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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/3718.rdf" xlink:actuate="onRequest">Accession numbers for Labyrinthulomycetes detected in sea fans collected in the Florida Keys and Puerto Rico from 2006-2010 (Climate_CoralDisease project)</gmx:Anchor>
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        <gco:CharacterString>Accession numbers for Labyrinthulomycetes detected in sea fans Dataset Description: &amp;lt;p&amp;gt;Accession numbers to NCBI's GenBank are provided for &amp;lt;i&amp;gt;Labyrinthulomycetes&amp;lt;/i&amp;gt; detected in sea fans collected in Florida and Puerto Rico. &amp;lt;b&amp;gt;&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
References:&amp;lt;/b&amp;gt;&amp;lt;br /&amp;gt;
Burge CA, Douglas N, Conti-Jerpe I, Weil E, Roberts S, Friedman CS &amp;amp;amp; CD Harvell. In press (May 2012) Friend or foe: the association of Labyrinthulomycetes with the Caribbean sea fan, &amp;lt;i&amp;gt;Gorgonia ventalina&amp;lt;/i&amp;gt;. Dis Aquat Org.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;b&amp;gt;Sampling and Analytical Methodology:&amp;lt;/b&amp;gt;&amp;lt;br /&amp;gt;
Healthy and diseased sea fans were collected from Florida and Puerto Rico. &amp;lt;i&amp;gt; Labyrinthulomycetes&amp;lt;/i&amp;gt; cells were isolated from a diseased sea fan from Florida;  DNA extracted, amplified, cloned, sequenced, and deposited with accession # JQ248602. Fragments of healthy and diseased sea fans were extracted, amplified, cloned and sequenced under accession numbers JQ248603 (Florida), JQ248604 (Florida), JQ248605 (Puerto Rico), and JQ248606 (Puerto Rico).&amp;lt;/p&amp;gt;
&amp;lt;p&amp;gt;Labyrinthulomycota small-subunit ribosomal DNA (SSU rRNA) specific primers, Laby-A and Laby-Y, were used (Stokes et al., 2002).  Those containing bands of the expected  (~ 430 bp) size were purified using the QIAquick PCR kit (Qiagen,) and sent to the Cornell University Life Sciences Core Laboratories for direct sequencing on an Applied Biosystems Automated 3730 DNA Analyzer. Although direct sequencing of all of the PCR products showed unambiguous DNA chromatographs throughout, the homogeneity of samples was additionally confirmed by cloning the PCR products into the TOPO-TA vector, using the TOPO TA cloning kit (Invitrogen) for sequencing of 2 to 5 clones of each isolate.&amp;lt;/p&amp;gt;</gco:CharacterString>
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                            <gco:CharacterString>&lt;p&gt;This award is funded under the American Recovery and Reinvestment Act of 2009 (Public Law 111-5).&lt;/p&gt;
&lt;p&gt;Coral reef ecosystems are highly endangered by recent increases in temperature and by projected increases in ocean acidification. Although temperature has been identified as a driver of some coral disease outbreaks, nothing is known about direct effects of acidification on host immunity and pathogen virulence, or the potential for synergism with temperature. Natural coral populations often suffer from simultaneous infection by multiple pathogens that can also influence host immune responses, but co-infection dynamics have not been investigated in invertebrate systems lacking classical adaptive immunity. Changing climate will very likely influence the outcome of single and co-infection.&lt;/p&gt;
&lt;p&gt;This project will investigate the influence of environmental stress on co-infection dynamics of the sea fan coral, &lt;i&gt;Gorgonia ventalina&lt;/i&gt;, with a fungal pathogen, &lt;i&gt;Aspergillus sydowii&lt;/i&gt; and a protist parasite, SPX. The goal is to identify the mechanisms through which multiple infections, temperature and acidification modify host resistance, leading to changes in within- and among-colony rates of disease spread.&lt;/p&gt;
&lt;p&gt;The objectives of this project are to:&lt;br /&gt;
(1) Identify incidence and co-infection frequency of &lt;i&gt;Aspergillus sydowii&lt;/i&gt; and SPX. Detailed field surveys of the two diseases will test the hypothesis that co-infection is significant, provide valuable information about drivers of aspergillosis, and will help to characterize an emerging new sea fan disease.&lt;br /&gt;
(2) Investigate how co-infection influences sea fan susceptibility, resistance, and within host disease dynamics.  Through manipulative lab inoculation experiments we will test the hypothesis that single infections increase susceptibility to a second pathogen.&lt;br /&gt;
(3) Examine the effects of temperature increase and ocean acidification on pathogen virulence, on underlying host resistance, and on the dynamics of single and co-infections.&lt;/p&gt;
&lt;p&gt;The hypotheses that acidification will increase pathogen virulence and host susceptibility will be tested in a temperature and pH controlled experimental system. This system will also allow the potential synergistic effects of temperature and acidification on host immunity and co-infection dynamics to be explored. The primary intellectual merit of the proposed work will be a greater understanding of how changing climate mediates co-infection and immunity in a non-model invertebrate. While fungal pathogens are primarily opportunistic, labyrinthulid protozoans are recognized as primary pathogens in shellfish. Even in shellfish, little is known about co-infections involving labyrinthulids, and these protists are entirely unstudied in corals.&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Publications associated with this project:&lt;/b&gt;&lt;br /&gt;
Burge CA, Douglas N, Conti-Jerpe I, Weil E, Roberts S, Friedman CS &amp;amp; CD Harvell. (May 2012) Friend or foe: the association of&lt;i&gt; Labyrinthulomycetes&lt;/i&gt; with the Caribbean sea fan,&lt;i&gt; Gorgonia ventalina&lt;/i&gt;. Dis Aquat Org. 101:1-12. doi: &lt;a href=&quot;http://dx.doi.org/10.3354/dao02487&quot; target=&quot;_blank&quot;&gt;10.3354/dao02487&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Burge CA, Mouchka, ME, Harvell, CD &amp;amp; S Roberts. (In review) Immune response of the Caribbean sea fan, &lt;i&gt;Gorgonia ventalina&lt;/i&gt; exposed to an &lt;i&gt;Aplanochytrium&lt;/i&gt; parasite as revealed by transcriptome sequencing.&lt;/p&gt;</gco:CharacterString>
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