154 research outputs found

    An innovative blazar classification based on radio jet kinematics

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    Blazars are usually classified following their synchrotron peak frequency (νF(ν)\nu F(\nu) scale) as high, intermediate, low frequency peaked BL Lacs (HBLs, IBLs, LBLs), and flat spectrum radio quasars (FSRQs), or, according to their radio morphology at large scale, FR~I or FR~II. However, the diversity of blazars is such that these classes seem insufficient to chart the specific properties of each source. We propose to classify a wide sample of blazars following the kinematic features of their radio jets seen in very long baseline interferometry (VLBI). For this purpose we use public data from the MOJAVE collaboration in which we select a sample of blazars with known redshift and sufficient monitoring to constrain apparent velocities. We selected 161 blazars from a sample of 200 sources. We identify three distinct classes of VLBI jets depending on radio knot kinematics: class I with quasi-stationary knots, class II with knots in relativistic motion from the radio core, and class I/II, intermediate, showing quasi-stationary knots at the jet base and relativistic motions downstream. A notable result is the good overlap of this kinematic classification with the usual spectral classification; class I corresponds to HBLs, class II to FSRQs, and class I/II to IBLs/LBLs. We deepen this study by characterizing the physical parameters of jets from VLBI radio data. Hence we focus on the singular case of the class I/II by the study of the blazar BL Lac itself. Finally we show how the interpretation that radio knots are recollimation shocks is fully appropriate to describe the characteristics of these three classes.Comment: 12 pages, 13 figures, accepted by A&

    Les géographes et le travail collectif : la recherche coopérative sur programme à l'œuvre

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    National audienceJusqu'à la fin des années 1960, le CNRS représentait principalement pour les géographes français un lieu d'hébergement dans le cadre duquel achever une thèse d'État. Mais à la fin de la décennie, une vision nouvelle du travail d'équipe, rompant avec l'individualisme universitaire jusque là de mise, s'est partiellement imposée

    Les géographes et le travail collectif

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    Jusqu’à la fin des années 1960, le CNRS représentait principalement pour les géographes français un lieu d’hébergement dans le cadre duquel ils pouvaient achever une thèse d’État. Mais à la fin de la décennie, une vision nouvelle du travail d’équipe, rompant avec l’individualisme universitaire jusque-là de mise, s’est partiellement imposée. Olivier Orain et Marie-Pierre Sol font un retour historique sur cette période.Until the end of the 1960s, French geographers were used to consider CNRS mainly as a place where to achieve their PhD. Later on, a new vision of teamwork appeared, quitting academic individualism. A flash back by Olivier Orain and Marie-Pierre Sol

    Generation and characterization of a stable cell population releasing fluorescent HIV-1-based Virus Like Particles in an inducible way

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    BACKGROUND: The availability of cell lines releasing fluorescent viral particles can significantly support a variety of investigations, including the study of virus-cell interaction and the screening of antiviral compounds. Regarding HIV-1, the recovery of such biologic reagents represents a very hard challenge due to the intrinsic cytotoxicity of many HIV-1 products. We sought to overcome such a limitation by using a cell line releasing HIV-1 particles in an inducible way, and by exploiting the ability of a HIV-1 Nef mutant to be incorporated in virions at quite high levels. RESULTS: Here, we report the isolation and characterization of a HIV-1 packaging cell line, termed 18-4s, able to release valuable amounts of fluorescent HIV-1 based Virus-Like Particles (VLPs) in an inducible way. 18-4s cells were recovered by constitutively expressing the HIV-1 NefG3C mutant fused with the enhanced-green fluorescent protein (NefG3C-GFP) in a previously isolated inducible HIV-1 packaging cell line. The G3C mutation creates a palmitoylation site which results in NefG3C-GFP incorporation into virions greatly exceeding that of the wild type counterpart. Upon induction of 18-4s cells with ponasterone A and sodium butyrate, up to 4 μg/ml of VLPs, which had incorporated about 150 molecules of NefG3C-GFP per viral particle, were released into the culture supernatant. Due to their intrinsic strong fluorescence, the 18-4s VLPs were easily detectable by a novel cytofluorometric-based assay developed here. The treatment of target cells with fluorescent 18-4 VLPs pseudotyped with different glycoprotein receptors resulted in these becoming fluorescent as early as two hours post-challenge. CONCLUSION: We created a stable cell line releasing fluorescent HIV-1 based VLPs upon induction useful for several applications including the study of virus-cell interactions and the screening of antiviral compounds

