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<title>Nature Reviews Microbiology</title>
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<title>Mathematical models of infectious disease transmission</title>
<link>http://dx.doi.org/10.1038/nrmicro1845</link>
<description>Mathematical analysis and modelling is central to infectious disease epidemiology. Here, we provide an intuitive introduction to the process of disease transmission, how this stochastic process can be represented mathematically and how this mathematical representation can be used to analyse the emergent dynamics of observed </description>
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<p>
<b>Mathematical models of infectious disease transmission</b>
</p>
<p>Nature Reviews Microbiology 6, 477 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1845">doi:10.1038/nrmicro1845</a>
</p>
<p>Authors: Nicholas C. Grassly
&amp; Christophe Fraser</p>
<p>Mathematical analysis and modelling is central to infectious disease epidemiology. Here, we provide an intuitive introduction to the process of disease transmission, how this stochastic process can be represented mathematically and how this mathematical representation can be used to analyse the emergent dynamics of observed </p>
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<dc:title>Mathematical models of infectious disease transmission</dc:title>
<dc:creator>Nicholas C. Grassly</dc:creator>
<dc:creator>Christophe Fraser</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1845</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 477 (2008)</dc:source>
<dc:date>2008-05-13</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
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<prism:endingPage>487</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrmicro1872">
<title>Microbial diversity and the genetic nature of microbial species</title>
<link>http://dx.doi.org/10.1038/nrmicro1872</link>
<description>The earth contains a huge number of largely uncharacterized Bacteria and Archaea. Microbiologists are struggling to summarize their genetic diversity and classify them, which has resulted in heated debates on methods for defining species, mechanisms that lead to speciation and whether microbial species even exist. </description>
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<p>
<b>Microbial diversity and the genetic nature of microbial species</b>
</p>
<p>Nature Reviews Microbiology 6, 431 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1872">doi:10.1038/nrmicro1872</a>
</p>
<p>Authors: Mark Achtman
&amp; Michael Wagner</p>
<p>The earth contains a huge number of largely uncharacterized Bacteria and Archaea. Microbiologists are struggling to summarize their genetic diversity and classify them, which has resulted in heated debates on methods for defining species, mechanisms that lead to speciation and whether microbial species even exist. </p>
]]></content:encoded>
<dc:title>Microbial diversity and the genetic nature of microbial species</dc:title>
<dc:creator>Mark Achtman</dc:creator>
<dc:creator>Michael Wagner</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1872</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 431 (2008)</dc:source>
<dc:date>2008-05-7</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-05-7</prism:publicationDate>
<prism:volume>6</prism:volume>
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<prism:startingPage>431</prism:startingPage>
<prism:endingPage>440</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrmicro1887">
<title>Coordinating assembly of a bacterial macromolecular machine</title>
<link>http://dx.doi.org/10.1038/nrmicro1887</link>
<description>The assembly of large and complex organelles, such as the bacterial flagellum, poses the formidable problem of coupling temporal gene expression to specific stages of the organelle-assembly process. The discovery that levels of the bacterial flagellar regulatory protein FlgM are controlled by its secretion from </description>
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<p>
<b>Coordinating assembly of a bacterial macromolecular machine</b>
</p>
<p>Nature Reviews Microbiology 6, 455 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1887">doi:10.1038/nrmicro1887</a>
</p>
<p>Authors: Fabienne F. V. Chevance
&amp; Kelly T. Hughes</p>
<p>The assembly of large and complex organelles, such as the bacterial flagellum, poses the formidable problem of coupling temporal gene expression to specific stages of the organelle-assembly process. The discovery that levels of the bacterial flagellar regulatory protein FlgM are controlled by its secretion from </p>
]]></content:encoded>
<dc:title>Coordinating assembly of a bacterial macromolecular machine</dc:title>
<dc:creator>Fabienne F. V. Chevance</dc:creator>
<dc:creator>Kelly T. Hughes</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1887</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 455 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>455</prism:startingPage>
<prism:endingPage>465</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrmicro1892">
<title>The ecology and biotechnology of sulphate-reducing bacteria</title>
<link>http://dx.doi.org/10.1038/nrmicro1892</link>
<description>Sulphate-reducing bacteria (SRB) are anaerobic microorganisms that use sulphate as a terminal electron acceptor in, for example, the degradation of organic compounds. They are ubiquitous in anoxic habitats, where they have an important role in both the sulphur and carbon cycles. SRB can cause a </description>
<content:encoded><![CDATA[

