Wheat is one of the main sources of calories and protein of the world's population and therefore the pathogens that cause rust diseases of the crop are a real threat to food security. Besides the continuous evolution of rust pathogens which repeatedly results in overcoming the resistance of commercial varieties throughout the world, plant breeders are also now challenged by the impacts of global climatic changes. Agricultural practices will need to keep pace with the intensification of sustainable food production in order to face the challenge of feeding a world population estimated to reach about nine billion by 2050. Contemporary wheat breeding has increasingly focused on the future, culminating in the emergence of a global partnership for breeding new wheat varieties with resistance to rust pathogens. Plant breeding now employs a wide range of both long-established and frontier technologies aimed at achieving the United Nations Millennium Development Goals of ending hunger and extreme poverty (MDG1), while concurrently promoting environmental sustainability (MDG7) through global partnerships for development (MDG8).

In this study we screened soil nematodes collected in the south region of Brazil for pathogenicity against S. frugiperda. Symbiotic bacteria associated with these nematodes were isolated and characterized. We also evaluated urease production by the symbiotic bacteria in vitro and along the course of infection in S. frugiperda and demonstrated that urease production correlated positively to their entomopathogenicity.

Xyloglucan is the major hemicellulosic polymer found in the primary cell walls of dicots. Xyloglucan tethers cellulose microfibrils conferring rigidity and strength for maintenance of cell integrity, and it is thought that its metabolism contributes to cell elongation and thus plant growth. Here, we have cloned and characterized a Eucalyptus grandis gene ortholog of the Arabidopsis thaliana MUR3 gene (xyloglucan galactosyltransferase), thus termed EgMUR3. EgMUR3 represents an intronless sequence of 1,854 bp predicted to encode a protein of 617 amino acid residues. It exhibits 73% identity and 82% similarity to the A. thaliana MUR3 gene. To demonstrate that this gene encodes a functional enzyme, the putative ORF was cloned into a binary vector under the control of a constitutive promoter and transformed into the A. thaliana mur3 mutant. The effect of the genetic complementation was investigated by xyloglucan oligosaccharide fingerprinting of wall material. The results confirmed that EgMUR3 represents indeed a xyloglucan galactosyltransferase of E. grandis able to use endogenous substrate(s) in A. thaliana, suggesting that both species share common steps in xyloglucan biosynthesis.

Low transformation efficiency is one of the main limiting factors in the establishment of genetic transformation of wheat via Agrobacterium tumefaciens. To determine more favorable conditions for T-DNA delivery and explant regeneration after infection, this study investigated combinations of acetosyringone concentration and pH variation in the inoculation and co-cultivation media and co-culture temperatures using immature embryos from two Brazilian genotypes (BR 18 Terena and PF 020037). Based on transient expression of uidA, the most favorable conditions for T-DNA delivery were culture media with pH 5.0 and 5.4 combined with co-culture temperatures of 22 °C and 25 °C, and a 400 μM acetosyringone supplement. These conditions resulted in blue foci in 81% of the embryos. Media with more acidic pH also presented reduced A. tumefaciens overgrowth during co-culture, and improved regeneration frequency of the inoculated explants. BR 18 Terena was more susceptible to infection by A. tumefaciens than PF 020037. We found that it is possible to improve T-DNA delivery and explant regeneration by adjusting factors involved in the early stages of A. tumefaciens infection. This can contribute to establishing a stable transformation procedure in the future.

These products were cloned and sequenced. The subgroup II 3' partial CP amino acid deduced sequences were identifi ed as BYDV-RMV (92 -93 % of identity with "Illinois" Z14123 isolate).The complete CP amino acid deduced sequences of subgroup I isolates were confi rmed as BYDV-PAV (94 -99 % of identity) and established a very homogeneous group (identity higher than 99 %). These results support the prevalence of BYDV-PAV in southern Brazil as previously diagnosed by Enzyme-Linked Immunosorbent Assay (ELISA) and suggest that this population is very homogeneous. To our knowledge, this is the fi rst report of BYDV-RMV in Brazil and the fi rst genetic diversity study on B/CYDV in South America.