Easter Lily Research Articles

Characterization of Lilium longiflorum cv. 'Nellie White' Infection with Root-lesion Nematode Pratylenchus penetrans by Bright-field and Transmission Electron Microscopy.

Lilium longiflorum cv. Nellie White, commonly known as Easter lily, is an important floral crop with an annual wholesale value of over $26 million in the United States. The root-lesion nematode, Pratylenchus penetrans, is a major pest of lily due to the significant root damage it causes. In this study, we investigated the cytological aspects of this plant-nematode interaction using bright-field and transmission electron microscopy. We took advantage of an in vitro culture method to multiply lilies and follow the nematode infection over time. Phenotypic reactions of roots inoculated with P. penetrans were evaluated from 0 to 60 d after nematode infection. Symptom development progressed from initial randomly distributed discrete necrotic areas to advanced necrosis along entire roots of each inoculated plant. A major feature characterizing this susceptible host response to nematode infection was the formation of necrosis, browning, and tissue death involving both root epidermis and cortical cells. Degradation of consecutive cell walls resulted in loss of cell pressure, lack of cytoplasmic integrity, followed by cell death along the intracellular path of the nematode's migration. Pratylenchus penetrans was never seen in the vascular cylinder as the layer of collapsed endodermal cells presumably blocked the progression of nematodes into this area of the roots. This study presents the first detailed cytological characterization of P. penetrans infection of Easter lily plants.

Flowering pathway is regulated by bulb size in Lilium longiflorum (Easter lily).

Lilium longiflorum (Easter lily) vegetative propagation occurs through production of underground bulbs containing apical and axillary meristems. In addition, sexual reproduction is achieved by flowering of elongated shoots above the bulb. It is generally accepted that L.longiflorum has an obligatory requirement for vernalisation and that long day (LD) regime hastens flowering. However, the effect of bulb size and origin, with respect to axillary or apical meristems on flowering, as well as the interactions between these meristems are largely unknown. The aim of this study was to explore the effect of bulb size, vernalisation and photoperiod on L.longiflorum flowering. To this end, we applied vernalisation and photoperiod treatments to the different bulb sizes and used a system of constant ambient temperature of 25°C, above vernalisation spectrum, to avoid cold-dependent floral induction during plant growth. Vernalisation and LD hasten flowering in all bulbs. Large, non-vernalised bulbs invariably remained at a vegetative stage. However, small non-vernalised bulbs flowered under LD conditions. These results demonstrate for the first time that cold exposure is not an obligatory prerequisite for L.longiflorum flowering, and that an alternative flowering pathway can bypass vernalisation in small bulbs. We suggest that apical dominance interactions determine the distinct flowering pathways of the apical and axillary meristems. Similar floral induction is achieved in propagated bulblets from scaling. These innovative findings in the field of geophyte floral induction represent valuable applicative knowledge for lily production.

Hepatoprotective Activity of Easter Lily (Lilium longiflorum Thunb.) Bulb Extracts.

The hepatoprotective activities of two different extracts, a hydroethanolic crude bulb extract (CB) and a steroidal glycoside-rich 1-butanol extract (BuOH), prepared from the bulbs of Easter lily (Lilium longiflorum Thunb.), were evaluated in a 24 week study in the female KK.Cg-A(y)/J Type 2 diabetic mouse model. Animals were divided into six groups (n = 16): control mice received Easter lily bulb extract-free drinking water together with a low- or high-fat diet (diabetic control); drinking water for the remaining groups was supplemented with CB extract (1%), BuOH extract (0.1 or 0.2%), and reference drug Metformin (0.001%), together with a high-fat diet. Both CB and BuOH extract treatment groups exhibited significantly improved liver function based on comparisons of triglycerides [diabetic 219 ± 34 mg/dL, CB 131 ± 27 mg/dL, BuOH(0.2%) 114 ± 35 mg/dL], CB total cholesterol (TC) (diabetic 196 ± 12 mg/dL, CB 159 ± 5 mg/dL), average liver mass [diabetic 2.96 ± 0.13 g, CB 2.58 ± 0.08 g, BuOH(0.1%) 2.48 ± 0.13 g], alanine transferase [diabetic 74 ± 5 units/L, CB 25 ± 1 units/L, BuOH(0.1%) 45 ± 1 units/L], and histological examinations. Glucose metabolism was improved only in CB, which was confirmed by oral glucose tolerance tests (OGTT) in diet-induced obese C57BL/6J mice exposed to CB extract. These data suggest that steroidal glycosides 1-5 might play a role in the hepatoprotective activity of the BuOH extracts, while the results of the TC measurements and OGTT study indicate that other constituents present in the CB extract are responsible for its hypocholesterolemic and hypoglycemic activity.

