Rumen-protected methionine supplementation alters lipid profile of preimplantation embryo and endometrial tissue of Holstein cows

Our objective is to evaluate the effects of feeding rumen-protected Met (RPM) throughout the transition period and early lactation on the lipid profile of the preimplantation embryos and the endometrial tissue of Holstein cows. Treatments consisted of feeding a total mixed ration with top-dressed RPM (Smartamine® M, Adisseo, Alpharetta, GA, United States; MET; n = 11; RPM at a rate of 0.08% of DM: Lys:Met = 2.8:1) or not (CON; n = 9, Lys:Met = 3.5:1). Endometrial biopsies were performed at 15, 30, and 73 days in milk (DIM). Prior to the endometrial biopsy at 73 DIM, preimplantation embryos were harvested via flushing. Endometrial lipid profiles were analyzed using multiple reaction monitoring-profiling and lipid profiles of embryos were acquired using matrix assisted laser desorption/ionization mass spectrometry. Relative intensities levels were used for principal component analysis. Embryos from cows in MET had greater concentration of polyunsaturated lipids than embryos from cows in CON. The endometrial tissue samples from cows in MET had lesser concentrations of unsaturated and monounsaturated lipids at 15 DIM, and greater concentration of saturated, unsaturated (specifically diacylglycerol), and monounsaturated (primarily ceramides) lipids at 30 DIM than the endometrial tissue samples from cows in CON. In conclusion, feeding RPM during the transition period and early lactation altered specific lipid classes and lipid unsaturation level of preimplantation embryos and endometrial tissue

Leptogenesis, Yukawa Textures and Weak Basis Invariants

We show that a large class of sets of leptonic texture zeros considered in the literature imply the vanishing of certain CP-odd weak-basis invariants. These invariant conditions enable one to recognize a flavour model corresponding to a set of texture zeros, when written in an arbitrary weak-basis where the zeros are not manifest. We also analyse the r\^ ole of texture zeros in allowing for a connection between leptogenesis and low-energy leptonic masses, mixing and CP violation. For some of the textures the variables relevant for leptogenesis can be fully determined in terms of low energy parameters and heavy neutrino masses.Comment: 16 pages, no figures. One reference added, version submitted for publicatio

La adquisición de islas de patogenicidad favorece la emergencia y potencial de virulencia de Escherichia coli productor de Shiga toxina (STEC) LEE-negativo

