Abstract:
:Animal studies with Candida albicans have provided models for understanding fungal virulence and antifungal drug development. To non-invasively monitor long-term Candida murine infections, clinical isolates were stably transformed with a codon-optimized luciferase gene to constitutively express luciferase. Chronic systemic infections were established in mice with engineered strains, and bioluminescent signals were apparent from kidneys by non-invasive imaging using charged-coupled device cameras. These infections were established in immune-competent mice, and bioluminescence was detectable in animals that showed no physiological consequence of infection, as well as those visually succumbing to the disease. Similarly, bioluminescence was measured from the vaginal tissue of mice infected vaginally. Fungal loads determined by plating vaginal lavages showed a similar pattern to the bioluminescent signals measured, and fungal infection could be detected in animals for over 30 days post infection by both modalities. The effect of the antifungal drug miconazole was tested in this model, and clearance in animals was apparent by both direct imaging and fungal load determination. The use of bioluminescence to monitor these and other models of Candida infections will greatly speed up the analysis of drug development studies, both in ease of visualizing infections and decreasing numbers of animals required to run such studies.
journal_name
Microb Pathogjournal_title
Microbial pathogenesisauthors
Doyle TC,Nawotka KA,Kawahara CB,Francis KP,Contag PRdoi
10.1016/j.micpath.2005.11.003subject
Has Abstractpub_date
2006-02-01 00:00:00pages
82-90issue
2eissn
0882-4010issn
1096-1208pii
S0882-4010(05)00137-3journal_volume
40pub_type
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journal_title:Microbial pathogenesis
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