Phytophthora infestans is the most destructive pathogen of potato and a model organism for the oomycetes, a distinct lineage of fungus-like eukaryotes that are related to organisms such as brown algae and diatoms. As the agent of the Irish potato famine in the mid-nineteenth century, P. infestans has had a tremendous effect on human history, resulting in famine and population displacement. To this day, it affects world agriculture by causing the most destructive disease of potato, the fourth largest food crop and a critical alternative to the major cereal crops for feeding the world's population. Current annual worldwide potato crop losses due to late blight are conservatively estimated at $6.7 billion. Management of this devastating pathogen is challenged by its remarkable speed of adaptation to control strategies such as genetically resistant cultivars. Here we report the sequence of the P. infestans genome, which at approximately 240 megabases (Mb) is by far the largest and most complex genome sequenced so far in the chromalveolates. Its expansion results from a proliferation of repetitive DNA accounting for approximately 74% of the genome. Comparison with two other Phytophthora genomes showed rapid turnover and extensive expansion of specific families of secreted disease effector proteins, including many genes that are induced during infection or are predicted to have activities that alter host physiology. These fast-evolving effector genes are localized to highly dynamic and expanded regions of the P. infestans genome. This probably plays a crucial part in the rapid adaptability of the pathogen to host plants and underpins its evolutionary potential.
Summary: Genome sequences of the soybean pathogen, Phytophthora sojae, and the sudden oak death pathogen, Phytophthora ramorum, suggest a photosynthetic past and reveal recent massive expansion and diversification of potential pathogenicity gene families.Abstract: Draft genome sequences of the soybean pathogen, Phytophthora sojae, and the sudden oak death pathogen, Phytophthora ramorum, have been determined. Oömycetes
Oomycetes form a deep lineage of eukaryotic organisms that includes a large number of plant pathogens which threaten natural and managed ecosystems. We undertook a survey to query the community for their ranking of plant-pathogenic oomycete species based on scientific and economic importance. In total, we received 263 votes from 62 scientists in 15 countries for a total of 33 species. The Top 10 species and their ranking are: (1) Phytophthora infestans; (2, tied) Hyaloperonospora arabidopsidis; (2, tied) Phytophthora ramorum; (4) Phytophthora sojae; (5) Phytophthora capsici; (6) Plasmopara viticola; (7) Phytophthora cinnamomi; (8, tied) Phytophthora parasitica; (8, tied) Pythium ultimum; and (10) Albugo candida. This article provides an introduction to these 10 taxa and a snapshot of current research. We hope that the list will serve as a benchmark for future trends in oomycete research.
The oomycete vegetable pathogen Phytophthora capsici has shown remarkable adaptation to fungicides and new hosts. Like other members of this destructive genus, P. capsici has an explosive epidemiology, rapidly producing massive numbers of asexual spores on infected hosts. In addition, P. capsici can remain dormant for years as sexually-recombined oospores, making it difficult to produce crops at infested sites, and allowing outcrossing populations to maintain significant genetic variation. Genome sequencing, development of a high-density genetic map, and integrative genomic/genetic characterization of P. capsici field isolates and intercross progeny revealed significant mitotic loss of heterozygosity (LOH) and higher levels of SNVs than those reported for humans, plants, and P. infestans. LOH was detected in clonally propagated field isolates and sexual progeny, cumulatively affecting >30% of the genome. LOH altered genotypes for more than 11,000 single nucleotide variant (SNV) sites and showed a strong association with changes in mating type and pathogenicity. Overall, it appears that LOH may provide a rapid mechanism for fixing alleles and may be an important component of adaptability for P. capsici.
This chapter describes the symptoms caused by various Phytophthora species on broadleaved tree hosts and overviews disease distributions across Europe. In addition, a historical perspective is provided and potential pathways and triggering factors are discussed. The ink disease of chestnut, beech (Fagus sylvatica) decline, oak decline, root and collar rot epidemic of alders are also discussed.
The potential for outcrossing, occurrence of oospores, and inheritance of mefenoxam sensitivity was assessed in naturally occurring populations of Phytophthora capsici. Between 1997 and 1998, 14 farms were sampled, with 473 isolates recovered from cucurbit hosts and 30 from bell pepper. The A1 and A2 compatibility types were recovered in a roughly 1:1 ratio in 8 of 14 farms with sample sizes larger than 15. In 1997, one isolate was designated as insensitive and four as sensitive to mefenoxam. In 1998, 55% of the 498 isolates sampled were sensitive, 32% were intermediate, and 13% were fully insensitive to mefenoxam. In vitro characterization of mefenoxam sensitivity was conducted by crossing field isolates. Chi-square analysis of crosses between sensitive, intermediately sensitive, and insensitive isolates indicate that mefenoxam insensitivity segregated as an incompletely dominant trait unlinked to compatibility type (P = 0.05). Oospores were observed in diseased cucurbit fruit from four farms in 1998, and 223 oospore progeny were recovered from a single diseased cucumber. All six mefenoxam sensitivity-compatibility type combinations were present in these oospore progeny and within single fields. Based on these findings, we conclude that oospores likely play a role in the survival of P. capsici and that sexual recombination may significantly influence population structure.
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