Use of Temperature for Standardizing the Progression of Francisella tularensis in Mice |
| |
Authors: | Claudia R. Molins Mark J. Delorey John W. Young Brook M. Yockey John T. Belisle Martin E. Schriefer Jeannine M. Petersen |
| |
Affiliation: | 1. Division of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, United State of America.; 2. Microbiology, Immunology, and Pathology Department, Colorado State University, Fort Collins, Colorado, United States of America.; Albany Medical College, United States of America, |
| |
Abstract: | The study of infectious agents, their pathogenesis, the host response and the evaluation of newly developed countermeasures often requires the use of a living system. Murine models are frequently used to undertake such investigations with the caveat that non-biased measurements to assess the progression of infection are underutilized. Instead, murine models predominantly rely on symptomology exhibited by the animal to evaluate the state of the animal''s health and to determine when euthanasia should be performed. In this study, we used subcutaneous temperature as a non-subjective measurement to follow and compare infection in mice inoculated with Francisella tularensis, a Gram-negative pathogen that produces an acute and fatal illness in mice. A reproducible temperature pattern defined by three temperature phases (normal, febrile and hypothermic) was identified in all mice infected with F. tularensis, regardless of the infecting strain. More importantly and for the first time a non-subjective, ethical, and easily determined surrogate endpoint for death based on a temperature, termed drop point, was identified and validated with statistical models. In comparative survival curve analyses for F. tularensis strains with differing virulence, the drop point temperature yielded the same results as those obtained using observed time to death. Incorporation of temperature measurements to evaluate F. tularensis was standardized based on statistical models to provide a new level of robustness for comparative analyses in mice. These findings should be generally applicable to other pathogens that produce acute febrile disease in animal models and offers an important tool for understanding and following the infection process. |
| |
Keywords: | |
|
|