Distinct responses of oomycete plant parasites according to their lifestyle in a landscape-scale metabarcoding survey

Oomycetes are an ubiquitous protistan lineage including devastating crop parasites. Although their ecology in agrosystems has been widely studied, little is known of their distribution in natural and semi-natural ecosystems. We provide here a baseline of the diversity and distribution of soil oomycetes, classified by lifestyles (biotrophy, hemibiotrophy and saprotrophy), at the landscape scale in temperate grassland and forest. From 600 soil samples, we obtained 1,148 Operational Taxonomy Units representing ∼20 million Illumina reads (region V4, 18S rRNA gene). We found a majority of hemibiotrophic plant pathogens, which are parasites spending part of their life cycle as saprotrophs after the death of the host. Overall both grassland and forest constitute an important reservoir of plant pathogens. In forests, relative abundances of obligate biotrophs and hemibiotrophs differed between regions and showed opposite responses to edaphic conditions and human-induced management intensification, suggesting different ecological requirements for these two functional guilds.

Whole-Genome Sequence of the Phlox Powdery Mildew Pathogen Golovinomyces magnicellulatus Strain FPH2017-1

Powdery mildew (PM) fungi are obligate biotrophs capable of infecting diverse plant hosts, ranging from monocotyledonous agricultural crops to dicotyledonous ornamental crops. The PM lifestyle poses significant challenges for studying these pathogens in isolation from their host. We present a draft genome of Golovinomyces magnicellulatus, a host-specific PM on Phlox species.

Signatures of Adaptation to Obligate Biotrophy in the Hyaloperonospora arabidopsidis Genome

Many oomycete and fungal plant pathogens are obligate biotrophs, which extract nutrients only from living plant tissue and cannot grow apart from their hosts. Although these pathogens cause substantial crop losses, little is known about the molecular basis or evolution of obligate biotrophy. Here, we report the genome sequence of the oomycete Hyaloperonospora arabidopsidis (Hpa), an obligate biotroph and natural pathogen of Arabidopsis thaliana. In comparison with genomes of related, hemibiotrophic Phytophthora species, the Hpa genome exhibits dramatic reductions in genes encoding (i) RXLR effectors and other secreted pathogenicity proteins, (ii) enzymes for assimilation of inorganic nitrogen and sulfur, and (iii) proteins associated with zoospore formation and motility. These attributes comprise a genomic signature of evolution toward obligate biotrophy.