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An anti-bacterial liaison

How communication between lysosomes and mitochondria controls Salmonella growth in macrophages

Freiburg/Würzburg, July 21, 2022 – Macrophages play a central role in our immune response. They can trap and digest invading pathogens. However, specific bacteria such as Salmonella or Mycobacteria can survive the digestive system of macrophages and escape the control of immune cells. Research from the Max Planck Institute of Immunobiology and Epigenetics (MPI-IE) in Freiburg and the Helmholtz Institute for RNA-based Infection Research (HIRI) in Würzburg reveals how different organelle systems communicate to activate a more effective anti-bacterial defense mechanism. Successful elimination of specific bacteria in the phago-lysosomal system depends on a signal controlling mitochondria. The yet unknown phago-lysosome-mitochondria crosstalk in macrophages leads to a better understanding of how immune cells work and may identify new intervention points for treating infectious diseases. 

Macrophages are key cells of our innate immune response. By populating almost all tissues in our body, these cells have an essential role in maintaining our organs in a healthy state, as they constantly remove dying cells or eliminate microbes that have invaded tissues. As cells specialized in eating and devouring, macrophages are exceptionally well adapted to take up, digest and destroy foreign material.

However, certain microorganisms and bacteria such as Salmonella have developed strategies to protect themselves from the macrophages’ digesting attempts, causing severe Typhoid infections and inflammations. Scientists from the Max Planck Institute of Immunobiology and Epigenetics (MPI-IE) in Freiburg and the Helmholtz Institute for RNA-based Infection Research (HIRI) in Würzburg now report in their latest study published in the scientific journal Nature Metabolism how the inter-organellar crosstalk between phago-lysosomes and mitochondria restricts the growth of such bacteria inside macrophages.

Signals from the digestion organelle

The interior of a macrophage, like most other cells, is subdivided into several distinct compartments. These so-called “organelles” each take over specific functions inside the cell, in analogy to the organ systems of humans, which fulfilling specific roles in our body. As professional scavenger cells, macrophages have a very prominent digestion organelle, the phago-lysosome, where engulfed microorganisms are commonly degraded into pieces and become inactivated. “It has long been known that the molecule TFEB (Transcription factor EB) is important for the regulation of the phago-lysosomal system. More recent evidence also suggested that TFEB supports the defense against bacteria,” says Max Planck group leader Angelika Rambold.

She and her team wanted to understand how exactly TFEB mediates its anti-bacterial role in macrophages. They confirmed earlier findings showing that a broad range of microbes, bacterial and inflammatory stimuli activate TFEB and thus the phago-lysosomal system. “It made sense that pathogen signals trigger TFEB as macrophages need a more active digestion system quickly after they devour a meal of bacteria. But, interestingly, the experiments also revealed an additional strong effect of TFEB activation on another intracellular organelle system—mitochondria. This was completely unexpected and novel to us,” says Angelika Rambold.

Instructing mitochondria to increase anti-microbial activity

Mitochondria are best known as “powerhouses of the cell”. Composed of an inner and outer mitochondrial membrane, these organelles are the primary sites of cellular respiration and release energy from nutrients. Moreover, the mitochondria in immune cells were recently identified as sources of anti-microbial metabolites.

By using a broad experimental tool set, including metabolomics, molecular biology, and imaging techniques, the Max Planck researchers identified the pathway controlling an unexpected crosstalk between lysosomes and mitochondria. “Macrophages make use of extensive inter-organellar communication: the lysosome activates TFEB, which shuttles into the nucleus where it controls the transcription of a protein called IRG1. This protein is imported into mitochondria, where it acts as a major enzyme to produce the anti-microbial metabolite itaconate,” explains Angelika Rambold.

Exploiting organelle communication to control bacterial infections

The researchers explored whether they could exploit this newly identified pathway to control bacterial growth. “We speculated that activating this pathway could be used to target certain bacterial species, such as Salmonella,” says Angelika Rambold. “Salmonella can escape the degradation by the phago-lysosomal system. They manage to grow inside macrophages, which can lead to the spreading of these bacteria to several organs in an infected body,” explains Alexander Westermann, HIRI group leader and junior professor at the University of Würzburg.

When the researchers activated TFEB in infected macrophages in mice, the TFEB-Irg1-itaconate pathway inhibited the growth of Salmonella inside the cells. These data show that the lysosome-to-mitochondria interplay represents an antibacterial defense mechanism to protect the macrophage from being exploited as a bacterial growth niche.

In light of the increasing emergence of multi-drug resistant bacteria, with more than 10 million expected deaths per year by 2050 according to the various expert groups, it becomes important to identify new strategies to control bacterial infections that escape immune mechanisms. Utilizing the TFEB-Irg1-itaconate pathway or itaconate itself to treat infections caused by itaconate-sensitive bacteria might be a promising path. According to the scientists from Freiburg and Würzburg, more work, however, is needed to assess whether these new intervention points can be successfully applied to humans.

Original Publication

TFEB induces mitochondrial itaconate synthesis to suppress bacterial growth in macrophages.
Schuster E-M, Epple MW, Glaser KM, Mihlan M, Lucht K, Zimmermann JA, Bremser A, Polyzou A, Obier N, Cabezas-Wallscheid N, Trompouki E, Ballabio A, Vogel J, Buescher JM, Westermann AJ, Rambold AS (2022). Nature Metabolism.

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