Density-dependent synthetic magnetism for ultracold atoms in optical lattices

10 pags.; 6 figs.; PACS number(s): 67.85.−d, 03.65.Vf, 03.75.Lm© 2015 American Physical Society. Raman-assisted hopping can allow for the creation of density-dependent synthetic magnetism for cold neutral gases in optical lattices. We show that the density-dependent fields lead to a nontrivial interplay between density modulations and chirality. This interplay results in a rich physics for atoms in two-leg ladders, characterized by a density-driven Meissner-superfluid to vortex-superfluid transition, and a nontrivial dependence of the density imbalance between the legs. Density-dependent fields also lead to intriguing physics in square lattices. In particular, it leads to a density-driven transition between a nonchiral and a chiral superfluid, both characterized by nontrivial charge density-wave amplitude. We finally show how the physics due to the density-dependent fields may be easily probed in experiments by monitoring the expansion of doublons and holes in a Mott insulator, which presents a remarkable dependence on quantum fluctuations.We acknowledge support by the cluster of excellence QUEST, the DFG Research Training Group 1729, the SUTD start-up grant (Grant No. SRG-EPD-2012-045), and the Spanish Ministry of Economy and Competitiveness through Grants No. FIS-2012- 34479, No. BES-2010-031607, and No. EEBB-14-09077.Peer Reviewe

Constructor paralelo de planificaciones

Scheduling es un área activa de investigación en Inteligencia Artificial Aplicada. El interés en esta área es planificar adecuadamente la asignación de un número limitado de recursos a determinadas tareas que se deben desarrollar en el tiempo. Existen un número de técnicas heurísticas que han realizado contribuciones notables al problema de scheduling, entre ellas los algoritmos genéticos y otras variantes de la Computación Evolutiva. Estos algoritmos tienen la capacidad de descubrir planificaciones cercanas a las óptimas mucho más rápido debido a su paralelismo implícito. Varias implementaciones ya realizadas en esta dirección muestran que los algoritmos genéticos trabajan mejor cuando en la representación del cromosoma que utilizan se incorpora conocimiento específico del problema de modo tal que permita trabajar con operadores de recombinación avanzados. La elección de este tipo de representación indirecta del cromosoma requiere de un decodificador o "schedulers builder ", el cual transforme la representación del cromosoma en una planificación legal. En otras palabras los schedule builder deben garantizar la factibilidad y consistencia de cada planificación.Eje: Procesamiento concurrente, paralelo y distribuido. Procesamiento de imágenes.Red de Universidades con Carreras en Informática (RedUNCI

Constructor paralelo de planificaciones

Scheduling es un área activa de investigación en Inteligencia Artificial Aplicada. El interés en esta área es planificar adecuadamente la asignación de un número limitado de recursos a determinadas tareas que se deben desarrollar en el tiempo. Existen un número de técnicas heurísticas que han realizado contribuciones notables al problema de scheduling, entre ellas los algoritmos genéticos y otras variantes de la Computación Evolutiva. Estos algoritmos tienen la capacidad de descubrir planificaciones cercanas a las óptimas mucho más rápido debido a su paralelismo implícito. Varias implementaciones ya realizadas en esta dirección muestran que los algoritmos genéticos trabajan mejor cuando en la representación del cromosoma que utilizan se incorpora conocimiento específico del problema de modo tal que permita trabajar con operadores de recombinación avanzados. La elección de este tipo de representación indirecta del cromosoma requiere de un decodificador o "schedulers builder ", el cual transforme la representación del cromosoma en una planificación legal. En otras palabras los schedule builder deben garantizar la factibilidad y consistencia de cada planificación.Eje: Procesamiento concurrente, paralelo y distribuido. Procesamiento de imágenes.Red de Universidades con Carreras en Informática (RedUNCI

Human Erythroid Progenitors Are Directly Infected by SARS-CoV-2: Implications for Emerging Erythropoiesis in Severe COVID-19 Patients

