Non-equilibrium entanglement in a driven Dicke model

We study the entanglement dynamics in the externally-driven single-mode Dicke model in the thermodynamic limit, when the field is in resonance with the atoms. We compute the correlations in the atoms-field ground state by means of the density operator that represents the pure state of the universe and the reduced density operator for the atoms, which results from taking the partial trace over the field coordinates. As a measure of bipartite entanglement, we calculate the linear entropy, from which we analyze the entanglement dynamics. In particular, we found a strong relation between the stability of the dynamical parameters and the reported entanglement.Comment: Contribution to the SLAFES XIX. This version to appear in J. Phys.: Conference Serie

Spin and charge optical conductivities in spin-orbit coupled systems

We study the frequency dependent spin- and charge- conductivity tensors of a two-dimensional electron gas (2DEG) with Rashba and Dresselhaus spin-orbit interaction. We show that the angular anisotropy of the spin-splitting energy induced by the interplay between the Rashba and Dresselhaus couplings gives rise to a characteristic spectral behavior of the spin and charge response which is significantly different from that of pure Rashba or Dresselhaus case. Such new spectral structures open the possibility for control of the optical response by applying an external bias and/or by adjusting the light frequency. In addition, it is shown that the relative strength of the spin-orbit coupling parameters can be obtained through optical probing.Comment: 13 pages, 4 figures. Revised versio

The Chlamydia trachomatis Type III Secretion Chaperone Slc1 Engages Multiple Early Effectors, Including TepP, a Tyrosine-phosphorylated Protein Required for the Recruitment of CrkI-II to Nascent Inclusions and Innate Immune Signaling

Chlamydia trachomatis, the causative agent of trachoma and sexually transmitted infections, employs a type III secretion (T3S) system to deliver effector proteins into host epithelial cells to establish a replicative vacuole. Aside from the phosphoprotein TARP, a Chlamydia effector that promotes actin re-arrangements, very few factors mediating bacterial entry and early inclusion establishment have been characterized. Like many T3S effectors, TARP requires a chaperone (Slc1) for efficient translocation into host cells. In this study, we defined proteins that associate with Slc1 in invasive C. trachomatis elementary bodies (EB) by immunoprecipitation coupled with mass spectrometry. We identified Ct875, a new Slc1 client protein and T3S effector, which we renamed TepP (Translocated early phosphoprotein). We provide evidence that T3S effectors form large molecular weight complexes with Scl1 in vitro and that Slc1 enhances their T3S-dependent secretion in a heterologous Yersinia T3S system. We demonstrate that TepP is translocated early during bacterial entry into epithelial cells and is phosphorylated at tyrosine residues by host kinases. However, TepP phosphorylation occurs later than TARP, which together with the finding that Slc1 preferentially engages TARP in EBs leads us to postulate that these effectors are translocated into the host cell at different stages during C.trachomatis invasion. TepP co-immunoprecipitated with the scaffolding proteins CrkI-II during infection and Crk was recruited to EBs at entry sites where it remained associated with nascent inclusions. Importantly, C. trachomatis mutants lacking TepP failed to recruit CrkI-II to inclusions, providing genetic confirmation of a direct role for this effector in the recruitment of a host factor. Finally, endocervical epithelial cells infected with a tepP mutant showed altered expression of a subset of genes associated with innate immune responses. We propose a model wherein TepP acts downstream of TARP to recruit scaffolding proteins at entry sites to initiate and amplify signaling cascades important for the regulation of innate immune responses to Chlamydia.Fil: Chen, Yi-Shan. University of Duke; Estados UnidosFil: Bastidas, Robert J.. University of Duke; Estados UnidosFil: Saka, Hector Alex. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. University of Duke; Estados UnidosFil: Carpenter, Victoria K.. Duke University Medical Center; . University of Duke; Estados UnidosFil: Richards, Kristian L.. Miami University; Estados UnidosFil: Plano, Gregory V.. Miami University; Estados UnidosFil: Valdivia, Raphael H.. University of Duke; Estados Unido

A 2-pyridone-amide inhibitor targets the glucose metabolism pathway of Chlamydia trachomatis.

UnlabelledIn a screen for compounds that inhibit infectivity of the obligate intracellular pathogen Chlamydia trachomatis, we identified the 2-pyridone amide KSK120. A fluorescent KSK120 analogue was synthesized and observed to be associated with the C. trachomatis surface, suggesting that its target is bacterial. We isolated KSK120-resistant strains and determined that several resistance mutations are in genes that affect the uptake and use of glucose-6-phosphate (G-6P). Consistent with an effect on G-6P metabolism, treatment with KSK120 blocked glycogen accumulation. Interestingly, KSK120 did not affect Escherichia coli or the host cell. Thus, 2-pyridone amides may represent a class of drugs that can specifically inhibit C. trachomatis infection.ImportanceChlamydia trachomatis is a bacterial pathogen of humans that causes a common sexually transmitted disease as well as eye infections. It grows only inside cells of its host organism, within a parasitophorous vacuole termed the inclusion. Little is known, however, about what bacterial components and processes are important for C. trachomatis cellular infectivity. Here, by using a visual screen for compounds that affect bacterial distribution within the chlamydial inclusion, we identified the inhibitor KSK120. As hypothesized, the altered bacterial distribution induced by KSK120 correlated with a block in C. trachomatis infectivity. Our data suggest that the compound targets the glucose-6-phosphate (G-6P) metabolism pathway of C. trachomatis, supporting previous indications that G-6P metabolism is critical for C. trachomatis infectivity. Thus, KSK120 may be a useful tool to study chlamydial glucose metabolism and has the potential to be used in the treatment of C. trachomatis infections

