Surface temperature changes indicate disease onset after pulmonary murine corona virus infection, but do not constitute a humane endpoint

TL;DR

The study found that changes in surface temperature can signal disease onset in mice infected with a coronavirus, but are not reliable for determining humane endpoints.

Contribution

The study evaluates thermal imaging as a potential humane endpoint during murine coronavirus infection.

Findings

BALB/c mice showed increased surface temperature and significant weight loss during MCoV infection.

C57BL/6J mice also showed temperature increases and weight loss, but fewer reached the termination point.

Surface temperature changes were not correlated with weight loss in individual animals.

Abstract

Mouse models are important contributors for understanding the immune system during infections. Objective parameters help to assess the course of infection and guarantee animal welfare. In this study we analyzed if surface temperature measured via thermal imaging of the dorsal area is a suitable marker to evaluate animal wellbeing during murine coronavirus (MCoV) infection. Infected BALB/c mice displayed severe symptoms whereas C57BL/6 mice were less affected. In BALB/c animals, temperature increased from 27.1 °C to 28.4 °C within 24 h with levels remaining slightly elevated over the observation period. In contrast, a decrease in body weight was consistent through the period with 60% of the animals reaching the previously set termination point of 20% weight loss (n = 6). Also, C57BL/6J animals showed a significant temperature increase from 27.1 °C to 28.4 °C within 24 h and a significant weight loss over time with two out of ten reached weight loss end point. However, temperature and weight changes were not related in individual animals. In contrast to temperature values, body weight clearly set a trajectory towards early termination. Taken together, our data indicate that superficial temperature did not serve as a predictive parameter for defining humane end points, but indicate disease onset after pulmonary virus infection.

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