtained using MACS microbeads (Miltenyi Biotec) conjugated with CD11b antibody.

Techniques: Infection, Bacteria, In Vitro