Updated June 16, 2024:
Uniform foliar fungicide trials have been planted at 15 locations across 11 states (AL, AR, DE, KY, LA, MS, NC, PA, TN, VA, WI). Growth stages at these locations vary from just recently planted to approaching R2 development stage. At least one location for each participating state has already or will be soon deploying spore traps at two different heights within a "no fungicide" area of the field. The spores will be collected throughout the season and will be analyzed via molecular quantification assays at the University of Wisconsin (Damon Smith Lab) and at Louisiana State University (Sara Thomas-Sharma Lab). Pathogens that will be quantified are Cercospora sojina (frogeye leaf spot pathogen), Corynespora cassiicola (target spot pathogen), and the different Cercospora species complex that cause Cercospora leaf blight. The Smith Lab recently hired Dr. Shalina Yerukala as a post-doc partially funded on this project. Dr. Yerukala is currently working to extract DNA from all spore trap samples. She is also working on developing a species-specific primer set for Cercospora sojina. The Smith Lab has a promising protocol they are working on and are hopeful that they will get the PCR protocol validated very soon. Once validated, they will begin processing spore trap DNA from all 2023 and 2024 samples. The Thomas-Sharma Lab is currently testing published qPCR assays to detect the target spot pathogen, Corynespora cassiicola, on soybean. The primers amplify an 85 bp product in the elongation factor 1 alpha (TEF1) gene of the pathogen. DNA extracted from 6 isolates of the pathogen from Kentucky was shared with their lab and were tested with the assay. An average DNA concentration of 20 ng/ul resulted in average cycle threshold values of 24.39. They are currently testing DNA of 6 more isolates collected in Arkansas. They are also going to collect isolates of the pathogen from Louisiana this growing season. Louisiana isolates together with isolates from Kentucky and Arkansas obtained from collaborators (once APHIS permits are obtained) will be used to develop standard curves of spore counts. The latter will allow them to determine spore counts of the pathogen collected on the spore trap samples.