Pro-Inflammatory Effect of Gliadins and Glutenins Extracted from Different Wheat Cultivars on an In Vitro 3D Intestinal Epithelium Model

There is a need to assess the relationship between improved rheological properties and the immunogenic potential of wheat proteins. The present study aimed to investigate the in vitro effects of total protein extracts from three modern and two landrace Triticum aestivum commercial flour mixes, with significant differences in gluten strength (GS), on cell lines. Cytotoxicity and innate immune responses induced by wheat proteins were investigated using Caco-2 monocultures, two dimensional (2D) Caco-2/U937 co-cultures, and three dimensional (3D) co-cultures simulating the intestinal mucosa with Caco-2 epithelial cells situated above an extra-cellular matrix containing U937 monocytes and L929 fibroblasts. Modern wheat proteins, with increased GS, significantly reduced Caco-2 cell proliferation and vitality in monoculture and 2D co-cultures than landrace proteins. Modern wheat proteins also augmented Caco-2 monolayer disruption and tight junction protein, occludin, redistribution in 3D co-cultures. Release of interleukin-8 into the cell medium and increased U937 monocyte migration in both 2D and 3D co-cultures were similarly apparent. Immuno-activation of migrating U937 cells was evidenced from cluster of differentiation 14 (CD14) staining and CD11b-related differentiation into macrophages. The modern wheat proteins, with gluten polymorphism relatedness and increased GS, were shown to be more cytotoxic and immunogenic than the landrace wheat proteins.     

Mussoorrie rock phosphate-pyrite mixture as phosphate fertilizer

Mussoorrie rock phosphate (MRP), MRP + pyrite (25% by weight), diammonium phosphate (DAP), ammonium polyphosphate (APP) and nitrophosphate (NP) were compared in a field experiment as fertilizers for wheat. At 20 kg P ha^–1, MRP was only 6 per cent as effective as DAP. However, when it was mixed with pyrite, the efficiency of MRP increased to 64 per cent at 20 kg P ha^–1 compared with 97 per cent at 40 kg P ha^–1. The P requirement for a targeted yield for 4.5 t ha^–1 decreased from 39.4 kg P ha^–1 as MRP to 23.7 kg P ha^–1 as MRP + pyrite. Of the other P fertilizers studied, NP was as effective as DAP, whereas APP was 9 to 37 per cent more effective than DAP. However, the P requirement as DAP, NP and APP for a targeted yield of 4.5 t ha^–1 was similar (11 ± 0.5 kg P ha^–1).     

The role of manganese and nitrogen nutrition in the susceptibility of wheat plants to take-all in Western Australia

Five field experiments are described which measured the effect of take-all on grain yield of wheat when 5 levels of manganese fertilizer were applied in a factorial combination with 5 different types of nitrogen fertilizer.Ammonium nitrogen fertilizer, either as ammonium sulphate or ammonium chloride, lowered the severity of take-all. By contrast, sodium nitrate had no effect on the incidence and severity of take-all. Ammonium chloride and ammonium sulphate were equally effective at controlling take-all, suggesting that the chloride or sulphate ion had little or no effect on the disease.Manganese sulphate decreased take-all severity at two trial sites. Where manganese was deficient, an application of manganese lowered the severity of take-all, had no effect on the incidence and increased the dry matter and grain yields of the wheat plants. There were no beneficial effects of applied manganese if the wheat plants were adequately supplied with soil manganese.The results suggest that take-all is more severe where plants are deficient in either manganese or nitrogen. The work also suggests that manganese deficiency is not necessarily the reason why the wheat plants grown on the acid soils of south-west Western Australia are prone to take-all.     

Incubating superphosphate in ‘dry’soil can reduce its effectiveness

Single superphosphate was incubated for six months at 25°C in soil which had been subject to one of three moisture treatments. These were: dried in a glasshouse, dried at a constant temperature of 25°C, or moist soil. Phosphorus (P) effectiveness was then compared with effectiveness of P from freshly-applied superphosphate using yields of wheat (Triticum aestivum) and triticale (×Triticosecale) tops in pot experiments.Incubation in soil which had been dried at 25°C did not decrease the effectiveness of the P. Incubation in moist soil decreased it to about 20% of the effectiveness of freshly-applied P in one case and to about 50% in the other case. Incubation in soil which had been dried in a glasshouse also decreased its effectiveness. The decrease varied with conditions, but in two cases the P was 70% as effective as freshly-applied P, and in one case only 45% as effective. Presumably sufficient moisture was present in the soil dried in the glasshouse to enable water-soluble P present in the fertilizer to react with the soil.     

Inhibitory effect of parthenium (Parthenium hysterophorus L.) residue on growth of water hyacinth (Eichhornia crassipes Mart Solms.) II. Relative effect of flower,leaf, stem,and root residue

The relative effect of residue of leaf, flower, stem, and root of parthenium (Parthenium hysterophorus L.) on growth of water hyacinth was studied. The inhibitory activity of the residue as shown by its effect on biomass and healthy leaf number (HLN) of treated plants was in the order: leaf and flower >stem >root. Total phenolic acids in the medium after 72 hr of suspending the plant part residue were maximum in flower followed by leaf, root, and stem, successively. The dry leaf powder (DLP) and dry flower powder (DFP) at and above 0.50% (w/v) and dry stem powder (DSP) at 1.00% (w/v) killed water hyacinth in about one month. Dry root powder (DRP) at the highest dose (1.25% w/v) reduced the growth of the treated plants drastically, but the plants recovered after about one month. The DSP at 0.50% (w/v) and DRP at 0.25–0.75% (w/v) supported growth of treated plants, probably due to lower levels of inhibitors, allowing utilization of constituents of the residue as nutrients. Using wheat seedlings as a reference material, it was observed that in aquaculture at different levels of parthenium plant parts residue, water hyacinth plants were much more sensitive to inhibitory activity. Thus, water hyacinth is suggested as a material for bioassay of inhibitory activity of the parthenium plant residue.     

