4.5 Article

Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv

期刊

VIRULENCE
卷 13, 期 1, 页码 1543-1557

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/21505594.2022.2119657

关键词

Tuberculosis; Mycobacterium tuberculosis; Galleria mellonella; infection model; innate immunity; mycobacteria

资金

  1. National Centre for the Replacement, Refinement, and Reduction of Animals in Research (NC3Rs) PhD studentship [NC/R001596/1]
  2. NC3Rs training Fellowship [NC/W002264/1]

向作者/读者索取更多资源

This study demonstrates the use of Galleria mellonella larvae as a low-cost, rapid, and ethically more acceptable model for tuberculosis research. The Gm-MTB model can mimic key aspects of the disease and can be used for anti-TB drug screening and comparing virulence of different strains.
Tuberculosis (TB), caused by Mycobacterium tuberculosis (MTB), is a leading cause of infectious disease mortality. Animal infection models have contributed substantially to our understanding of TB, yet their biological and non-biological limitations are a research bottleneck. There is a need for more ethically acceptable, economical, and reproducible TB infection models capable of mimicking key aspects of disease. Here, we demonstrate and present a basic description of how Galleria mellonella (the greater wax moth, Gm) larvae can be used as a low cost, rapid, and ethically more acceptable model for TB research. This is the first study to infect Gm with the fully virulent MTB H37Rv, the most widely used strain in research. Infection of Gm with MTB resulted in a symptomatic lethal infection, the virulence of which differed from both attenuated Mycobacterium bovis BCG and auxotrophic MTB strains. The Gm-MTB model can also be used for anti-TB drug screening, although CFU enumeration from Gm is necessary for confirmation of mycobacterial load reducing activity of the tested compound. Furthermore, comparative virulence of MTB isogenic mutants can be determined in Gm. However, comparison of mutant phenotypes in Gm against conventional models must consider the limitations of innate immunity. Our findings indicate that Gm will be a practical, valuable, and advantageous additional model to be used alongside existing models to advance tuberculosis research.

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