<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" media="screen" href="/~d/styles/rss1full.xsl"?><?xml-stylesheet type="text/css" media="screen" href="http://feeds.nature.com/~d/styles/itemcontent.css"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/basic/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns="http://purl.org/rss/1.0/" xmlns:admin="http://webns.net/mvcb/" xmlns:feedburner="http://rssnamespace.org/feedburner/ext/1.0">
<channel rdf:about="http://www.nature.com/nrmicro/current_issue/rss">
<title>Nature Reviews Microbiology - Issue - nature.com science feeds</title>
<description />
<link>http://www.nature.com/nrmicro/current_issue/</link>
<admin:generatorAgent rdf:resource="http://www.nature.com/" />
<admin:errorReportsTo rdf:resource="mailto:feedback@nature.com" />
<dc:publisher>Nature Publishing Group</dc:publisher>
<dc:language>en</dc:language>
<dc:rights>© 2009 Nature Publishing Group</dc:rights>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:issn>1740-1526</prism:issn>
<prism:eIssn>1740-1534</prism:eIssn>
<prism:copyright>© 2009 Nature Publishing Group</prism:copyright>
<prism:rightsAgent>permissions@nature.com</prism:rightsAgent>
<image rdf:resource="http://www.nature.com/includes/rj_globnavimages/nrmicro_logo.gif" />
<items>
<rdf:Seq>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2258" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2246" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2250" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2247" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2252" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2255" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2256" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2251" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2254" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2253" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2257" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2220" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2221" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2222" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2223" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2219" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2202" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2235" />
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nrmicro2244" />
</rdf:Seq>
</items>
<atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" href="http://feeds.nature.com/nrmicro/rss/current" type="application/rss+xml" /><feedburner:emailServiceId>nrmicro/rss/current</feedburner:emailServiceId><feedburner:feedburnerHostname>http://feedburner.google.com</feedburner:feedburnerHostname><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com" /></channel>
<image rdf:about="http://www.nature.com/includes/rj_globnavimages/nrmicro_logo.gif">
<title>Nature Reviews Microbiology</title>
<url>http://www.nature.com/includes/rj_globnavimages/nrmicro_logo.gif</url>
<link>http://www.nature.com/nrmicro/</link>
</image>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2258">
<title>In this issue</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/vUcWuNB3zKE/nrmicro2258</link>
<description>To survive in a host, a pathogen must avoid detection by the host immune system or stay one step ahead of it. One way that HIV avoids detection and clearance is by establishing a latent reservoir in resting memory CD4+ T cells. Several </description>
<content:encoded><![CDATA[

<p>
<b>In this issue</b>
</p>
<p>Nature Reviews Microbiology 7, 757 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2258">doi:10.1038/nrmicro2258</a>
</p>
<p>To survive in a host, a pathogen must avoid detection by the host immune system or stay one step ahead of it. One way that HIV avoids detection and clearance is by establishing a latent reservoir in resting memory CD4+ T cells. Several </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/vUcWuNB3zKE" height="1" width="1"/>]]></content:encoded>
<dc:title>In this issue</dc:title>
<dc:identifier>doi:10.1038/nrmicro2258</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 757 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2258</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2258</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>In This Issue</prism:section>
<prism:startingPage>757</prism:startingPage>
<prism:endingPage>757</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2258</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2246">
<title>Giving microbial diversity a home</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/04aqNLpO-J8/nrmicro2246</link>
<description>Efforts to house environmental microbial culture collections, resources and data are lagging behind the speed of discovery in the scientific community. Emerson and Wilson explain the need to increase the investment in biological resource centres to meet this growing challenge.</description>
<content:encoded><![CDATA[

