Two experiments were conducted in separate locations, one at Université Laval in eastern Canada (Québec) and one at the Agassiz Research Station in western Canada (British Columbia), in an attempt to determine the effectiveness of soluble silicon (Si) against cucumber root disease caused by Pythium aphanidermatum Edson. Long English cucumber (Cucumis sativus L. cv. Corona) plants were grown either in a standard nutrient solution or in nutrient solutions supplemented with 1.7 mm (100 ppm) Si and inoculated or not with the pathogen. Supplying the solutions with 1.7 mm Si significantly reduced mortality and disease symptoms attributed to infection by P. aphanidermatum. Grown in presence of Si, plants infected with P. aphanidermatum showed a significant increase in yield, marketable fruit, and plant dry weight compared to Si-nonamended and infected plants. These beneficial effects were observed under both experimental conditions. The fruit yield of noninoculated plants was not affected by the presence of Si in the Agassiz experiment. However, Si-amended control plants were more productive in the experiment conducted at Laval, apparently because of contamination problems, which indicates that Si beneficial effects are most likely related to disease management.
M. Chérif, J.G. Menzies, D.L. Ehret, C. Bogdanoff, and R.R. Bélanger
Edward W. Bush, Don R. LaBonte, Ann L. Gray, and Arthur Q. Villordon
Production of disease-free sweetpotato [Ipomoea batatas (L.) Lam.] transplants is of major importance to certified and foundation seed programs and producers. Sweetpotato roots are traditionally planted and cuttings are harvested from propagation beds. The objective of this study was to investigate the efficiency of producing cuttings in nursery containers. Virus-tested and virus-infected `Beauregard' sweetpotato transplants were harvested from planting beds for the purpose of producing cuttings for transplants. Cuttings were established in 3.7-L plastic nursery containers filled with 100% pine bark amended with either low, medium, or high rates of Osmocote 14-14-14 and dolomitic lime. Resulting transplants produced a greater number of cuttings and greater plant biomass with higher fertilizer rates. Increasing fertilizer rates also had a positive effect on cutting production and biomass. Dry weight and stem growth were similar for both virus-infected and virus-tested transplants following first and second harvests. Producing foundation cuttings in nursery containers filled with a pine bark medium proved to be an efficient method of increasing virus-tested sweetpotato cuttings.
A. Smigocki and F. Hammerschlag
Immature `Redhaven' peach (Prunus persica L. Batsch) embryos were infected with Agrobacterium tumefaciens strain tms328::Tn5 carrying the functional cytokinin gene. Shoots were regenerated from callus grown on MS medium without added phytohormones and subsequently rooted on half-strength MS medium with 2.8 -naphthaleneacetic acid. These plants exhibited an increased frequency of branching in vitro. Low levels of cytokinin gene transcripts were detected in these cells by Northern analysis, and using an ELISA assay, the cytokinins zeatin and zeatinriboside were determined to be on the average 30-fold higher. From these results, the expression of the cytokinin gene appears to promote growth of cells in the absence of phytohormones thus serving as a marker for transformation and a promoter of morphogenesis without a 2,4-dichlorophenoxyacetic acid inductive step.
Ann C. Smigocki and Freddi A. Hammerschlag
Immature `Redhaven' peach [Prunus persica (L.) Batsch] embryos were infected with a shooty mutant strain of Agrobacterium tumefaciens, tms328::Tn5, which carries an octopine-type Ti plasmid with a functional cytokinin gene and a mutated auxin gene. Shoots were regenerated from embryo-derived callus that was initiated on MS medium lacking phytohormones. Shoots exhibited increased frequency of branching and were more difficult to root than the noninfected. Transcripts of the tms328::Tn5-cytokinin gene were detected using northern analyses of total plant RNA. Polymerase chain reaction of genomic DNA and cDNA resulted in amplification of DNA fragments specific for the cytokinin gene, as determined by restriction enzyme and Southern analyses. The concentrations of the cytokinins zeatin and zeatin riboside in the leaves of regenerated plants were on the average 51-fold higher than in leaves taken from nontransformed plants. None of the shoots or callus tissues were postive for octopine. The expression of the T-DNA encoded cytokinin gene promotes growth of peach cells in the absence of phytohormones, thus serving as a marker for transformation. In addition, this gene appears to promote morphogenesis without an auxin inductive step.
Kenneth L. Deahl, Richard W. Jones, Frances M. Perez, David S. Shaw, and Louise R. Cooke
The oomycete, Phytophthora infestans, is a devastating pathogen of potato worldwide. Several genotypes of P. infestans are able to infect other cultivated and weed species of the family Solanaceae and cause symptoms similar to late blight. Changes in P. infestans populations have stimulated investigations to determine if potato strains from new immigrant populations infect nonpotato hosts more often than those from the older population. Expansion of the effective host range may be one of the mechanisms involved in pathogenic changes in natural populations of P. infestans and to determine its significance, it is necessary to establish if the pathogen strains on nonpotato hosts represent distinct genotypes/populations or are freely exchanging with those on potato. This article reports characterization of P. infestans isolates from four solanaceous hosts (black nightshade, hairy nightshade, petunia, and tomato) growing within and around fields of blighted potatoes in four U.S. locations and one U.K. location and their comparison with isolates collected from adjacent infected potatoes. Isolates were characterized for mitochondrial DNA haplotype, mating type, metalaxyl resistance, allozymes of glucose-6-phosphate isomerase and peptidase, and DNA fingerprint with the RG57 probe. Analysis showed close similarity of the petunia, hairy and black nightshade isolates to potato isolates. However, tomatoes from New Jersey and Pennsylvania, respectively, were infected by two distinct and previously unreported pathogen genotoypes, which had quite different fingerprints from P. infestans isolates recovered from nearby infected potatoes. Potato growers should be aware that both weed and cultivated solanaceous species can be infected with P. infestans and may serve as clandestine reservoirs of inoculum. Because some of these plants do not show conspicuous symptoms, they may escape detection and fail to be either removed or treated and so may play a major role in the introduction and spread of pathogens to new locations.
