Optimizing molecular assays for glyphosate and ALS-inhibitor resistance diagnostics in four weed species

Abstract

Herbicide-resistant weeds pose a threat to food production in modern agriculture, causing US$32 billion dollars in crop production losses worldwide. In Michigan, highly troublesome and widespread weeds include waterhemp, Palmer amaranth, common ragweed, and horseweed, with accessions that are resistant to glyphosate (Group 9) and ALS-inhibitors (Group 2), major herbicide sites of action utilized in soybean and corn cropping systems. Molecular assays for rapid resistance diagnostics to confirm the in-field status of herbicide resistance can assist with more effective, timely, and proactive management. In this research, we developed and tested PCR-based assays to identify target-site resistance mechanisms to both herbicide groups through Sanger sequencing and EPSPS copy number variation. Nine different SNPs were identified in five ALS positions known to confer herbicide resistance among all species surveyed. Pro197Ser was the most frequent in horseweed and common ragweed accessions, whereas Trp574Leu was the predominant mutation in Palmer amaranth and waterhemp. Four horseweed accessions contained the Pro106Ser mutation in the EPSPS gene, which confers resistance to glyphosate. Additionally, waterhemp and Palmer amaranth had 2-7 and 20-160 copies of EPSPS, respectively. The assays were validated by comparing genotyping of several field-collected accessions of unknown resistance status with known resistant and susceptible accessions. The efficacy of genotyping assays was > 98%, and required only two days, confirming that molecular assays are a robust tool for rapid resistance diagnostics. These assays can help growers evaluate herbicide resistance status in weed populations within the same growing season, allowing them to adopt effective management practices.