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      <src>https://www.socictopen.socict.org/files/original/606a89277f095400f66e9f6e8757b851.pdf</src>
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            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Coronavirus</text>
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            <name>Description</name>
            <description>An account of the resource</description>
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                <text>Dominio científico: Coronavirus</text>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>Spike Protein Fusion Peptide and Feline Coronavirus Virulence</text>
            </elementText>
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          <name>Creator</name>
          <description>An entity primarily responsible for making the resource</description>
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              <text>Hui-Wen Chang, Herman  F. Egberink, Rebecca Halpin, David J Spiro, Peter J.M. Rottier</text>
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        <element elementId="41">
          <name>Description</name>
          <description>An account of the resource</description>
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              <text>Coronaviruses are well known for their potential to change their host or tissue tropism, resulting in unpredictable new diseases and changes in pathogenicity; severe acute respiratory syndrome and feline coronaviruses, respectively, are the most recognized examples. Feline coronaviruses occur as 2 pathotypes: nonvirulent feline enteric coronaviruses (FECVs), which replicate in intestinal epithelium cells, and lethal feline infectious peritonitis viruses (FIPVs), which replicate in macrophages. Evidence indicates that FIPV originates from FECV by mutation, but consistent distinguishing differences have not been established. We sequenced the full genome of 11 viruses of each pathotype and then focused on the single most distinctive site by additionally sequencing hundreds of viruses in that region. As a result, we identified 2 alternative amino acid differences in the putative fusion peptide of the spike protein that together distinguish FIPV from FECV in &gt;95% of cases. By these and perhaps other mutations, the virus apparently acquires its macrophage tropism and spreads systemically.</text>
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          <name>Date</name>
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              <text>2012</text>
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          <name>Subject</name>
          <description>The topic of the resource</description>
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              <text>Zoonoses, Virulence, pathogenesis, virus tropism, Feline coronavirus, Feline infectious peritonitis virus</text>
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          <name>Identifier</name>
          <description>An unambiguous reference to the resource within a given context</description>
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              <text>DOI: 10.3201/eid1807.120143</text>
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          <name>Source</name>
          <description>A related resource from which the described resource is derived</description>
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              <text>Emerging Infectious Diseases</text>
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          <name>Publisher</name>
          <description>An entity responsible for making the resource available</description>
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              <text>Centers for Disease Control and Prevention</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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            <elementText elementTextId="18519">
              <text>Infectious and parasitic diseases, Medicine</text>
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          <name>Language</name>
          <description>A language of the resource</description>
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            <elementText elementTextId="18520">
              <text>EN</text>
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