We document here that intensive care COVID-19 patients suffer a profound decline in hemoglobin levels but show an increase of circulating nucleated red cells, suggesting that SARS-CoV-2 infection either directly or indirectly induces stress erythropoiesis. We show that ACE2 expression peaks during erythropoiesis and renders erythroid progenitors vulnerable to infection by SARS-CoV-2. Early erythroid progenitors, defined as CD34-CD117+CD71+CD235a-, show the highest levels of ACE2 and constitute the primary target cell to be infected during erythropoiesis. SARS-CoV-2 causes the expansion of colony formation by erythroid progenitors and can be detected in these cells after 2 weeks of the initial infection. Our findings constitute the first report of SARS-CoV-2 infectivity in erythroid progenitor cells and can contribute to understanding both the clinical symptoms of severe COVID-19 patients and how the virus can spread through the circulation to produce local inflammation in tissues, including the bone marrow

Activation of the Receptor Tyrosine Kinase, RET, improves long-term Hematopoietic Stem Cell outgrowth and potency

Expansion of Human Hematopoietic Stem Cells (HSCs) is a rapidly advancing field showing great promise for clinical applications. Recent evidence has implicated the nervous system and glial family ligands (GFLs) as potential drivers of hematopoietic survival and self-renewal in the bone marrow niche, but how to apply this to HSC maintenance and expansion is yet to be explored. We demonstrate a role for the GFL receptor, RET, at the cell surface of HSCs, in mediating sustained cellular growth, resistance to stress and improved cell survival throughout in vitro expansion. HSCs treated with the key RET ligand/co-receptor complex, GDNF/GFRa1, show improved progenitor function at primary transplantation and improved long-term HSC function at secondary transplantation. Finally, we demonstrate that RET drives a multi-faceted intracellular signalling pathway, including key signalling intermediates AKT, ERK1/2, NFkB and p53, responsible for a wide range of cellular and genetic responses which improve cell growth and survival under culture conditions

Good immune restitution but unsatisfactory viral suppression in children on ART in a remote Western Kenya area

Mexico AIDS Conference 200

Performance of the 2007 WHO Algorithm to diagnose Smear-negative Pulmonary Tuberculosis in a HIV prevalent setting

The 2007 WHO algorithm for diagnosis of smear-negative pulmonary tuberculosis (PTB) including Mycobacterium tuberculosis (MTB) culture was evaluated in a HIV prevalent area of Kenya

Loss of TET2 in human hematopoietic stem cells alters the development and function of neutrophils

Somatic mutations commonly occur in hematopoietic stem cells (HSCs). Some mutant clones outgrow through clonal hematopoiesis (CH) and produce mutated immune progenies shaping host immunity. Individuals with CH are asymptomatic but have an increased risk of developing leukemia, cardiovascular and pulmonary inflammatory diseases, and severe infections. Using genetic engineering of human HSCs (hHSCs) and transplantation in immunodeficient mice, we describe how a commonly mutated gene in CH, TET2, affects human neutrophil development and function. TET2 loss in hHSCs produce a distinct neutrophil heterogeneity in bone marrow and peripheral tissues by increasing the repopulating capacity of neutrophil progenitors and giving rise to low-granule neutrophils. Human neutrophils that inherited TET2 mutations mount exacerbated inflammatory responses and have more condensed chromatin, which correlates with compact neutrophil extracellular trap (NET) production. We expose here physiological abnormalities that may inform future strategies to detect TET2-CH and prevent NET-mediated pathologies associated with CH

Diagnostic accuracy of WHO screening criteria to guide lateral-flow lipoarabinomannan testing among HIV-positive inpatients: A systematic review and individual participant data meta-analysis

