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      Sensitive and broadly reactive reverse transcription-PCR assays to detect novel paramyxoviruses.

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          Abstract

          We have developed a set of reverse transcription-PCR assays for the detection and identification of known and novel paramyxoviruses in clinical specimens. Primers were designed from the conserved motifs of the polymerase pol gene sequences to detect members of the Paramyxovirinae or Pneumovirinae subfamily or groups of genera within the Paramyxovirinae subfamily. The consensus-degenerate hybrid oligonucleotide primer design and seminested or nested PCR assay design were used to enhance the breadth of reactivity and sensitivity of the respective assays. Using expressed RNA and 10-fold dilution series of virus-infected tissue culture isolates from different members of the family or genera, these assays were able to detect on average between 100 and 500 copies of template RNA. The assays were specific to the respective group of genera or subfamily viruses. This set of primers enhances our ability to look for novel viruses in outbreaks and diseases of unknown etiology.

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          Author and article information

          Journal
          J Clin Microbiol
          Journal of clinical microbiology
          American Society for Microbiology
          1098-660X
          0095-1137
          Aug 2008
          : 46
          : 8
          Affiliations
          [1 ] Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA. sot1@cdc.gov
          Article
          JCM.00192-08
          10.1128/JCM.00192-08
          2519498
          18579717
          ace2a002-4d36-4e63-aa04-2ad3336eece9
          History

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