STEC causa diarrea, disentería y síndrome hemolítico urémico (SHU). La Shiga toxina es el principal factor de virulenciade STEC, pero la capacidad de la bacteria para adherirse y colonizar el intestino humano es fundamental para causarenfermedad. La Isla de Patogenicidad (PAI) Locus of Enterocyte Effacement (LEE) contiene genes que median elfenotipo de adhesión de un grupo de cepas STEC (LEE-positivo) que son clínicamente relevantes debido a su asociacióncon SHU. No obstante, cepas STEC que carecen de LEE (LEE-negativo) también han sido aisladas de casos de SHU,indicando que factores de virulencia adicionales están involucrados en la patogenicidad de estas bacterias. De hecho,tres PAIs, denominadas como ?Locus of Proteolysis Activity?, ?Subtilase-Encoding Pathogenicity Island? y el ?Locus ofAdhesion and Autoaggregation? (LAA), han sido reportadas como exclusivamente presentes en STEC LEE-negativo. Sinembargo, se desconocen los mecanismos de patogénesis mediados por estas PAIs. Recientemente, la incidencia degastroenteritis causada por cepas STEC LEE-negativo ha aumentado en varios países. Por lo tanto, en este estudioinvestigamos la base genética para su emergencia y realizamos un análisis de genómica comparativa utilizando 367genomas de cepas STEC LEE-negativo aisladas a nivel mundial. Como resultado, identificamos tres nuevos elementosgenéticos, incluyendo dos PAIs y un Elemento Integrativo y Conjugativo. Además, encontramos que LAA fue la PAI másfrecuente, sugiriendo que juega un papel importante en la biología de STEC. En consecuencia, LAA fue eliminada delcromosoma de la cepa STEC E045 mediante reemplazo alélico. Posteriormente, se realizaron ensayos in vitro e in vivopara determinar si la deleción de LAA afecta la capacidad de adhesión, colonización y virulencia de la cepa E045. Sepresenta evidencia en apoyo a la participación de LAA en la colonización intestinal de un modelo murino de infecciónpor STEC. Finalmente, análisis filogenéticos indicaron que clados en los que se agrupan cepas con dos o más PAIs estángeográficamente más diseminados en comparación con clados filogenéticamente cercanos en los que se agrupan cepasque carecen o contienen una sola PAI. Este estudio es un paso adelante en el conocimiento de la evolución y virulenciade STEC.Fil: Montero, David A.. Universidad de Chile. Facultad de Medicina; ChileFil: Del Canto, Felipe. Universidad de Chile. Facultad de Medicina; ChileFil: Salazar, Juan C.. Universidad de Chile. Facultad de Medicina; ChileFil: Velasco, Juliana. Universidad de Chile. Facultad de Medicina; ChileFil: Colello, Rocío. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Padola, Nora Lía. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Oñate, Angel. Universidad de Chile. Facultad de Medicina; ChileFil: Puente, José L.. Universidad Nacional Autónoma de México. Instituto de Biotecnología; MéxicoFil: Vidal, Roberto. Universidad de Chile. Facultad de Medicina; ChileXXIV Congreso Latinoamericano de Microbiología; XL Congreso Chileno de Microbiología; II Reunión Anual de la Asociación Chilena de Inmunología y IX Reunión de la Sociedad Latinoamericana de Tuberculosis y otras MicobacteriosisSantiago de ChileChileAsociación Latinoamericana de Microbiologí

Leptonic CP Violation and Neutrino Mass Models

We discuss leptonic mixing and CP violation at low and high energies, emphasizing possible connections between leptogenesis and CP violation at low energies, in the context of lepton flavour models. Furthermore we analyse weak basis invariants relevant for leptogenesis and for CP violation at low energies. These invariants have the advantage of providing a simple test of the CP properties of any lepton flavour model.Comment: 26 pages, no figures, submitted to the Focus Issue on `Neutrino Physics` edited by F. Halzen, M. Lindner and A. Suzuki, to be published in New Journal of Physic

Genomic transformation and social organization during the Copper Age–Bronze Age transition in southern Iberia

The emerging Bronze Age (BA) of southeastern Iberia saw marked social changes. Late Copper Age (CA) settlements were abandoned in favor of hilltop sites, and collective graves were largely replaced by single or double burials with often distinctive grave goods indirectly reflecting a hierarchical social organization, as exemplified by the BA El Argar group. We explored this transition from a genomic viewpoint by tripling the amount of data available for this period. Concomitant with the rise of El Argar starting ~2200 cal BCE, we observe a complete turnover of Y-chromosome lineages along with the arrival of steppe-related ancestry. This pattern is consistent with a founder effect in male lineages, supported by our finding that males shared more relatives at sites than females. However, simple two-source models do not find support in some El Argar groups, suggesting additional genetic contributions from the Mediterranean that could predate the BA.Introduction Results - Genetic substructure in the Iberian CA - Genetic turnover in the southern Iberian BA and the rise of El Argar - Mediterranean and central European ancestries shaped the genetic profile of southeastern BA groups in Iberia - A late Argar genetic outlier makes links to North Africa and the central Mediterranean - Insights into phenotypic variation, demography, and social correlates of CA and EBA El Argar societies Discussion Material and method

The insecticides permethrin and chlorpyrifos show limited genotoxicity and no leukemogenic potential in human and murine hematopoietic stem progenitor cells