The complete chloroplast genome sequence of Lilium hansonii Leichtlin ex D.D.T.Moore

Lilium hansonii is a lily species native to Korea and an important wild species for lily breeding. The chloroplast genome of L. hansonii was completed by de novo assembly using the small amount of whole genome sequencing data. The chloroplast genome of L. hansonii was 152 655 bp long and consisted of large single copy region (82 051 bp), small single copy region (17 620 bp) and a pair of inverted repeat regions (26 492 bp). A total of 115 genes were annotated, which included 81 protein-coding genes, 30 tRNA genes and 4 rRNA genes. Phylogenetic analysis with the reported chloroplast genomes revealed that L. hansonii is most closely related to L. superbum (Turk’s-cap lily) and L. longiflorum (Easter lily).

Whole transcriptome profiling of the vernalization process in Lilium longiflorum (cultivar White Heaven) bulbs.

BackgroundVernalization is an obligatory requirement of extended exposure to low temperatures to induce flowering in certain plants. It is the most important factor affecting flowering time and quality in Easter lily (Lilium longiflorum). Exposing the bulbs to 4 °C gradually decreases flowering time up to 50 % compared to non-vernalized plants. We aim to understand the molecular regulation of vernalization in Easter lily, for which we characterized the global expression in lily bulb meristems after 0, 2, 5, 7 and 9 weeks of incubation at 4 °C.ResultsWe assembled de-novo a transcriptome which, after filtering, yielded 121,572 transcripts and 42,430 genes which hold 15,414 annotated genes, with up to 3,657 GO terms. This extensive annotation was mapped to the more general GO slim plant with a total of 94 terms. The response to cold exposure was summarized in 6 expression clusters, providing useful patterns for dissecting the dynamics of vernalization in lily. The functional annotation (GO and GO slim plant) was used to group transcripts in gene sets. Analysis of these gene sets and profiles revealed that most of the enriched functions among genes up-regulated by cold exposure were related to epigenetic processes and chromatin remodeling. Candidate vernalization genes in lily were selected based on their sequence similarity to known regulators of flowering in other species.ConclusionsWe present a detailed analysis of gene expression dynamics during vernalization in Lilium, covering several time points and accounting for biological variation by the use of replicates. The resulting collection of transcripts and novel isoforms provides a useful resource for studying the changes occurring during vernalization at a fine level. The selected potential candidate genes can shed light on the regulation of this process.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1675-1) contains supplementary material, which is available to authorized users.

Two plant pathogenic species of Phytophthora associated with stem blight of Easter lily and crown rot of lettuce in Japan

New diseases of Easter lily and lettuce were noticed in Japan and the pathogens were identified initially as Phytophthora megasperma and Phytophthora sp., respectively, based on morphological characteristics. We re-examined these isolates using phylogenetical and morphological analysis. In a detailed phylogenetic analysis of all clade members that was based on the sequences of eight genomic regions, Easter lily isolates formed a monophyletic group with high bootstrap support. The unique colony pattern supported this result. In separate analyses of Phytophthora clade 8 based on rRNA gene ITS and the cox1 gene sequences, the lettuce isolates grouped with P. lactucae (described from lettuce in Greece) in the rRNA gene ITS tree but formed a distinct group in the cox1 tree. The sporangia of Japanese lettuce isolates germinated directly, an uncommon feature in clade 8b. These results suggested that the Easter lily and lettuce isolates are novel species that we formally describe as Phytophthora lilii sp. nov. and P. pseudolactucae sp. nov., respectively. Moreover, P. lilii appears to represent a new Phytophthora clade.

