Researchers at CSU and University of Minnesota have developed a DNA genotyping assay that identifies the presence of Palmer amaranth seeds in a mixture of seeds, for the purpose of detecting noxious weed seed contamination. The test can be used by seed producers to determine if their seed may be sold in locations were Palmer amaranth (Ameranthus palmeri) is a prohibited noxious weed, and they must certify their clean seed.
Amaranthus is a genus of between 60-70 annual or short-lived perennial plants and include many classifications. Some amaranth species are cultivated as leaf vegetables, pseudocereals, and ornamental plants. Unfortunately, some amaranth species are extremely invasive and are classified as noxious weeds, such as Palmer amaranth. This weed poses a serious economic threat to crops such as corn and soybeans and is classified as a prohibited noxious weed in multiple Midwestern states.
Thus, several states that are experiencing large crop loss due to Palmer amaranth require certified Palmer amaranth-free seed to be able to grow any amaranth type. Seed producers and sellers must test their seeds and seed mixtures to prove there is no threat of such an invasive weed in them, as all of the Amaranthus genus have very similar, small black seeds and it is impossible to visually distinguish the species. Typical testing involves growing a sample of seeds to show plant identification, which is slow and unreliable. Other testing offered includes testing individual seeds using DNA sequencing, which is expensive and burdensome. There is a need for a highly sensitive, specific field assay for the detection of Palmer amaranth seeds in a mixture of other Amaranthus seeds and debris.
Researchers have identified several single nucleotide polymorphisms (SNPs) that can be used to identify Palmer amaranth from a mixed pool of Amaranthus species DNA. This assay is more accurate and robust than any commercially available test. By using these SNPs, this assay is capable of detecting Amaranthus species from multiple geographic locations, including regional US populations as well as South American and African populations. Furthermore, the test is easy to perform and more efficient that other molecular diagnostic tests available for Palmer amaranth detection.
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TRL: 6
US 9,963,750
US 11,866,793
Todd Gaines
Eric Patterson
Crystal Sparks
Anthony Brusa
Kevin Dorn
Jessy McGowan
Jessy.McGowan@colostate.edu
970-491-7100