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      GC content-based pan-pox universal PCR assays for poxvirus detection.

      Journal of Clinical Microbiology
      Animals, Base Composition, Base Sequence, Chordopoxvirinae, genetics, isolation & purification, DNA, Viral, chemistry, Humans, Molecular Diagnostic Techniques, methods, Molecular Sequence Data, Phylogeny, Polymerase Chain Reaction, Poxviridae Infections, diagnosis, veterinary, virology, Sequence Alignment, Vertebrates, Virology

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          Abstract

          Chordopoxviruses of the subfamily Chordopoxvirinae, family Poxviridae, infect vertebrates and consist of at least eight genera with broad host ranges. For most chordopoxviruses, the number of viral genes and their relative order are highly conserved in the central region. The GC content of chordopoxvirus genomes, however, evolved into two distinct types: those with genome GC content of more than 60% and those with a content of less than 40% GC. Two standard PCR assays were developed to identify chordopoxviruses based on whether the target virus has a low or high GC content. In design of the assays, the genus Avipoxvirus, which encodes major rearrangements of gene clusters, was excluded. These pan-pox assays amplify DNA from more than 150 different isolates and strains, including from primary clinical materials, from all seven targeted genera of chordopoxviruses and four unclassified new poxvirus species. The pan-pox assays represent an important advance for the screening and diagnosis of human and animal poxvirus infections, and the technology used is accessible to many laboratories worldwide.

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