Characterization of anthocyanins from the fruits of baguaçu (Eugenia umbelliflora Berg)

Anthocyanin pigments in the berries of bagua?u (Eugenia umbelliflora Berg), a tropical fruit from Brazil, were extracted with 0.1% HCl in ethanol, and the crude anthocyanin extract was purified by Amberlite XAD-7 open-column chromatography. Six major anthocyanins were isolated by preparative HPLC, and their chemical structures were identified by spectroscopic methods (TLC, UV-vis, MS, and (1)H NMR). Delphinidin 3-O-beta-glucopyranoside, cyanidin 3-O-beta-glucopyranoside, petunidin 3-O-beta-glucopyranoside, pelargonidin 3-O-beta-glucopyranoside, peonidin 3-O-beta-glucopyranoside, and malvidin 3-O-beta-glucopyranoside were identified. On the basis of chromatographic data the total anthocyanin content was 342 mg/100 g of fresh bagua?u berries. Therefore, the concomitant presence of six anthocyanins in a single plant species makes this product promising as a new pigment source.     

Prevalence and risk factors for Trichomonas foetus infection in cattle in northeastern Costa Rica

Two studies (one pilot and one cross-sectional) were conducted in the two main livestock-rearing areas of Costa Rica using an improved method (In-Pouch TF) for the detection of Trichomonas foetus infection in bulls. Herd prevalence rates of 6.7% (6/98) and 15.9% (10/63), and bull prevalence rates of 3.9% (6/153) and 6.2% (14/225) were found in the pilot and cross-sectional studies, respectively. Adjusted prevalences in the cross-sectional study were 18.4% and 7.2% for aarms and bulls, respectively. Breed (Bos taurus) and age (over 4 years) were the main risk factors identified using random-effects logistics regression. The nature of the disease and the high prevalence indicated that trichomoniasis could have a serious economic impact on cattle production in Costa Rica.     

Cerebellar degeneration in cattle grazing Solanum bonariense ("Naranjillo") in Western Uruguay.

Cattle in western Uruguay that were eating Solanum bonariense developed periodic episodes of ataxia, hypermetria, hyperesthesia, head and thoracic limb extension, opisthotonus, nystagmus, and falling to the side or backward. Similar clinical signs were experimentally reproduced in cattle by administration of S. bonariense via rumen cannula at a dose of 1,024 g/kg body mass. No significant gross lesions were observed in field cases or experimentally induced cases. Spontaneous and induced histologic lesions were similar and included vacuolation, degeneration, and loss of Purkinje cells. Axonal spheroids, microcavitations, and other changes of wallerian-type degeneration in cerebellar white matter were also observed. Ultrastructural changes included increased number of electron-dense residual storage bodies in membrane-bound vesicles in affected Purkinje cells, and similar vesicles and mitochondria in axonal spheroids. No histologic lesions were detected in the other examined tissues. The Purkinje-cell swelling and vacuolation with subsequent cerebellar degeneration are suggestive of Purkinje-cell specific toxin that produces abnormal lysosome function and cell specific axonal transport. This is the first report of S. bonariense toxicity.     

Prospecting for pig single nucleotide polymorphisms in the human genome: have we struck gold?

Gene‐to‐gene variation in the frequency of single nucleotide polymorphisms (SNPs) has been observed in humans, mice, rats, primates and pigs, but a relationship across species in this variation has not been described. Here, the frequency of porcine coding SNPs (cSNPs) identified by in silico methods, and the frequency of murine cSNPs, were compared with the frequency of human cSNPs across homologous genes. From 150 000 porcine expressed sequence tag (EST) sequences, a total of 452 SNP‐containing sequence clusters were found, totalling 1394 putative SNPs. All the clustered porcine EST annotations and SNP data have been made publicly available at http://sputnik.btk.fi/project?name=swine . Human and murine cSNPs were identified from dbSNP and were characterized as either validated or total number of cSNPs (validated plus non‐validated) for comparison purposes. The correlation between in silico pig cSNP and validated human cSNP densities was found to be 0.77 (p < 0.00001) for a set of 25 homologous genes, while a correlation of 0.48 (p < 0.0005) was found for a primarily random sample of 50 homologous human and mouse genes. This is the first evidence of conserved gene‐to‐gene variability in cSNP frequency across species and indicates that site‐directed screening of porcine genes that are homologous to cSNP‐rich human genes may rapidly advance cSNP discovery in pigs.     

Ustilago maydis Infection of the Nonnatural Host Arabidopsis thaliana

ABSTRACT The experimental infection of Arabidopsis thaliana by the maize phytopathogenic hemibasidiomycete Ustilago maydis under axenic conditions is described. When plantlets were inoculated with mixtures of compatible haploids, the fungus was able to grow on the plant surface of inoculated seedlings in the form of white mycelium and invade the tissues, probably penetrating through stomata; however, it did not form teliospores. Symptoms of disease were increased anthocyanin formation, development of chlorosis, increased formation of secondary roots, induction of malformations in the leaves and petioles, induction of tissue necrosis, and stunting. In several cases, death of the invaded plants occurred. Interestingly, inoculation of single U. maydis haploid strains produced similar symptoms in Arabidopsis plantlets. In contrast, several mutants avirulent to maize also were avirulent or less virulent than wildtype strains on Arabidopsis. Collectively, the reported data suggest that the U. maydis-Arabidopsis pathosystem may constitute a useful experimental model for the analysis of some aspects of the virulence factors of the fungus. With the study of nonhost responses and their comparison to those occurring during maize infection, we will be able to elucidate some obscure aspects of U. maydis pathogenicity in the future.     

Development of a Suitable Maintenance Diet for Anodonta cygnea

Selenastrum, Chlorella and the Cyanophyta groups, important components of the phytoplankton in the natural habitat of Anodonta cygnea in Mira Lagoon, were used separately as experimental diet for Anodonta cygnea. To assess the effects of the different diets, several organic and inorganic compounds of the haemolymph and extrapallial fluid were measured. Protein content was significantly reduced with experimental Non Feed, and carbohydrate content with Non Feed, Selenastrum, Chlorella , and Cyanophyta diets compared to the control in the lagoon. Lipid contents in body fluids were similar among the different diet groups, with the exception of the Chlorella diet, which showed a higher value. In all diets, the inorganic elements, magnesium and chloride, presented a non-significant variation profile. The concentration of sodium and potassium was significantly affected in Selenastrum and Chlorella diets, observing in the Non Feed diet a minimum value for potassium. The non-significant variation of osmolality suggests the presence of a specific osmotic regulatory mechanism independent of the diet. A particular regulation mechanism seems to exist for both calcium and manganese ion inducing similar profiles for all experimental diets with higher contents in Selenastrum and Cyanophyta diets, respectively. The higher calcium ion concentration appears associated with lower protein-carbohydrate contents, probably due to weak calcium aggregation and deposition mechanism, except for the control and Mixture diets. In general, the concentrations of organic and inorganic compounds in the body fluids of Mixture-fed A. cygnea , were more similar to those found in the control diet group. This suggests that an equal mixture of the three algae, Selenastrum, Chlorella , and Cyanophyta, is more appropriate diet to provide the necessary nutrients for a normal maintenance of A. cygnea in the wild.     

Genetic Diversity and Structure of the Apiosporina morbosa Populations on Prunus spp

ABSTRACT Populations of Apiosporina morbosa collected from 15 geographic locations in Canada and the United States and three host species, Prunus virginiana, P. pensylvanica, and P. padus, were evaluated using the sequence-related amplified polymorphism (SRAP) technique to determine their genetic diversity and population differentiation. Extensive diversity was detected in the A. morbosa populations, including 134 isolates from Canada and the United States, regardless of the origin of the population. The number of polymorphic loci varied from 6.9 to 82.8% in the geographic populations, and from 41.4 to 79.3% in the populations from four host genotypes based on 58 polymorphic fragments. In all, 44 to 100% of isolates in the geographic populations and 43.6 to 76.2% in populations from four host genotypes represented unique genotypes. Values of heterozygosity (H) varied from 2.8 to 28.3% in the geographic populations and 10.2 to 26.1% in the populations from four host genotypes. In general, the A. morbosa populations sampled from wild chokecherry showed a higher genetic diversity than those populations collected from other host species, whereas the populations isolated from cultivated chokecherry, P. virginiana 'Shubert Select', showed a reduction of genetic diversity compared with populations from wild P. virginiana. Significant population differentiation was found among both the geographic populations (P < 0.05) and populations from different host genotypes (P < 0.02). In the geographic populations, most of populations from cultivated and wild P. virginiana were closely clustered, and no population differentiation was detected except for the populations from Morris, Morden, and Winnipeg, Manitoba, Canada. Furthermore, the populations from P. virginiana in the same geographic locations had higher genetic identity and closer genetic distance to each other compared with those from different locations. Four populations from P. virginiana, P. pensylvanica, and P. padus, were significantly differentiated from each other (P < 0.02), except there was no differentiation between the Shubert Select and wild chokecherry populations (>P> = 0.334). Indirect estimation of gene flow showed that significant restricted gene flow existed between populations from different regions and host species. Gene flow rates (Nm) varied from <1 to 12.5, with higher gene flow rates among population pairs from the same host species (P = 1.000). The analysis of molecular variance revealed that a major genetic variance source came from the genetic variation among isolates within populations regardless of the origin and host genotype of the population. Although some locations had a limited number of isolates, the results of this study clearly showed that the genetic diversity and population differentiation of A. morbosa were closely associated with host genotypes and geographic locations, but mostly with the former.