PsAAT3, an oomycete-specific aspartate aminotransferase, is required for full pathogenicity of the oomycete pathogen Phytophthora sojae

Fungal Biol. 2016 Apr;120(4):620-630. doi: 10.1016/j.funbio.2016.01.005. Epub 2016 Jan 18.

Abstract

Pathogen nutrient acquisition and metabolism are critical for successful infection and colonization. However, the nutrient requirements and metabolic pathways related to pathogenesis in oomycete pathogens are unknown. In this study, we bioinformatically identified Phytophthora sojae aspartate aminotransferases (AATs), which are key enzymes that coordinate carbon and nitrogen metabolism. We demonstrated that P. sojae encodes more AATs than the analysed fungi. Some of the AATs contained additional prephenate dehydratase and/or prephenate dehydrogenase domains in their N-termini, which are unique to oomycetes. Silencing of PsAAT3, an infection-inducible expression gene, reduced P. sojae pathogenicity on soybean plants and affected the growth under N-starving condition, suggesting that PsAAT3 is involved in pathogen pathogenicity and nitrogen utilisation during infection. Our results suggest that P. sojae and other oomycete pathogens may have distinct amino acid metabolism pathways and that PsAAT3 is important for its full pathogenicity.

Keywords: Amino acid metabolism; Aspartate aminotransferase; Oomycetes; Phytophthora.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspartate Aminotransferases / genetics
  • Aspartate Aminotransferases / metabolism*
  • Computational Biology
  • Gene Knockdown Techniques
  • Glycine max / microbiology*
  • Nitrogen / metabolism
  • Phytophthora / enzymology*
  • Phytophthora / genetics
  • Phytophthora / growth & development
  • Phytophthora / pathogenicity*
  • Plant Diseases / microbiology*
  • Protein Domains

Substances

  • Aspartate Aminotransferases
  • Nitrogen