<p>
<b>The ecology and biotechnology of sulphate-reducing bacteria</b>
</p>
<p>Nature Reviews Microbiology 6, 441 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1892">doi:10.1038/nrmicro1892</a>
</p>
<p>Authors: Gerard Muyzer
&amp; Alfons J. M. Stams</p>
<p>Sulphate-reducing bacteria (SRB) are anaerobic microorganisms that use sulphate as a terminal electron acceptor in, for example, the degradation of organic compounds. They are ubiquitous in anoxic habitats, where they have an important role in both the sulphur and carbon cycles. SRB can cause a </p>
]]></content:encoded>
<dc:title>The ecology and biotechnology of sulphate-reducing bacteria</dc:title>
<dc:creator>Gerard Muyzer</dc:creator>
<dc:creator>Alfons J. M. Stams</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1892</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 441 (2008)</dc:source>
<dc:date>2008-05-07</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-05-07</prism:publicationDate>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>441</prism:startingPage>
<prism:endingPage>454</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrmicro1893">
<title>Proteorhodopsins: an array of physiological roles?</title>
<link>http://dx.doi.org/10.1038/nrmicro1893</link>
<description>Metagenomic analyses have revealed widespread and diverse retinal-binding rhodopsin proteins (named proteorhodopsins) among numerous marine bacteria and archaea, which has challenged the notion that solar energy can only enter marine ecosystems by chlorophyll-based photosynthesis. Most marine proteorhodopsins share structural and functional similarities with archaeal bacteriorhodopsins, </description>
<content:encoded><![CDATA[

<p>
<b>Proteorhodopsins: an array of physiological roles?</b>
</p>
<p>Nature Reviews Microbiology 6, 488 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1893">doi:10.1038/nrmicro1893</a>
</p>
<p>Authors: Jed A. Fuhrman, Michael S. Schwalbach
&amp; Ulrich Stingl</p>
<p>Metagenomic analyses have revealed widespread and diverse retinal-binding rhodopsin proteins (named proteorhodopsins) among numerous marine bacteria and archaea, which has challenged the notion that solar energy can only enter marine ecosystems by chlorophyll-based photosynthesis. Most marine proteorhodopsins share structural and functional similarities with archaeal bacteriorhodopsins, </p>
]]></content:encoded>
<dc:title>Proteorhodopsins: an array of physiological roles?</dc:title>
<dc:creator>Jed A. Fuhrman</dc:creator>
<dc:creator>Michael S. Schwalbach</dc:creator>
<dc:creator>Ulrich Stingl</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1893</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 488 (2008)</dc:source>
<dc:date>2008-05-13</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-05-13</prism:publicationDate>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Perspective</prism:section>
<prism:startingPage>488</prism:startingPage>
<prism:endingPage>494</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrmicro1900">
<title>The surprisingly diverse ways that prokaryotes move</title>
<link>http://dx.doi.org/10.1038/nrmicro1900</link>
<description>Prokaryotic cells move through liquids or over moist surfaces by swimming, swarming, gliding, twitching or floating. An impressive diversity of motility mechanisms has evolved in prokaryotes. Movement can involve surface appendages, such as flagella that spin, pili that pull and Mycoplasma 'legs' that walk. </description>
<content:encoded><![CDATA[

