<?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>T. J. O'Shea</dc:contributor>
  <dc:contributor>L.M. Oko</dc:contributor>
  <dc:contributor>K.V. Holmes</dc:contributor>
  <dc:creator>S.R. Dominguez</dc:creator>
  <dc:date>2007</dc:date>
  <dc:description>The epidemic of severe acute respiratory syndrome (SARS) was caused by a newly emerged coronavirus (SARS-CoV). Bats of several species in southern People's Republic of China harbor SARS-like CoVs and may be reservoir hosts for them. To determine whether bats in North America also harbor coronaviruses, we used reverse transcription-PCR to detect coronavirus RNA in bats. We found coronavirus RNA in 6 of 28 fecal specimens from bats of 2 of 7 species tested. The prevalence of viral RNA shedding was high: 17% in Eptesicus fuscus and 50% in Myotis occultus. Sequence analysis of a 440-bp amplicon in gene 1b showed that these Rocky Mountain bat coronaviruses formed 3 clusters in phylogenetic group 1 that were distinct from group 1 coronaviruses of Asian bats. Because of the potential for bat coronaviruses to cause disease in humans and animals, further surveillance and characterization of bat coronaviruses in North America are needed.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.3201/eid1309.070491</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>National Center for Biotechnology Information</dc:publisher>
  <dc:title>Detection of group 1 coronaviruses in bats in North America</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>