In Vivo Bacterial Imaging Using Bioluminescence.

Mariette Barbier, Justin Bevere, F Heath Damron
Author Information
  1. Mariette Barbier: Department of Microbiology, Immunology and Cell Biology, West Virginia University School of Medicine, Morgantown, WV, USA.
  2. Justin Bevere: Department of Microbiology, Immunology and Cell Biology, West Virginia University School of Medicine, Morgantown, WV, USA.
  3. F Heath Damron: Department of Microbiology, Immunology and Cell Biology, West Virginia University School of Medicine, Morgantown, WV, USA. fdamron@hsc.wvu.edu.

Abstract

Bacterial luminescence allows for noninvasive continuous monitoring of promoter activity in a wide range of model systems. This chapter details various examples of use of the lux reporter system to measure promoter activity in bacteria using the vector pUC18T-mini-Tn7T-lux-Tp. Here, we describe the construction of promoter fusions with bacterial luciferase, and how to quantify promoter activity in real time in vitro and in vivo in plant, insect, and murine infection models.

Keywords

MeSH Term

Animals
Bacteria
Insecta
Luciferases
Luminescence
Luminescent Measurements
Mice
Molecular Imaging
Plants
Plasmids
Promoter Regions, Genetic

Chemicals

Luciferases

Word Cloud

Created with Highcharts 10.0.0promoteractivityBacterialsystemvivoBioluminescenceluminescenceallowsnoninvasivecontinuousmonitoringwiderangemodelsystemschapterdetailsvariousexamplesuseluxreportermeasurebacteriausingvectorpUC18T-mini-Tn7T-lux-TpdescribeconstructionfusionsbacterialluciferasequantifyrealtimevitroplantinsectmurineinfectionmodelsVivoImagingUsingBacteriapathogenesisimagingPathogen-hostinteractionPromoterReporter

Similar Articles

Cited By