<p>
<b>Giving microbial diversity a home</b>
</p>
<p>Nature Reviews Microbiology 7, 758 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2246">doi:10.1038/nrmicro2246</a>
</p>
<p>Authors: David Emerson &amp; Willie Wilson</p>
<p>Efforts to house environmental microbial culture collections, resources and data are lagging behind the speed of discovery in the scientific community. Emerson and Wilson explain the need to increase the investment in biological resource centres to meet this growing challenge.</p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/04aqNLpO-J8" height="1" width="1"/>]]></content:encoded>
<dc:title>Giving microbial diversity a home</dc:title>
<dc:creator>David Emerson</dc:creator>
<dc:creator>Willie Wilson</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2246</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 758 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2246</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2246</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Editorial</prism:section>
<prism:startingPage>758</prism:startingPage>
<prism:endingPage>758</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2246</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2250">
<title>Bacterial physiology: Mirror signal, manoeuvre</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/xRVLCS5pnIg/nrmicro2250</link>
<description>A recent Science paper from the Waldor laboratory provides evidence that bacteria use D-amino acids to remodel the cell wall during the adaptation to stationary phase.Almost all naturally occurring proteinogenic amino acids are chiral and, as such, can exist as L- </description>
<content:encoded><![CDATA[

<p>
<b>Bacterial physiology: Mirror signal, manoeuvre</b>
</p>
<p>Nature Reviews Microbiology 7, 759 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2250">doi:10.1038/nrmicro2250</a>
</p>
<p>Author: Sheilagh Molloy</p>
<p>A recent Science paper from the Waldor laboratory provides evidence that bacteria use D-amino acids to remodel the cell wall during the adaptation to stationary phase.Almost all naturally occurring proteinogenic amino acids are chiral and, as such, can exist as L- </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/xRVLCS5pnIg" height="1" width="1"/>]]></content:encoded>
<dc:title>Bacterial physiology: Mirror signal, manoeuvre</dc:title>
<dc:creator>Sheilagh Molloy</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2250</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 759 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2250</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2250</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>759</prism:startingPage>
<prism:endingPage>759</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2250</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2247">
<title>Fungal physiology: Stressed fungi are not highly sprung</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/OyivszplVDI/nrmicro2247</link>
<description>Saccharomyces cerevisiae maintains cellular integrity in the presence of cell wall stress by upregulating cell wall-remodelling pathways. Such stresses are detected by a group of five transmembrane sensor proteins, Wsc1–Wsc3, Mid2 and Mtl2. In an article published online in Nature Chemical Biology, Dupres </description>
<content:encoded><![CDATA[

<p>
<b>Fungal physiology: Stressed fungi are not highly sprung</b>
</p>
<p>Nature Reviews Microbiology 7, 760 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2247">doi:10.1038/nrmicro2247</a>
</p>
<p>Author: Andrew Jermy</p>
<p>Saccharomyces cerevisiae maintains cellular integrity in the presence of cell wall stress by upregulating cell wall-remodelling pathways. Such stresses are detected by a group of five transmembrane sensor proteins, Wsc1&#8211;Wsc3, Mid2 and Mtl2. In an article published online in Nature Chemical Biology, Dupres </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/OyivszplVDI" height="1" width="1"/>]]></content:encoded>
<dc:title>Fungal physiology: Stressed fungi are not highly sprung</dc:title>
<dc:creator>Andrew Jermy</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2247</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 760 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2247</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2247</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>760</prism:startingPage>
<prism:endingPage>760</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2247</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2252">
<title>Bacterial pathogenesis: A 'hijacked' regulatory mechanism</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/TxL8-cu6C08/nrmicro2252</link>
<description>To disseminate between host cells, Listeria monocytogenes polymerizes host cell actin using ActA, a bacterial protein that mimics the action of Wiscott–Aldrich syndrome protein (WASP) and recruits the actin-nucleating ARP2/3 complex to the bacterial surface. This results in the formation of actin tails, which </description>
<content:encoded><![CDATA[