<p>
<b>The surprisingly diverse ways that prokaryotes move</b>
</p>
<p>Nature Reviews Microbiology 6, 466 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1900">doi:10.1038/nrmicro1900</a>
</p>
<p>Authors: Ken F. Jarrell
&amp; Mark J. McBride</p>
<p>Prokaryotic cells move through liquids or over moist surfaces by swimming, swarming, gliding, twitching or floating. An impressive diversity of motility mechanisms has evolved in prokaryotes. Movement can involve surface appendages, such as flagella that spin, pili that pull and Mycoplasma 'legs' that walk. </p>
]]></content:encoded>
<dc:title>The surprisingly diverse ways that prokaryotes move</dc:title>
<dc:creator>Ken F. Jarrell</dc:creator>
<dc:creator>Mark J. McBride</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1900</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 466 (2008)</dc:source>
<dc:date>2008-05-07</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-05-07</prism:publicationDate>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>466</prism:startingPage>
<prism:endingPage>476</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1901">
<title>Microbiology in the post-genomic era</title>
<link>http://dx.doi.org/10.1038/nrmicro1901</link>
<description>Genomics has revolutionized every aspect of microbiology. Now, 13 years after the first bacterial genome was sequenced, it is important to pause and consider what has changed in microbiology research as a consequence of genomics. In this article, we review the evolving field of bacterial </description>
<content:encoded><![CDATA[

<p>
<b>Microbiology in the post-genomic era</b>
</p>
<p>Nature Reviews Microbiology 6, 419 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1901">doi:10.1038/nrmicro1901</a>
</p>
<p>Authors: Duccio Medini, Davide Serruto, Julian Parkhill, David A. Relman, Claudio Donati, Richard Moxon, Stanley Falkow
&amp; Rino Rappuoli</p>
<p>Genomics has revolutionized every aspect of microbiology. Now, 13 years after the first bacterial genome was sequenced, it is important to pause and consider what has changed in microbiology research as a consequence of genomics. In this article, we review the evolving field of bacterial </p>
]]></content:encoded>
<dc:title>Microbiology in the post-genomic era</dc:title>
<dc:creator>Duccio Medini</dc:creator>
<dc:creator>Davide Serruto</dc:creator>
<dc:creator>Julian Parkhill</dc:creator>
<dc:creator>David A. Relman</dc:creator>
<dc:creator>Claudio Donati</dc:creator>
<dc:creator>Richard Moxon</dc:creator>
<dc:creator>Stanley Falkow</dc:creator>
<dc:creator>Rino Rappuoli</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1901</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 419 (2008)</dc:source>
<dc:date>2008-05-13</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-05-13</prism:publicationDate>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>419</prism:startingPage>
<prism:endingPage>430</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1911">
<title>DNA replication: Follow the path</title>
<link>http://dx.doi.org/10.1038/nrmicro1911</link>
<description>According to the prevailing view of DNA replication, DNA is delivered to, and then replicated in, fixed cellular 'replication factories'. However, the movement of replisomes (the replication machinery that is located at the replication forks) in live Escherichia coli cells, report David Sherratt and </description>
<content:encoded><![CDATA[

<p>
<b>DNA replication: Follow the path</b>
</p>
<p>Nature Reviews Microbiology 6, 412 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1911">doi:10.1038/nrmicro1911</a>
</p>
<p>Author: Asher Mullard</p>
<p>According to the prevailing view of DNA replication, DNA is delivered to, and then replicated in, fixed cellular 'replication factories'. However, the movement of replisomes (the replication machinery that is located at the replication forks) in live Escherichia coli cells, report David Sherratt and </p>
]]></content:encoded>
<dc:title>DNA replication: Follow the path</dc:title>
<dc:creator>Asher Mullard</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1911</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 412 (2008)</dc:source>
<dc:date>2008-04-28</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-04-28</prism:publicationDate>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>412</prism:startingPage>
<prism:endingPage>412</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1914">
<title>Viral pathogenesis: Turning virus spread on its head</title>
<link>http://dx.doi.org/10.1038/nrmicro1914</link>
<description>Understanding how viruses spread from the initial site of infection to become systemic and cause symptoms in a host is an important aspect of viral pathogenesis. Reporting in Cell Host &amp; Microbe, Sacher et al. reveal that although murine cytomegalovirus (MCMV) replicates to </description>
<content:encoded><![CDATA[

