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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: Antiviral Res. 2016 Nov 10;137:14–22. doi: 10.1016/j.antiviral.2016.11.003

Table 2.

Tissue infectious assay and histopathologic diagnoses of adult AG129 mice infected with ZIKV.

Days post-infection Tissue infectious assay on indicator Vero 76 cells Histopathologic lesionsa ZIKV immunohistochemistryb

Kidney pos./totalc Liver pos./total Testis pos./total Brain pos./total Brain pos./total Testis pos./total Epididymis pos./total
Sham 0/3 0/3 0/3 0/3 0/3 0/3 0/3
3 0/4 N/A N/A N/A 0/3 0/2 0/2
5 0/4 N/A N/A N/A 0/4 2/2 0/2
7 3/4 2/4 0/2 2/4 0/4 2/2 2/2
9 0/4 1/4 2/2 3/4 4/4d 0/1 0/1
11 2/4 0/4 2/2 2/4 4/4d 0/2 0/2
13 N/A N/A N/A N/A 2/2d 1/1 1/1

N/A: Not available.

a

Histopathologic analysis of kidney, spleen, liver and testis/uterus were also processed and did not have any histopathologic lesions as assessed by a board-certified veterinary pathologist.

b

Various tissues, including testis and attached epididymis, brain, spleen, liver and kidney were processed. In addition to the results above, spleen also stained positive for ZIKV immunoreactivity after 5 dpi in 2 animals.

c

Samples that stained positive for ZIKV foci per total number of samples assayed.

d

Meningoencephalitis was the primary lesion observed in brain sections of ZIKV-infected mice.