HIV-1 tolerates changes in A-count in a small segment of the pol gene

Retrovirology. 2017 Sep 5;14(1):43. doi: 10.1186/s12977-017-0367-0.

Abstract

Background: The HIV-1 RNA genome has a biased nucleotide composition with a surplus of As. Several hypotheses have been put forward to explain this striking phenomenon, but the A-count of the HIV-1 genome has thus far not been systematically manipulated. The reason for this reservation is the likelihood that known and unknown sequence motifs will be affected by such a massive mutational approach, thus resulting in replication-impaired virus mutants. We present the first attempt to increase and decrease the A-count in a relatively small polymerase (pol) gene segment of HIV-1 RNA.

Results: To minimize the mutational impact, a new mutational approach was developed that is inspired by natural sequence variation as present in HIV-1 isolates. This phylogeny-instructed mutagenesis allowed us to create replication-competent HIV-1 mutants with a significantly increased or decreased local A-count. The local A-count of the wild-type (wt) virus (40.2%) was further increased to 46.9% or reduced to 31.7 and 26.3%. These HIV-1 variants replicate efficiently in vitro, despite the fact that the pol changes cause a quite profound move in HIV-SIV sequence space.

Conclusions: Extrapolating these results to the complete 9 kb RNA genome, we may cautiously suggest that the A-rich signature does not have to be maintained. This survey also provided clues that silent codon changes, in particular from G-to-A, determine the subtype-specific sequence signatures.

Keywords: A-rich; Evolution; HIV-1 evolution; Mutagenesis; Nucleotide composition; Phylogeny; RNA genome; Silent codon changes; Subtypes.

MeSH terms

  • AT Rich Sequence / genetics*
  • AT Rich Sequence / physiology
  • Base Composition / genetics*
  • Base Composition / physiology
  • Cells, Cultured
  • Evolution, Molecular
  • Genes, pol / genetics*
  • Genetic Variation
  • HEK293 Cells
  • HIV Infections / virology
  • HIV Reverse Transcriptase / chemistry
  • HIV Reverse Transcriptase / genetics
  • HIV-1 / classification
  • HIV-1 / genetics*
  • Humans
  • Phylogeny
  • RNA, Viral / chemistry
  • RNA, Viral / genetics
  • Silent Mutation
  • Virus Replication / genetics

Substances

  • RNA, Viral
  • HIV Reverse Transcriptase