Bioassay-guided fractionation of extracts from Easter lily (Lilium longiflorum) flowers reveals unprecedented structural variability of steroidal glycoalkaloids

Several Lilium species are nephrotoxic in cats (Felis silvestris catus), among them Easter lilies (Lilium longiflorum). Although clinical trials have been carried out, the causative toxic phytochemicals have not yet been identified. We thus aimed to determine the toxic constituents of Easter lily flowers applying a bioassay-guided approach based on a feline kidney cell line model. The bioassay-guided fractionation traced the observed cytotoxicity to a complex mixture of compounds that were tentatively identified as steroidal glycoalkaloids of the solasodine-type, based on multiple-fragmentation ion trap and high-resolution mass spectrometry. The glycoalkaloids in the active fraction possessed trisaccharide chains, and at least 16 different congeners could be separated using liquid chromatography-mass spectrometry. The two principal compounds were solasodine trisaccharides containing two hexose and one deoxy-hexose unit. In the remaining 14 analogues, one or two of the hydroxyl groups of the second hexose from the aglycone were acetylated. In addition, some of the analogues appeared to be carbonate esters. Esterification of steroidal glycoalkaloids in plants has only been reported once and was in accordance with higher antifungal activity of the acetylated versus the parent congener. Our pilot study shows that esterification of steroidal glycoalkaloids in Lilium species might be common resulting in an array of different analogues with largely unexplored structural variability and bioactivity.

Growth and flowering physiology, and developing new technologies to increase the flower numbers in the Genus Lilium

The genus Lilium is important as potted plants or cut flowers for horticultural trade and for gardens. However, most of the extensive research on the growth and flowering of this genus was conducted with L. longiflorum Thunb. (Easter lily) forcing large bulbs grown in the field for at least one or two years. Dormancy had to be broken to induce flowering by cold treatment which was given to mature bulbs (vernalization). It would be desirable if the bulb production phase could be bypassed to shorten the total production time, ideally by manipulating the temperature during the bulb programming phase (vernalization methods) and the early greenhouse forcing phase (from potting to flower bud initiation). Information on the physiology of bulb development, controlled flowering, and timing for the Easter, and to certain extent for the Asiatic hybrid lily is readily available. However, information on LA, L. longiflorum × Oriental (LO), and Oriental × Trumpet (OT) hybrid lilies, is not available. The objective of this article is to review factors that control flower numbers and speed of flowering, and to present outlines for producing quality plants of L. longiflorum, L. ×elegans, and LA hybrids, starting from seeds, stem bulbils, and tissue cultured plants, respectively, in a year. Detailed information on the production of L. ×elegans starting from stem bulbils is presented. Cut flowers of Asiatic hybrid ‘Beni no Mai’ with 2 to 3 flowers and strong 60 cm stems were produced in less than a year when mature bulbils, weighing about 400 mg harvested 40 to 50 days after flowering, are treated with a sequential temperature treatment (SEQ CD) 14 to 20 days each at 5°C-15°C-5°C. This production period can be divided into plug production phase from potting the treated bulbils shoot emergence lasting about 200 to 230 days and the second phase from shoot emergence to flowering requiring 90 to 100 days. The increase in the number of flowers could result from the increased shoot apex size and not from the changes in soluble and cell wall neutral sugars.

