Michigan ranks third in the United States for the wholesale value of floriculture products, with an estimated value of $375.7 million. Seedling damping-off and root and crown rot are commonly caused by Pythium spp. and are important problems for greenhouse growers. Pythium spp. associated with Michigan’s floriculture crops were characterized as a means to improve current management strategies. During 2011 and 2012, potted poinsettias with root rot symptoms were sampled from nine greenhouses located in Kent, Kalamazoo, and Wayne counties. In 2013, from the same three counties, symptomatic geranium and snapdragon bedding plants were sampled from 12 greenhouses. Additionally, symptomatic hibiscus and lantana plants were sampled at one greenhouse facility. Isolates were confirmed to be Pythium spp. via morphology and sequencing of the ITS region. A total of 287 Pythium spp. isolates were obtained from poinsettias and 726 isolates from geranium, snapdragon, hibiscus, and lantana. Seven Pythium spp., and a group of isolates determined as Pythium sp. 1 were identified. The most prevalent species were P. irregulare, P. ultimum, and P. aphanidermatum. A subset of isolates was chosen for pathogenicity and mefenoxam sensitivity testing. Six of the species were virulent to germinating geranium seeds. Most P. ultimum and P. cylindrosporum isolates tested were intermediate to highly resistant to mefenoxam, whereas most P. aphanidermatum isolates were sensitive. This study suggests that Pythium spp. recovered from Michigan greenhouses may vary depending on the host, and that mefenoxam may not be effective to control P. ultimum or P. cylindrosporum.

In containerized (potted) annual nursery and greenhouse crops, set point-controlled irrigation allows adaptation to increasing water insecurity by precisely reducing water inputs. A key factor influencing adoption is lack of information on disease risk. To facilitate adaptive water use, effects of set-point substrate moisture (SM) control on disease risk and water savings in containerized annual production were evaluated using the Phytophthora capsici–tomato pathosystem (a model system for water stress predisposition to pathogen infection), comparing outcomes of imposing midrange SM (15% volumetric water content [VWC]) and low-range SM (10% VWC) with well-watered (20% VWC) plants. Reducing soil moisture to 10% VWC differentially reduced stem water potential (P < 0.05) and enhanced rate of wilt progress (P = 0.006) and root rot severity (P = 0.03) in P. capsici inoculated plants compared with noninoculated plants. Furthermore, incidence of fine root infections in inoculated asymptomatic plants was greater under reduced SM (10% VWC) compared with in well-watered plants (P < 0.05). Mild reductions to 15% VWC did not influence plant performance (root and shoot weights and plant height) or pathogen infection in either inoculated or noninoculated plants compared with well-watered plants and reduced water inputs by 17%, indicating potential for reducing water usage without increasing disease risk. Furthermore, P. capsici inoculated plants had lower shoot biomass and greater root infection incidence when 15% VWC was applied to older compared with younger plants; the inverse was true for root rot severity, although root rot development was minor overall (P < 0.05). These results indicate that water use reductions pose disease risks, but there is potential to reduce water use and effectively manage plant pathogens in containerized production. Overall, this study indicates that physiological indices should not be solely relied on to develop water reduction methods.

No abstract

Five Phytophthora species comprising a total of 243 isolates (77 P. cinnamomi, 23 P. citrophthora, 18 P. multivora, 18 P. pini, and 107 P. plurivora) were screened for sensitivity to mefenoxam, fosetyl-Al, dimethomorph, dimethomorph + ametoctradin and fluoxastrobin using amended agar assays. Mefenoxam-insensitive isolates were detected within P. cinnamomi (4%), P. multivora (11%), and P. plurivora (12%) even at approximately 2.5x the recommended label rate. These isolates were also insensitive to higher (off-label) concentrations of fluoxastrobin. Concentrations of dimethomorph (400 g/mL) and dimethomorph + ametoctradin (100 g/mL) were mostly effective in mycelial growth inhibition, but two P. plurivora isolates were insensitive, suggesting that resistance management is required. All mefenoxam-insensitive isolates were sensitive to fosetyl-Al at the label rate. Surprisingly, the populations of P. cinnamomi from mid-Atlantic oak forests included insensitive isolates. With almost all species, isolates recovered from asymptomatic hosts (e.g., soil/potting media collected of randomly selected asymptomatic hosts) had a significantly greater relative growth rate when compared to isolates recovered from symptomatic hosts (e.g., isolates recovered from lesions or wilted plants). These findings suggest that mefenoxam should no longer be used to manage oomycetes in Maryland ornamental nurseries and that the use of fluoxastrobin should be limited.

Root rot caused by Pythium spp. is a significant disease on greenhouse-grown crops and negatively affects the floriculture industry. To develop strategies that limit Pythium root rot on geranium and snapdragon, greenhouse trials were conducted to test plant protectants and cultivars. Seven fungicides and two biological control agents were evaluated on plants inoculated with P. aphanidermatum, P. irregulare, or P. ultimum. Disease severity was assessed using a scale of 1 (healthy, no disease symptoms) to 5 (plant death) from 5 to 45 day postinoculation (dpi). The area under disease progress curve (AUDPC) values differed significantly (P < 0.0001) among Pythium spp. and treatment. The interaction between plant protectants and Pythium spp. was also significant. For geranium, mefenoxam (trade name: Subdue Maxx) and Streptomyces lydicus WYEC108 (trade name: Actinovate) effectively controlled Pythium root rot. For snapdragon, treatment efficacy varied depending on the Pythium sp. When 11 geranium cultivars were inoculated with P. aphanidermatum, none were completely resistant to the pathogen. However, when P. irregulare was used to inoculate these geranium cultivars, Nano White Hybrid and Bulls Eye Cherry were similar to the uninoculated control. When 12 snapdragon cultivars were inoculated with P. aphanidermatum or P. irregulare, no cultivar was completely resistant to either pathogen, but Twinny White and Candy Showers Yellow were least susceptible to both. Integrating effective fungicides with less susceptible cultivars can limit disease caused by Pythium spp.

