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However, when looking through the literature, we were unable to find information on using body temperature BT measurements as a predictor of death in an animal model similar to our intranasal inoculation of Aspergillus. The publications we found mostly focused on bacterial 12 , 13 , 15 , 19 , 20 or viral infections, 18 , 19 , 22 with only one fungal model that involved Candida albicans.
For example, a study evaluating a staphylococcal enterotoxic shock model found that mice reaching a body temperature as low as Given the variety of endpoints recommended for the various infectious diseases and animal models, we decided that data directly from our model were necessary to independently evaluate the usefulness of a hypothermic endpoint for our particular model of interest.
BT measurements were already incorporated into the design of these studies, so we retrospectively analyzed the data in an attempt to identify a specific hypothermic endpoint for this murine model of IPA. All experiments had taken place before the decision was made to evaluate BT data as a humane endpoint; therefore the current study is a retrospective assessment of mice inoculated with A.
Data from 4 independent experiments comprising a total of mice were included in the current study. Mice were designated by the vendor as SPF for Sendai virus, pneumonia virus of mice, mouse hepatitis virus, minute virus of mice, mouse parvovirus, mouse norovirus, Theiler murine enchephalomyelitis virus, mouse reovirus type 3, mouse rotavirus, lymphocytic choriomeningitis virus, ectromelia virus, mouse adenovirus 1 and 2, mouse cytomegalovirus, polyoma virus, K virus, mouse thymic virus, Hantaan virus, Prospect Hill virus, cilia-associated respiratory bacillus, E.
They were also free of Helicobacter spp. Mice were kept on a h light:dark cycle and allowed to acclimate for at least 1 wk prior to beginning the experiment.
Study design. Data were collected retrospectively from 4 independent experiments performed by a single investigator from one research group.
Aspergillus strain and vaccination reagents.
Conidia were prepared as described by the laboratory in previous publications. There were 6 different experimental scenarios prior to Aspergillus challenge. Mice subcutaneously received either an aspergillosis vaccine an initial injection followed by a booster 2 wk later , or PBS plus adjuvant at the same site and time points. Six weeks after injection, mice were either immunosuppressed or not and placed prophylactically on sulfamethoxazole 0.
For immunosuppression, mice either received a subcutaneous injection of cortisone acetate 2.
The day after completion of the immunosuppression regimen, mice were weighed and their BT recorded; mice were then anesthetized with ketamine—xylazine and intranasally inoculated with A. The mice were monitored every 2 h during the day for 7 d after inoculation and at least once daily thereafter until euthanasia. Body weight was recorded daily, and BT was recorded as many as 3 times daily.