山羊草及普通小麦遗传多样性的研究

使用微卫星荧光标记-全自动基因分析仪(3700 DNA Analyzer)，用43对D染色体组引物标记76份普通小麦、粗山羊草、拟斯卑尔脱山羊草和尾状山羊草品种和材料，将其结果进行聚类分析，共聚成四类：普通小麦被聚成一类，粗山羊草被聚成两类，拟斯卑尔脱山羊草、尾状山羊草和部分来自巴基斯坦的粗山羊草聚成一类。聚类结果与现有的植物学分类的结果相一致。     

The Plastome Sequences of Triticum sphaerococcum (ABD) and Triticum turgidum subsp. durum (AB) Exhibit Evolutionary Changes,Structural Characterization,Comparative Analysis,Phylogenomics and Time Divergence

The mechanism and course of Triticum plastome evolution is currently unknown; thus, it remains unclear how Triticum plastomes evolved during recent polyploidization. Here, we report the complete plastomes of two polyploid wheat species, Triticum sphaerococcum (AABBDD) and Triticum turgidum subsp. durum (AABB), and compare them with 19 available and complete Triticum plastomes to create the first map of genomic structural variation. Both T. sphaerococcum and T. turgidum subsp. durum plastomes were found to have a quadripartite structure, with plastome lengths of 134,531 bp and 134,015 bp, respectively. Furthermore, diploid (AA), tetraploid (AB, AG) and hexaploid (ABD, AGA^m) Triticum species plastomes displayed a conserved gene content and commonly harbored an identical set of annotated unique genes. Overall, there was a positive correlation between the number of repeats and plastome size. In all plastomes, the number of tandem repeats was higher than the number of palindromic and forward repeats. We constructed a Triticum phylogeny based on the complete plastomes and 42 shared genes from 71 plastomes. We estimated the divergence of Hordeum vulgare from wheat around 11.04–11.9 million years ago (mya) using a well-resolved plastome tree. Similarly, Sitopsis species diverged 2.8–2.9 mya before Triticum urartu (AA) and Triticum monococcum (AA). Aegilops speltoides was shown to be the maternal donor of polyploid wheat genomes and diverged ~0.2–0.9 mya. The phylogeny and divergence time estimates presented here can act as a reference framework for future studies of Triticum evolution.     

Mining the Wheat Grain Proteome

Bread wheat is the most widely cultivated crop worldwide, used in the production of food products and a feed source for animals. Selection tools that can be applied early in the breeding cycle are needed to accelerate genetic gain for increased wheat production while maintaining or improving grain quality if demand from human population growth is to be fulfilled. Proteomics screening assays of wheat flour can assist breeders to select the best performing breeding lines and discard the worst lines. In this study, we optimised a robust LC–MS shotgun quantitative proteomics method to screen thousands of wheat genotypes. Using 6 cultivars and 4 replicates, we tested 3 resuspension ratios (50, 25, and 17 µL/mg), 2 extraction buffers (with urea or guanidine-hydrochloride), 3 sets of proteases (chymotrypsin, Glu-C, and trypsin/Lys-C), and multiple LC settings. Protein identifications by LC–MS/MS were used to select the best parameters. A total 8738 wheat proteins were identified. The best method was validated on an independent set of 96 cultivars and peptides quantities were normalised using sample weights, an internal standard, and quality controls. Data mining tools found particularly useful to explore the flour proteome are presented (UniProt Retrieve/ID mapping tool, KEGG, AgriGO, REVIGO, and Pathway Tools).     

Fusarium graminearum Infection Strategy in Wheat Involves a Highly Conserved Genetic Program That Controls the Expression of a Core Effectome

Fusarium graminearum, the main causal agent of Fusarium Head Blight (FHB), is one of the most damaging pathogens in wheat. Because of the complex organization of wheat resistance to FHB, this pathosystem represents a relevant model to elucidate the molecular mechanisms underlying plant susceptibility and to identify their main drivers, the pathogen’s effectors. Although the F. graminearum catalog of effectors has been well characterized at the genome scale, in planta studies are needed to confirm their effective accumulation in host tissues and to identify their role during the infection process. Taking advantage of the genetic variability from both species, a RNAseq-based profiling of gene expression was performed during an infection time course using an aggressive F. graminearum strain facing five wheat cultivars of contrasting susceptibility as well as using three strains of contrasting aggressiveness infecting a single susceptible host. Genes coding for secreted proteins and exhibiting significant expression changes along infection progress were selected to identify the effector gene candidates. During its interaction with the five wheat cultivars, 476 effector genes were expressed by the aggressive strain, among which 91% were found in all the infected hosts. Considering three different strains infecting a single susceptible host, 761 effector genes were identified, among which 90% were systematically expressed in the three strains. We revealed a robust F. graminearum core effectome of 357 genes expressed in all the hosts and by all the strains that exhibited conserved expression patterns over time. Several wheat compartments were predicted to be targeted by these putative effectors including apoplast, nucleus, chloroplast and mitochondria. Taken together, our results shed light on a highly conserved parasite strategy. They led to the identification of reliable key fungal genes putatively involved in wheat susceptibility to F. graminearum, and provided valuable information about their putative targets.