2017
DOI: 10.1099/jgv.0.000772
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Revisiting the genotyping scheme for varicella-zoster viruses based on whole-genome comparisons

Abstract: We report whole-genome sequences (WGSs) for four varicella-zoster virus (VZV) samples from a shingles study conducted by Kaiser Permanente of Southern California. Comparative genomics and phylogenetic analysis of all published VZV WGSs revealed that strain KY037798 is in clade IX, which shall henceforth be designated clade 9. Previously published single nucleotide polymorphisms (SNP)-based genotyping schemes fail to discriminate between clades 6 and VIII and employ positions that are not clade-specific. We pro… Show more

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Cited by 35 publications
(31 citation statements)
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“…However, most studies of recombination in human herpesviruses have focused on naturally circulating variants and have inferred historical sites of recombination and phylogenetic relationships from the comparison of disparate strains. For example, increased genomic surveillance of VZV has expanded the number of known phylogenetic clades for this species in recent years; this has provided evidence for ancient, interclade recombination as well as for modern recombination between individual strains ( 28 32 ). For the beta-herpesvirus HCMV, multiple groups have confirmed the finding of rampant genome-wide recombination among different HCMV strains ( 19 , 33 , 34 ).…”
Section: Recombination As a Driving Force In Dna Virus Evolutionmentioning
confidence: 99%
See 1 more Smart Citation
“…However, most studies of recombination in human herpesviruses have focused on naturally circulating variants and have inferred historical sites of recombination and phylogenetic relationships from the comparison of disparate strains. For example, increased genomic surveillance of VZV has expanded the number of known phylogenetic clades for this species in recent years; this has provided evidence for ancient, interclade recombination as well as for modern recombination between individual strains ( 28 32 ). For the beta-herpesvirus HCMV, multiple groups have confirmed the finding of rampant genome-wide recombination among different HCMV strains ( 19 , 33 , 34 ).…”
Section: Recombination As a Driving Force In Dna Virus Evolutionmentioning
confidence: 99%
“…The norm for HTS studies has now shifted to include either comparisons of a large number of viral strains at a time or a deeper investigation of viral setting or outbreak. This expansion of known diversity has driven the definition of new phylogenetic clades and facilitated the reconstruction of the evolutionary history of VZV ( 28 , 30 32 ), HSV-1 ( 23 , 36 , 70 72 ), HSV-2 ( 73 76 ), HCMV ( 20 , 33 , 34 , 77 ), HHV 6A/6B ( 119 ), EBV ( 78 , 79 ), and KSHV ( 80 ), as well as animal herpesviruses ( 41 ). While it is clear that increasing the number of fully sequenced genomes for each species widens our knowledge of viral diversity, the next challenge lies in dissecting the phenotypic impacts of the observed genetic differences in these viral populations.…”
Section: Capturing and Cataloging The Diversity Of Herpesvirusesmentioning
confidence: 99%
“…For a small proportion of cases (3%), samples were tested for VZV only at CDC. For VZV PCR testing at CDC, four different PCR protocols were performed on every sample, each of which can detect <10 copies/reaction . VZV genotyping was also performed at CDC on a subset of VZV‐positive samples.…”
Section: Methodsmentioning
confidence: 99%
“…The classifications of these samples are similar to those found in the US except that European clades (clades 1 and 3) predominate, followed by clade 5 (CDC, unpublished observation). VZV molecular epidemiology varies by geographical region, likely reflecting climatic conditions and the geographic isolation of populations, although this trend does not hold in countries with widespread immigration [6][7][8][9][10] . Clade 5 is the dominant genotype in Africa, and its dominance in Brazil may reflect large influxes of people from sub-Saharan Africa.…”
Section: /4mentioning
confidence: 99%
“…Seven isolates were determined to be clade 5 viruses (50%), 5 were clade 1 (36%), and 2 were clade 3 (14%) ( Table 1). Depletion of the samples precluded the use of the recently-published revisions to our SNPbased genotyping method 8 . The method used fails to distinguish clade 6 from clade VIII, but since no clade 6/VIII viruses were identified, it was not relevant to this study.…”
mentioning
confidence: 99%