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Updated: Aug 17, 2026

Using Mycobacterium smegmatis as a Bioindicator for Zinc-Limited Growth Conditions in Mycobacteria
Published on: September 20, 2024
Porins limit the intracellular persistence of Mycobacterium smegmatis
Soroush Sharbati-Tehrani1, Joachim Stephan2, Gudrun Holland1
1Robert Koch-Institut, Nordufer 20, 13353 Berlin, Germany.
Abstract:
The genus Mycobacterium comprises highly pathogenic as well as opportunistic or apathogenic species exhibiting a great variability with respect to their ability to persist or multiply within monocytic host cells. The impact of the permeability of the mycobacterial outer membrane on intracellular persistence was studied. For this purpose, a Mycobacterium smegmatis mutant with a deletion of the major porin gene mspA and a second mutant lacking mspA and the homologous porin gene mspC were used. Deletion of mspA together with mspC significantly enhanced intracellular persistence in murine bone marrow macrophages, the mouse macrophage cell line J774A.1 and Acanthamoeba castellanii. Complementation of mspA in the porin mutant strains resulted in restoration of the wild-type phenotype with respect to intracellular persistence. This is the first report to show that the deletion of porins of mycobacteria results in improved persistence in eukaryotic cells, demonstrating that the intracellular persistence of M. smegmatis depends upon the permeability of the outer membrane.
Insights
Deleting porin genes in Mycobacterium smegmatis enhances its ability to survive inside host cells. This suggests that the outer membrane
Area of Science:
- Microbiology
- Cell Biology
- Immunology
Background:
- Mycobacterium species display varied abilities to persist within host cells.
- The mycobacterial outer membrane's role in intracellular survival is not fully understood.
Purpose of the Study:
- To investigate the impact of outer membrane permeability on intracellular persistence of Mycobacterium smegmatis.
- To determine if porin deletions affect mycobacterial survival in eukaryotic cells.
Main Methods:
- Generated Mycobacterium smegmatis mutants with deletions in porin genes mspA and mspC.
- Assessed intracellular persistence of wild-type and mutant strains in murine macrophages and Acanthamoeba castellanii.
- Complemented the mspA deletion to confirm gene function.
Main Results:
- Deletion of both mspA and mspC significantly enhanced intracellular persistence.
- Complementation restored wild-type levels of persistence.
- Outer membrane permeability is critical for M. smegmatis intracellular survival.
Conclusions:
- Porin-mediated permeability of the mycobacterial outer membrane is essential for limiting intracellular persistence.
- Targeting porins could be a strategy to control mycobacterial infections.
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