Profile of IL-2, IL-4, IL-10, IFN- ? , TNF- ? and KC-like cytokines in pregnant bitches

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Gestión del ranking para una asociación canina de perros de exposición

[ES] Esta aplicación web realizada en Ruby on Rails, tiene como objetivo principal la gestión del ranking para una asociación de perros de exposición. Dicha asociación es la “Asociación Española para el Fomento de la Raza Bulldog Francés”. En dicha asociación, los perros participan en exposiciones caninas y de acuerdo con una tabla y los resultados, les adjudican puntos a los perros. La tabla de asignación de puntos puede variar cada año.  El perro que más puntos obtiene gana el ranking, hay un ganador hembra y otro ganador macho. Por otra parte, los posibles roles de usuarios son: el rol de administrador, los cuales pueden manejar todos los recursos; el rol de socio, que puede crear nuevos perfiles de perros, enviar resultados de sus perros y demás acciones posibles para este rol; el rol de usuarios registrado, que son usuarios que fueron socios y que ya no lo son. Dicho tipo de usuario puede modificar su perfil, pero ya no podría hacer cambios o eliminar sus perros de la aplicación. Y tampoco podría borrar resultados de sus perros que ya hubiesen sido enviados cuando era socio;  y el rol de usuario no registrado que sólo pueden ver los listados de perros, ver sus perfiles y demás acciones que sólo sean ver pero no crear, modificar ni borrar nada. Como resultado final a este trabajo de fin de grado se ha obtenido una aplicación con los requisitos necesarios para cubrir las necesidades para la asociación de perros de exposición, en el cual se gestiona el ranking, también se gestionan los perfiles tanto de perros como de usuarios, control de accesos según el rol del usuario, gestión de las exposiciones, etc.

Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1

Background Lethal chondrodysplasia (bulldog syndrome) is a well-known congenital syndrome in cattle and occurs sporadically in many breeds. In 2015, it was noticed that about 12 % of the offspring of the phenotypically normal Danish Holstein sire VH Cadiz Captivo showed chondrodysplasia resembling previously reported bulldog calves. Pedigree analysis of affected calves did not display obvious inbreeding to a common ancestor, suggesting the causative allele was not a rare recessive. The normal phenotype of the sire suggested a dominant inheritance with incomplete penetrance or a mosaic mutation. Results Three malformed calves were examined by necropsy, histopathology, radiology, and computed tomography scanning. These calves were morphologically similar and displayed severe disproportionate dwarfism and reduced body weight. The syndrome was characterized by shortening and compression of the body due to reduced length of the spine and the long bones of the limbs. The vicerocranium had severe dysplasia and palatoschisis. The bones had small irregular diaphyses and enlarged epiphyses consisting only of chondroid tissue. The sire and a total of four affected half-sib offspring and their dams were genotyped with the BovineHD SNP array to map the defect in the genome. Significant genetic linkage was obtained for several regions of the bovine genome including chromosome 5 where whole genome sequencing of an affected calf revealed a COL2A1 point mutation (g.32473300 G > A). This private sequence variant was predicted to affect splicing as it altered the conserved splice donor sequence GT at the 5’-end of COL2A1 intron 36, which was changed to AT. All five available cases carried the mutant allele in heterozygous state and all five dams were homozygous wild type. The sire VH Cadiz Captivo was shown to be a gonadal and somatic mosaic as assessed by the presence of the mutant allele at levels of about 5 % in peripheral blood and 15 % in semen. Conclusions The phenotypic and genetic findings are comparable to a previously reported COL2A1 missense mutation underlying lethal chondrodysplasia in the offspring of a mosaic French Holstein sire (Igale Masc). The identified independent spontaneous splice site variant in COL2A1 most likely caused chondrodysplasia and must have occurred during the early foetal development of the sire. This study provides a first example of a dominant COL2A1 splice site variant as candidate causal mutation of a severe lethal chondrodysplasia phenotype. Germline mosaicism is a relatively frequent mechanism in the origin of genetic disorders and explains the prevalence of a certain fraction of affected offspring. Paternal dominant de novo mutations are a risk in cattle breeding, especially because the ratio of defective offspring may be very high and be associated with significant animal welfare problems.

Schwartz /

I. Schwartz: a history. Young Mr. Barter's repentance.--II. Bulldog and Butterfly. Julia and her Romeo: a chronicle of castle Barfield.

Brachycephalic obstructive airway syndrome : a review with six clinical cases

Dissertação de Mestrado Integrado em Medicina Veterinária

Estudo retrospetivo sobre traqueostomia permanente como tratamento cirúrgico em cães com síndrome braquicefálica obstrutiva

Dissertação de Mestrado Integrado em Medicina Veterinária