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. 2018 Oct 22;19(10):3274. doi: 10.3390/ijms19103274

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© 2018 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Percentages of CD4 and CD8 T-lymphocytes in the peripheral blood in the control group (Con), which received saline, and in the treatment group (LPS), which received LPS from S. Enteritidis at a dose of 5 μg/kg b.w.; n = 5 pigs/group. Bars represent mean ± SD (standard deviation). The statistical analysis was performed by one-way ANOVA and Tukey’s tests. Statistically different at p = 0.044 (for the percentage of plasma CD8 T-lymphocytes) and p < 0.001(for the percentage of plasma CD4 T-lymphocytes) as compared with the control group. Panels A and B present exemplary dot plots with distribution of CD4 and CD8 T-lymphocytes of the control and treatment group. Samples were stained with FITC Anti-Pig CD4a (BD) and PE Anti-Pig CD8a (BD) and analysed on flow cytometer (Beckman Coulter).

Percentages of CD4 and CD8 T-lymphocytes in the peripheral blood in the control group (Con), which received saline, and in the treatment group (LPS), which received LPS from S. Enteritidis at a dose of 5 μg/kg b.w.; n = 5 pigs/group. Bars represent mean ± SD (standard deviation). The statistical analysis was performed by one-way ANOVA and Tukey’s tests. Statistically different at p = 0.044 (for the percentage of plasma CD8 T-lymphocytes) and p < 0.001(for the percentage of plasma CD4 T-lymphocytes) as compared with the control group. Panels A and B present exemplary dot plots with distribution of CD4 and CD8 T-lymphocytes of the control and treatment group. Samples were stained with FITC Anti-Pig CD4a (BD) and PE Anti-Pig CD8a (BD) and analysed on flow cytometer (Beckman Coulter).