Pythium ultimum causes seedling damping-off and root and crown rot in greenhouse ornamental plants. To understand the population dynamics and assess population structure of P. ultimum in Michigan floriculture crops, simple sequence repeats (SSRs) were developed using the previously published P. ultimum predicted transcriptome. A total of 166 isolates sampled from 2011 to 2013 from five, one, and three greenhouses in Kalamazoo, Kent, and Wayne Counties, respectively, were analyzed using six polymorphic and fluorescently labeled SSR markers. The average unbiased Simpson’s index (λu, 0.95), evenness (E5, 0.56), and recovery of 12 major clones out of the 65 multilocus genotypes obtained, suggests that P. ultimum is not a recent introduction into Michigan greenhouses. Analyses revealed a clonal population, with limited differentiation among seasons, hosts, and counties sampled. Results also indicated the presence of common genotypes among years, suggesting that sanitation measures should be enhanced to eradicate resident P. ultimum populations. Finally, the presence of common genotypes among counties suggests that there is an exchange of infected plant material among greenhouse facilities, or that there is a common source of inoculum coming to the region. Continued monitoring of pathogen populations will enhance our understanding of population dynamics of P. ultimum in Michigan and facilitate improvement of control strategies.

No abstract

Industrial hemp (Cannabis sativa) is a newly legal crop in California that is grown for cannabidiol oil, fiber and seed. In August 2019, whole plant decline and root rot were observed affecting <5% of plants in two industrial fields in Fresno County, CA. Symptoms included chlorotic, collapsed foliage, stem vascular discoloration, and root rot with abundant mycelial growth. Stem and root segments (1-2 cm) from three to five diseased plants were agitated in 0.1% tween-20 and soaked in 70% ethanol for 30 s and 1% NaOCl for 2 min. After incubating for 5 to 7 days on 1:10 potato dextrose agar (PDA) amended with tetracycline, Fusarium selective medium (FSM), and PARP (pimaricin + ampicillin + rifampicin + pentachloronitrobenzene [PCNB] agar) medium, white to pale cream aerial mycelium emerged from tissue of all plants on PDA and FSM but not PARP. Isolates cultured on 0.1% potassium chloride agar formed heads of microconidia on long monophialides consistent with the Fusarium solani species complex (FSSC) (Leslie and Summerell 2008). To obtain pure cultures of two isolates (CS529 and CS530), a single-hyphal tip was excised and grown on PDA. DNA was extracted from actively growing mycelium (PrepMan Ultra kit). The translation elongation factor gene (EF-1α) was amplified via PCR using EF1/EF2 primers (O’Donnell et al. 1998). Sequences of the two isolates were identical and deposited under accession number MW892973 in GenBank. The 599 bp sequence was 99.33% identical to FSSC 3 + 4 (Fusarium falciforme) accessions FD_01443_EF-1a based on FUSARIUM-ID BLAST analysis. To evaluate pathogenicity, stems of hemp plants (cv. ‘Berry Blossom’; n=8 plants per isolate) were wounded by penetrating the epidermis in an area about 0.5-cm square by 1-mm deep and 8-inches above the soil line. A 0.5 cm-diameter plug of 7-day old F. falciforme-colonized PDA was placed against the wound. Inoculation sites were loosely wrapped with parafilm for 2 days. A negative control consisted of a sterile PDA plug (n=3). Treatments were arranged in a completely randomized design in a greenhouse. The experiment was conducted once, due to regulatory restrictions at campus facilities. At 61 days post-inoculation, external stem lesions were significantly larger in diameter (P < 0.05; Tukey’s HSD) in plants inoculated with CS529 (8 ± 1 mm) compared to the control (2 ± 0 mm), and larger but not significant for CS530 (6 ± 1 mm). Internal stem lesions (i.e., rot in stele) were observed in plants inoculated with CS529 (9 ± 3 mm); stem rot was very minor in plants treated with CS530 (1 ± 1 mm) and nonexistent for control plants. No other disease symptoms were observed. F. falciforme was isolated from stems of CS529- and C530-inoculated plants. Sequences of re-isolates matched 100% with accession MW892973. These results suggest that F. falciforme causes rot in hemp in California. These studies specifically confirm stem rot abilities; field observations of root rot indicate root rotting abilities, but further tests are needed for confirmation. This is the first report of F. falciforme causing disease in industrial hemp. FSSC was described as causing foot rot in hemp in Italy (Sorrentino et al. 2019), but these isolates belonged to phylogenetic species 5 (F. solani) not F. falciforme. In addition, F. falciforme was reported as causing root rot in hydroponically grown cannabis (Punja and Rodriguez 2018). These studies provide the foundation for development of management tools for hemp disease.