4.6 Article

Three Small Cysteine-Free Proteins (CFP1-3) Are Required for Insect-Pathogenic Lifestyle of Metarhizium robertsii

Journal

JOURNAL OF FUNGI
Volume 8, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/jof8060606

Keywords

Hypocreales; asexual insect pathogens; cysteine-free proteins; gene expression and regulation; insect pathogenicity; insecticidal activity

Funding

  1. National Natural Science Foundation of China [31772218]
  2. Zhejiang Provincial RD Program [2022C02058]

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This study identified a unique protein called CFP as a virulence factor in Beauveria bassiana, a main source of fungal insecticides. The study also showed the essential roles of CFP homologs in Metarhizium robertsii in cuticle infection and virulence. Transcriptomic analysis revealed dysregulation of genes involved in virulence-related processes, providing insight into genetic improvement of fungal insecticidal activity.
Unique CFP (cysteine-free protein; 120 aa) has been identified as an extraordinary virulence factor in Beauveria bassiana (Cordycipitaceae), a main source of wide-spectrum fungal insecticides. Its homologs exclusively exist in wide-spectrum insect pathogens of Hypocreales, suggesting their importance for a fungal insect-pathogenic lifestyle. In this study, all three CFP homologs (CFP1-3, 128-145 aa) were proven essential virulence factors in Metarhizium robertsii (Clavicipitaceae). Despite limited effects on asexual cycles in vitro, knockout mutants of cfp1, cfp2 and cfp3 were severely compromised in their capability for normal cuticle infection, in which most tested Galleria mellonella larvae survived. The blocked cuticle infection concurred with reduced secretion of extracellular enzymes, including Pr1 proteases required cuticle penetration. Cuticle-bypassing infection by intrahemocoel injection of similar to 250 conidia per larva resulted in a greater reduction in virulence in the mutant of cfp1 (82%) than of cfp2 (21%) or cfp3 (25%) versus the parental wild-type. Transcriptomic analysis revealed dysregulation of 604 genes (up/down ratio: 251:353) in the Delta cfp1 mutant. Many of them were involved in virulence-related cellular processes and events aside from 154 functionally unknown genes (up/down ratio: 56:98). These results reinforce the essential roles of small CFP homologs in hypocrealean fungal adaptation to insect-pathogenic lifestyle and their exploitability for the genetic improvement of fungal insecticidal activity.

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