Biased Nucleotide Composition and Differential Codon Usage Pattern in HIV-1 and HIV-2

HIV-1 and HIV-2 are closely related retroviruses with differences in pathogenicity and geographic distribution. HIV-2 infection is associated with slower disease progression and transmission, longer latency period, low or undetectable plasmatic viral loads, and reduced likelihood of progression to A...

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Published inAIDS research and human retroviruses Vol. 33; no. 3; p. 298
Main Authors Vidyavijayan, K K, Hassan, Sameer, Precilla, Lucia K, Ashokkumar, Manickam, Chandrasekeran, Padmapriyadharshini, Swaminathan, Soumya, Hanna, Luke Elizabeth
Format Journal Article
LanguageEnglish
Published United States 01.03.2017
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ISSN1931-8405
DOI10.1089/AID.2015.0320

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Abstract HIV-1 and HIV-2 are closely related retroviruses with differences in pathogenicity and geographic distribution. HIV-2 infection is associated with slower disease progression and transmission, longer latency period, low or undetectable plasmatic viral loads, and reduced likelihood of progression to AIDS, compared to HIV-1. In this investigation, we analyzed HIV-2 genes and genomes and compared them with that of HIV-1 belonging to various subtypes. Comparative analysis of the effective number of codons (ENC) for each of the nine genes of the two viruses revealed that the tat gene of HIV-2 had a higher ENC value compared to HIV-1 tat, reflecting lower levels of expression of HIV-2 tat. Lower levels of tat protein particularly during the early stages of infection could result in a lower viral load, lower viral set point, and delayed progression of disease in HIV-2-infected individuals compared to HIV-1-infected subjects. Furthermore, the GC3 composition of the regulatory genes of HIV-2 was ≥50%, suggesting a firm effort by these viruses to adapt themselves to evolutionary survival. We hypothesize that differential codon usage could be one of the possible factors that could contribute to the diminished pathogenicity of HIV-2 in the host as compared to HIV-1.
AbstractList HIV-1 and HIV-2 are closely related retroviruses with differences in pathogenicity and geographic distribution. HIV-2 infection is associated with slower disease progression and transmission, longer latency period, low or undetectable plasmatic viral loads, and reduced likelihood of progression to AIDS, compared to HIV-1. In this investigation, we analyzed HIV-2 genes and genomes and compared them with that of HIV-1 belonging to various subtypes. Comparative analysis of the effective number of codons (ENC) for each of the nine genes of the two viruses revealed that the tat gene of HIV-2 had a higher ENC value compared to HIV-1 tat, reflecting lower levels of expression of HIV-2 tat. Lower levels of tat protein particularly during the early stages of infection could result in a lower viral load, lower viral set point, and delayed progression of disease in HIV-2-infected individuals compared to HIV-1-infected subjects. Furthermore, the GC3 composition of the regulatory genes of HIV-2 was ≥50%, suggesting a firm effort by these viruses to adapt themselves to evolutionary survival. We hypothesize that differential codon usage could be one of the possible factors that could contribute to the diminished pathogenicity of HIV-2 in the host as compared to HIV-1.
Author Hanna, Luke Elizabeth
Chandrasekeran, Padmapriyadharshini
Swaminathan, Soumya
Vidyavijayan, K K
Precilla, Lucia K
Ashokkumar, Manickam
Hassan, Sameer
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  fullname: Hanna, Luke Elizabeth
  organization: 1 Department of HIV/AIDS, National Institute for Research in Tuberculosis (ICMR) , Chennai, India
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Keywords nucleotide composition
HIV/AIDS pathogenesis
codon usage
virus evolution/diversity
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Snippet HIV-1 and HIV-2 are closely related retroviruses with differences in pathogenicity and geographic distribution. HIV-2 infection is associated with slower...
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StartPage 298
SubjectTerms Base Composition
Codon
Gene Expression
Genes, Viral
Genome, Viral
HIV-1 - genetics
HIV-2 - genetics
Humans
Nucleotides - analysis
Title Biased Nucleotide Composition and Differential Codon Usage Pattern in HIV-1 and HIV-2
URI https://www.ncbi.nlm.nih.gov/pubmed/27599904
Volume 33
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