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Galleria mellonella as an infection model for the virulent Mycobacterium tuberculosis H37Rv
被引:8
作者:
Asai, Masanori
[1
]
Li, Yanwen
[1
]
Spiropoulos, John
[2
]
Cooley, William
[2
]
Everest, David J.
[2
]
Kendall, Sharon L.
[3
]
Martin, Carlos
[4
]
Robertson, Brian D.
[5
]
Langford, Paul R.
[1
]
Newton, Sandra M.
[1
]
机构:
[1] Imperial Coll London, Dept Infect Dis, Sect Paediat Infect Dis, London, England
[2] Anim & Plant Hlth Agcy, Dept Pathol, Addlestone, Surrey, England
[3] Royal Vet Coll, Ctr Emerging Endem & Exot Dis Pathobiol & Populat, Hartfield, England
[4] Univ Zaragoza, Dept Microbiol, Fac Med, Zaragoza, Spain
[5] Imperial Coll London, MRC Ctr Mol Bacteriol & Infect, Dept Infect Dis, London, England
来源:
基金:
英国国家替代、减少和改良动物研究中心;
关键词:
Tuberculosis;
Mycobacterium tuberculosis;
Galleria mellonella;
infection model;
innate immunity;
mycobacteria;
GREATER WAX MOTH;
IN-VITRO;
HOST;
LARVAE;
IDENTIFICATION;
NODULATION;
HEMOCYTES;
DELETION;
IMMUNITY;
SYSTEM;
D O I:
10.1080/21505594.2022.2119657
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
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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页码:1543 / 1557
页数:15
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