ABSTRACT
Cnaphalocrocis medinalis Guenée is a noxious rice pest during cultivated periods. Cnaphalocrocis medinalis moths lay eggs on leaf surfaces, and larvae longitudinally roll the leaves to hide inside the leaf buds and feed on the upper epidermis and mesophyll tissues. In this study, we evaluated the female oviposition preference and larval performance of C. medinalis on six insect-resistant and six insect-susceptible rice genotypes. Female moth choice and no-choice oviposition preferences were studied. The number of eggs laid on the leaf varies among selected rice genotypes; however, female adults prefer to lay more eggs on both some resistant and susceptible rice genotypes. Furthermore, newly hatched larvae showed no observed differences in preference for both specific resistant and susceptible rice genotypes. The time taken by larvae for leaf selection varied significantly after inoculation on different genotypes at the maximum tillering and heading stages of rice plants. Compared with susceptible genotypes, leaf selection time was prolonged in resistant genotypes. In addition, the time taken for folding primary vegetative and flag leaves by larvae varied among the selected rice genotypes; larvae required more time to fold leaves of resistant than susceptible genotypes. In host antibiosis tests, larval and pupal survival and pupal weight were higher in susceptible than resistant genotypes. The results showed that the time required by larvae for leaf rolling and host antibiosis should be considered as the most crucial factors for rice genotypes resistant to C. medinalis.
Subject(s)
Antibiosis , Life History Traits , Moths/physiology , Oryza/genetics , Oviposition , Animals , Feeding Behavior , Larva/growth & development , Larva/physiology , Moths/growth & development , Pupa/growth & development , Pupa/physiologyABSTRACT
The bacterial genus "Candidatus Phytoplasma" contains a group of insect-transmitted plant pathogens in the class Mollicutes. Here, we report a draft genome assembly and annotation of strain NCHU2014, which belongs to the 16SrII-A subgroup within this genus and is associated with purple coneflower witches' broom disease in Taiwan.
ABSTRACT
This study used a simulated in vitro gastrointestinal digestion procedure to assess the bioavailability of a freeze-dried cranberry bean hydroalcoholic extract (polyphenol content of 28.73mgg-1). The amount of polyphenols in 200mg of cranberry bean extract increased from 5.73 (non-digested original) to 11.39mg following gastric digestion, but decreased to 6.05mg during intestinal digestion. When cranberry bean extract was accompanied with starch for the digestion tests, the added cranberry bean extract exhibited a potent inhibitory effect against glucose release during simulated intestinal digestion, with IC50 values of 472mg cranberry bean extract or 13mg polyphenols. A significant decrease in polyphenols was observed for the sample collected from dialysis phase, with only 11% of non-digested original polyphenols permeating through the dialysis membrane (0.63mg) and preserving an inhibitory effect against α-glucosidase to some extent. Therefore, polyphenol-rich cranberry bean extract may be used to manage postprandial hyperglycemia.
ABSTRACT
Dendrobium tosaense is one of the most valuable Chinese medicines and well developed health food. Atopic dermatitis (AD) is a chronic skin disease that occurs mainly in childhood. The pathogenesis of atopic dermatitis had been studied in BALB/c mice modeling by skin-inoculated ovalbumin (OVA) with 2,4,6-trinitro-1-chrolobenzene (TNCB). These mice exhibit features of chronic dermatitis, including skin rash, mast cells infiltration, and elevated serum anti-OVA specific IgE and cytokines modulation. In this study, a standardized ethyl acetate extract of D. tosaense (DtE) was used to protect these mice from the OVA/TNCB-induced skin lesions of atopic dermatitis. The results indicated an increased population of natural T regulatory cell was accompanied by immunosuppression in cytokine profiles and anti-OVA IgE level to significantly reduce Th2 polarization. Finally, toluidine blue staining indicated mast cell infiltration and degranulation was reduced in skin lesion. Our results were shed light on the usage of D. tosaense in AD.
