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Molecular evolution of human adenoviruses

  • Christopher M. Robinson
  • , Gurdeep Singh
  • , Jeong Yoon Lee
  • , Shoaleh Dehghan
  • , Jaya Rajaiya
  • , Elizabeth B. Liu
  • , Mohammad A. Yousuf
  • , Rebecca A. Betensky
  • , Morris S. Jones
  • , David W. Dyer
  • , Donald Seto
  • , James Chodosh*
  • *Corresponding author for this work
  • Harvard University
  • George Mason University
  • American University Washington DC
  • Naval Medical Center San Diego
  • University of Oklahoma

Research output: Contribution to journalJournal articlepeer-review

Abstract

The recent emergence of highly virulent human adenoviruses (HAdVs) with new tissue tropisms underscores the need to determine their ontogeny. Here we report complete high quality genome sequences and analyses for all the previously unsequenced HAdV serotypes (n = 20) within HAdV species D. Analysis of nucleotide sequence variability for these in conjunction with another 40 HAdV prototypes, comprising all seven HAdV species, confirmed the uniquely hypervariable regions within species. The mutation rate among HAdV-Ds was low when compared to other HAdV species. Homologous recombination was identified in at least two of five examined hypervariable regions for every virus, suggesting the evolution of HAdV-Ds has been highly dependent on homologous recombination. Patterns of alternating GC and AT rich motifs correlated well with hypervariable region recombination sites across the HAdV-D genomes, suggesting foci of DNA instability lead to formulaic patterns of homologous recombination and confer agility to adenovirus evolution.

Original languageEnglish
Article number1812
JournalScientific Reports
Volume3
DOIs
StatePublished - 2013

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