BACKGROUND: WHO recommends urine lateral-flow lipoarabinomannan (LF-LAM) testing with AlereLAM in HIV-positive inpatients only if screening criteria are met. We assessed the performance of WHO screening criteria and alternative screening tests/strategies to guide LF-LAM testing and compared diagnostic accuracy of the WHO AlereLAM algorithm (WHO screening criteria → AlereLAM) with AlereLAM and FujiLAM (a novel LF-LAM test). METHODS: We searched MEDLINE, Embase, and Cochrane Library from Jan 1, 2011 to March 1, 2020 for studies among adult/adolescent HIV-positive inpatients regardless of tuberculosis signs and symptoms. The reference standards were 1) AlereLAM or FujiLAM for screening tests/strategies and 2) culture or Xpert for AlereLAM/FujiLAM. We determined proportion of inpatients eligible for AlereLAM using WHO screening criteria; assessed accuracy of WHO criteria and alternative screening tests/strategies to guide LF-LAM testing; compared accuracy of WHO AlereLAM algorithm with AlereLAM/FujiLAM in all; and determined diagnostic yield of AlereLAM, FujiLAM, and Xpert MTB/RIF (Xpert). We estimated pooled proportions with a random-effects model, assessed diagnostic accuracy using random-effects bivariate models, and assessed diagnostic yield descriptively. FINDINGS: We obtained data from all 5 identified studies (n=3,504). The pooled proportion of inpatients eligible for AlereLAM using WHO criteria was 93% (95%CI 91, 95). Among screening tests/strategies to guide LF-LAM testing, WHO criteria, C-reactive protein (≥5 mg/L), and CD4 count (<200 cells/μL) had high sensitivities but low specificities; cough (≥2 weeks), haemoglobin (<8 g/dL), body mass index (<18.5 kg/m2), lymphadenopathy, and WHO-defined danger signs had higher specificities but suboptimal sensitivities. AlereLAM in all had the same sensitivity (62%) and specificity (88%) as WHO AlereLAM algorithm. Sensitivity of FujiLAM and AlereLAM was 69% and 48%, while specificity was 48% and 96%, respectively. Diagnostic yield of sputum Xpert was 29-41%, AlereLAM was 39-76%, and urine Xpert was 35-62%. In one study, FujiLAM diagnosed 80% of tuberculosis cases (vs 39% for AlereLAM), and sputum Xpert combined with AlereLAM, urine Xpert, or FujiLAM diagnosed 69%, 81%, and 92% of all cases, respectively. INTERPRETATION: WHO criteria and alternative screening tests/strategies have limited utility in guiding LF-LAM testing, suggesting that AlereLAM testing in all HIV-positive medical inpatients be implemented. Routine FujiLAM may improve tuberculosis diagnosis. FUNDING: None

Phospholipids and sports performance

Phospholipids are essential components of all biological membranes. Phosphatidylcholine (PC) and Phosphatidylserine (PS) are Phosphatidyl-phospholipids that are required for normal cellular structure and function. The participation in physical activity often challenges a variety of physiological systems; consequently, the ability to maintain normal cellular function during activity can determine sporting performance. The participation in prolonged intense exercise has been shown to reduce circulatory choline concentrations in some individuals. As choline is a pre-cursor to the neurotransmitter Acetylcholine, this finding has encouraged researchers to investigate the hypothesis that supplementation with PC (or choline salts) could enhance sporting performance. Although the available data that evaluates the effects of PC supplementation on performance are equivocal, acute oral supplementation with PC (~0.2 g PC per kg body mass) has been demonstrated to improve performance in a variety of sporting activities where exercise has depleted circulatory choline concentrations. Short term oral supplementation with soy-derived PS (S-PS) has been reported to attenuate circulating cortisol concentrations, improve perceived well-being, and reduce perceived muscle soreness after exercise. More recently, short term oral supplementation (750 mg per day of S-PS for 10 days) has been demonstrated to improve exercise capacity during high intensity cycling and tended to increase performance during intermittent running. Although more research is warranted to determine minimum dietary Phospholipid requirements for optimal sporting performance, these findings suggest that some participants might benefit from dietary interventions that increase the intakes of PC and PS