Cargando…
A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella
Mammalian infection models have contributed significantly to our understanding of the host-mycobacterial interaction, revealing potential mechanisms and targets for novel antimycobacterial therapeutics. However, the use of conventional mammalian models such as mice, are typically expensive, high mai...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550006/ https://www.ncbi.nlm.nih.gov/pubmed/32530737 http://dx.doi.org/10.1080/21505594.2020.1781486 |
_version_ | 1783592883074367488 |
---|---|
author | Asai, Masanori Li, Yanwen Spiropoulos, John Cooley, William Everest, David Robertson, Brian D. Langford, Paul R. Newton, Sandra M. |
author_facet | Asai, Masanori Li, Yanwen Spiropoulos, John Cooley, William Everest, David Robertson, Brian D. Langford, Paul R. Newton, Sandra M. |
author_sort | Asai, Masanori |
collection | PubMed |
description | Mammalian infection models have contributed significantly to our understanding of the host-mycobacterial interaction, revealing potential mechanisms and targets for novel antimycobacterial therapeutics. However, the use of conventional mammalian models such as mice, are typically expensive, high maintenance, require specialized animal housing, and are ethically regulated. Furthermore, research using Mycobacterium tuberculosis (MTB), is inherently difficult as work needs to be carried out at biosafety level 3 (BSL3). The insect larvae of Galleria mellonella (greater wax moth), have become increasingly popular as an infection model, and we previously demonstrated its potential as a mycobacterial infection model using Mycobacterium bovis BCG. Here we present a novel BSL2 complaint MTB infection model using G. mellonella in combination with a bioluminescent ΔleuDΔpanCD double auxotrophic mutant of MTB H37Rv (SAMTB lux) which offers safety and practical advantages over working with wild type MTB. Our results show a SAMTB lux dose dependent survival of G. mellonella larvae and demonstrate proliferation and persistence of SAMTB lux bioluminescence over a 1 week infection time course. Histopathological analysis of G. mellonella, highlight the formation of early granuloma-like structures which matured over time. We additionally demonstrate the drug efficacy of first (isoniazid, rifampicin, and ethambutol) and second line (moxifloxacin) antimycobacterial drugs. Our findings demonstrate the broad potential of this insect model to study MTB infection under BSL2 conditions. We anticipate that the successful adaptation and implementation of this model will remove the inherent limitations of MTB research at BSL3 and increase tuberculosis research output. |
format | Online Article Text |
id | pubmed-7550006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75500062020-10-22 A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella Asai, Masanori Li, Yanwen Spiropoulos, John Cooley, William Everest, David Robertson, Brian D. Langford, Paul R. Newton, Sandra M. Virulence Research Paper Mammalian infection models have contributed significantly to our understanding of the host-mycobacterial interaction, revealing potential mechanisms and targets for novel antimycobacterial therapeutics. However, the use of conventional mammalian models such as mice, are typically expensive, high maintenance, require specialized animal housing, and are ethically regulated. Furthermore, research using Mycobacterium tuberculosis (MTB), is inherently difficult as work needs to be carried out at biosafety level 3 (BSL3). The insect larvae of Galleria mellonella (greater wax moth), have become increasingly popular as an infection model, and we previously demonstrated its potential as a mycobacterial infection model using Mycobacterium bovis BCG. Here we present a novel BSL2 complaint MTB infection model using G. mellonella in combination with a bioluminescent ΔleuDΔpanCD double auxotrophic mutant of MTB H37Rv (SAMTB lux) which offers safety and practical advantages over working with wild type MTB. Our results show a SAMTB lux dose dependent survival of G. mellonella larvae and demonstrate proliferation and persistence of SAMTB lux bioluminescence over a 1 week infection time course. Histopathological analysis of G. mellonella, highlight the formation of early granuloma-like structures which matured over time. We additionally demonstrate the drug efficacy of first (isoniazid, rifampicin, and ethambutol) and second line (moxifloxacin) antimycobacterial drugs. Our findings demonstrate the broad potential of this insect model to study MTB infection under BSL2 conditions. We anticipate that the successful adaptation and implementation of this model will remove the inherent limitations of MTB research at BSL3 and increase tuberculosis research output. Taylor & Francis 2020-06-24 /pmc/articles/PMC7550006/ /pubmed/32530737 http://dx.doi.org/10.1080/21505594.2020.1781486 Text en © 2020 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 Robertson, Brian D. Langford, Paul R. Newton, Sandra M. A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella |
title | A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella |
title_full | A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella |
title_fullStr | A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella |
title_full_unstemmed | A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella |
title_short | A novel biosafety level 2 compliant tuberculosis infection model using a ΔleuDΔpanCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella |
title_sort | novel biosafety level 2 compliant tuberculosis infection model using a δleudδpancd double auxotroph of mycobacterium tuberculosis h37rv and galleria mellonella |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550006/ https://www.ncbi.nlm.nih.gov/pubmed/32530737 http://dx.doi.org/10.1080/21505594.2020.1781486 |
work_keys_str_mv | AT asaimasanori anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT liyanwen anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT spiropoulosjohn anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT cooleywilliam anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT everestdavid anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT robertsonbriand anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT langfordpaulr anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT newtonsandram anovelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT asaimasanori novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT liyanwen novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT spiropoulosjohn novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT cooleywilliam novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT everestdavid novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT robertsonbriand novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT langfordpaulr novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella AT newtonsandram novelbiosafetylevel2complianttuberculosisinfectionmodelusingadleuddpancddoubleauxotrophofmycobacteriumtuberculosish37rvandgalleriamellonella |