Subject(s)
Anti-Inflammatory Agents/therapeutic use , Dendrobium , Dermatitis, Atopic/drug therapy , Plant Extracts/therapeutic use , Allergens , Animals , Anti-Inflammatory Agents/pharmacology , Cell Degranulation/drug effects , Cytokines/immunology , Dermatitis, Atopic/blood , Dermatitis, Atopic/chemically induced , Dermatitis, Atopic/immunology , Disease Models, Animal , Female , Immunoglobulin E/blood , Lymph Nodes/cytology , Mast Cells/drug effects , Mast Cells/physiology , Mice , Mice, Inbred BALB C , Ovalbumin , Phytotherapy , Picryl Chloride , Plant Extracts/pharmacology , Plant Stems , Skin/drug effects , Skin/immunology , Skin/pathology , Spleen/cytology , T-Lymphocytes/drug effects , T-Lymphocytes/immunologyABSTRACT
BACKGROUND: Echinacea purpurea L. (EP) is a popular herbal antioxidant and immunomodulator. The present study was conducted to evaluate the effects of EP on meat quality and oxidative status in broilers. Two hundred and fifty (1-day-old) male broilers (Arbor Acres) were randomly allocated to five groups including the control (corn-soybean meal diet) and 0.1, 0.5, 1.0 and 2.0% EP powder groups, with two replicates per treatment group. RESULTS: The results indicated that the addition of 0.5% and 1.0% EP significantly increased water-holding capacity and decreased storage loss of breast and thigh fillets at 35 days old. For fillet colour, L* (lightness) values were lower, and a* (redness) and b* (yellowness) values were higher with EP supplementation. Lower crude fat contents were observed in EP groups in comparison with control at 35 days of age in breast and thigh fillets, respectively. Production of malondialdehyde was slightly reduced in serum of EP supplemented birds compared to the control group. Results for Trolox equivalent antioxidant capacity, catalase and superoxide dismutase were significantly higher for the 0.5, 1.0 and 2.0% EP supplemental groups than control group in serum. Liver and spleen tissues results showed that the antioxidative enzymes activities were higher with EP powder at 35 days of age. CONCLUSION: Dried EP can be used as a feed additive to improve the meat quality and oxidative status in Arbor Acres broilers.
Subject(s)
Antioxidants/pharmacology , Color , Dietary Supplements , Echinacea , Lipid Peroxidation/drug effects , Meat/analysis , Plant Preparations/pharmacology , Animals , Antioxidants/metabolism , Catalase/blood , Chickens , Dietary Fats/analysis , Humans , Liver/metabolism , Malondialdehyde/blood , Meat/standards , Spleen/metabolism , Superoxide Dismutase/metabolism , WaterABSTRACT
This study was performed to investigate the free radical scavenging active components from in vitro propagated medicinal herbs of the genus Dendrobium, namely, Dendrobium tosaense Makino and Dendrobium moniliforme SW, using a 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical antioxidative assay. Seeds of the capsules derived after 12 weeks of hand-pollination germinated asymbiotically (50-74%) on half-strength Murashige and Skoog's (MS) basal medium with 3% sucrose and solidified with 0.9% Difco agar. Active growth in the germinated seedlings was achieved by reculturing on full-strength MS basal medium supplemented with 8% banana homogenate, 8% potato homogenate, 8% coconut water, 1.5% sucrose, and 0.9% Difco agar. Healthy plantlets transferred to plastic trays containing moss or moss and tree fern successfully acclimatized (84-100%) in the greenhouse. Extracts were prepared from plants grown in the greenhouse for a period of 6 months. Methanolic extracts of D. tosaense and D. moniliforme scavenged DPPH at 95.9 and 83.4%, respectively, at a concentration of 0.4 mg/mL. Therefore, methanolic solubles of D. tosaense and D. moniliforme were subjected to bioguided fractionation and separation by column chromatographic methods individually. After chromatographic separation of these crude extracts, the obtained fractions (Dm 1, Dm 2, Dm 3, Dt 1, Dt 2, and Dt 3) were tested for their activity. Among them, fractions Dm 2 and Dt 1 showed significant antioxidant activity by DPPH radical antioxidative assay. Active fractions were purified further by column chromatography and resulted in identification of the antioxidant components alkyl ferulates from D. moniliforme and quercetin from D. tosaense.
