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

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 mor...

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Autores principales: Asai, Masanori, Li, Yanwen, Spiropoulos, John, Cooley, William, Everest, David J., Kendall, Sharon L., Martín, Carlos, Robertson, Brian D., Langford, Paul R., Newton, Sandra M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481108/
https://www.ncbi.nlm.nih.gov/pubmed/36052440
http://dx.doi.org/10.1080/21505594.2022.2119657
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author Asai, Masanori
Li, Yanwen
Spiropoulos, John
Cooley, William
Everest, David J.
Kendall, Sharon L.
Martín, Carlos
Robertson, Brian D.
Langford, Paul R.
Newton, Sandra M.
author_facet Asai, Masanori
Li, Yanwen
Spiropoulos, John
Cooley, William
Everest, David J.
Kendall, Sharon L.
Martín, Carlos
Robertson, Brian D.
Langford, Paul R.
Newton, Sandra M.
author_sort Asai, Masanori
collection PubMed
description 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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spelling pubmed-94811082022-09-17 Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv Asai, Masanori Li, Yanwen Spiropoulos, John Cooley, William Everest, David J. Kendall, Sharon L. Martín, Carlos Robertson, Brian D. Langford, Paul R. Newton, Sandra M. Virulence Research Paper 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. Taylor & Francis 2022-09-11 /pmc/articles/PMC9481108/ /pubmed/36052440 http://dx.doi.org/10.1080/21505594.2022.2119657 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Asai, Masanori
Li, Yanwen
Spiropoulos, John
Cooley, William
Everest, David J.
Kendall, Sharon L.
Martín, Carlos
Robertson, Brian D.
Langford, Paul R.
Newton, Sandra M.
Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv
title Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv
title_full Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv
title_fullStr Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv
title_full_unstemmed Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv
title_short Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv
title_sort galleria mellonella as an infection model for the virulent mycobacterium tuberculosis h37rv
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481108/
https://www.ncbi.nlm.nih.gov/pubmed/36052440
http://dx.doi.org/10.1080/21505594.2022.2119657
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