Arginine Auxotrophy Affects Siderophore Biosynthesis and Attenuates Virulence of <i>Aspergillus fumigatus</i>

• Main Authors: Anna-Maria Dietl, Ulrike Binder, Ingo Bauer, Yana Shadkchan, Nir Osherov, Hubertus Haas
• Format: Article
• Language: English
• Published: MDPI AG 2020-04-01
• Series: Genes
• Subjects: <i>Aspergillus fumigatus</i>; virulence; arginine; ornithine; siderophores
• Online Access: https://www.mdpi.com/2073-4425/11/4/423

<i>Aspergillus fumigatus</i> is an opportunistic human pathogen mainly infecting immunocompromised patients. The aim of this study was to characterize the role of arginine biosynthesis in virulence of <i>A. fumigatus</i> via genetic inactivation of two key arginine biosynthetic enzymes, the bifunctional acetylglutamate synthase/ornithine acetyltransferase (<i>argJ</i>/AFUA_5G08120) and the ornithine carbamoyltransferase (<i>argB</i>/AFUA_4G07190). Arginine biosynthesis is intimately linked to the biosynthesis of ornithine, a precursor for siderophore production that has previously been shown to be essential for virulence in <i>A. fumigatus</i>. ArgJ is of particular interest as it is the only arginine biosynthetic enzyme lacking mammalian homologs. Inactivation of either ArgJ or ArgB resulted in arginine auxotrophy. Lack of ArgJ, which is essential for mitochondrial ornithine biosynthesis, significantly decreased siderophore production during limited arginine supply with glutamine as nitrogen source, but not with arginine as sole nitrogen source. In contrast, siderophore production reached wild-type levels under both growth conditions in ArgB null strains. These data indicate that siderophore biosynthesis is mainly fueled by mitochondrial ornithine production during limited arginine availability, but by cytosolic ornithine production during high arginine availability via cytosolic arginine hydrolysis. Lack of ArgJ or ArgB attenuated virulence of <i>A. fumigatus</i> in the insect model <i>Galleria mellonella</i> and in murine models for invasive aspergillosis, indicating limited arginine availability in the investigated host niches.