Budesonide and Poractant Alfa prevent bronchopulmonary dysplasia via triggering SIRT1 signaling pathway.

OBJECTIVE: This study aimed to evaluate effect of budesonide combining Poractant Alfa on preventing bronchopulmonary dysplasia (BPD). PATIENTS AND METHODS: A total of 120 preterm infants were involved. pH value, partial pressure of oxygen (PO2), and blood gas analysis were evaluated. Peripheral blood was collected and mononuclear cells were isolated. Reactive oxygen species (ROS) in peripheral blood mononuclear cells (PBMCs) were detected with laser confocal. Sirtuin 1 (SIRT1) in PBMCs was detected using immunofluorescence. SIRT1 and small ubiquitin-like modifier (SUMO)-specific protease 1 (SENP1) were detected with Western blot. RESULTS: Compared with group B, pH value and PO2 were improved significantly in group C and D (p<0.01). Compared with group B, oxygen inhalation duration, rate of having a respirator assisted ventilation, and using pulmonary surfactant (PS) again, and BPD incidence were significantly decreased in other groups (p<0.05). BPD incidence in group D was less than group C (χ2=4.00, p<0.05). Compared with control group, ROS level of neonatal respiratory distress syndrome (NRDS) group was significantly increased, SENP1 was increased, and SIRT1 was decreased in SIRT1 group. Compared with NRDS, when budesonide combined with Poractant Alfa, ROS decreased, SENP1 decreased, SIRT1 nuclear pulp shuttling rate reduced, nuclear SIRT1 increased (p<0.01). Compared with control, ROS level of NRDS group was significantly increased, SENP1 increased, and SIRT1 in nucleus decreased (p<0.05). Compared with NRDS group, when treated with budesonide and Poractant Alfa, ROS levels decreased, SENP1 decreased, nuclear SIRT1 increased (p<0.01). CONCLUSIONS: Budesonide combining Poractant Alfa can prevent BPD in preterm infants by activating the SIRT1 signaling pathway.

Molecular detection of QTL controlling plant height components in a doubled haploid barley population.

Yield losses caused by lodging in barley can be partially controlled by reducing plant height. In order to understand dwarfing mechanisms and efficiently use new dwarf germplasms for a breeding program, it is important to identify QTL of plant height components. QTL analysis was performed for seven plant height component traits using a DH population of 122 lines derived from the cross of Huaai 11 x Huadamai 6. Composite interval mapping procedures detected 20 QTL, which were mapped onto chromosomes 2H, 3H, 5H, 6H, and 7H. Eleven QTL were detected in 3 years and four QTL were detected in 2 years. QTL controlling all seven plant height component traits were found near the dwarfing gene btwd1 on chromosome 7H. These QTL accounted for 27.19 to 59.73% of phenotypic variation in seven plant height component traits. Positive transgressive segregation was found for all traits. Some of the QTL identified in this study will be useful for understanding the dwarfing mechanism and for developing new dwarf varieties using marker-assisted selection.

Management of Daylily Rust with Different Fungicides and Application Methods.

The objectives of this study were to assess the efficacy of various fungicides applied as root dips, soil drenches, or foliar sprays to daylily plants grown in containers and planted in the field to manage rust caused by Puccinia hemerocallidis. Soil drenches and foliar sprays were evaluated in field experiments in Griffin, GA in 2010 and 2011. Dipping bare-root daylily plants for 5 min in azoxystrobin, tebuconazole, or thiophanate-methyl significantly reduced lesion development compared with nontreated control plants. Drenches with azoxystrobin, fluoxastrobin, or tebuconazole, each at three rates (0.06, 0.12, and 0.24 g of active ingredient [a.i.]/container), significantly reduced development of rust lesions on container-grown daylily plants for up to 9 weeks after treatment and 6 weeks after inoculation. One early-season drench of azoxystrobin at 0.12 g a.i‥/plant provided season-long reduction in disease incidence and disease progress that was comparable with foliar sprays with azoxystrobin or chlorothalonil applied at 14-day intervals. Dip or drench applications of fungicides would allow growers to diversify rust management options and could reduce the number of foliar fungicide applications.

