Figure 1.
In vitro growth kinetics of tick-borne flaviviruses.
BHK21 cells were infected with either OHFV Guriev, KFDV P9605, AHFV 2003, or AHFV Zaki-1 at an MOI of 0.01, and supernatant (A) and cell-associated (B) fractions were harvested daily for 5 days. Titers are expressed as TCID50 ml−1, and error bars represent standard deviations.
Figure 2.
Virulence of KFDV and AHFV in mice.
Groups of 5 mice were infected via footpad inoculation with 2×103 TCID50 per animal of either KFDV P9605, AHFV 2003, or AHFV Zaki-1. (A) Survival curve. Death of an animal is indicated by a step down on the curve. (B) Temperature. Mice were implanted with subdermal transponders as detailed in the Materials and Methods, and the temperature was monitored daily. (C) Weight change. Mice were weighed daily, and the change in weight is shown as a percentage of the initial study weight on the day of infection. Error bars in (B) and (C) represent standard deviations.
Figure 3.
Groups of 20 mice were infected with 2×103 TCID50 per animal of either KFDV P9605 or AHFV Zaki-1 via footpad inoculation. Two additional control groups of 5 mice each were inoculated with serum-free MEM. Five mice from each group were sacrificed at days 2, 4, 6, and 8 post-infection, and the controls groups were sacrificed at the end of study. Organs were harvested and homogenized as described in the Materials and Methods, and homogenates were titrated on BHK21 cells by limiting dilution. Results for the lung (A), brain (B), kidney (C), spleen (D), liver (E), and plasma (F) are shown. Each symbol represents one animal. Background cut-offs of 101 TCID50 mg−1 (lung in [A]), 102 TCID50 mg−1 (brain, kidney, spleen, and liver in [B–E]), and 103 TCID50 ml−1 (plasma in [F]) were applied to organ and plasma titrations based on the control groups, and are shown as dashed lines on the lower axes of the respective graphs. Note in (F) that no animals were viremic. Each symbol represents one animal, and geometric means are indicated by horizontal black lines.
Figure 4.
Histopathologic changes in BALB/c mice experimentally infected with KFDV P9605 and AHFV Zaki-1.
(A and B) H&E stain of the brain at day 8 post-infection. (A) Mock. (B) KFDV P9605-infected mouse. Meninges are expanded by an inflammatory infiltrate (arrows), perivaculitis is characterized by infiltrations of mononuclear cells and neutrophils (inset). (C and D) H&E stain of the liver at day 4 post-infection. (C) Mock. (D) AHFV Zaki-1-infected mouse. Scattered foci of inflammatory cells (arrows), foci are composed of macrophages and lymphocytes (inset). (E and F) H&E stain of the kidney at day 6 post-infection. (E) Mock. (F) AHFV Zaki-1-infected mouse. Congested kidney tissue and an increased cellularity of glomeruli (arrow head) with mononuclear inflammatory cells in proximity (inset).
Figure 5.
Immunohistochemical findings in BALB/c mice experimentally infected with KFDV P9605 and AHFV Zaki-1.
(A and B) Immunohistochemistry of the brain. (A) Mock. (B) Foci of positive immunostaining for KFDV P9605 (brown) within neurons and some astrocytes at day 8 post-infection. (C and D) Immunohistochemistry of the kidney at day 4 post-infection. (C) Mock. (D) AHFV Zaki-1-infected mouse, viral antigen (brown) can be found scattered in the cortex and the medulla. Positive immunostaining for AHFV Zaki-1 in mesangial cells of the glomeruli (inset). (E and F) Immunohistochemistry of the liver on day 6 post-infection. (E) Mock. (F) AHFV Zaki-1-infected mouse. AHFV Zaki-1 immunostaining (brown) in sinusoids and Kupffer cells (inset).
Figure 6.
White blood cell (WBC) abnormalities induced by KFDV P9605 and AHFV Zaki-1 infection.
(A) Total WBC counts from whole blood. Each symbol represents one animal. (B) Lymphocyte counts from whole blood. Each symbol represents one animal. Arithmetic means in (A) and (B) are indicated by horizontal black lines. (C) Composite graph showing average absolute counts of lymphocytes, neutrophils, monocytes, eosinophils, and basophils from 5 mice per day for each virus, and 10 uninfected control animals. (D) Composite graph showing average population proportions for lymphocytes, neutrophils, monocytes, eosinophils, and basophils from 5 mice per day for each virus, and 10 uninfected control animals.
Figure 7.
Hematologic abnormalities induced by KFDV P9605 and AHFV Zaki-1 infection.
(A) Total RBC counts from whole blood. (B) Hemoglobin (Hb) levels from whole blood. (C) Hematocrit levels from whole blood. (D) Platelet counts from whole blood. Each symbol represents one animal, and arithmetic means are indicated by horizontal black lines.
Figure 8.
Differential cytokine induction by KFDV P9605 and AHFV Zaki-1.
Organ homogenates were analyzed by Bio-Plex Pro Mouse Cytokine Assay as described in the Materials and Methods. Results for IL-6, IL-10, IFN-γ, MCP-1, and TNF-α are shown for the brain (A), kidney (B), and spleen (C). All cytokine concentrations were normalized to the amount of the respective tissue that was homogenized in each sample. Error bars represent standard deviations. Statistical significance is indicated by * for p<0.05 and ** for p<0.01.