Steroidal glycosides from the bulbs of Easter lily (Lilium longiflorum Thunb.) promote dermal fibroblast migration in vitro

Ethnopharmacological relevancePreparations derived from bulbs of various Lilium species have been used to promote the healing of skin abrasions, sores and burns and to aid in healing wounds in Traditional Chinese and Greco-Roman Medicine. Aim of the studyTo evaluate fractionated Easter lily bulb extracts and their steroidal glycosides (1–5) for the promotion of dermal fibroblast migration in vitro, a model for the early events in wound healing. Materials and methodsAn activity-guided screening approach was used by coupling sequential solvent extraction, gel permeation chromatography (GPC), and semi-preparative reverse-phase high performance liquid chromatography (RP-HPLC) with an in vitro dermal fibroblast migration assay. Cytotoxicity was evaluated with methyl thiazole tetrazolium (MTT). To gain insight into the mode of action of the steroidal glycosides, nitric oxide (NO) production, and expression of genes for transforming growth factor beta-1 (TGF-β) and its receptors were evaluated. ResultsFractionated bulb extracts and the two isolated steroidal glycoalkaloids (1) and (2) induced NO production and TGF-β receptor I mRNA expression in fibroblast cell culture. In a cytotoxicity assay, steroidal glycosides (1) and (3) had IC50 values of 8.2 and 8.7µM, but the natural acetylation of the C-6″′ hydroxy of the terminal glucose unit in (2) resulted in a 3-fold decrease in cell cytotoxicity when compared with (1). Results from the dermal fibroblast migration assay revealed that the steroidal glycoalkaloids (1) and (2), and the furostanol saponin (3) promoted fibroblast migration from the range of 23.7±5.7 to 37.7±5.1%, as compared with the control. ConclusionCollectively, our data demonstrate that the steroidal glycosides present in Easter lily bulbs induce, at least in part, the observed dermal fibroblast migration activity of the bulb extracts. This is the first evidence that steroidal glycosides from Lilium longiflorum may potentially play a role in the wound healing process and may provide a scientific basis for the historical use of lily bulbs for this purpose.

Substrate Drenches Containing Flurprimidol Suppress Height of ‘Nellie White’ Easter Lilies

The objective of this research was to quantify how flurprimidol substrate drenches applied to ‘Nellie White’ easter lilies (Lilium longiflorum) affected height at flowering, time to flower, and flower number. In Expt. 1, size 9/10 ‘Nellie White’ easter lilies were treated with a 4-fl oz drench applied to the surface of the substrate when shoots were ≈3 inches tall providing 0.0, 0.02, 0.04, 0.08, 0.16, or 0.24 mg flurprimidol per pot or 0.03 or 0.06 mg uniconazole per pot. In Expt. 2, size 10/12 ‘Nellie White’ easter lilies were treated with 4-fl oz drenches applied to the surface of the substrate when shoots were ≈3 inches tall providing 0.0, 0.01, 0.02, 0.04, 0.06, or 0.08 mg flurprimidol per pot. In Expt. 1, plants treated with flurprimidol or uniconazole were up to 38.9 cm (59%) shorter than untreated plants, while time to flower and flower number remained unaffected by plant growth retardant (PGR) treatments. In Expt. 2, as the amount of flurprimidol increased from 0.01 to 0.08 mg/pot, plant height was suppressed linearly (r2 = 0.63), by up to 23.2 cm (28%), while time to flower and flower number remained unaffected. Additionally, the chemical cost for drenches containing flurprimidol is less than the cost of uniconazole required to achieve comparable height control. Flurprimidol substrate drenches appear to be an effective and economical alternative to control easter lily height.

Donaldson v United Kingdom: No Right for Prisoners to Wear Easter Lilies

In the recent case of Donaldson v United Kingdom the European Court denied a claim from an imprisoned Irish Republican that HMP Maghaberry prison violated Article 102 and Article 143 of the European Convention on Human Rights when it asked him to remove an Easter lily from his clothing. The Easter lily has long been regarded as a symbol commemorating Irish Republican combatants who died during or were executed after the 1916 Easter Rising, a rebellion against the British Government’s rule in Ireland. In this case, the applicant, who is currently serving a 12-year sentence at Roe House, a segregated wing of HMP Maghaberry for Republican prisoners, affixed an Easter lily to his outer clothing on Easter Sunday in March 2008. A prison officer asked him to remove the Easter lily and when he refused he was charged with disobeying a lawful order under the Prison and Young Offenders Centre Rules (Northern Ireland) 1995, which prohibits prisoners from wearing emblems outside their cells. In HMP Maghaberry an exception was made with respect to the wearing of a shamrock on St Patrick’s Day and the wearing of poppies on Remembrance Sunday as these emblems were deemed to be ‘non-political and non-sectarian’