<p>
<b>Bacterial pathogenesis: A 'hijacked' regulatory mechanism</b>
</p>
<p>Nature Reviews Microbiology 7, 760 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2252">doi:10.1038/nrmicro2252</a>
</p>
<p>Author: Rachel David</p>
<p>To disseminate between host cells, Listeria monocytogenes polymerizes host cell actin using ActA, a bacterial protein that mimics the action of Wiscott&#8211;Aldrich syndrome protein (WASP) and recruits the actin-nucleating ARP2/3 complex to the bacterial surface. This results in the formation of actin tails, which </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/TxL8-cu6C08" height="1" width="1"/>]]></content:encoded>
<dc:title>Bacterial pathogenesis: A 'hijacked' regulatory mechanism</dc:title>
<dc:creator>Rachel David</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2252</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 760 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2252</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2252</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>760</prism:startingPage>
<prism:endingPage>760</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2252</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2255">
<title>Symbiosis: A partnership cast in iron</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/P9DFBR_cTgI/nrmicro2255</link>
<description>Many species of bloom-forming algae in the phytoplankton form beneficial or obligate associations with marine bacteria. Such partnerships are thought to enable the sharing of metabolites and nutrients, although a detailed understanding of most of these interactions is lacking. The acquisition of iron may be </description>
<content:encoded><![CDATA[

<p>
<b>Symbiosis: A partnership cast in iron</b>
</p>
<p>Nature Reviews Microbiology 7, 760 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2255">doi:10.1038/nrmicro2255</a>
</p>
<p>Author: Andrew Jermy</p>
<p>Many species of bloom-forming algae in the phytoplankton form beneficial or obligate associations with marine bacteria. Such partnerships are thought to enable the sharing of metabolites and nutrients, although a detailed understanding of most of these interactions is lacking. The acquisition of iron may be </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/P9DFBR_cTgI" height="1" width="1"/>]]></content:encoded>
<dc:title>Symbiosis: A partnership cast in iron</dc:title>
<dc:creator>Andrew Jermy</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2255</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 760 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2255</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2255</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>760</prism:startingPage>
<prism:endingPage>760</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2255</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2256">
<title>In Brief</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/i3PuV3E3s5s/nrmicro2256</link>
<description>Environmental microbiology</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Microbiology 7, 761 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2256">doi:10.1038/nrmicro2256</a>
</p>
<p>Environmental microbiology</p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/i3PuV3E3s5s" height="1" width="1"/>]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nrmicro2256</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 761 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2256</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2256</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>761</prism:startingPage>
<prism:endingPage>761</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2256</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2251">
<title>Bacterial immune evasion: An evasive surface</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/4e4UckizEuA/nrmicro2251</link>
<description>Gram-positive bacterial pathogens can evade the host innate immune response by using a cell surface protein to synthesize adenosine, a potent suppressor of inflammation, according to a new report in the Journal of Experimental Medicine.Gram-positive pathogens such as Staphylococcus aureus use various </description>
<content:encoded><![CDATA[

<p>
<b>Bacterial immune evasion: An evasive surface</b>
</p>
<p>Nature Reviews Microbiology 7, 762 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2251">doi:10.1038/nrmicro2251</a>
</p>
<p>Author: Sheilagh Molloy</p>
<p>Gram-positive bacterial pathogens can evade the host innate immune response by using a cell surface protein to synthesize adenosine, a potent suppressor of inflammation, according to a new report in the Journal of Experimental Medicine.Gram-positive pathogens such as Staphylococcus aureus use various </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/4e4UckizEuA" height="1" width="1"/>]]></content:encoded>
<dc:title>Bacterial immune evasion: An evasive surface</dc:title>
<dc:creator>Sheilagh Molloy</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2251</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 762 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2251</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2251</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>762</prism:startingPage>
<prism:endingPage>762</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2251</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2254">
<title>Fungal physiology: Candida puts RNA at the tip</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/Yz-w7vra7zs/nrmicro2254</link>
<description>The generation of cell polarity is a fundamental feature of eukaryotic cells and the basis for many biological processes, such as cell division and differentiation. One mechanism for achieving cell polarity is through the localization of specific mRNAs. In yeast, RNA localization is best exemplified </description>
<content:encoded><![CDATA[

