Sensitivity of recently naturalised Digitaria spp. populations to 4-hydroxyphenyl pyruvate dioxygenase- and acetolactate synthase-inhibiting herbicides in maize

Until recently, Digitaria aequiglumis var. aequiglumis, native to South America, and Digitaria ciliaris subsp. nubica, native to Northeast Africa, were completely overlooked in Belgium due to their close morphological resemblance to Digitaria sanguinalis and Digitaria ischaemum. One of the possible reasons for their expansion in maize fields, besides for example the lack of crop rotation, might be a lower sensitivity to post-emergence herbicides acting against panicoid grasses. Dose-response pot experiments were conducted in the glasshouse to evaluate the effectiveness of four foliar-applied HPPD-inhibiting herbicides (mesotrione, sulcotrione, tembotrione, topramezone) and two foliar-applied ALS-inhibiting herbicides (foramsulfuron, nicosulfuron) for controlling Belgian populations of D. aequiglumis and D. ciliaris subsp. Nubica, as well as local D. sanguinalis and D. ischaemum populations. In another dose-response pot experiment, the influence of growth stage at time of herbicide application on efficacy of topramezone and nicosulfuron for Digitaria spp. control was evaluated. In general, D. aequiglumis and D. ciliaris subsp. nubica populations were less sensitive to HPPD inhibitors than D. ischaemum and D. sanguinalis populations, except for D. aequiglumis treated with topramezone. Contrary to other herbicides tested, topramezone adequately controlled all D. aequiglumis populations at doses well below maximum authorised field dose. All species tested showed a progressive decrease in sensitivity to topramezone and nicosulfuron with seedling age. A satisfactory post-emergence control of Digitaria species in the field will require appropriate choice of herbicide and dose, as well as more timely application

Detection of Fusarium oxysporum f.sp. lactucae race 1 and 4 via race-specific real-time PCR and target enrichment

Fusarium oxysporum f.sp. lactucae (Fol) causes a vascular disease in lettuce that results in significant yield losses. Race-specific and sensitive real-time PCR assays were developed for Fol races 1 and 4, which are prevalent in Europe. Using genotyping-by-sequencing, unique DNA loci specific to each race were identified and subsequently used for the design of primers and hydrolysis probes. Two assays per race were developed to ensure specificity. The two assays of each race could be run in duplex format, while still giving a sensitivity of 100 fg genomic DNA for all assays. Sample preparation methods were developed for plant tissue, soil, and surfaces, with an extra enrichment step when additional sensitivity was required. By controlling the incubation conditions during the enrichment step, the real-time PCR signal could be matched to the number of spore equivalents in the original sample. When enriching naturally infested soil, down to six conidiospore equivalents L-1 soil could be detected. As enrichment ensures sensitive detection and focuses on living Fol propagules, it facilitates the evaluation of control measures. The developed detection methods for soil and surfaces were applied to samples from commercial lettuce farms and confirmed the prevalence of Fol race 4 in Belgium. Monitoring of soil disinfestation events revealed that despite a dramatic decrease in quantity, the pathogen could still be detected either immediately after sheet steaming or after harvesting the first new crop. The detection method for plant tissue was successfully used to quantify Fol in lettuce inoculated with race 1, race 4 or a combination of both. Under the temperature conditions used, race 4 was more aggressive than race 1, as reflected in larger amounts of DNA of race 4 detected in the roots. These newly developed assays are a promising tool for epidemiological research as well as for the evaluation of control measures