<p>
<b>Viral pathogenesis: Turning virus spread on its head</b>
</p>
<p>Nature Reviews Microbiology 6, 413 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1914">doi:10.1038/nrmicro1914</a>
</p>
<p>Author: Susan Jones</p>
<p>Understanding how viruses spread from the initial site of infection to become systemic and cause symptoms in a host is an important aspect of viral pathogenesis. Reporting in Cell Host &amp; Microbe, Sacher et al. reveal that although murine cytomegalovirus (MCMV) replicates to </p>
]]></content:encoded>
<dc:title>Viral pathogenesis: Turning virus spread on its head</dc:title>
<dc:creator>Susan Jones</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1914</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 413 (2008)</dc:source>
<dc:date>2008-05-13</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-05-13</prism:publicationDate>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>413</prism:startingPage>
<prism:endingPage>413</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1915">
<title>In brief</title>
<link>http://dx.doi.org/10.1038/nrmicro1915</link>
<description>SymbiosisFree-living tubeworm endosymbionts found at deep-sea ventsHarmer, T. L.et al. Appl. Environ. Microbiol.11 Apr 2008 (doi: 10.1128/AEM.02470-07)Bacterial symbionts can be transmitted by vertical (parent to offspring), horizontal (between individuals in the same niche) or environmental (acquisition </description>
<content:encoded><![CDATA[

<p>
<b>In brief</b>
</p>
<p>Nature Reviews Microbiology 6, 412 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1915">doi:10.1038/nrmicro1915</a>
</p>
<p>SymbiosisFree-living tubeworm endosymbionts found at deep-sea ventsHarmer, T. L.et al. Appl. Environ. Microbiol.11 Apr 2008 (doi: 10.1128/AEM.02470-07)Bacterial symbionts can be transmitted by vertical (parent to offspring), horizontal (between individuals in the same niche) or environmental (acquisition </p>
]]></content:encoded>
<dc:title>In brief</dc:title>
<dc:identifier>doi:10.1038/nrmicro1915</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 412 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>412</prism:startingPage>
<prism:endingPage>412</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1917">
<title>Fungal metabolism: Dissecting catalysis</title>
<link>http://dx.doi.org/10.1038/nrmicro1917</link>
<description>The catalytic mechanism of iterative polyketide synthases (IPKSs) is now more clearly understood thanks to the work of Townsend, Kelleher, Crawford and colleagues. Reporting in Science, they describe how &#8212; by using product analysis and mass spectrometry to characterize the intermediates that were bound </description>
<content:encoded><![CDATA[

<p>
<b>Fungal metabolism: Dissecting catalysis</b>
</p>
<p>Nature Reviews Microbiology 6, 414 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1917">doi:10.1038/nrmicro1917</a>
</p>
<p>Author: Rachel Smallridge</p>
<p>The catalytic mechanism of iterative polyketide synthases (IPKSs) is now more clearly understood thanks to the work of Townsend, Kelleher, Crawford and colleagues. Reporting in Science, they describe how &#8212; by using product analysis and mass spectrometry to characterize the intermediates that were bound </p>
]]></content:encoded>
<dc:title>Fungal metabolism: Dissecting catalysis</dc:title>
<dc:creator>Rachel Smallridge</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1917</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 414 (2008)</dc:source>
<dc:date>2008-05-13</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2008-05-13</prism:publicationDate>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>414</prism:startingPage>
<prism:endingPage>415</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1920">
<title>Techniques and applications: A model infection</title>
<link>http://dx.doi.org/10.1038/nrmicro1920</link>
<description>Reporting in a recent issue of PLoS Biology, Andrew Grant and colleagues describe a new method of modelling the within-host spatiotemporal dynamics of an infection with an intracellular bacterial pathogen.Grant et al. chose to study Salmonella enterica serovar Typhimurium (S. </description>
<content:encoded><![CDATA[

