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Figure 1.

SHIVSF162P4 loads in plasma (A), CD4+ T cell counts in peripheral blood (B), relative CCL3 (C), CCL4 (D) and CCL5 (E) gene expression levels in PBMCs at PID 0-180 with SHIVSF162P4.

Each point on the graph represents the mean fold change in gene expression relative to pre-infection level±SE (n = 5).

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Figure 1 Expand

Figure 2.

Relative CCL3 (A), CCL4 (B) and CCL5 (C) expression levels in GALT tissues at different stages of SHIVSF162P4 infection (n = 5).

PID 0 was used as the calibrator (value = 1).

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Figure 2 Expand

Figure 3.

Triple-label confocal microscopy of CCL4+ cells in mesenteric lymph nodes obtained from control (PID 0) and SHIVSF162P4-inoculated macaques at PID 14.

T lymphocytes (CD3+) are red, CCL4+ cells are green, SHIVSF162P4-infected cells (p28+) are blue. Overlap of red and green fluorescence is seen as yellow, overlap of red and blue as pink. Higher number of CD3+CCL4+ cells was seen at PID 0 than at PID 14 (Table 1) while CD3+p28+ cells could be seen at PID 14 but not at PID 0 indicating the successful spread of virus into GALTs following mucosal inoculation.

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Figure 3 Expand

Figure 4.

Macrophages were also identified as CCL4+ cells.

Macrophages (CD68+) are red, CCL4+ cells are green, overlap of red and green fluorescence is seen as yellow.

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Figure 4 Expand

Table 1.

Absolute (counts) and relative (%) levels of CCL4+ cells in MLN following SHIVSF162P4 inoculation

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Table 1 Expand

Figure 5.

The proportions of peripheral blood CD3+CD4+CCL4+ and CD3+CD8+CCL4+ T lymphocytes were compared at PID 0 and PID 14 with SHIVSF162P4 by flow cytometry (A).

Gating was performed via CD3+ lymphocyte population. Statistically significant differences between CD3+CD4+CCL4+ and CD3+CD8+CCL4+ cells over CD3+ lymphocytes at PID 0 vs. PID 14 (n = 5) are shown (B).

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Figure 5 Expand

Figure 6.

Comparison of SHIVSF162P4 and SHIVKu1 primary infection in peripheral blood.

Viral loads in plasma (A), CD4+ T cell counts (B), Fold-changes of CCL3, CCL4 and CCL5 gene expression levels in SHIVSF162P4- and SHIVKu1–infected macaques at PID 0 vs. PID 14 (C) (n = 5 for each group). Negative sample cut-off for viral load measurements in plasma was <30 copies/ml e.g. PID 0 value.

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Figure 6 Expand

Table 2.

Rhesus macaque-specific primers for real-time PCR

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Table 2 Expand