    Characterization of Reemerging Chikungunya Virus

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    An unprecedented epidemic of chikungunya virus (CHIKV) infection recently started in countries of the Indian Ocean area, causing an acute and painful syndrome with strong fever, asthenia, skin rash, polyarthritis, and lethal cases of encephalitis. The basis for chikungunya disease and the tropism of CHIKV remain unknown. Here, we describe the replication characteristics of recent clinical CHIKV strains. Human epithelial and endothelial cells, primary fibroblasts and, to a lesser extent, monocyte-derived macrophages, were susceptible to infection and allowed viral production. In contrast, CHIKV did not replicate in lymphoid and monocytoid cell lines, primary lymphocytes and monocytes, or monocyte-derived dendritic cells. CHIKV replication was cytopathic and associated with an induction of apoptosis in infected cells. Chloroquine, bafilomycin-A1, and short hairpin RNAs against dynamin-2 inhibited viral production, indicating that viral entry occurs through pH-dependent endocytosis. CHIKV was highly sensitive to the antiviral activity of type I and II interferons. These results provide a general insight into the interaction between CHIKV and its mammalian host

    Tetherin Restricts Productive HIV-1 Cell-to-Cell Transmission

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    The IFN-inducible antiviral protein tetherin (or BST-2/CD317/HM1.24) impairs release of mature HIV-1 particles from infected cells. HIV-1 Vpu antagonizes the effect of tetherin. The fate of virions trapped at the cell surface remains poorly understood. Here, we asked whether tetherin impairs HIV cell-to-cell transmission, a major means of viral spread. Tetherin-positive or -negative cells, infected with wild-type or ΔVpu HIV, were used as donor cells and cocultivated with target lymphocytes. We show that tetherin inhibits productive cell-to-cell transmission of ΔVpu to targets and impairs that of WT HIV. Tetherin accumulates with Gag at the contact zone between infected and target cells, but does not prevent the formation of virological synapses. In the presence of tetherin, viruses are then mostly transferred to targets as abnormally large patches. These viral aggregates do not efficiently promote infection after transfer, because they accumulate at the surface of target cells and are impaired in their fusion capacities. Tetherin, by imprinting virions in donor cells, is the first example of a surface restriction factor limiting viral cell-to-cell spread

    Innate Sensing of HIV-Infected Cells

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    Cell-free HIV-1 virions are poor stimulators of type I interferon (IFN) production. We examined here how HIV-infected cells are recognized by plasmacytoid dendritic cells (pDCs) and by other cells. We show that infected lymphocytes are more potent inducers of IFN than virions. There are target cell-type differences in the recognition of infected lymphocytes. In primary pDCs and pDC-like cells, recognition occurs in large part through TLR7, as demonstrated by the use of inhibitors and by TLR7 silencing. Donor cells expressing replication-defective viruses, carrying mutated reverse transcriptase, integrase or nucleocapsid proteins induced IFN production by target cells as potently as wild-type virus. In contrast, Env-deleted or fusion defective HIV-1 mutants were less efficient, suggesting that in addition to TLR7, cytoplasmic cellular sensors may also mediate sensing of infected cells. Furthermore, in a model of TLR7-negative cells, we demonstrate that the IRF3 pathway, through a process requiring access of incoming viral material to the cytoplasm, allows sensing of HIV-infected lymphocytes. Therefore, detection of HIV-infected lymphocytes occurs through both endosomal and cytoplasmic pathways. Characterization of the mechanisms of innate recognition of HIV-infected cells allows a better understanding of the pathogenic and exacerbated immunologic events associated with HIV infection

    Quality of Life in Sarcopenia and Frailty

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    The reduced muscle mass and impaired muscle performance that define sarcopenia in older individuals are associated with increased risk of physical limitation and a variety of chronic diseases. They may also contribute to clinical frailty. A gradual erosion of quality of life (QoL) has been evidenced in these individuals, although much of this research has been done using generic QoL instruments, particularly the SF-36, which may not be ideal in older populations with significant comorbidities. This review and report of an expert meeting presents the current definitions of these geriatric syndromes (sarcopenia and frailty). It then briefly summarizes QoL concepts and specificities in older populations and examines the relevant domains of QoL and what is known concerning QoL decline with these conditions. It calls for a clearer definition of the construct of disability, argues that a disease-specific QoL instrument for sarcopenia/frailty would be an asset for future research, and discusses whether there are available and validated components that could be used to this end and whether the psychometric properties of these instruments are sufficiently tested. It calls also for an approach using utility weighting to provide some cost estimates and suggests that a time trade-off study could be appropriat
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