|KODIN, KAROLINA - Longwood University|
Submitted to: American Society of Horticulture Science Meeting
Publication Type: Abstract Only
Publication Acceptance Date: 4/24/2015
Publication Date: 8/7/2015
Citation: Kisha, T.J., Kodin, K. 2105. Genetic variation in the USDA Chamaecrista Fasciculata collection. American Society of Horticulture Science Meeting. meeting abstract.
Technical Abstract: North American wild kidney bean or thicket bean (Phaseolus polystachios (L.) Britton, Sterns, & Poggenb.) is a perennial vine found in the eastern United States from Texas to Connecticut. Habitat destruction and urbanization are limiting its distribution: e.g., it was once prevalent in the Detroit River International Wildlife Refuge, but has not been seen there since the late 1800’s. Crop wild relatives are a critical source of genetic diversity, often holding untapped genes for breeding of domesticated plants in agriculture for disease resistance, yield, quality, and adaptation to climate change, as well as ecologically important members of natural habitat. The closest cultivated relative of P. polystachios is P. lunatus, the lima bean. Through coevolution in its natural habitat, P. polystachios may have acquired true resistance to the ubiquitous pathogen white mold (Sclerotinia sclerotiorum) and provide a source for interspecific transfer. The Western Regional Plant Introduction Station of the National Plant Germplasm System holds over 17,000 accessions of Phaseolus from 47 species groups, but has only 10 accessions of the wild Phaseolus polystachios, 5 of which were only recently collected in Florida. Planning is underway for a collection trip throughout the Midwest to increase the diversity of P. polystachios within the collection. Understanding genetic diversity is critical for identifying areas to target for recovering maximum genetic representation. Molecular markers are an important tool for analyzing the extent and distribution of genetic diversity within and among wild populations and are important for identifying geographic gaps for collecting underrepresented genotypes. We analyzed nine accessions from the USDA collection along with sixteen herbarium samples provided by the Smithsonian Institution using 231 AFLP molecular markers from six primer combinations. While the DNA from the herbarium samples was somewhat degraded, markers at and below 200 bp were readily discernible and showed four distinct clusters. One herbarium sample from Florida was distinct from the others and, because of the lobed leaves, is likely P. smilacifolius. The USDA accession from Texas was very unique and has been reclassified as P. texensis. The level of distinction among the samples studied here reinforces the need for continued collection of this diverse species.