Abstract

Aspergillus fumigatus is an important fungal pathogen that represents a major threat for severely immunocompromised patients. Cases of invasive aspergillosis are associated with a high mortality rate, which reflects the limited treatment options that are currently available. The development of novel therapeutic approaches is therefore an urgent task. An interesting compound is fludioxonil, a derivative of the bacterial secondary metabolite pyrrolnitrin. Both agents possess potent antimicrobial activity against A. fumigatus and trigger a lethal activation of the group III hybrid histidine kinase TcsC, the major sensor kinase of the High Osmolarity Glycerol (HOG) pathway in A. fumigatus. In the current study, we have characterized proteins that operate downstream of TcsC and analyzed their roles in the antifungal activity of fludioxonil and in other stress situations. We found that the SskA-SakA axis of the HOG pathway and Skn7 can independently induce an increase of the internal glycerol concentration, but each of these individual responses amounts for only half of the level found in the wild type. The lethal fludioxonil-induced ballooning occurs in the sskA and the sakA mutant, but not in the skn7-deficient strain, although all three strains show comparable glycerol responses. This indicates that an elevated osmotic pressure is necessary, but not sufficient and that a second, decisive and Skn7-dependent mechanism mediates the antifungal activity. We assume that fludioxonil triggers a reorganization in the fungal cell wall that reduces its rigidity, which in combination with the elevated osmotic pressure executes the lethal expansion of the fungal cells. Two findings link Skn7 to the cell wall of A. fumigatus: (1) the fludioxonil-induced massive increase in the chitin content depends on Skn7 and (2) the skn7 mutant is more resistant to the cell wall stressor Calcofluor white. In conclusion, our data suggest that the antifungal activity of fludioxonil in A. fumigatus relies on two distinct and synergistic processes: A high internal osmotic pressure and a weakened cell wall. The involvement of Skn7 in both processes most likely accounts for its particular importance in the antifungal activity of fludioxonil.

Highlights

  • Group III hybrid histidine kinases (HHK) have been characterized in several pathogenic fungi

  • In order to investigate the role of individual components of the A. fumigatus High Osmolarity Glycerol (HOG) pathway for the antifungal activity of fludioxonil, we have generated single deletion mutants in sskA (Afu5g08390), sakA (Afu1g12940) and skn[7] (Afu6g12522) as well as a double mutant in skn[7] and sakA (Δskn[7] ΔsakA)

  • The damaging activity of fludioxonil is mediated by interference with the fungal two-component signaling, a conserved sensing mechanism that enables fungi to adapt to various stress situations and environmental ­changes[1]

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Summary

Introduction

Group III HHKs have been characterized in several pathogenic fungi. Mutants in the corresponding genes are viable indicating that these proteins are not essentially required under normal lab conditions. Fludioxonil and fenpiclonil are synthetic derivatives of pyrrolnitrin that are more photo-stable and currently used as antifungal agents in agriculture to protect leaves, fruits and seeds at pre- and post-harvest stages. Even though these agents have been utilized for decades, resistance in the field is rarely observed, resistant mutants can be readily isolated under lab ­conditions[7]. These mutants commonly carry point mutations in their group III HHK, which apparently have a negative impact on their overall f­itness[7]. Apart from the classical HOG pathway that runs from SskA to SakA, we have included Skn[7] in this analysis and consider this response regulator as a side branch of the HOG pathway

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