Manejo del agua en las acequias privadas Garrapatal y el Tambo en la provincia del Carchi, Ecuador

Como parte de las actividades que el Instituto Internacional del Manejo del Agua (IWMI, por su sigla en Inglés) adelantó en la Región Andina se llevó a cabo el estudio que aquí se presenta. El Banco Interamericano de Desarrollo otorgó una donación al Intituto a fin de valuar, entre otras cosas, el manejo de los sistemas de riego privados en las partes altas del Ecuador. Fue así como se escogieron dos acequias en la Provincia del Carchi: Garrapatal y el Tambo. El estudio representa un esfuerzo significativo por parte de los autores ya que las condiciones geográficas del área constituyen de por sí una gran barrera para la ejecución de este tipo de trabajos. Tanto el acceso a las bocatomas de estas acequias andinas como el recorrido de las mismas representan buenas horas de camino, en el mejor de los casos. Sin embargo, debe decirse que ese esfuerzo se ve más compensado por la espectacular belleza del paisaje y la amabilidad de los habitantes de la zona. El trabajo cubre no solo los aspectos técnicos relacionados con la disponibilidad, distribución y eficiencia en el manejo del agua sino también que fue mas allá al mirar factores relacionados con la producción agrícola, factores institucionales y organizativos de las juntas de agua, los rendimientos económicos de las diferentes zonas de riego ---incluyendo lo relacionado con las tarifas de agua---, así como aspectos ambientales de estos pequeños sistemas de riego en las laderas andinas. Finalmente, es bueno anotar que en este trabajo también el Instituto aplica los indicadores de desempeño que ha venido promoviendo en otros estudios a nivel global lo que permitirá eventualmente comparar los comportamientos de sistemas de riego similares pero bajo diferentes condiciones y ambientes geográficos una meta a mediano plazo del Instituto

Photonic quantum signatures of chaos and boson sampling

Boson sampling is a paradigmatic example of a task that can be performed by a quantum photonic computer yet is hard for digital classical computers. In a typical boson sampling experiment, the scattering amplitude is determined by the permanent of a submatrix of a unitary drawn from an ensemble of random matrices. Random matrix theory plays a very important role in quite diverse fields while at the same time being intimately related to quantum signatures of chaos. Within this framework, a chaotic quantum system exhibits level statistics characteristic of ensembles of random matrices. Such quantum signatures are encoded in the unitary evolution and so in this work we combine the dynamics of chaotic systems with boson sampling. One of the key results of our work is that we demonstrate the intimate relation between out-of-time-order correlators and boson sampling. We show that the unitary dynamics of a Floquet system may be exploited to perform sampling tasks with identical particles using single-mode phase shifters and multiport beamsplitters. At the end of our paper propose a photonic implementation of the multiparticle kicked rotor, which provides a concrete example of our general approach.Comment: 17 pages, 7 figures. Comments are welcom

Ptr/CTL0175 is required for the efficient recovery of chlamydia trachomatisfrom stress induced by gamma-interferon

Chlamydia trachomatis is the most common sexually transmitted bacterial pathogen in humans and a frequent cause of asymptomatic, persistent infections leading to serious complications, particularly in young women. Chlamydia displays a unique obligate intracellular lifestyle involving the infectious elementary body and the replicative reticulate body. In the presence of stressors such as gamma-interferon (IFNγ) or beta-lactam antibiotics, C. trachomatis undergoes an interruption in its replication cycle and enters a viable but non-cultivable state. Upon removal of the stressors, surviving C. trachomatis resume cell division and developmental transitions. In this report, we describe a genetic screen to identify C. trachomatis mutants with defects in recovery from IFNγ- and/or penicillin-induced stress and characterized a chemically derived C. trachomatis mutant strain that exhibited a significant decrease in recovery from IFNγ- but not penicillin-induced stress. Through lateral gene transfer and targeted insertional gene inactivation we identified ptr, encoding a predicted protease, as a gene required for recovery from IFNγ-induced stress. A C. trachomatis LGV-L2 ptr-null strain displayed reduced generation of infectious progeny and impaired genome replication upon removal of IFNγ. This defect was restored by introducing a wild type copy of ptr on a plasmid, indicating that Ptr is required for a rapid growth upon removal of IFN?. Ptr was expressed throughout the developmental cycle and localized to the inclusion lumen. Overall, our findings indicate that the putative secreted protease Ptr is required for C. trachomatis to specifically recover from IFNγ- but not penicillin-induced stress.Fil: Panzetta, Maria Emilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; ArgentinaFil: Lujan, Agustin Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Bastidas, Robert J.. University of Duke; Estados UnidosFil: Damiani, Maria Teresa. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza; Argentina. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Valdivia, Raphael H.. University of Duke; Estados UnidosFil: Saka, Hector Alex. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentin