RESUMEN
Eucalyptus urophylla is an important species in the Brazilian forest sector due to its rapid growth rates and resistance to disease. The aim of this study was to verify Mendelian inheritance, genetic linkage, and genotypic disequilibrium for 15 microsatellite loci, with the goal of producing a robust set of genetic markers. Mendelian inheritance and genetic linkage analyses were carried out using genotypes from maternal trees, and their open-pollinated seeds and genotypic disequilibrium were assessed using adult trees. By comparing heterozygous maternal genotypes and their seeds, we found no significant deviations from the expected 1:1 Mendelian segregation and the expected 1:1:1:1 segregation hypothesis for pairwise loci. For adult trees, we did not find strong evidence of genotypic imbalance for pairwise loci. Our results indicated that the analyzed set of microsatellite loci could be used to carry out analyses of genetic diversity, mating system, and parentage in E. urophylla.
Asunto(s)
Eucalyptus/genética , Desequilibrio de Ligamiento , Repeticiones de Microsatélite , Frecuencia de los Genes , Genotipo , Polimorfismo GenéticoRESUMEN
BACKGROUND: Greyhounds are known to have a higher systemic arterial blood pressure (BP) than non-Greyhound dogs. OBJECTIVES: The purpose of this study was to determine whether the high systemic BP was because of the white-coat effect. ANIMALS: Twenty-two healthy retired racing Greyhounds (RRG) enrolled in a blood donation program. MATERIALS/METHODS: We prospectively measured systemic BP in 3 environments: in the hospital by the investigator (Hosp), in the home by the investigator (H/I), and in the home by the owner (H/O). Five serial measurements of systolic, diastolic, and mean arterial pressures (SAP, DAP, MAP) as well as heart rate (HR) were measured by an oscillometric method on the distal forelimb and distal hind limb in all 3 environments. RESULTS: There was a significant difference for SAP, MAP, and HR between the Hosp and both H/I and H/O (P < .001); there were no significant differences for any of the parameters between the H/I and H/O environments. HR, but not SAP, MAP, or DAP (P < .05) decreased in RRG with multiple hospital visits for blood donation before this study. The hind limb SAP was significantly higher than the forelimb SAP (P < .05). CONCLUSIONS AND CLINICAL IMPORTANCE: We conclude that the high SAP, MAP, and HR seen in the hospital setting are likely because of a white-coat effect. Furthermore, consideration should be given to defining the parameters of normal BP in RRG according to the environment in which they are obtained.
Asunto(s)
Presión Sanguínea/fisiología , Perros/fisiología , Hipertensión de la Bata Blanca/veterinaria , Animales , Perros/psicología , Femenino , Masculino , Estudios Prospectivos , Factores Sexuales , Estadísticas no ParamétricasRESUMEN
Leptospira species colonize a significant proportion of rodent populations worldwide and produce life-threatening infections in accidental hosts, including humans. Complete genome sequencing of Leptospira interrogans serovar Copenhageni and comparative analysis with the available Leptospira interrogans serovar Lai genome reveal that despite overall genetic similarity there are significant structural differences, including a large chromosomal inversion and extensive variation in the number and distribution of insertion sequence elements. Genome sequence analysis elucidates many of the novel aspects of leptospiral physiology relating to energy metabolism, oxygen tolerance, two-component signal transduction systems, and mechanisms of pathogenesis. A broad array of transcriptional regulation proteins and two new families of afimbrial adhesins which contribute to host tissue colonization in the early steps of infection were identified. Differences in genes involved in the biosynthesis of lipopolysaccharide O side chains between the Copenhageni and Lai serovars were identified, offering an important starting point for the elucidation of the organism's complex polysaccharide surface antigens. Differences in adhesins and in lipopolysaccharide might be associated with the adaptation of serovars Copenhageni and Lai to different animal hosts. Hundreds of genes encoding surface-exposed lipoproteins and transmembrane outer membrane proteins were identified as candidates for development of vaccines for the prevention of leptospirosis.
Asunto(s)
Genoma Bacteriano , Genómica , Leptospira interrogans/fisiología , Leptospira interrogans/patogenicidad , Animales , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Cricetinae , Humanos , Leptospira interrogans/clasificación , Leptospira interrogans/genética , Leptospirosis/microbiología , Ratones , Datos de Secuencia Molecular , Análisis de Secuencia de ADN , Serotipificación , Virulencia/genéticaRESUMEN
Xylella fastidiosa is a xylem-dwelling, insect-transmitted, gamma-proteobacterium that causes diseases in many plants, including grapevine, citrus, periwinkle, almond, oleander, and coffee. X. fastidiosa has an unusually broad host range, has an extensive geographical distribution throughout the American continent, and induces diverse disease phenotypes. Previous molecular analyses indicated three distinct groups of X. fastidiosa isolates that were expected to be genetically divergent. Here we report the genome sequence of X. fastidiosa (Temecula strain), isolated from a naturally infected grapevine with Pierce's disease (PD) in a wine-grape-growing region of California. Comparative analyses with a previously sequenced X. fastidiosa strain responsible for citrus variegated chlorosis (CVC) revealed that 98% of the PD X. fastidiosa Temecula genes are shared with the CVC X. fastidiosa strain 9a5c genes. Furthermore, the average amino acid identity of the open reading frames in the strains is 95.7%. Genomic differences are limited to phage-associated chromosomal rearrangements and deletions that also account for the strain-specific genes present in each genome. Genomic islands, one in each genome, were identified, and their presence in other X. fastidiosa strains was analyzed. We conclude that these two organisms have identical metabolic functions and are likely to use a common set of genes in plant colonization and pathogenesis, permitting convergence of functional genomic strategies.
Asunto(s)
Citrus/microbiología , Gammaproteobacteria/genética , Genoma Bacteriano , Enfermedades de las Plantas/microbiología , Secuencia de Bases , Datos de Secuencia MolecularRESUMEN
Com o propósito de determinar a relaçäo filogenética entre a cana-de-açúcar e membros da subtribo Saccharinae,a regiäo gênica nuclear ITS1-5,8S-ITS2 (ITS: espaçador interno transcrito; 5,8S: DNA ribossomal 5.8S), com alta taxa evolutiva, foi identificada no banco de dados do projeto genoma "Sugarcane Expressed Sequence Tag" (SUCEST). Uma análise através do método de parcimônia, utilizando esta regiäo e seqüências homólogas de 23 Andropogoneae retiradas da base de dados GenBank, indicou que a cana-de-açúcar é o grupo-irmäo de Saccharum sinense. No entanto, devido à pequena quantidade de caracteres informativos para parcimônia e à homoplasia presentes na regiäo ITS1-5,8S-ITS2, näo foi possível determinar com segurança a relaçäo filogenética entre a cana-de-açúcar e alguns dos demais membros da tribo Saccharine. Como alternativa para esta baixa resoluçäo, dezessete regiões gênicas nucleares, cloroplasmáticas ou mitocondriais foram selecionadas a partir do banco de dados SUCEST com o objetivo de encontrar marcadores mais apropriados para a reconstruçäo da filogenia da cana-de-açúcar. Entre elas, aquelas correspondentes à alfa-tubulina, rpl16, a rpoC2 apresentaram baixa incidência de polimorfismo e taxas de evoluçäo equivalentes ou mesmo maiores do que a observada para a regiäo ITS1-5,8S-ITS2. Estes marcadores säo propostos como preferenciais para estudos filogenéticos da subtribo Saccharinae.
Asunto(s)
Etiquetas de Secuencia Expresada , Filogenia , Plantas , Bases de Datos como AsuntoRESUMEN
Restriction fragment length polymorphism (RFLP) maps of chromosomes 6A, 6B, and 6D of hexaploid wheat (Triticum aestivum L. em. Thell.) have been produced. They were constructed using a population of F7-8 recombinant inbred lines derived from a synthetic wheat x bread wheat cross. The maps consist of 74 markers assigned to map positions at a LOD >= 3 (29 markers assigned to 6A, 24 to 6B, and 21 to 6D) and 2 markers assigned to 6D ordered at a LOD of 2.7. Another 78 markers were assigned to intervals on the maps. The maps of 6A, 6B, and 6D span 178, 132, and 206 cM, respectively. Twenty-one clones detected orthologous loci in two homoeologues and 3 detected an orthologous locus in each chromosome. Orthologous loci are located at intervals of from 1.5 to 26 cM throughout 70% of the length of the linkage maps. Within this portion of the maps, colinearity (homosequentiality) among the three homoeologues is strongly indicated. The remainder of the linkage maps consists of three segments ranging in length from 47 to 60 cM. Colinearity among these chromosomes and other Triticeae homoeologous group 6 chromosomes is indicated and a consensus RFLP map derived from maps of the homoeologous group 6 chromosomes of hexaploid wheat, tetraploid wheat, Triticum tauschii, and barley is presented. Key words : RFLP, wheat, linkage maps, molecular markers.