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. 2022 Jan 29;59(4):602–612. doi: 10.1177/03009858211071016

Table 2.

Lesions and viral RNA (in situ hybridization) and nucleocapsid immunolabeling in the nasal passages of K18-hACE2 Tg mice (n = 3), hACE2 Tg mice (n = 3), and hamsters (n = 3 per time point) infected with SARS-CoV-2.

K18-hACE2 Tg mice hACE2 Tg mice Syrian hamsters
3 dpi 5 dpi 7 dpi 14 dpi
Moderate Mild Severe Mild
Epithelial lesion scores Squamous 0 0 0 0
Respiratory 1 0 3 0
Olfactory 2 0 4 0
ISH (viral RNA) Squamous
Respiratory + +/−
Olfactory ++ +/− +
IHC (viral nucleocapsid) Squamous + +/− +
Respiratory ++ +/− ++
Olfactory ++ +/− ++

Lesion severity was scored by the distribution or extent of lesions as follows: 0, no visible changes; 1, mild focal or multifocal changes; 2, moderate multifocal changes; 3, moderate diffuse changes; 4, severe diffuse changes. The intensity of positive IHC or ISH signals in nasal cavities was scored as follows: −, no detectable signal; +/−, weak or faint signal; + moderate, readily detectable signal; ++, strong, intense signal.

Abbreviations: hACE2, human angiotensin-converting enzyme 2; Tg, transgenic; SARS-CoV-2, severe acute respiratory syndrome coronavirus-2; IHC, immunohistochemistry; ISH, in situ hybridization.