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. 2020 Apr 6;27(5):704–709.e2. doi: 10.1016/j.chom.2020.03.023

Figure 1.

Figure 1

Temperature Changes, Weight Loss, Survival, Viral Shedding, and Immunohistochemistry of Tissues of NMC-nCoV02-Infected Ferrets

(A–C) Six ferrets were inoculated intranasally with 105.5 TCID50 of virus. (A) Temperature changes, (B) number of viral RNA copies, and (C) infectious virus titers were measured in tissues of NMC-nCoV02-infected ferrets (n = 6/group). Each tissue (n = 3 per group) was collected at 4, 8, and 12 dpi. Viral loads in nasal turbinate, trachea, lung, kidney, and intestine were titered using quantitative real-time PCR and TCID50. Data are presented as mean ± SEM.

(D) Serum neutralizing (SN) antibody titers (GMT) against NMC-nCoV02 (100 TCID50) were measured onto Vero cells after 12 days of experiment (n = 6 per group). Data are presented as geometric mean ± SD. Tissues were harvested on day 4 after inoculation and immunohistochemistry was performed with a mouse polyclonal antibody.

(E–H) Tissues of PBS control ferrets; (E) nasal turbinate, (F) trachea, (G) lung, and (H) intestine.

(I–L) Tissues of NMC-nCoV02 infected ferrets: (I) Nasal turbinate, (J) Trachea, (K) lung, and (L) Intestine.

The presence of NMC-nCoV02 antigen was determined by IHC with mouse polyclonal antibody. Magnification ×400. Asterisks indicate statistical significance compared with PBS control group by the two-way ANOVA with Sidaks multiple comparisons test (A), the two way ANOVA with Dunnett’s multiple comparisons test (B and C), or one-way ANOVA Dunnett’s multiple comparisons test ( indicates p < 0.05, ∗∗ indicates p < 0.001, and ∗∗∗ indicates p < 0.0001).