Ed Stover and Greg McCollum
consistent with either reduced likelihood of ‘Temple’ and ‘Fallglo’ becoming initially infected, so that infections begin later but progress at the same rate after initiation, or reduced proliferation once infection occurs. Differences between cultivars in
Flavia T. Zambon, Davie M. Kadyampakeni, and Jude W. Grosser
deficiency of micronutrients known to be cofactors in enzymatic reactions that protect cell integrity ( Hänsch and Mendel, 2009 ) from excessive reactive oxygen species (ROS) when infected with C Las ( Pitino et al., 2017 ). Several approaches have been
Davie M. Kadyampakeni, Kelly T. Morgan, Arnold W. Schumann, and Peter Nkedi-Kizza
et al., 2009 ). Intensive fertigation practices are being devised primarily to manage HLB disease and increase yields so growers break-even within a few years of establishing a grove. Graham et al. (2013) found that HLB-infected trees had up to 40
A.Q. Villordon, C.A. Clark, R.A. Valverde, R.L. Jarret, and D.R. LaBonte
Previous work by our group has detected the presence of a heterogeneous population of Ty1-copia-like reverse transcriptase retrotransposon sequences in the sweetpotato genome. Recently, we detected the presence of putatively active Ty1-copia-like reverse transcriptase sequences from a virus-infected `Beauregard' sweetpotato clone. In the current study, we report the differential detection of putatively stress-activated sequences in clones from seedling 91-189. The clones were infected with different combinations of virus isolates followed by extraction of leaf RNA samples at three sampling dates (weeks 2, 4, and 6) after inoculation. After repeated DNAse treatments to eliminate contaminating DNA, the RNA samples were subjected to first strand cDNA synthesis using random decamer primers followed by PCR analysis utilizing Ty1-copia reverse transcriptase-specific primers. Through this approach, we detected amplified fragments within the expected size range (280-300 bp) from clones infected with isolates of sweetpotato leaf curl (SPLC) and feathery mottle viruses (FMV) (week 2 and 6) and FMV (week 4). We were unable to detect PCR products from the noninfected clones or the other infected samples. The data suggests that specific viruses may be involved in the expression of these Ty1-copia-related reverse transcriptase sequences. It also appears that sampling at various dates is necessary to detect putative activity over time. This preliminary information is essential before proceeding to the construction and screening of cDNA libraries to isolate and fully characterize the putatively active sweetpotato Ty1-copia-like retrotransposon sequences. Through the partial or complete characterization of sweetpotato Ty1-copia elements, sequences that correspond to cis-regulatory element(s) can be identified and further studied for their roles in responding to specific stress factors.
Wei Li, Rongcai Yuan, Jacqueline K. Burns, L.W. Timmer, and Kuang-Ren Chung
Colletotrichum acutatum J. H. Simmonds infects citrus flower petals, causing brownish lesions, young fruit drop, production of persistent calyces, and leaf distortion. This suggests that hormones may be involved in symptom development. To identify the types of hormones, cDNA clones encoding proteins related to ethylene and jasmonate (JA) biosynthesis, indole-3-acetic acid (IAA) regulation, cell-wall modification, signal transduction, or fruit ripening were used to examine differential gene expressions in calamondin (Citrus madurensis Lour) and/or `Valencia' sweet orange (Citrus sinensis Osbeck) after C. acutatum infection. Northern-blot analyses revealed that the genes encoding 1-aminocyclopropane-1-carboxylate (ACC) oxidase and 12-oxophytodienoate required for ethylene and JA biosynthesis, respectively, were highly up-regulated in both citrus species. Both gene transcripts increased markedly in petals, young fruit and stigmas, but not in calyces. The transcripts of the genes encoding IAA glucose transferase and auxin-responsive GH3-like protein, but not IAA amino acid hydrolyase, also markedly increased in both species 5 days after inoculation. The expansin and chitinase genes were slightly up-regulated, whereas the senescence-induced nuclease and ß-galactosidase genes were down-regulated in calamondin. No differential expression of transcripts was detected for the genes encoding expansin, polygalacturonase, and serine-threonine kinase in sweet orange. As compared to the water controls, infection of C. acutatum increased ethylene and IAA levels by 3- and 140-fold. In contrast, abscisic acid (ABA) levels were not significantly changed. Collectively, the results indicate that infection by C. acutatum of citrus flowers triggered differential gene expressions, mainly associated with IAA, ethylene, and JA production and regulation, and increased hormone concentrations, consistent with the hypothesis of the involvement of phytohormones in postbloom fruit drop.