| Title | Increase in the genetic polymorphism of varicella-zoster virus after passaging in in vitro cell culture |
|---|---|
| Author | Hye Rim Hwang, Seok Cheon Kim, Se Hwan Kang, and Chan Hee Lee* |
| Address | Department of Microbiology, Chungbuk National University, Cheongju 28644, Republic of Korea |
| Bibliography | Journal of Microbiology, 57(11),1033–1039, 2019, |
| DOI | 10.1007/s12275-019-9429-4 |
| Key Words | varicella-zoster virus, genetic polymorphism, passaging |
| Abstract | Primary infections with the varicella-zoster virus (VZV) result in varicella, while latent reactivation leads to herpes zoster. Both varicella and zoster can be prevented by live attenuated vaccines. There have been reports suggesting that both clinical VZV strains and those in vaccine preparations are genetically polymorphic, containing mixtures of both wild-type and vaccine-type sequences at certain vaccine-specific sites. In this study, the genetic polymorphism of the VZV genome was examined by analyzing the frequencies of minor alleles at each nucleotide position. Next-generation sequencing of the clinical VZV strain YC02 passaged in an in vitro cell culture was used to identify genetically polymorphic sites (GPS), where the minor allele frequency (MAF) exceeded 5%. The number of GPS increased by 7.3-fold at high passages (p100) when compared to low passages (p17), although the average MAF remained similar. GPS were found in 6 open reading frames (ORFs) in p17, 35, and 54 ORFs in p60 and p100, respectively. GPS were found more frequently in the dispensable gene group than the essential gene group, but the average MAF was greater in the essential gene group. The most common two major/minor base pairs were A/g and T/c. GPS were found in all three passages at 16 positions, all located in the reiterated (R) region. The population diversity as measured by Shannon entropy increased in p60 and p100. However, the entropy remained unchanged in the R regions. |