<p>
<b>Techniques and applications: A model infection</b>
</p>
<p>Nature Reviews Microbiology 6, 413 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1920">doi:10.1038/nrmicro1920</a>
</p>
<p>Author: Sheilagh Molloy</p>
<p>Reporting in a recent issue of PLoS Biology, Andrew Grant and colleagues describe a new method of modelling the within-host spatiotemporal dynamics of an infection with an intracellular bacterial pathogen.Grant et al. chose to study Salmonella enterica serovar Typhimurium (S. </p>
]]></content:encoded>
<dc:title>Techniques and applications: A model infection</dc:title>
<dc:creator>Sheilagh Molloy</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1920</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 413 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>413</prism:startingPage>
<prism:endingPage>413</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1921">
<title>Immune evasion: Overcoming defensins</title>
<link>http://dx.doi.org/10.1038/nrmicro1921</link>
<description>Human cells rely on various antimicrobial peptides, including defensins, to prevent the spread of pathogenic bacteria. For example, defensins can induce chemotaxis of dendritic cells, and expression of defensins correlates with inhibition of bacterial RNA, DNA and protein synthesis, as well as with reduced bacterial </description>
<content:encoded><![CDATA[

<p>
<b>Immune evasion: Overcoming defensins</b>
</p>
<p>Nature Reviews Microbiology 6, 415 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1921">doi:10.1038/nrmicro1921</a>
</p>
<p>Author: Asher Mullard</p>
<p>Human cells rely on various antimicrobial peptides, including defensins, to prevent the spread of pathogenic bacteria. For example, defensins can induce chemotaxis of dendritic cells, and expression of defensins correlates with inhibition of bacterial RNA, DNA and protein synthesis, as well as with reduced bacterial </p>
]]></content:encoded>
<dc:title>Immune evasion: Overcoming defensins</dc:title>
<dc:creator>Asher Mullard</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1921</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 415 (2008)</dc:source>
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<prism:number>6</prism:number>
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<prism:endingPage>415</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1922">
<title>Virtual networking for microbiologists</title>
<link>http://dx.doi.org/10.1038/nrmicro1922</link>
<description>The advent of Web 2.0 applications, which enable information sharing and virtual networking, could revolutionize science. But are microbiologists taking advantage?</description>
<content:encoded><![CDATA[

<p>
<b>Virtual networking for microbiologists</b>
</p>
<p>Nature Reviews Microbiology 6, 410 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1922">doi:10.1038/nrmicro1922</a>
</p>
<p>The advent of Web 2.0 applications, which enable information sharing and virtual networking, could revolutionize science. But are microbiologists taking advantage?</p>
]]></content:encoded>
<dc:title>Virtual networking for microbiologists</dc:title>
<dc:identifier>doi:10.1038/nrmicro1922</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 410 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Editorial</prism:section>
<prism:startingPage>410</prism:startingPage>
<prism:endingPage>410</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1923">
<title>Cellular microbiology: Virus plays dead</title>
<link>http://dx.doi.org/10.1038/nrmicro1923</link>
<description>Vaccinia virus is a large, complex, enveloped DNA virus that belongs to the Poxviridae family of viruses, which includes variola, the causative agent of smallpox. The infectious mature virus (MV) form of vaccinia has been shown to bind to actin-containing finger-like protrusions (filopodia) of the </description>
<content:encoded><![CDATA[

