Human herpesvirus 6 infects cervical epithelial cells and transactivates human papillomavirus gene expression

  • Chen M
  • Popescu N
  • Woodworth C
  • et al.
84Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

To examine whether human herpesvirus 6 (HHV-6) is capable of infecting human cervical epithelial cells and altering expression of human papillomavirus (HPV) genes, HPV-immortalized or -transformed carcinoma cell lines were infected with HHV-6 variant A. No cytopathic effect was observed in infected cervical cells. However, immunofluorescence indicated that infected cells expressed early-late proteins of HHV-6 by day 3 postinfection. HHV-6 DNA was also detected by Southern blot hybridization after infection and persisted through continued subculture in an episomal state as proven by Gardella gel electrophoresis and fluorescence in situ hybridization. HHV-6 infection enhanced expression of HPV RNAs encoding the viral oncoproteins E6 and E7. Transient transfection assays showed that two HHV-6 molecular clones, pZVB-70 and pZVH-14, upregulated transcription 9- to 15-fold from a receptor plasmid containing the HPV type 18 regulatory sequences which control transcription in vivo. Cervical carcinoma cells infected with HHV-6 induced more rapid development of tumors in mice than did noninfected cells. These results are the first evidence that human cervical epithelial cells can be infected with HHV-6 and that HHV-6 contains transactivators which stimulate the HPV-transforming genes.

Cite

CITATION STYLE

APA

Chen, M., Popescu, N., Woodworth, C., Berneman, Z., Corbellino, M., Lusso, P., … DiPaolo, J. A. (1994). Human herpesvirus 6 infects cervical epithelial cells and transactivates human papillomavirus gene expression. Journal of Virology, 68(2), 1173–1178. https://doi.org/10.1128/jvi.68.2.1173-1178.1994

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free