Department of Plant Pathology
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The Department of Plant Pathology at the University of Minnesota has a strong research and teaching emphasis in disease resistance, molecular genetics and genomics, control of diseases caused by biotic pathogens, wood deterioration, effect of air pollution on plants, biological control, ecology and evolution of plant-associated microbes, and in the physiology and molecular biology of plant-microbe interactions. The department also has a strong outreach emphasis through the extension service, plant disease clinic, and other avenues.
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Browsing Department of Plant Pathology by Type "Presentation"
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Item Alfalfa leaf protein concentrate: A sustainable protein source for aquaculture feeds(2019) Samac, Deborah A; Coburn, Jessica E M; Phelps, Nicholas; Wells, M ScottInterest in local, sustainable aquaculture is continuing to expand across the United States. To ensure profitability and high consumer acceptance, a plant-based non-GMO source of protein is needed for replacing fishmeal in aquaculture diets. Most replacements in current use are derived from seeds, and often contain undesirable antinutritional components. Alfalfa (Medicago sativa) is a high biomass perennial legume that is grown across the U.S. for use in animal feeds. We evaluated the yield and composition of protein concentrates derived from fresh alfalfa foliage. Furthermore, a commercial alfalfa protein concentrate (APC) was used to replace fishmeal in diets for yellow perch (Perca flavescens) and rainbow trout (Oncorhynchus mykiss). Weight gains, growth rate, and feed conversion ratios were measured.Item Genome editing in alfalfa (Medicago sativa) to hyper-accumulate phosphate(2019) Samac, Deborah A; Miller, Susan S; Dornbusch, Melinda R; Curtin, Shaun JRock phosphate, the main source of phosphate (P) for crop fertilizers, is a finite resource that is predicted to be depleted in 50-100 years. P is a critical nutrient in agriculture and its application can dramatically improve plant productivity. However, many soils have excess amounts of P from application of animal manures and runoff of phosphate from agricultural lands is the major source of nonpoint water pollution in the Midwestern US. The goal of this project is to create mutations by gene editing in the ubiquitin E2 conjugating enzyme PHO2, involved in P signaling and P homeostasis in alfalfa so that plants hyper-accumulate phosphate. Such plants could be used to reduce soil P levels and reclaim P for use as a fertilizer. From a draft diploid Medicago sativa genome scaffold sequence and the alfalfa transcriptome database (AGED), three PHO2 genes were identified. The genes, two of which are >99% homologous (a/b), each have seven exons interspersed by six introns. The open reading frames are 912 amino acids except when an alternate splice site is used in a/b gene transcript resulting in a 902 amino acid sequence. Alfalfa plants grown under P limiting conditions expressed low levels of the a/b transcripts with higher levels seen for PHO2c, while application of higher P induced increased expression mainly of the a/b transcripts. Under high P conditions, roots and shoots accumulated 4.1x and 2.5x more P than in low P conditions, respectively. An initial CRISPR/Cas9/Cys4 reagent targeting all three genes was generated and used to transform alfalfa cv. RegenSY. A total of 67 verified transgenic plants were screened by acrylamide gel shift assays, cloning, and sequencing to identify plants with mutations. Mutations ranging from a 1 bp insertion to a 25 bp deletion were identified in a total of 10 plants and some plants had multiple targets hit. Recently, a second attempt at CRISPR/Cas9 mutation utilized a cassette vector system with either the tRNA or Cys4 splicing system and exonuclease components. Initial screening results indicate that the tRNA splicing system may have yielded greater numbers of mutations. TaqMan probes were designed to identify plants with changes in the target sites and were verified by restriction digestions, cloning, and sequencing. Data on inheritance of mutations and phosphate accumulation in edited plants will be presented. The results of these experiments demonstrate that editing of multiple targets can be accomplished in alfalfa, although the tetraploid inheritance of genes complicates analysis.Item Lignin reduction in alfalfa (Medicago sativa) does not affect foliar disease resistance(2018) Samac, Deborah A; Ao, Samadangla; Dornbusch, Melinda R; Grev, Amanda M; Wells, M Scott; Martinson, Krishona; Sheaffer, Craig CDisruptions in the lignin biosynthetic pathway have been shown to reduce disease resistance in a number of crops. Recently, genetically modified alfalfa (Medicago sativa) varieties have been marketed with reduced lignin and improved forage quality traits, including increased digestibility by ruminants at later stages of plant maturity. The objective of this study was to compare foliar disease resistance in three reference alfalfa varieties, 54R02, DKA43-22RR, WL355.RR, and the reduced lignin variety, 54HVX41, to evaluate the effect of the reduced lignin trait on foliar disease resistance. Alfalfa plants in research plots at three locations in Minnesota were evaluated for percent defoliation caused by foliar pathogens at four maturity stages; early bud, bud, early flower, and flowering; with natural inoculum. Spring black stem and leaf spot, Leptosphaerulina leaf spot, and common leaf spot were observed from June through September in all locations on all varieties. Summer black stem and leaf spot was most prevalent in August on all varieties at one location. The amount of defoliation increased with maturity stage for all varieties. When harvest was delayed until the flowering stage, moderate to severe (32 to 64%) leaf loss occurred, depending on location. Alfalfa varieties did not differ in percent defoliation at any maturity stage indicating that the reduced lignin trait did not affect foliar disease resistance.