Agronomic performance and genetic dissimilarity among cherry tomato genotypes

<div><p>ABSTRACT The genotypes evaluation in a germplasm bank is essential to determine their commercial or usefulness, as potential parents, in a breeding program. We aimed to detect the genetic diversity of 42 tomato genotypes of cherry type, belonging to the germplasm bank of the Federal University of Uberlândia and, also evaluate their behavior. The experiment was conducted in a greenhouse in randomized block design with 42 treatments and two replications. Ten quantitative traits of agronomic importance were evaluated. The genetic divergence was obtained by multivariate analysis, using the Mahalanobis distance with different clustering methods (UPGMA and Tocher). The hybrids performance was compared by Scott-Knott (p= 0.05) and Dunnett’s test (p= 0.05). UPGMA and Tocher grouped the genotypes similarly, representing genetic divergence satisfactorily. The genotypes UFU 29, UFU 21 and UFU 07 were more productive, earlier and also divergent from the pre-commercial treatment (UFU 200), being able to be used as potential parents.</p></div

Agronomic potential and selection of okra hybrids to obtain potential genitors

<div><p>ABSTRACT Evaluation of pre-commercial hybrids in a germplasm bank is essential for determining its commercial potential or its utility as a potential genitor in a breeding program. The objective of this study was to determine genetic divergence and per se behavior of 47 pre-commercial hybrids from okra germplasm bank of the Universidade Federal de Uberlândia. Precocity index (%), number of fruits (fruits per plant), average fruit mass (g) and productivity (g per plant) were evaluated. Analysis of genetic divergence was performed by multivariate analysis using Mahalanobis distance with different clustering methods (UPGMA and canonical analysis). The performance of hybrids was compared by Scott-Knott (p= 0.05). A significant genetic variability among okra hybrids was observed. UPGMA and canonical analysis grouped the hybrids similarly, being satisfactory to represent genetic divergence. Ten hybrids presented higher performance than the commercial hybrids. Among them, UFU-QB16 stood out as the most promising hybrid for being used as a potential parent in breeding programs after auto pollination.</p></div

Peroxiredoxins play a major role in protecting Trypanosoma cruzi against macrophage- and endogenously-derived peroxynitrite.

There is increasing evidence that Trypanosoma cruzi antioxidant enzymes play a key immune evasion role by protecting the parasite against macrophage-derived reactive oxygen and nitrogen species. Using T. cruzi transformed to overexpress the peroxiredoxins TcCPX (T. cruzi cytosolic tryparedoxin peroxidase) and TcMPX (T. cruzi mitochondrial tryparedoxin peroxidase), we found that both cell lines readily detoxify cytotoxic and diffusible reactive oxygen and nitrogen species generated in vitro or released by activated macrophages. Parasites transformed to overexpress TcAPX (T. cruzi ascorbate-dependent haemoperoxidase) were also more resistant to H2O2 challenge, but unlike TcMPX and TcCPX overexpressing lines, the TcAPX overexpressing parasites were not resistant to peroxynitrite. Whereas isolated tryparedoxin peroxidases react rapidly (k=7.2 x 10(5) M(-1) x s(-1)) and reduce peroxynitrite to nitrite, our results demonstrate that both TcMPX and TcCPX peroxiredoxins also efficiently decompose exogenous- and endogenously-generated peroxynitrite in intact cells. The degree of protection provided by TcCPX against peroxynitrite challenge results in higher parasite proliferation rates, and is demonstrated by inhibition of intracellular redox-sensitive fluorescence probe oxidation, protein 3-nitrotyrosine and protein-DMPO (5,5-dimethylpyrroline-N-oxide) adduct formation. Additionally, peroxynitrite-mediated over-oxidation of the peroxidatic cysteine residue of peroxiredoxins was greatly decreased in TcCPX overexpressing cells. The protective effects generated by TcCPX and TcMPX after oxidant challenge were lost by mutation of the peroxidatic cysteine residue in both enzymes. We also observed that there is less peroxynitrite-dependent 3-nitrotyrosine formation in infective metacyclic trypomastigotes than in non-infective epimastigotes. Together with recent reports of up-regulation of antioxidant enzymes during metacyclogenesis, our results identify components of the antioxidant enzyme network of T. cruzi as virulence factors of emerging importance