Skip to main content
NC3Rs: National Centre for the Replacement Refinement & Reduction of Animals in Research
Project grant

Reduction and refinement of murine models of bacterial infection

Two researchers looking at a screen. One is sitting and the other is standing pointing to the screen

At a glance

Completed
Award date
January 2009
Grant amount
£276,759
Principal investigator
Professor Shiranee Sriskandan

Co-investigator(s)

Institute
Imperial College London

R

  • Reduction
  • Refinement

Overview

Aims

This research aimed to reduce the use of animals in the investigation of clinically-relevant bacterial diseases by developing and implementing a method of monitoring infection using bioluminescence.

Background

Infectious diseases are a major cause of mortality and morbidity worldwide. Mice are often used to investigate disease pathogenesis and to develop treatments. Traditionally, infected animals are killed at defined time points and tissues removed to determine localisation and degree of infection, and response to treatment; a six time point experiment would use up to 36 animals. Non-invasive detection of bacteria within live animals enables longitudinal monitoring and reduces the number of mice used by avoiding culling cohorts at various time points and allowing each animal to act as its own control.

Research details and methods

Plasmid vectors were developed for expression of luciferase in the targeted bacteria.  Infection and disease progression were monitored in real time in mice by bioluminescence imaging.

Key impacts and findings

The project developed a clinically-relevant bioluminescent strain of Streptococcus pyogenes, a Gram positive bacterium associated with a range of human diseases. By monitoring the bioluminescence, infected mice could be studied for around four days without the need to cull groups at pre-determined time points. This allowed the number of animals to be reduced by four-fold. The technique also provided more precise quantitation of the bacterial infectious dose, and revealed previously unknown niches of infection. The ability to identify mice in which the disease was progressing rapidly enabled the use of improved humane endpoints to minimise suffering. 

Publications

Alam FM et al. (2013). Non-invasive monitoring of Streptococcus pyogenes vaccine efficacy using biophotonic imaging. PLoS ONE 8(11):e82123. doi: 10.1371/journal.pone.0082123

Alam FM et al. (2013). Inactivation of the CovR/S virulence regulator impairs infection in an improved murine model of Streptococcus pyogenes naso-pharyngeal infection. PLoS ONE 8(4):e61655. doi: 10.1371/journal.pone.0061655

Andreu N et al. (2011). Non-invasive biophotonic imaging for studies of infectious disease. FEMS Microbiology Reviews 35(2):360-394. doi: 10.1111/j.1574-6976.2010.00252.x

Impacts