<p>
<b>Fungal physiology: Candida puts RNA at the tip</b>
</p>
<p>Nature Reviews Microbiology 7, 762 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2254">doi:10.1038/nrmicro2254</a>
</p>
<p>Author: Christiaan van Ooij</p>
<p>The generation of cell polarity is a fundamental feature of eukaryotic cells and the basis for many biological processes, such as cell division and differentiation. One mechanism for achieving cell polarity is through the localization of specific mRNAs. In yeast, RNA localization is best exemplified </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/Yz-w7vra7zs" height="1" width="1"/>]]></content:encoded>
<dc:title>Fungal physiology: Candida puts RNA at the tip</dc:title>
<dc:creator>Christiaan van Ooij</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2254</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 762 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2254</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2254</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>762</prism:startingPage>
<prism:endingPage>762</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2254</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2253">
<title>Unity in diversity: lessons from Candida</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/MTdoKmF8Qno/nrmicro2253</link>
<description>This month's Genome Watch showcases the use of genomic comparisons at different depths to investigate pathogenicity within the Candida clade.</description>
<content:encoded><![CDATA[

<p>
<b>Unity in diversity: lessons from Candida</b>
</p>
<p>Nature Reviews Microbiology 7, 763 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2253">doi:10.1038/nrmicro2253</a>
</p>
<p>Authors: Christiane Hertz-Fowler &amp; Arnab Pain</p>
<p>This month's Genome Watch showcases the use of genomic comparisons at different depths to investigate pathogenicity within the Candida clade.</p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/MTdoKmF8Qno" height="1" width="1"/>]]></content:encoded>
<dc:title>Unity in diversity: lessons from Candida</dc:title>
<dc:creator>Christiane Hertz-Fowler</dc:creator>
<dc:creator>Arnab Pain</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2253</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 763 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2253</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2253</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>763</prism:startingPage>
<prism:endingPage>763</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2253</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2257">
<title>In the News</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/V-TSWTAonwA/nrmicro2257</link>
<description>CEACAM6 and Crohn's DiseaseInvestigators have found that expression of human carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) makes mice susceptible to infection by adhesive and invasive Escherichia coli (AIEC), which has been linked to Crohn's disease in humans. Crohn's disease is thought to </description>
<content:encoded><![CDATA[

<p>
<b>In the News</b>
</p>
<p>Nature Reviews Microbiology 7, 764 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2257">doi:10.1038/nrmicro2257</a>
</p>
<p>CEACAM6 and Crohn's DiseaseInvestigators have found that expression of human carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) makes mice susceptible to infection by adhesive and invasive Escherichia coli (AIEC), which has been linked to Crohn's disease in humans. Crohn's disease is thought to </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/V-TSWTAonwA" height="1" width="1"/>]]></content:encoded>
<dc:title>In the News</dc:title>
<dc:identifier>doi:10.1038/nrmicro2257</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 764 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2257</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2257</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>764</prism:startingPage>
<prism:endingPage>764</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2257</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2220">
<title>Structural biology of the chaperone–usher pathway of pilus biogenesis</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/ffW6CCYdh0s/nrmicro2220</link>
<description>The chaperone–usher (CU) pathway of pilus biogenesis is the most widespread of the five pathways that assemble adhesive pili at the surface of Gram-negative bacteria. Recent progress in the study of the structural biology of the CU pathway has unravelled the molecular basis of chaperone </description>
<content:encoded><![CDATA[

<p>
<b>Structural biology of the chaperone&#8211;usher pathway of pilus biogenesis</b>
</p>
<p>Nature Reviews Microbiology 7, 765 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2220">doi:10.1038/nrmicro2220</a>
</p>
<p>Authors: Gabriel Waksman &amp; Scott J. Hultgren</p>
<p>The chaperone&#8211;usher (CU) pathway of pilus biogenesis is the most widespread of the five pathways that assemble adhesive pili at the surface of Gram-negative bacteria. Recent progress in the study of the structural biology of the CU pathway has unravelled the molecular basis of chaperone </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/ffW6CCYdh0s" height="1" width="1"/>]]></content:encoded>
<dc:title>Structural biology of the chaperone–usher pathway of pilus biogenesis</dc:title>
<dc:creator>Gabriel Waksman</dc:creator>
<dc:creator>Scott J. Hultgren</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2220</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 765 (2009)</dc:source>
<dc:date>2009-10-12</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2009-10-12</prism:publicationDate>
<prism:doi>10.1038/nrmicro2220</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2220</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>765</prism:startingPage>
<prism:endingPage>774</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2220</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2221">
<title>The trypanosome flagellar pocket</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/GzthsLKMOQU/nrmicro2221</link>
<description>Trypanosomes are important disease agents and excellent models for the study of evolutionary cell biology. The trypanosome flagellar pocket is a small invagination of the plasma membrane where the flagellum exits the cytoplasm and participates in many cellular processes. It is the only site of </description>
<content:encoded><![CDATA[

