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| TABLE OF CONTENTS | |||||||||||||||||||||||||||||||||||||
| July 2013 Volume 11 Number 7 | |||||||||||||||||||||||||||||||||||||
| In this issue
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| EDITORIAL | Top | ||||||||||||||||||||||||||||||||||||
| It's microbiology, citizens p427 | doi:10.1038/nrmicro3065 The rise of the 'citizen science' movement in microbiology provides an opportunity for public engagement and the chance to gather essential data on a large scale. Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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| NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||
| GENOME WATCH Culture-free club Josephine M. Bryant p434 | doi:10.1038/nrmicro3052 This month's Genome Watch highlights recent studies demonstrating that genomic analyses of pathogens in clinical samples are not limited to culture-friendly bacteria. | |||||||||||||||||||||||||||||||||||||
| PROGRESS | Top | ||||||||||||||||||||||||||||||||||||
Transposon insertion sequencing: a new tool for systems-level analysis of microorganisms Tim van Opijnen & Andrew Camilli p435 | doi:10.1038/nrmicro3033 The combination of transposon mutagenesis with next-generation sequencing has emerged as a useful tool for identifying putative gene function in a high-throughput manner. Here, van Opijnen and Camilli describe the four main techniques that are used for this purpose, with a focus on their application for uncovering bacterial gene function. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
| REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
| The molecular mechanisms and physiological consequences of oxidative stress: lessons from a model bacterium James A. Imlay p443 | doi:10.1038/nrmicro3032 To survive in oxic environments, all organisms require mechanisms to degrade toxic reactive oxygen species (ROS). In this Review, James Imlay describes the oxidative stress response of Escherichia coli and considers the damage caused by ROS and the adaptive strategies used by this bacterium to minimize intracellular ROS accumulation. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
| Systems virology: host-directed approaches to viral pathogenesis and drug targeting G. Lynn Law, Marcus J. Korth, Arndt G. Benecke & Michael G. Katze p455 | doi:10.1038/nrmicro3036 Katze and colleagues provide an overview of the evolution of systems virology and the insights obtained from using such methodologies to study virus-host interactions. Combining systems, mathematical and computational approaches with traditional virology research will offer a better understanding of how viruses cause disease and will help in the development of therapeutics. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
| Fortifying the barrier: the impact of lipid A remodelling on bacterial pathogenesis Brittany D. Needham & M. Stephen Trent p467 | doi:10.1038/nrmicro3047 Lipid A is the bioactive component of the Gram-negative outer membrane and is extensively remodelled to enable the bacterium to subvert the immune system of the host. Here, Needham and Trent describe the regulation of lipid A-modifying enzymes, the host defences that target lipid A and the strategies that bacterial pathogens use to avoid immune detection. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
| The molecular and structural basis of advanced antiviral therapy for hepatitis C virus infection Ralf Bartenschlager, Volker Lohmann & Francois Penin p482 | doi:10.1038/nrmicro3046 Hepatitis C virus infection is a major cause of liver cirrhosis and cancer, and current therapies are often ineffective or have severe side effects. Here, Bartenschlager and colleagues review how structural and functional insights into the viral life cycle have allowed the development of novel direct-acting antiviral agents. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
| ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||
| The abundance and variety of carbohydrate-active enzymes in the human gut microbiota Abdessamad El Kaoutari, Fabrice Armougom, Jeffrey I. Gordon, Didier Raoult & Bernard Henrissat p497 | doi:10.1038/nrmicro3050 The human genome encodes very few enzymes involved in the digestion of complex polysaccharides, and this deficit is compensated for by the myriad of carbohydrate-active enzymes (CAZymes) encoded by members of the gut microbiome. In this Analysis article, Henrissat and colleagues characterize the CAZymes present in a representative human mini-microbiome. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
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| *2011 Journal Citation Report (Thomson Reuters, 2012) |
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