Subject(s)
Dendrobium/chemistry , Free Radical Scavengers/isolation & purification , Biphenyl Compounds , Chemical Fractionation , Dendrobium/growth & development , Picrates/chemistry , Plant Extracts/chemistryABSTRACT
A simple and efficient plant propagation system has been developed by asymbiotic germination of seeds in three medicinally important Dendrobium species, namely, Dendrobium tosaense, Dendrobium moniliforme, and Dendrobium linawianum. Plants obtained from natural habitats were grown in the greenhouse. The flowers were hand pollinated. Seeds of the capsules derived after 12 weeks of hand-pollination germinated asymbiotically (50-74%) on half strength Murashige and Skoog's (MS) basal medium with 3% sucrose and solidified with 0.9% Difco agar. Active growth in the germinated seedlings was achieved by re-culturing on full strength MS basal medium supplemented with 8% banana homogenate, 8% potato homogenate, 8% coconut water, 1.5% sucrose and 0.9% Difco agar. Healthy plantlets, transferred to plastic trays containing moss or moss and tree fern, successfully acclimatized (84-100%) in the greenhouse. A marked varied response was observed in the free radical scavenging activity of methanolic extracts of in vitro propagated plants, on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical using a UV spectrophotometer assay. Methanolic extracts were prepared by dissolving the powdered plant material, obtained from six months old in vitro propagated plants, each about 5 g, in boiling methanol. The percentage of scavenging effect of D. tosaense extract was 95.9% at 0.4 mg/ml concentration, whereas D. monoliforme, and D. linawianum extracts scavenged 83.4% and 92.3%, respectively, at a concentration of 0.4 mg/ml. All the extracts scavenged DPPH radical significantly in a concentration dependent manner.
Subject(s)
Biphenyl Compounds/pharmacology , Dendrobium/drug effects , Free Radical Scavengers/pharmacology , Germination/drug effects , Hydrazines/pharmacology , Seeds/drug effects , Biphenyl Compounds/metabolism , Dendrobium/growth & development , Free Radical Scavengers/metabolism , Germination/physiology , Hydrazines/metabolism , Picrates , Plant Extracts/metabolism , Plant Extracts/pharmacology , Plants, Medicinal/drug effects , Plants, Medicinal/growth & development , Seeds/growth & development , Symbiosis/drug effects , Tissue Culture TechniquesABSTRACT
Effect of N(6)-benzyladenine (BA) on tanshinone formation in callus cultures of Salvia miltiorrhiza was examined in an attempt to increase the productivity of the medicinal compound, cryptotanshinone. Primary callus was induced by culturing leaf explants on Murashige and Skoog's (MS) basal medium supplemented with 1.0 mg l(-1) of 2,4-dichlorophenoxyacetic acid (2,4-D) in darkness. The callus proliferated further on MS basal medium containing 1.0 mg l(-1) 2,4-D and 0.5 mg l(-1) BA and was analyzed for cryptotanshinone by high performance liquid chromatography (HPLC). The HPLC results indicated that it contained small amounts of cryptotanshinone (0.26+/-0.05 mg/g dry wt). Omission of 2,4-D from the medium resulted in a marked increase in the content of cryptotanshinone in callus. The HPLC analysis revealed that the content of cryptotanshinone in the callus cultured on the MS basal medium supplemented with 0.1, 0.2, 0.5, 1.0, and 2.0 mg l(-1) of BA was significantly higher than the marketed crude drug (processed underground parts of S. miltiorrhiza). Maximum yield of cryptotanshinone (4.59+/-0.09 mg/g dry wt) was observed in the callus cultured on MS basal medium supplemented with 0.2 mg l(-1) BA for 60 d. Cryptotanshinone was isolated from callus through silica gel column chromatography followed by preparative TLC and characterized based on NMR and mass spectral data.