Antifungal Activity and Fungal Metabolism of Steroidal Glycosides of Easter Lily (Lilium longiflorum Thunb.) by the Plant Pathogenic Fungus, Botrytis cinerea

Botrytis cinerea Pers. Fr. is a plant pathogenic fungus and the causal organism of blossom blight of Easter lily (Lilium longiflorum Thunb.). Easter lily is a rich source of steroidal glycosides, compounds which may play a role in the plant-pathogen interaction of Easter lily. Five steroidal glycosides, including two steroidal glycoalkaloids and three furostanol saponins, were isolated from L. longiflorum and evaluated for fungal growth inhibition activity against B. cinerea, using an in vitro plate assay. All of the compounds showed fungal growth inhibition activity; however, the natural acetylation of C-6''' of the terminal glucose in the steroidal glycoalkaloid, (22R,25R)-spirosol-5-en-3β-yl O-α-L-rhamnopyranosyl-(1→2)-[6-O-acetyl-β-D-glucopyranosyl-(1→4)]-β-D-glucopyranoside (2), increased antifungal activity by inhibiting the rate of metabolism of the compound by B. cinerea. Acetylation of the glycoalkaloid may be a plant defense response to the evolution of detoxifying mechanisms by the pathogen. The biotransformation of the steroidal glycoalkaloids by B. cinerea led to the isolation and characterization of several fungal metabolites. The fungal metabolites that were generated in the model system were also identified in Easter lily tissues infected with the fungus by LC-MS. In addition, a steroidal glycoalkaloid, (22R,25R)-spirosol-5-en-3β-yl O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside (6), was identified as both a fungal metabolite of the steroidal glycoalkaloids and as a natural product in L. longiflorum for the first time.

Quantitative Analysis of Steroidal Glycosides in Different Organs of Easter Lily (Lilium longiflorum Thunb.) by LC-MS/MS

The bulbs of the Easter lily ( Lilium longiflorum Thunb.) are regularly consumed in Asia as both food and medicine, and the beautiful white flowers are appreciated worldwide as an attractive ornamental. The Easter lily is a rich source of steroidal glycosides, a group of compounds that may be responsible for some of the traditional medicinal uses of lilies. Since the appearance of recent reports on the role steroidal glycosides in animal and human health, there is increasing interest in the concentration of these natural products in plant-derived foods. A LC-MS/MS method performed in multiple reaction monitoring (MRM) mode was used for the quantitative analysis of two steroidal glycoalkaloids and three furostanol saponins, in the different organs of L. longiflorum. The highest concentrations of the total five steroidal glycosides were 12.02 ± 0.36, 10.09 ± 0.23, and 9.36 ± 0.27 mg/g dry weight in flower buds, lower stems, and leaves, respectively. The highest concentrations of the two steroidal glycoalkaloids were 8.49 ± 0.3, 6.91 ± 0.22, and 5.83 ± 0.15 mg/g dry weight in flower buds, leaves, and bulbs, respectively. In contrast, the highest concentrations of the three furostanol saponins were 4.87 ± 0.13, 4.37 ± 0.07, and 3.53 ± 0.06 mg/g dry weight in lower stems, fleshy roots, and flower buds, respectively. The steroidal glycoalkaloids were detected in higher concentrations as compared to the furostanol saponins in all of the plant organs except the roots. The ratio of the steroidal glycoalkaloids to furostanol saponins was higher in the plant organs exposed to light and decreased in proportion from the aboveground organs to the underground organs. Additionally, histological staining of bulb scales revealed differential furostanol accumulation in the basal plate, bulb scale epidermal cells, and vascular bundles, with little or no staining in the mesophyll of the bulb scale. An understanding of the distribution of steroidal glycosides in the different organs of L. longiflorum is the first step in developing insight into the role these compounds play in plant biology and chemical ecology and aids in the development of extraction and purification methodologies for food, health, and industrial applications. In the present study, (22R,25R)-spirosol-5-en-3β-yl O-α-l-rhamnopyranosyl-(1→2)-β-d-glucopyranosyl-(1→4)-β-d-glucopyranoside, (22R,25R)-spirosol-5-en-3β-yl O-α-l-rhamnopyranosyl-(1→2)-[6-O-acetyl-β-d-glucopyranosyl-(1→4)]-β-d-glucopyranoside, (25R)-26-O-(β-d-glucopyranosyl)furost-5-ene-3β,22α,26-triol 3-O-α-l-rhamnopyranosyl-(1→2)-β-d-glucopyranosyl-(1→4)-β-d-glucopyranoside, (25R)-26-O-(β-d-glucopyranosyl)furost-5-ene-3β,22α,26-triol 3-O-α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranosyl-(1→3)-β-d-glucopyranoside, and (25R)-26-O-(β-d-glucopyranosyl)furost-5-ene-3β,22α,26-triol 3-O-α-l-rhamnopyranosyl-(1→2)-α-l-xylopyranosyl-(1→3)-β-d-glucopyranoside were quantified in the different organs of L. longiflorum for the first time.

