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ABSTRACT: Objectives
In vivo experimentation is costly and time-consuming, and presents a major bottleneck in anti-tuberculosis drug development. Conventional methods rely on the enumeration of bacterial colonies, and it can take up to 4 weeks for Mycobacterium tuberculosis to grow on agar plates. Light produced by recombinant bacteria expressing luciferase enzymes can be used as a marker of bacterial load, and disease progression can be easily followed non-invasively in live animals by using the appropriate imaging equipment. The objective of this work was to develop a bioluminescence-based mouse model of tuberculosis to assess antibiotic efficacy against M. tuberculosis in vivo.Methods
We used an M. tuberculosis strain carrying a red-shifted derivative of the firefly luciferase gen
SUBMITTER: Andreu N
PROVIDER: S-EPMC3743513 | biostudies-literature | 2013 Sep
REPOSITORIES: biostudies-literature