Altres ajuts: European Food and Safety Authority, EFSA.PRAS.2018.04-CT1; Consejo Nacional de Ciencia y Tecnología, CB-2012-01-183467; Centro de Investigación Biomédica en Red en Cáncer, PID2019-104695RBI00; Asociación Española Contra el Cáncer, AECC INVES211226MOLI

Genomic transformation and social organization during the Copper Age-Bronze Age transition in southern Iberia

The emerging Bronze Age (BA) of southeastern Iberia saw marked social changes. Late Copper Age (CA) settlements were abandoned in favor of hilltop sites, and collective graves were largely replaced by single or double burials with often distinctive grave goods indirectly reflecting a hierarchical social organization, as exemplified by the BA El Argar group. We explored this transition from a genomic viewpoint by tripling the amount of data available for this period. Concomitant with the rise of El Argar starting ~2200 cal BCE, we observe a complete turnover of Y-chromosome lineages along with the arrival of steppe-related ancestry. This pattern is consistent with a founder effect in male lineages, supported by our finding that males shared more relatives at sites than females. However, simple two-source models do not find support in some El Argar groups, suggesting additional genetic contributions from the Mediterranean that could predate the BA

BCR-ABL1-induced expression of HSPA8 promotes cell survival in chronic myeloid leukaemia

In order to determine new signal transduction pathways implicated in chronic myeloid leukaemia (CML), we performed a gene expression profile comparison between CD34+ cells from CML patients and healthy donors. Functional studies were performed using the Mo7e and Mo7e-p210 cell lines. Expression of CCND1 (Cyclin D1), as well as the chaperone HSPA8, which is important for regulation of CCND1, were significantly upregulated in CD34+ CML cells. Upregulation of HSPA8 was dependent, at least in part, on STAT5 (signal transducer and activator of transcrition 5)-dependent transcriptional activation, as demonstrated by chromatin immunoprecipitation. The presence of HSPA8 in the nuclear protein fraction as well as its binding to CCND1 suggests that it may contribute to stabilization of the CCND1/CDK4 complex, which, in turn, may participate in proliferation of CML cells. Treatment of CML cells with the specific HSPA8 inhibitor 15-deoxyspergualin induced inhibition of CML cell viability but did not induce apoptosis. In conclusion, our studies suggest that STAT5-mediated activation of HSPA8 induces nuclear translocation and activation of the CCND1/CDK4 complex leading to increased proliferation of CML cells, deciphering a new pathway implicated in CML and supporting a potential role of chaperone inhibitors in the treatment of CML

Genomic transformation and social organization during the Copper Age-Bronze Age transition in southern Iberia

The emerging Bronze Age (BA) of southeastern Iberia saw marked social changes. Late Copper Age (CA) settlements were abandoned in favor of hilltop sites, and collective graves were largely replaced by single or double burials with often distinctive grave goods indirectly reflecting a hierarchical social organization, as exemplified by the BA El Argar group. We explored this transition from a genomic viewpoint by tripling the amount of data available for this period. Concomitant with the rise of El Argar starting ∼2200 cal BCE, we observe a complete turnover of Y-chromosome lineages along with the arrival of steppe-related ancestry. This pattern is consistent with a founder effect in male lineages, supported by our finding that males shared more relatives at sites than females. However, simple two-source models do not find support in some El Argar groups, suggesting additional genetic contributions from the Mediterranean that could predate the BA.This work was supported by the Max Planck Society (V.V.-M. and W.H.); European Research Council (ERC) grant 771234—PALEoRIDER (W.H.); Spanish Ministry of Economy, Industry and Competitiveness project HAR2017-85962-P (C.O., C.R.-H., M.I.F., E.C.B., C.V.-F., V.L., R.M., and R.R.); AGAUR 2017SGR1044 (C.O., C.R.-H., M.I.F., E.C.B., C.V.-F., V.L., R.M., and R.R.); ICREA Academia program (R.R.); John Templeton Foundation grant 61220 (D.R.); and Paul Allen Family Foundation (D.R.). D.R. is an Investigator of the Howard Hughes Medical Institute