<p>
<b>The trypanosome flagellar pocket</b>
</p>
<p>Nature Reviews Microbiology 7, 775 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2221">doi:10.1038/nrmicro2221</a>
</p>
<p>Authors: Mark C. Field &amp; Mark Carrington</p>
<p>Trypanosomes are important disease agents and excellent models for the study of evolutionary cell biology. The trypanosome flagellar pocket is a small invagination of the plasma membrane where the flagellum exits the cytoplasm and participates in many cellular processes. It is the only site of </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/GzthsLKMOQU" height="1" width="1"/>]]></content:encoded>
<dc:title>The trypanosome flagellar pocket</dc:title>
<dc:creator>Mark C. Field</dc:creator>
<dc:creator>Mark Carrington</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2221</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 775 (2009)</dc:source>
<dc:date>2009-10-06</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2009-10-06</prism:publicationDate>
<prism:doi>10.1038/nrmicro2221</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2221</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>775</prism:startingPage>
<prism:endingPage>786</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2221</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2222">
<title>The evolutionary conundrum of pathogen mimicry</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/Id1BKGgt5lk/nrmicro2222</link>
<description>Evolutionary conflicts involving mimicry are found throughout nature. Diverse pathogens produce a range of 'mimics' that resemble host components in both form and function. Such mimics subvert crucial cellular processes, including the cell cycle, apoptosis, cytoskeletal dynamics and immunity. Here, we review the mounting evidence </description>
<content:encoded><![CDATA[

<p>
<b>The evolutionary conundrum of pathogen mimicry</b>
</p>
<p>Nature Reviews Microbiology 7, 787 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2222">doi:10.1038/nrmicro2222</a>
</p>
<p>Authors: Nels C. Elde &amp; Harmit S. Malik</p>
<p>Evolutionary conflicts involving mimicry are found throughout nature. Diverse pathogens produce a range of 'mimics' that resemble host components in both form and function. Such mimics subvert crucial cellular processes, including the cell cycle, apoptosis, cytoskeletal dynamics and immunity. Here, we review the mounting evidence </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/Id1BKGgt5lk" height="1" width="1"/>]]></content:encoded>
<dc:title>The evolutionary conundrum of pathogen mimicry</dc:title>
<dc:creator>Nels C. Elde</dc:creator>
<dc:creator>Harmit S. Malik</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2222</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 787 (2009)</dc:source>
<dc:date>2009-10-06</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2009-10-06</prism:publicationDate>
<prism:doi>10.1038/nrmicro2222</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2222</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>787</prism:startingPage>
<prism:endingPage>797</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2222</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2223">
<title>Understanding HIV-1 latency provides clues for the eradication of long-term reservoirs</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/OM5yFYWgUns/nrmicro2223</link>
<description>HIV-1 can infect both activated and resting, non-dividing cells, following which the viral genome can be permanently integrated into a host cell chromosome. Latent HIV-1 reservoirs are established early during primary infection and constitute a major barrier to eradication, even in the presence of highly </description>
<content:encoded><![CDATA[

