Mecanismos inductores y vías de la apoptosis en la diarrea vírica bovina

La apoptosis es una forma de muerte celular inducida por una gran variedad de estímulos, considerada como el resultado final de una cascada en la que intervienen una serie de enzimas denominadas caspasas, inducidas tanto por estímulos externos como internos. Entre éstas destacan las denominadas caspasas iniciadoras (2, 8, 9 y 10) y las caspasas ejecutoras o efectoras (3, 6 y 7). Existen dos vías principales reguladoras de la apoptosis: la vía extrínseca, inducida y mediada por receptores, la cual se inicia cuando un ligando apropiado se une a receptores de muerte localizados en la superficie celular, de modo que estas uniones ligando-receptor hacen que los dominios de muerte celular intracelulares y su unión a ciertas proteínas del citosol activen a las caspasas iniciadoras de esta vía (pe: caspasa 8), y la vía intrínseca o mitocondrial, gobernada por proteínas de la familia del Bcl-2 que agrupa un grupo de moléculas involucradas en la permeabilidad de la mitocondria, pudiéndose distinguir entre moléculas anti-apoptóticas y pro-apoptóticas. El desequilibrio en la expresión de estas moléculas incrementa la permeabilidad de la membrana mitocondrial, favoreciendo la liberación de proteínas al citosol y la activación de las caspasas iniciadora de esta vía (pe: caspasa 9). Una vez activadas las caspasas iniciadoras, éstas ejercerán su actividad proteolítica sobre las denominadas caspasas efectoras o ejecutoras (3, 6 y 7), las cuales, una vez activadas ejecutarán la muerte de forma irreversible. Junto a aspectos generales relacionados con los mecanismos y vías de la apoptosis, en este trabajo se abordan aspectos relacionados con dichos mecanismos en el transcurso de la diarrea vírica bovina, donde la apoptosis parece ser la responsable de la depleción linfoide y la leucopenia que caracterizan a esta enfermedad

El virus de la lengua azul como modelo para el estudio de los orbivirus

Al género Orbivirus pertenecen tres virus transmitidos a través de vector, que afectan al ganado domestico y a animales de vida libre (Lengua Azul, Peste Equina Africana y Enfermedad Hemorrágica Epizoótica de los Ciervos), y que han causado en las dos últimas décadas, especialmente el virus de la Lengua Azul (vLA), pérdidas económicas cuantiosas en prácticamente toda Europa y en los países del sur y el este del Mediterráneo. Es importante, por tanto, profundizar en el conocimiento sobre los mecanismos de actuación de estos virus, tomando como base al vLA considerado como el virus modelo para el estudio de este género, y en los mecanismos que modulan la respuesta inmunológica del hospedador para poder mejorar el control de la enfermedad mediante vacunas más eficaces. Hasta el momento se desconocen aspectos tan importantes como la duración de la viremia en animales infectados, el papel de la inmunidad celular desencadenada en el hospedador o los mecanismos de “hibernación” que permitan al vLA “reaparecer” tras un periodo de ausencia del vector. Además, el hecho de que los tres compartan los mismos vectores, hace necesario analizar el riesgo de entrada de los virus de la Peste Equina Africana y dela Enfermedad Hemorrágica Epizoótica de los Ciervos en España, -que actualmente se detectan en los países del África Subsahariana y en el sur y este del Mediterráneo, respectivamente-. Por último, se considera también imprescindible mejorar las técnicas de diagnóstico para el virus de la Enfermedad Hemorrágica Epizoótica de los Ciervos y el virus de la Peste Equina Africana y desarrollar nuevos ensayos basados en las cepas circulantes por el área mediterránea

Células presentadoras de antígeno: células dendríticas y su papel en la lengua azul

Las células presentadoras de antígeno (CPA) desempeñan un papel fundamental en el desarrollo de la respuesta inmunitaria mediante el procesamiento y la presentación de antígenos, así como a través de distintos estímulos que favorecen la proliferación y diferenciación linfocitaria. Entre las CPA, las células dendríticas (CDs) son consideradas como las más eficientes en las funciones de presentación. En este trabajo se abordan aspectos generales relacionados con la localización, estructura y función de estas células, así como con su importante papel en la instauración de la repuesta inmunitaria. Junto a las células endoteliales y a los macrófagos, las CDs son consideradas células blanco del virus de la lengua azul (vLA), desempeñando un importante papel en la diseminación orgánica de éste. Además, las CDs parecen jugar un importante papel como productoras o inductoras de sustancias vasoactivas responsables de los cambios vasculares que caracterizan a la enfermedad, quedando aún por determinar la influencia de estos mediadores químicos en la instauración de la respuesta inmunológica frente al virus, aspecto fundamental para el desarrollo y mejora de vacunas

Ab initio alpha-alpha scattering

Processes involving alpha particles and alpha-like nuclei comprise a major part of stellar nucleosynthesis and hypothesized mechanisms for thermonuclear supernovae. In an effort towards understanding alpha processes from first principles, we describe in this letter the first ab initio calculation of alpha-alpha scattering. We use lattice effective field theory to describe the low-energy interactions of nucleons and apply a technique called the adiabatic projection method to reduce the eight-body system to an effective two-cluster system. We find good agreement between lattice results and experimental phase shifts for S-wave and D-wave scattering. The computational scaling with particle number suggests that alpha processes involving heavier nuclei are also within reach in the near future.Comment: 6 pages, 6 figure