Intersimple Sequence Repeats Distinguish Genetic Differences in Easter Lily ‘Nellie White’ Clonal Ramets within and among Bulb Growers over Years

The large genome size of easter lily [Lilium longiflorum (77.1 pg/2C nucleus)], coupled with repetitive DNA sequences, makes it difficult to use molecular techniques to identify or fingerprint lily (Lilium) species, hybrids, and clones. Previous research demonstrated that amplified fragment length polymorphisms could not be optimized for consistency and repeatability to obtain reliable genetic variation assessments of lily species and clones. The objective of this research was to analyze the effectiveness and stringency of intersimple sequence repeats (ISSRs) to determine genetic differences between L. longiflorum ‘Nellie White’ clonal ramet populations from bulb growers over years. DNA from closely related clones of L. longiflorum ‘Nellie White’ included 2002 (n = 11 bulb lots) and 2003 (n = 12 bulb lots). Comparison cultivars and species were also included. Five University of British Columbia (UBC) primers (P808, P810, P811, P814, and P818) that were used produced 56 polymorphic loci. ISSR banding patterns were consistent among three replications within ‘Nellie White’ clonal genotypes. ‘Nellie White’ clones differed significantly within (82%) and among (18%) growers in 2002 and 2003. ‘Nellie White’ clones are not uniform or part of a single ramet population. Principal clades within years separated at Nei's genetic distances (GDs) of GD = 0.6 (growers 2, 4, and 12) to GD = 0.82 (grower 6) in 2002 and GD = 0.51 (grower 4) to GD = 0.78 (grower 14). The most closely related ‘Nellie White’ clones within growers ranged from GD = 0.8 to 0.95 in 2002 and GD = 0.7 to 0.91 for 2003. Five top-performing growers (1, and 3–6) from previous morphological studies and, particularly growers 3 and 5, were in similar clades, cosegregating with phenotypic traits of stem emergence and flowering dates. The lack of a meiotic sieve (Muller's ratchet) may be responsible for the high level of mutational differences present in the ‘Nellie White’ clones and significantly affects the ability of commercial greenhouse growers to produce a uniform easter lily crop, particularly in years when the Easter holiday is early.

Isolation and Structural Determination of Steroidal Glycosides from the Bulbs of Easter Lily (Lilium longiflorum Thunb.)