<p>
<b>Understanding HIV-1 latency provides clues for the eradication of long-term reservoirs</b>
</p>
<p>Nature Reviews Microbiology 7, 798 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2223">doi:10.1038/nrmicro2223</a>
</p>
<p>Authors: Mayte Coiras, Mar&#237;a Rosa L&#243;pez-Huertas, Mayte P&#233;rez-Olmeda &amp; Jos&#233; Alcam&#237;</p>
<p>HIV-1 can infect both activated and resting, non-dividing cells, following which the viral genome can be permanently integrated into a host cell chromosome. Latent HIV-1 reservoirs are established early during primary infection and constitute a major barrier to eradication, even in the presence of highly </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/OM5yFYWgUns" height="1" width="1"/>]]></content:encoded>
<dc:title>Understanding HIV-1 latency provides clues for the eradication of long-term reservoirs</dc:title>
<dc:creator>Mayte Coiras</dc:creator>
<dc:creator>María Rosa López-Huertas</dc:creator>
<dc:creator>Mayte Pérez-Olmeda</dc:creator>
<dc:creator>José Alcamí</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2223</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 798 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2223</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2223</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>798</prism:startingPage>
<prism:endingPage>812</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2223</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2219">
<title>Humans and evolutionary and ecological forces shaped the phylogeography of recently emerged diseases</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/okdGipLD6Dc/nrmicro2219</link>
<description>The development of human civilizations and global commerce has led to the emergence and worldwide circulation of many infectious diseases. Anthrax, plague and tularaemia are three zoonotic diseases that have been intensely studied through genome characterization of the causative species and phylogeographical analyses. A few </description>
<content:encoded><![CDATA[

<p>
<b>Humans and evolutionary and ecological forces shaped the phylogeography of recently emerged diseases</b>
</p>
<p>Nature Reviews Microbiology 7, 813 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2219">doi:10.1038/nrmicro2219</a>
</p>
<p>Authors: Paul S. Keim &amp; David M. Wagner</p>
<p>The development of human civilizations and global commerce has led to the emergence and worldwide circulation of many infectious diseases. Anthrax, plague and tularaemia are three zoonotic diseases that have been intensely studied through genome characterization of the causative species and phylogeographical analyses. A few </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/okdGipLD6Dc" height="1" width="1"/>]]></content:encoded>
<dc:title>Humans and evolutionary and ecological forces shaped the phylogeography of recently emerged diseases</dc:title>
<dc:creator>Paul S. Keim</dc:creator>
<dc:creator>David M. Wagner</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2219</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 813 (2009)</dc:source>
<dc:date>2009-10-12</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2009-10-12</prism:publicationDate>
<prism:doi>10.1038/nrmicro2219</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2219</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>813</prism:startingPage>
<prism:endingPage>821</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2219</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2202">
<title>Metabolism, cell growth and the bacterial cell cycle</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/YWN1B-TQBOA/nrmicro2202</link>
<description>Adaptation to fluctuations in nutrient availability is a fact of life for single-celled organisms in the 'wild'. A decade ago our understanding of how bacteria adjust cell cycle parameters to accommodate changes in nutrient availability stemmed almost entirely from elegant physiological studies completed in the </description>
<content:encoded><![CDATA[

<p>
<b>Metabolism, cell growth and the bacterial cell cycle</b>
</p>
<p>Nature Reviews Microbiology 7, 822 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2202">doi:10.1038/nrmicro2202</a>
</p>
<p>Authors: Jue D. Wang &amp; Petra A. Levin</p>
<p>Adaptation to fluctuations in nutrient availability is a fact of life for single-celled organisms in the 'wild'. A decade ago our understanding of how bacteria adjust cell cycle parameters to accommodate changes in nutrient availability stemmed almost entirely from elegant physiological studies completed in the </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/YWN1B-TQBOA" height="1" width="1"/>]]></content:encoded>
<dc:title>Metabolism, cell growth and the bacterial cell cycle</dc:title>
<dc:creator>Jue D. Wang</dc:creator>
<dc:creator>Petra A. Levin</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2202</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 822 (2009)</dc:source>
<dc:date>2009-10-06</dc:date>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:publicationDate>2009-10-06</prism:publicationDate>
<prism:doi>10.1038/nrmicro2202</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2202</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Perspectives</prism:section>
<prism:startingPage>822</prism:startingPage>
<prism:endingPage>827</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2202</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2235">
<title>Explaining microbial population genomics through phage predation</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/a8Z-QviVPrQ/nrmicro2235</link>
<description>The remarkable differences that have been detected by metagenomics in the genomes of strains of the same bacterial species are difficult to reconcile with the widely accepted paradigm that periodic selection within bacterial populations will regularly purge genomic diversity by clonal replacement. We have found </description>
<content:encoded><![CDATA[

