Identification of a fungal antibacterial endopeptidase that cleaves peptidoglycan

Zugehörigkeit
Microbial Immunology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Machata, Silke;
ORCID
0000-0002-1897-5557
Zugehörigkeit
University of Hohenheim Core Facility - Module 1 Mass Spectrometry Unit Stuttgart Germany
Bertsche, Ute;
GND
1179981464
Zugehörigkeit
Department of Otorhinolaryngology Jena University Hospital Jena Germany
Hoffmann, Franziska;
Zugehörigkeit
Microbial Immunology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Fattal, Zaher M;
ORCID
0009-0003-3681-3433
Zugehörigkeit
Microbial Immunology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Kage, Franziska;
Zugehörigkeit
Molecular and Applied Microbiology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Flak, Michal;
Zugehörigkeit
Evolution of Microbial Interactions Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Iliou, Alexander N J;
ORCID
0000-0002-5493-930X
Zugehörigkeit
Evolution of Microbial Interactions Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Hillmann, Falk;
GND
1236649745
ORCID
0000-0002-8062-6999
Zugehörigkeit
Department of Otorhinolaryngology Jena University Hospital Jena Germany
von Eggeling, Ferdinand;
Zugehörigkeit
Department of Respiratory Medicine and Infectious Diseases Hannover Medical School, German Center for Lung Research (DZL), BREATH Hannover Germany
Slevogt, Hortense;
GND
1138445681
ORCID
0000-0002-8814-4193
Zugehörigkeit
Molecular and Applied Microbiology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Brakhage, Axel A;
GND
130267279
ORCID
0000-0002-6033-9984
Zugehörigkeit
Microbial Immunology Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute Jena Germany
Jacobsen, Ilse D

Abstract Aspergillus fumigatus is a saprophytic fungus dwelling in soil and on decaying plant material, but also an opportunistic pathogen in immunocompromised patients. In its environmental niche, A. fumigatus faces competition from other microorganisms including bacteria. Here, we describe the discovery of the first secreted antibacterial protein in A. fumigatus . We identify a secreted fungal endopeptidase, designated CwhA, that cleaves peptidoglycan of Gram-positive bacteria at specific residues within the peptidoglycan stem peptide. Cleavage leads to bacterial lysis and the release of peptidoglycan cleavage products. Expression of cwhA is induced by the presence of bacteria. Furthermore, CwhA is highly abundant in murine lungs during invasive pulmonary aspergillosis and peptidoglycan cleavage products generated by CwhA stimulate cytokine production of human immune cells in vitro. Although CwhA does not affect human cells directly, this novel player in fungal-bacterial interactions could affect A. fumigatus infections by inhibiting Gram-positive bacteria in its vicinity, and possibly modulate the immune system.

Synopsis CwhA, a secreted endopeptidase from Aspergillus fumigatus , targets bacterial peptidoglycan and lyses Gram-positive bacteria. Induced within the lung and by bacterial contact, CwhA may enable A. fumigatus to shape its microbial environment. Aspergillus fumigatus expresses CwhA inside the host and upon contact with bacteria, but not in liquid culture. CwhA is an endopeptidase cleaving peptidoglycan of Gram-positive bacteria with L-lysine at position 3 of the stem peptide. CwhA is not toxic to amoeba, host cells and fungal cells but can lead to lysis of Gram-positive bacteria. Peptidoglycan cleavage products can be recognized by the host and lead to cytokine production of TNFα and IL-1β.

CwhA, a secreted endopeptidase from Aspergillus fumigatus , targets bacterial peptidoglycan and lyses Gram-positive bacteria. Induced within the lung and by bacterial contact, CwhA may enable A. fumigatus to shape its microbial environment.

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