Resistance in Peanut Cultivars and Breeding Lines to Three Root-Knot Nematode Species.

Three major species of root-knot nematode infect peanut: Meloidogyne arenaria race 1, M. hapla, and M. javanica race 3. Sources of resistance to all three nematodes are needed for developing novel peanut cultivars with broad resistance to Meloidogyne spp. Cultivars and breeding lines of peanut were evaluated for resistance to M. arenaria, M. hapla, and M. javanica in the greenhouse and in the laboratory. Twenty-six genotypes with some resistance to M. arenaria, M. javanica, or M. hapla were identified from 60 accessions based on average eggs per gram of root and gall index relative to a susceptible control. Among these, 14 genotypes were moderately to highly resistant to all three species, 5 genotypes were resistant to M. arenaria and M. javanica, 2 genotypes were resistant to M. javanica and M. hapla, 1 genotype was resistant M. arenaria alone, and 4 genotypes were resistant to M. hapla alone. Reproduction of M. arenaria on lines NR 0817, C724-19-11, and D108 was highly variable, indicating that these genotypes likely were heterogeneous for resistance. COAN, NemaTAM, C724-25-8, and the M. arenaria-resistant plants of C724-19-11 contained the dominant sequence-characterized amplified region marker (197/909) for nematode resistance. Results with the molecular markers indicate that the high resistance to M. arenaria in GP-NC WS 6 may be different from the resistance in COAN, NemaTAM, and C724-25-8. Resistance to M. arenaria was correlated with resistance to M. javanica in peanut, whereas resistance to M. hapla was not correlated with the resistance to either M. arenaria or M. javanica. The resistant selections should be valuable sources for pyramiding resistance genes to develop new cultivars with broad and durable resistance to Meloidogyne spp.

[Determination of glucosinolates in rapeseed by reversed-phase ion-pair liquid chromatography].

This paper presents a method for the direct determination of intact glucosinolates in rapeseed by reversed-phase ion-pair liquid chromatography (RILC). The catechin, mercaptoethanol and phytic acid was adopted respectively in sample pretreatment to prevent indole glucosinolates being oxidized. Among them, the effect of mercaptoethanol was the most obvious. The effects of composition and concentration of the mobile phase, the pH of the mobile phase and the column temperature on the retention and the capacity factor of the glucosinolates were studied. The condition of this method by RILC has been set up: column, YWG-C18 H37(10 microns, 250 mm x 4 mm i.d.); mobile phase, 0.02 mol/L KH2PO4 buffer(pH 6) containing 4.5 mmol/L (C4H8)4NBr and CH3CN(90/10, V/V); flow rate, 1 mL/min; detector, UV-226 nm; column temperation, 30 degrees C. In this condition, six glucosinolates were separated completely. The relative correction factors were determined by using sinigrin or benzoic acid as the internal standard. The characteristics of glucosinolates in different kinds of Chinese rapeseed can be determined by this RILC method.

[Insect-resistant transgenic plants of Brassica napus and analysis of resistance in the plants].

Cotyledons, each with a 1-2 mm petiole at its base, were cut from axenic seedlings and infected with Agrobacterium tumefaciens. After 2-3 days of cocultivation, the cotyledon explants were transferred to MS selection medium containing 15 mg/L kanamycin and 4.5 mg/L 6-BA to induce shoot differentiation. Kanamycin-resistant shoots were subcultured on selection medium with 20-50 mg/L kanamycin for 3-6 months for eliminating escaped non-transformants, and then rooted on MS medium containing 25 mg/L kanamycin and 0.1 mg/L NAA. Whole plants were transplanted into soil and grew in the field. DNA Southern blot hybridization and polymerase chain reaction showed that some of the plants were positive when probed with the insecticidal crystal protein gene. The transgenic plants exhibited tolerant to pest insects such as Laphygma exigua and Pieris rapae in leaf feeding experiments Kanamycin-resistance and insect-resistance were maintained in the progeny. The foreign genes were delivered to the progeny according to Mendelian Law of single gene segregation.