Ownership and control in a competitive industry

We study a differentiated product market in which an investor initially owns a controlling stake in one of two competing firms and may acquire a non-controlling or a controlling stake in a competitor, either directly using her own assets, or indirectly via the controlled firm. While industry profits are maximized within a symmetric two product monopoly, the investor attains this only in exceptional cases. Instead, she sometimes acquires a noncontrolling stake. Or she invests asymmetrically rather than pursuing a full takeover if she acquires a controlling one. Generally, she invests indirectly if she only wants to affect the product market outcome, and directly if acquiring shares is profitable per se. --differentiated products,separation of ownership and control,private benefits of control

Comparative studies on the pathogenicity and tissue distribution of three virulence variants of classical swine fever virus, two field isolates and one vaccine strain, with special regard to immunohistochemical investigations

<p>Abstract</p> <p>Background</p> <p>The aim of this study was to compare the tissue distribution and pathogenicity of three virulence variants of classical swine fever virus (CSFV) and to investigate the applicability of various conventional diagnostic procedures.</p> <p>Methods</p> <p>64 pigs were divided into three groups and infected with the highly virulent isolate ISS/60, the moderately virulent isolate Wingene'93 and the live attenuated vaccine strain Riems, respectively. Clinical signs, gross and histopathological changes were compared in relation to time elapsed post infection. Virus spread in various organs was followed by virus isolation, by immunohistochemistry, applying monoclonal antibodies in a two-step method and by <it>in situ </it>hybridisation using a digoxigenin-labelled riboprobe.</p> <p>Results</p> <p>The tissue distribution data are discussed in details, analyzing the results of the various diagnostic approaches. The comparative studies revealed remarkable differences in the onset of clinical signs as well as in the development of the macro- and microscopical changes, and in the tissue distribution of CSFV in the three experimental groups.</p> <p>Conclusion</p> <p>The present study demonstrates that in the case of highly and moderately virulent virus variants the virulence does not affect the pattern of the viral spread, however, it influences the outcome, the duration and the intensity of the disease. Immunohistochemistry has the advantage to allow the rapid detection and localisation of the virus, especially in cases of early infection, when clinical signs are still absent. Compared to virus isolation, the advantage of this method is that no cell culture facilities are required. Thus, immunohistochemistry provides simple and sensitive tools for the prompt detection of newly emerging variants of CSFV, including the viruses of very mild virulence.</p

Differentiation stage of myeloma plasma cells: biological and clinical significance

[EN] The notion that plasma cells (PCs) are terminally differentiated has prevented intensive research in multiple myeloma (MM) about their phenotypic plasticity and differentiation. Here, we demonstrated in healthy individuals (n = 20) that the CD19 − CD81 expression axis identifies three bone marrow (BM)PC subsets with distinct age-prevalence, proliferation, replication-history, immunoglobulin-production, and phenotype, consistent with progressively increased differentiation from CD19+CD81+ into CD19 − CD81+ and CD19 − CD81 − BMPCs. Afterwards, we demonstrated in 225 newly diagnosed MM patients that, comparing to normal BMPC counterparts, 59% had fully differentiated (CD19 − CD81 −) clones, 38% intermediate-differentiated (CD19 − CD81+) and 3% less-differentiated (CD19+CD81+) clones. The latter patients had dismal outcome, and PC differentiation emerged as an independent prognostic marker for progression-free (HR: 1.7; P = 0.005) and overall survival (HR: 2.1; P = 0.006). Longitudinal comparison of diagnostic vs minimal-residual-disease samples (n = 40) unraveled that in 20% of patients, less-differentiated PCs subclones become enriched after therapy-induced pressure. We also revealed that CD81 expression is epigenetically regulated, that less-differentiated clonal PCs retain high expression of genes related to preceding B-cell stages (for example: PAX5), and show distinct mutation profile vs fully differentiated PC clones within individual patients. Together, we shed new light into PC plasticity and demonstrated that MM patients harbouring less-differentiated PCs have dismal survival, which might be related to higher chemoresistant potential plus different molecular and genomic profiles

Protection of Spanish Ibex (Capra pyrenaica) against Bluetongue Virus Serotypes 1 and 8 in a Subclinical Experimental Infection

Many wild ruminants such as Spanish ibex (Capra pyrenaica) are susceptible to Bluetongue virus (BTV) infection, which causes disease mainly in domestic sheep and cattle. Outbreaks involving either BTV serotypes 1 (BTV-1) and 8 (BTV-8) are currently challenging Europe. Inclusion of wildlife vaccination among BTV control measures should be considered in certain species. In the present study, four out of fifteen seronegative Spanish ibexes were immunized with a single dose of inactivated vaccine against BTV-1, four against BTV-8 and seven ibexes were non vaccinated controls. Seven ibexes (four vaccinated and three controls) were inoculated with each BTV serotype. Antibody and IFN-gamma responses were evaluated until 28 days after inoculation (dpi). The vaccinated ibexes showed significant (P<0.05) neutralizing antibody levels after vaccination compared to non vaccinated ibexes. The non vaccinated ibexes remained seronegative until challenge and showed neutralizing antibodies from 7 dpi. BTV RNA was detected in the blood of non vaccinated ibexes from 2 to the end of the study (28 dpi) and in target tissue samples obtained at necropsy (8 and 28 dpi). BTV-1 was successfully isolated on cell culture from blood and target tissues of non vaccinated ibexes. Clinical signs were unapparent and no gross lesions were found at necropsy. Our results show for the first time that Spanish ibex is susceptible and asymptomatic to BTV infection and also that a single dose of vaccine prevents viraemia against BTV-1 and BTV-8 replication