<p>
<b>Explaining microbial population genomics through phage predation</b>
</p>
<p>Nature Reviews Microbiology 7, 828 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2235">doi:10.1038/nrmicro2235</a>
</p>
<p>Authors: Francisco Rodriguez-Valera, Ana-Belen Martin-Cuadrado, Beltran Rodriguez-Brito, Lejla Pa&#353;i&#263;, T. Frede Thingstad, Forest Rohwer &amp; Alex Mira</p>
<p>The remarkable differences that have been detected by metagenomics in the genomes of strains of the same bacterial species are difficult to reconcile with the widely accepted paradigm that periodic selection within bacterial populations will regularly purge genomic diversity by clonal replacement. We have found </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/a8Z-QviVPrQ" height="1" width="1"/>]]></content:encoded>
<dc:title>Explaining microbial population genomics through phage predation</dc:title>
<dc:creator>Francisco Rodriguez-Valera</dc:creator>
<dc:creator>Ana-Belen Martin-Cuadrado</dc:creator>
<dc:creator>Beltran Rodriguez-Brito</dc:creator>
<dc:creator>Lejla Pašić</dc:creator>
<dc:creator>T. Frede Thingstad</dc:creator>
<dc:creator>Forest Rohwer</dc:creator>
<dc:creator>Alex Mira</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2235</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 828 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2235</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2235</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Perspectives</prism:section>
<prism:startingPage>828</prism:startingPage>
<prism:endingPage>836</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2235</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrmicro2244">
<title>The biology and future prospects of antivirulence therapies</title>
<link>http://feeds.nature.com/~r/nrmicro/rss/current/~3/FAKpWSXbuiA/nrmicro2244</link>
<description>Nature Reviews Microbiology6, 17–27 (2008), doi: 10.1038/nrmicro1818In the above article, a mistake was introduced in figure 4. The correct figure is shown below. We wish to apologize to the authors, and to readers, for any confusion </description>
<content:encoded><![CDATA[

<p>
<b>The biology and future prospects of antivirulence therapies</b>
</p>
<p>Nature Reviews Microbiology 7, 836 (2009). <a href="http://dx.doi.org/10.1038/nrmicro2244">doi:10.1038/nrmicro2244</a>
</p>
<p>Author: Lynette Cegelski, Garland R. Marshall, Gary R. Eldridge &amp; Scott J. Hultgren</p>
<p>Nature Reviews Microbiology6, 17&#8211;27 (2008), doi: 10.1038/nrmicro1818In the above article, a mistake was introduced in figure 4. The correct figure is shown below. We wish to apologize to the authors, and to readers, for any confusion </p>
<img src="http://feeds.feedburner.com/~r/nrmicro/rss/current/~4/FAKpWSXbuiA" height="1" width="1"/>]]></content:encoded>
<dc:title>The biology and future prospects of antivirulence therapies</dc:title>
<dc:creator>Lynette Cegelski</dc:creator>
<dc:creator>Garland R. Marshall</dc:creator>
<dc:creator>Gary R. Eldridge</dc:creator>
<dc:creator>Scott J. Hultgren</dc:creator>
<dc:identifier>doi:10.1038/nrmicro2244</dc:identifier>
<dc:source>Nature Reviews Microbiology 7, 836 (2009)</dc:source>
<prism:publicationName>Nature Reviews Microbiology</prism:publicationName>
<prism:doi>10.1038/nrmicro2244</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrmicro2244</prism:url>
<prism:volume>7</prism:volume>
<prism:number>11</prism:number>
<prism:section>Erratum</prism:section>
<prism:startingPage>836</prism:startingPage>
<prism:endingPage>836</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrmicro2244</feedburner:origLink></item>
</rdf:RDF>