<p>
<b>Cellular microbiology: Virus plays dead</b>
</p>
<p>Nature Reviews Microbiology 6, 411 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1923">doi:10.1038/nrmicro1923</a>
</p>
<p>Author: Arianne Heinrichs</p>
<p>Vaccinia virus is a large, complex, enveloped DNA virus that belongs to the Poxviridae family of viruses, which includes variola, the causative agent of smallpox. The infectious mature virus (MV) form of vaccinia has been shown to bind to actin-containing finger-like protrusions (filopodia) of the </p>
]]></content:encoded>
<dc:title>Cellular microbiology: Virus plays dead</dc:title>
<dc:creator>Arianne Heinrichs</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1923</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 411 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>411</prism:startingPage>
<prism:endingPage>411</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1924">
<title>Cellular microbiology: All aboard the cell-wall shuttle</title>
<link>http://dx.doi.org/10.1038/nrmicro1924</link>
<description>The coordination of bacterial cell-wall synthesis has been hotly debated for almost 40 years. A recent paper in Molecular Microbiology now sheds new light on this topic by revealing how the cell elongation&#8211;division cycle is controlled in Bacillus subtilis.In rod-shaped bacteria, such </description>
<content:encoded><![CDATA[

<p>
<b>Cellular microbiology: All aboard the cell-wall shuttle</b>
</p>
<p>Nature Reviews Microbiology 6, 414 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1924">doi:10.1038/nrmicro1924</a>
</p>
<p>Author: Sheilagh Molloy</p>
<p>The coordination of bacterial cell-wall synthesis has been hotly debated for almost 40 years. A recent paper in Molecular Microbiology now sheds new light on this topic by revealing how the cell elongation&#8211;division cycle is controlled in Bacillus subtilis.In rod-shaped bacteria, such </p>
]]></content:encoded>
<dc:title>Cellular microbiology: All aboard the cell-wall shuttle</dc:title>
<dc:creator>Sheilagh Molloy</dc:creator>
<dc:identifier>doi:10.1038/nrmicro1924</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 414 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>414</prism:startingPage>
<prism:endingPage>415</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1925">
<title>In this issue</title>
<link>http://dx.doi.org/10.1038/nrmicro1925</link>
<description>Bacteria and archaea are able to move both in liquids and on solid surfaces, and the mechanisms that they use to do so have long been a fascination of many microbiologists. On page 466, Ken Jarrell and Mark McBride describe the many different methods </description>
<content:encoded><![CDATA[

<p>
<b>In this issue</b>
</p>
<p>Nature Reviews Microbiology 6, 409 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1925">doi:10.1038/nrmicro1925</a>
</p>
<p>Bacteria and archaea are able to move both in liquids and on solid surfaces, and the mechanisms that they use to do so have long been a fascination of many microbiologists. On page 466, Ken Jarrell and Mark McBride describe the many different methods </p>
]]></content:encoded>
<dc:title>In this issue</dc:title>
<dc:identifier>doi:10.1038/nrmicro1925</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 409 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>In This Issue</prism:section>
<prism:startingPage>409</prism:startingPage>
<prism:endingPage>409</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro1926">
<title>In the News</title>
<link>http://dx.doi.org/10.1038/nrmicro1926</link>
<description>New fungicide foundInsects such as Drosophila spp. produce a range of antimicrobial peptides to protect against infection. One of the antimicrobial peptides that is produced by Drosophila spp. is drosomycin, which has been shown to be highly active against filamentous fungi and </description>
<content:encoded><![CDATA[

<p>
<b>In the News</b>
</p>
<p>Nature Reviews Microbiology 6, 416 (2008). <a href="http://dx.doi.org/10.1038/nrmicro1926">doi:10.1038/nrmicro1926</a>
</p>
<p>New fungicide foundInsects such as Drosophila spp. produce a range of antimicrobial peptides to protect against infection. One of the antimicrobial peptides that is produced by Drosophila spp. is drosomycin, which has been shown to be highly active against filamentous fungi and </p>
]]></content:encoded>
<dc:title>In the News</dc:title>
<dc:identifier>doi:10.1038/nrmicro1926</dc:identifier>
<dc:source>Nature Reviews Microbiology 6, 416 (2008)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:volume>6</prism:volume>
<prism:number>6</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>416</prism:startingPage>
<prism:endingPage>417</prism:endingPage>
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