Sequencing three crocodilian genomes to illuminate the evolution of archosaurs and amniotes

The International Crocodilian Genomes Working Group (ICGWG) will sequence and assemble the American alligator (Alligator mississippiensis), saltwater crocodile (Crocodylus porosus) and Indian gharial (Gavialis gangeticus) genomes. The status of these projects and our planned analyses are described

Host hindrance to HIV-1 replication in monocytes and macrophages

Monocytes and macrophages are targets of HIV-1 infection and play critical roles in multiple aspects of viral pathogenesis. HIV-1 can replicate in blood monocytes, although only a minor proportion of circulating monocytes harbor viral DNA. Resident macrophages in tissues can be infected and function as viral reservoirs. However, their susceptibility to infection, and their capacity to actively replicate the virus, varies greatly depending on the tissue localization and cytokine environment. The susceptibility of monocytes to HIV-1 infection in vitro depends on their differentiation status. Monocytes are refractory to infection and become permissive upon differentiation into macrophages. In addition, the capacity of monocyte-derived macrophages to sustain viral replication varies between individuals. Host determinants regulate HIV-1 replication in monocytes and macrophages, limiting several steps of the viral life-cycle, from viral entry to virus release. Some host factors responsible for HIV-1 restriction are shared with T lymphocytes, but several anti-viral mechanisms are specific to either monocytes or macrophages. Whilst a number of these mechanisms have been identified in monocytes or in monocyte-derived macrophages in vitro, some of them have also been implicated in the regulation of HIV-1 infection in vivo, in particular in the brain and the lung where macrophages are the main cell type infected by HIV-1. This review focuses on cellular factors that have been reported to interfere with HIV-1 infection in monocytes and macrophages, and examines the evidences supporting their role in vivo, highlighting unique aspects of HIV-1 restriction in these two cell types

Syndromics: A Bioinformatics Approach for Neurotrauma Research

Substantial scientific progress has been made in the past 50 years in delineating many of the biological mechanisms involved in the primary and secondary injuries following trauma to the spinal cord and brain. These advances have highlighted numerous potential therapeutic approaches that may help restore function after injury. Despite these advances, bench-to-bedside translation has remained elusive. Translational testing of novel therapies requires standardized measures of function for comparison across different laboratories, paradigms, and species. Although numerous functional assessments have been developed in animal models, it remains unclear how to best integrate this information to describe the complete translational “syndrome” produced by neurotrauma. The present paper describes a multivariate statistical framework for integrating diverse neurotrauma data and reviews the few papers to date that have taken an information-intensive approach for basic neurotrauma research. We argue that these papers can be described as the seminal works of a new field that we call “syndromics”, which aim to apply informatics tools to disease models to characterize the full set of mechanistic inter-relationships from multi-scale data. In the future, centralized databases of raw neurotrauma data will enable better syndromic approaches and aid future translational research, leading to more efficient testing regimens and more clinically relevant findings

Probing the Standard Model with Higgs signal rates from the Tevatron, the LHC and a future ILC

We explore the room for possible deviations from the Standard Model (SM) Higgs boson coupling structure in a systematic study of Higgs coupling scale factor benchmark scenarios using the latest signal rate measurements from the Tevatron and LHC experiments. We employ chi-squared fits performed with HiggsSignals, which takes into account detailed information on signal efficiencies and major correlations of theoretical and experimental uncertainties. All considered scenarios allow for additional non-standard Higgs boson decay modes, and various assumptions for constraining the total decay width are discussed. No significant deviations from the SM Higgs boson coupling structure are found in any of the investigated benchmark scenarios. We derive upper limits on an additional (undetectable) Higgs decay mode under the assumption that the Higgs couplings to weak gauge bosons do not exceed the SM prediction. We furthermore discuss the capabilities of future facilities for probing deviations from the SM Higgs couplings, comparing the high luminosity upgrade of the LHC with a future International Linear Collider (ILC), where for the latter various energy and luminosity scenarios are considered. At the ILC model-independent measurements of the coupling structure can be performed, and we provide estimates of the precision that can be achieved.Comment: 64 pages, 25 figures, 17 tables; v2: minor corrections in the text, references added. Matches published version on JHE