Related Experiment Video
Updated: Sep 26, 2026

Measuring Bacterial Load and Immune Responses in Mice Infected with Listeria monocytogenes
Published on: August 9, 2011
Low-level iron-dependent mutants of Listeria monocytogenes and their virulence in macrophages
Philippe Andre1, Stéphanie Oberle, Véronique Specklin
1Laboratoire de Bactériologie et Cryptogamie INSERM U-392, Université Louis Pasteur, U.F.R. des Sciences Pharmaceutiques, 74 route du Rhin, B.P. 24, F-67401 Illkirch cedex, France. andre@pharma.u-strasbg.fr
Abstract:
Listeria monocytogenes is an opportunistic intracellular pathogen capable of growth that requires iron for growth within phagocytic cells and virulence expression. In the presence of an appropriate concentration tropolone, an iron-chelating agent, growth of L. monocytogenes is completely inhibited. However, this inhibition can be relieved by addition of dopamine, norepinephrine, or ferric citrate. By selection on streptonigrin medium supplemented with tropolone and norepinephrine, we have obtained two spontaneous mutants, Lm-8 and Lm-15, with the same iron dependence but lower iron dependence than the wild-type Lm-B38. The association between iron requirement and virulence of the two mutants and the wild type was studied in the J774 macrophage cell line. One hour after phagocytosis by the J774 macrophage cell line, the two mutants and the parental strain displayed no difference in the number of phagocytosed bacteria. Twenty-four hours after phagocytosis, the number of bacteria within the surviving macrophages was identical for the wild strain and the two clones. However, only 40% of macrophage cells infected with Lm-8 and 90% of those infected with Lm-15 were alive after 24 h in comparison with macrophage cells infected with the parental strain Lm-B38. These data demonstrate that there is no direct correlation between iron requirement and virulence of L. monocytogenes in the J774 macrophage cell line.
Insights
Iron is essential for Listeria monocytogenes growth and virulence. Mutants with altered iron dependence showed reduced virulence in macrophages, indicating no direct correlation between iron requirement and pathogenicity.
Area of Science:
- Microbiology
- Pathogen-host interactions
- Bacterial physiology
Background:
- Listeria monocytogenes requires iron for intracellular growth and virulence.
- Iron chelators like tropolone inhibit L. monocytogenes growth.
- This inhibition can be reversed by iron sources or specific compounds.
Purpose of the Study:
- To investigate the relationship between iron requirement and virulence in Listeria monocytogenes.
- To characterize spontaneous mutants with altered iron dependence.
Main Methods:
- Generation of spontaneous mutants (Lm-8, Lm-15) with reduced iron dependence using streptonigrin and tropolone.
- Assessment of bacterial uptake and survival within J774 macrophage cell line.
- Evaluation of macrophage viability post-infection with wild-type and mutant strains.
Main Results:
- Mutants Lm-8 and Lm-15 exhibited reduced iron dependence compared to wild-type Lm-B38.
- No significant difference in initial phagocytosis or intracellular bacterial numbers was observed between strains.
- Macrophage survival was significantly lower in cultures infected with mutants Lm-8 (40% survival) and Lm-15 (90% survival) compared to wild-type Lm-B38 (100% survival).
Conclusions:
- There is no direct correlation between the iron requirement of Listeria monocytogenes and its virulence in the J774 macrophage model.
- Altered iron metabolism in mutants may impact host cell interactions differently than initially hypothesized.
Related Concept Videos
Regulation of Bacterial Virulence
Colonisation of Pathogens