The bulbs of the Easter lily ( Lilium longiflorum Thunb.) are used as a food and medicine in several Asian cultures, and they are cultivated as an ornamental plant throughout the world. A new steroidal glycoalkaloid and two new furostanol saponins, along with two known steroidal glycosides, were isolated from the bulbs of L. longiflorum. The new steroidal glycoalkaloid was identified as (22R,25R)-spirosol-5-en-3beta-yl O-alpha-l-rhamnopyranosyl-(1-->2)-[6-O-acetyl-beta-d-glucopyranosyl-(1-->4)]-beta-d-glucopyranoside. The new furostanol saponins were identified as (25R)-26-O-(beta-d-glucopyranosyl)-furost-5-en-3beta,22alpha,26-triol 3-O-alpha-l-rhamnopyranosyl-(1-->2)-alpha-l-arabinopyranosyl-(1-->3)-beta-d-glucopyranoside and (25R)-26-O-(beta-d-glucopyranosyl)-furost-5-en-3beta,22alpha,26-triol 3-O-alpha-l-rhamnopyranosyl-(1-->2)-alpha-l-xylopyranosyl-(1-->3)-beta-d-glucopyranoside. The previously known steroidal glycosides, (22R,25R)-spirosol-5-en-3beta-yl O-alpha-l-rhamnopyranosyl-(1-->2)-beta-d-glucopyranosyl-(1-->4)-beta-d-glucopyranoside and (25R)-26-O-(beta-d-glucopyranosyl)-furost-5-en-3beta,22alpha,26-triol 3-O-alpha-l-rhamnopyranosyl-(1-->2)-beta-d-glucopyranosyl-(1-->4)-beta-d-glucopyranoside were identified in L. longiflorum for the first time. These new compounds from L. longiflorum and the isolation methodologies employed can be used for studies on the biological role of steroidal glycosides in plant development and plant-pathogen interactions, as well as for studies in food and human health, for which little is known.

Paclobutrazol Pre-plant Bulb Dips Effectively Control Height of ‘Nellie White’ Easter Lily

The influence of pre-plant bulb dips in paclobutrazol solutions on final plant height, days to flower, and flower bud number were evaluated for easter lily (Lilium longiflorum). ‘Nellie White’ easter lily bulbs were placed in solutions of paclobutrazol containing 0, 30, 60, or 120 mg·L−1 for 15 min preceding planting. Days to flower and flower bud number were unaffected by paclobutrazol. Plant height at flowering for bulbs dipped in paclobutrazol solutions was 15% to 26% shorter compared with untreated bulbs. Additionally, dipping bulbs in 120 mg·L−1 paclobutrazol resulted in plants that met target height specifications for commercially grown easter lily. Based on these results, dipping easter lily bulbs in paclobutrazol solutions can be an effective strategy for reducing stem elongation without negatively impacting days to flower or flower bud number for commercially grown easter lily.

Effects of N–P–K deficiency and temperature regime on the growth and development of Lilium longiflorum ‘Nellie White’ during bulb production under phytotron conditions

One-year-old scale bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown under a combination of six constant day/night temperature regimes and five N–P–K nutrient treatments under short days for 107 d (growing period 1 or GP-1) to compare the effects on growth and development and bulb production. Results during GP-1 were as follows: failure of bulblets to produce a shoot (“no-shows”) was found at high temperatures (30/26 and 26/22 °C) and not influenced by the nutrient treatments. Flower bud abortion was observed in the minus-N, minus-P, and minus-N–P–K treatments at high temperatures (30/26 or 26/22 °C), but not observed at any temperatures in the complete and minus-K treatments. The loss of bulb fresh weight in minus-N treated bulblets was less than in the other treatments resulting in less root and shoot growth in the minus-N treatment. At the intermediate temperatures where growth was highest, omission of N, P, K, or all three resulted in losses in stem bulb fresh weight, stem plus leaf fresh weight, number of flowers, and stem root fresh weight. Omission of N, P, or all three nutrients resulted in lowest basal root fresh weight. Bulb N and K concentrations were lowest in plants grown with complete nutrient solution at the two coldest temperature regimes (14/10 and 10/6 °C). Bulb P concentration was lowest at the three coldest (18/14, 14/10 and 10/6 °C) and the warmest (30/26 °C) temperature regimes. Stem length was shorter when P was omitted. Omission of any of the three nutrients resulted in lower concentrations of the other nutrients. The one exception was where low K did not affect N concentration. In the second phase of the experiment, plants grown at 18/14 °C and irrigated with the complete nutrient solution for 107 d (GP-1) were continued at this day/night temperature regime and five N–P–K nutrient treatments for another 89 d under long days (growing period 2 or GP-2). Results during GP-2 were as follows. Basal bulb yield was not impacted by omission of N, P, or K, or all three. Of all growth measurements, only stem plus leaf fresh weight was lower and only when all three nutrients (minus-N–P–K) were omitted. At the end of GP-2, basal bulb concentrations of N and P did not differ from the concentrations in bulbs at the beginning of GP-1; however, K concentration was lower at the end of GP-2. Omission of N or P further resulted in lower bulb K concentration, suggesting that a moderate supply of N, P, and K be applied during GP-2 since an additional year of bulb production is needed to produce forcing-sized bulbs.

