Efficient identification of inherited chromosomally integrated human herpesvirus 6 using specimen pooling

J Clin Virol. 2016 Apr:77:71-6. doi: 10.1016/j.jcv.2016.02.016. Epub 2016 Feb 20.

Abstract

Background: Human herpesvirus 6 (HHV-6) has a unique ability to integrate into chromosomal telomeres. Vertical transmission via germ cell integration results in offspring with inherited chromosomally integrated (ci)HHV-6 in all nucleated cells, affecting ∼1% of the population.

Objectives: Inherited ciHHV-6 may be a direct or indirect mediator of human disease, but efficient identification of affected individuals is a fundamental roadblock to larger studies exploring the clinical importance of this condition.

Study design: A group testing strategy was designed to efficiently identify individuals with inherited ciHHV-6. DNA was extracted from 2496 cellular samples from hematopoietic cell transplant (HCT) donor-recipient pairs. Pools of 12 samples were screened for HHV-6 DNA with quantitative (q)PCR. Individual samples from high positive pools were tested with qPCR, and high positive individual samples were tested for inherited ciHHV-6 using droplet digital (dd)PCR to determine HHV-6 DNA copies/cellular genome.

Results: Thirty-one pools had high positive HHV-6 DNA detection with >10(3) HHV-6 DNA copies/μg. Each pool had one sample with >10(4) copies/μg HHV-6 DNA. Inherited ciHHV-6 was confirmed by ddPCR in every high positive sample (>10(3) HHV-6 DNA copies/μg), yielding a prevalence of 1.5% in HCT recipients and 0.96% in donors. We performed 580 qPCR tests to screen 2496 samples for inherited ciHHV-6, a 77% reduction in testing.

Conclusions: Inherited ciHHV-6 can be efficiently identified by specimen pooling coupled with modern molecular techniques. This algorithm can be used to facilitate cost-effective identification of patients with inherited ciHHV-6, thereby removing a major hurdle for large-scale study of its clinical impact.

Keywords: Chromosomally integrated; Diagnostic; HHV-6; Herpes; PCR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • DNA, Viral
  • Germ Cells / virology
  • Herpesvirus 6, Human / physiology*
  • Humans
  • Infectious Disease Transmission, Vertical*
  • Mass Screening
  • Real-Time Polymerase Chain Reaction
  • Reproducibility of Results
  • Roseolovirus Infections / diagnosis
  • Roseolovirus Infections / epidemiology
  • Roseolovirus Infections / transmission*
  • Roseolovirus Infections / virology*
  • Sensitivity and Specificity
  • Virus Integration*

Substances

  • DNA, Viral