<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Brock Kingstad-Bakke</dc:contributor>
  <dc:contributor>Marcel Wuthrich</dc:contributor>
  <dc:contributor>Ben Stading</dc:contributor>
  <dc:contributor>Rachel C. Abbott</dc:contributor>
  <dc:contributor>Marcos Isidoro Ayza</dc:contributor>
  <dc:contributor>Hannah E. Dobson</dc:contributor>
  <dc:contributor>Lucas dos Santos Dias</dc:contributor>
  <dc:contributor>Kevin Galles</dc:contributor>
  <dc:contributor>Julia S. Lankton</dc:contributor>
  <dc:contributor>Elizabeth Falendysz</dc:contributor>
  <dc:contributor>Jeffrey M. Lorch</dc:contributor>
  <dc:contributor>J. Scott Fites</dc:contributor>
  <dc:contributor>Jaime Lopera-Madrid</dc:contributor>
  <dc:contributor>Bruce Klein</dc:contributor>
  <dc:contributor>Jorge E. Osorio</dc:contributor>
  <dc:contributor>J. Paul White</dc:contributor>
  <dc:creator>Tonie E. Rocke</dc:creator>
  <dc:date>2019</dc:date>
  <dc:description>&lt;div id="Abs1-section" class="serif article-section js-article-section cleared clear"&gt;&lt;div id="Abs1-content" class="pl20 mq875-pl0 js-collapsible-section"&gt;&lt;p&gt;&lt;span&gt;White-nose syndrome (WNS) caused by the fungus,&amp;nbsp;&lt;/span&gt;&lt;i&gt;Pseudogymnoascus destructans&lt;/i&gt;&lt;span&gt;&amp;nbsp;(&lt;/span&gt;&lt;i&gt;Pd&lt;/i&gt;&lt;span&gt;) has killed millions of North American hibernating bats. Currently, methods to prevent the disease are limited. We conducted two trials to assess potential WNS vaccine candidates in wild-caught&amp;nbsp;&lt;/span&gt;&lt;i&gt;Myotis lucifugus&lt;/i&gt;&lt;span&gt;. In a pilot study, we immunized bats with one of four vaccine treatments or phosphate-buffered saline (PBS) as a control and challenged them with&amp;nbsp;&lt;/span&gt;&lt;i&gt;Pd&lt;/i&gt;&lt;span&gt;&amp;nbsp;upon transfer into hibernation chambers. Bats in one vaccine-treated group, that received raccoon poxviruses (RCN) expressing&amp;nbsp;&lt;/span&gt;&lt;i&gt;Pd&lt;/i&gt;&lt;span&gt;&amp;nbsp;calnexin (CAL) and serine protease (SP), developed WNS at a lower rate (1/10) than other treatments combined (14/23), although samples sizes were small. The results of a second similar trial provided additional support for this observation. Bats vaccinated orally or by injection with RCN-CAL and RCN-SP survived&amp;nbsp;&lt;/span&gt;&lt;i&gt;Pd&lt;/i&gt;&lt;span&gt;&amp;nbsp;challenge at a significantly higher rate (P = 0.01) than controls. Using RT-PCR and flow cytometry, combined with fluorescent&amp;nbsp;&lt;/span&gt;&lt;i&gt;in situ&lt;/i&gt;&lt;span&gt;&amp;nbsp;hybridization, we determined that expression of IFN-γ transcripts and the number of CD4 + T-helper cells transcribing this gene were elevated (P &amp;lt; 0.10) in stimulated lymphocytes from surviving vaccinees (n = 15) compared to controls (n = 3). We conclude that vaccination with virally-vectored&amp;nbsp;&lt;/span&gt;&lt;i&gt;Pd&lt;/i&gt;&lt;span&gt;antigens induced antifungal immunity that could potentially protect bats against WNS.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1038/s41598-019-43210-w</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Nature</dc:publisher>
  <dc:title>Virally-vectored vaccine candidates against white-nose syndrome induce anti-fungal immune response in little brown bats (Myotis lucifugus)</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>