沖永良部島のテッポウユリ「ひのもと」の茎に発生した赤すじ症状の発生実態調査と血清学的検討

In 2001, a new symptom was observed on the stem of Japanese Easter lily (Lilium longiflorum Thunb. “ Hinomoto” ), which was characterized by reddish-brown streaks (“ aka-suji” in Japanese) in Okinoerabu Island, Kagoshima Prefecture, Japan. It seemed that first chlorotic stripes (“ shiro- suji” in Japanese) appeared and these later turned reddish-brown when the lily approached the flowering stage in the seasonal cycle. Double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) detected Cucumber mosaic virus (CMV) and Lily symptomless virus (LSV) in lily with reddish-brown streaks. However, these 2 viruses were also detected in symptomless lily plants, indicating that additional factors might exist that induce the symptom. Further, we determined that the reddish-brown streaks were transmitted by the vegetative propagation of lilies. Taken together, these results suggested a viral etiology of the reddish-brown streaks.

Pollen proteolytic enzymes degrade tight junctions

Asthma and allergic rhinitis are significant, increasing causes of morbidity worldwide. Pollen, a major cause of seasonal rhinitis/conjunctivitis, carries proteolytic enzymes on its surface. We showed previously that peptidase allergens from house dust mites compromise epithelial barrier function by degrading the extracellular domains of the tight junction proteins, occludin and claudin, thus facilitating allergen delivery across epithelial layers. In this study, we aimed to determine whether peptidases from allergenic pollens should similarly be considered to have a role in disrupting tight junctions. Diffusates from stored pollen of Giant Ragweed, White Birch and Kentucky Blue Grass, and fresh pollen from Easter Lily were applied to confluent monolayers of Madin-Darby canine kidney (MDCK) and Calu-3 cells in serum-free medium. Immunofluorescence was performed for the tight junction proteins, occludin, claudin-1 and ZO-1. The effect of pollen diffusate on occludin was studied by Western blotting, and enzymatic activity in the diffusates was demonstrated by zymography. The ability of protease inhibitors to block the action of the diffusate on tight junctions was investigated. Diffusates from all four allergenic pollens caused loss of immunofluorescence labelling for tight junction proteins on MDCK and Calu-3 cells. The effect was blocked by inhibitors of serine and cysteine proteases. Degradation of occludin was demonstrated by Western blotting and zymography indicated that diffusates contain proteolytic activity. Pollen peptidases directly or indirectly disrupt epithelial tight junctions, and this activity should be considered as a possible mechanism for facilitating allergen delivery across epithelia.

Light Activation of Contractile Roots of Easter Lily

Contractile roots provide for a type of movement in plants that occurs in many plant species but has been given little attention. In the case of Easter lily (Lilium longiflorum Thunb. cv. Nelly White), root contraction serves to pull a bulb down into the soil where environmental conditions are more constant. The contraction is evidenced by a formation of epidermal wrinkles, starting at the base of the root and advancing toward the root tip. The movement function occurs in shallowly planted materials, is lessened at deeper locations, and ceases at a vermiculite depth of ≈15 cm. Examination of the cell shapes and volumes in the contracting sector indicates that movement of the bulb in the soil is achieved by a hydraulic shift in cortical cells. Root contraction is stimulated by light. Perception of the light stimulus does not occur in the root but occurs in the bulblet or possibly in the subtending leaf. Responsiveness to light fades with aging of the root, and experiments with light of different wavelengths indicate that the contraction response is preferentially triggered by blue light.