4.6 Article

Torque Teno Virus Primary Infection Kinetics in Early Childhood

Journal

VIRUSES-BASEL
Volume 14, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/v14061277

Keywords

anellovirus; TTV primary infection; infants; genoprevalence; viremia

Categories

Funding

  1. Finnish-Norwegian Medical Foundation
  2. Sigrid Juselius Foundation
  3. Life and Health Medical Support Association
  4. Swedish Cultural Fund
  5. Juvenile Diabetes Research Foundation International [4-1998-274, 4-1999-731, 4-2001-435]
  6. European Union [BMH4-CT98-3314]
  7. Academy of Finland [68292, 1122539]
  8. Novo Nordisk Foundation
  9. Finnish Funding Agency for Technology and Innovation (Tekes)
  10. Special Research Funds for University Hospitals in Finland
  11. Finnish Office for Health Technology Assessment
  12. Diabetes Research Foundation in Finland
  13. Emil Aaltonen Foundation
  14. Signe and Ane Gyllenberg Foundation
  15. Foundation for Pediatric Research
  16. Paivikki and Sakari Sohlberg Foundation
  17. University of Helsinki

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Human torque teno viruses (TTVs) are common nonenveloped viruses found in human blood, with infections primarily occurring during the first two years after birth. There is significant individual variation in viral load and strain diversity during the infection process.
Human torque teno viruses (TTVs) are a diverse group of small nonenveloped viruses with circular, single-stranded DNA genomes. These elusive anelloviruses are harbored in the blood stream of most humans and have thus been considered part of the normal flora. Whether the primary infection as a rule take(s) place before or after birth has been debated. The aim of our study was to determine the time of TTV primary infection and the viral load and strain variations during infancy and follow-up for up to 7 years. TTV DNAs were quantified in serial serum samples from 102 children by a pan-TTV quantitative PCR, and the amplicons from representative time points were cloned and sequenced to disclose the TTV strain diversity. We detected an unequivocal rise in TTV-DNA prevalence, from 39% at 4 months of age to 93% at 2 years; all children but one, 99%, became TTV-DNA positive before age 4 years. The TTV-DNA quantities ranged from 5 x 10(1) to 4 x 10(7) copies/mL, both within and between the children. In conclusion, TTV primary infections occur mainly after birth, and increase during the first two years with high intra- and interindividual variation in both DNA quantities and virus strains.

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