MaNmrA, a Negative Transcription Regulator in Nitrogen Catabolite Repression Pathway, Contributes to Nutrient Utilization, Stress Resistance, and Virulence in Entomopathogenic Fungus Metarhizium acridum

• Published in: Biology (Basel, Switzerland) Switzerland), 2021-11, Vol.10 (11), p.1167
• Main Authors: Li, Chaochuang, Zhang, Qipei, Xia, Yuxian, Jin, Kai
• Format: Article
• Language: English
• Subjects: Adaptability; Agricultural production; Bacteria; Binding sites; Carbon; Carbon sources; Catabolite repression; Cell walls; Cognition; Conserved sequence; Entomopathogenic fungi; Fungi; Genes; Germination; Hemolymph; Hydrogen peroxide; Infections; Inoculation; MaNmrA; Mannose; Metabolism; Metabolites; Metarhizium acridum; NAD; NADP; Nitrogen; Nitrogen sources; Nutrient utilization; nutrition utilization; Oxidative stress; Pathogenicity; Proteins; Sorbitol; stress response; Sucrose; Transcription; Transcription factors; Trehalose; Turgor; Virulence
• ISSN: 2079-7737; 2079-7737
• DOI: 10.3390/biology10111167

The NCR pathway plays an important regulatory role in the nitrogen metabolism of filamentous fungi. NmrA, a central negative regulatory protein in the NCR pathway and a key factor in sensing to the carbon metabolism, plays important roles in pathogenic fungal nutrition metabolism. In this study, we characterized the functions of MaNmrA in the insect pathogenic fungus M. acridum. Multiple sequence alignments found that the conserved domain (NAD/NADP binding domain) of MaNmrA was highly conservative with its homologues proteins. Deletion of MaNmrA improved the utilization of multiple carbon sources (such as glucose, mannose, sucrose, and trehalose) and non-preferred nitrogen sources (such as NaNO3 and urea), significantly delayed the conidial germination rate and reduced the conidial yield. The MaNmrA-disruption strain (ΔMaNmrA) significantly decreased tolerances to UV-B and heat-shock, and it also increased the sensitivity to the hypertonic substance sorbitol, oxygen stress substance H2O2, and cell wall destroyer calcofluor white, indicating that loss of MaNmrA affected cell wall integrity, tolerances to hypertonic and oxidative stress. Bioassays demonstrated that disruption of MaNmrA decreased the virulence in both topical inoculation and intrahemocoel injection tests. Further studies revealed that the appressorium formation, turgor pressure, and colonization in hemolymph were significantly reduced in the absence of MaNmrA. Our work will deepen the functional cognition of MaNmrA and make a contribution to the study of its homologous proteins.