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Retrovirology. 2008 Aug 7;5:74. doi: 10.1186/1742-4690-5-74.

Natural variation of HIV-1 group M integrase: implications for a new class of antiretroviral inhibitors.

Author information

1
Division of Infectious Diseases, Department of Medicine, Stanford University, Stanford, CA, USA. syrhee@stanford.edu

Abstract

HIV-1 integrase is the third enzymatic target of antiretroviral (ARV) therapy. However, few data have been published on the distribution of naturally occurring amino acid variation in this enzyme. We therefore characterized the distribution of integrase variants among more than 1,800 published group M HIV-1 isolates from more than 1,500 integrase inhibitor (INI)-naïve individuals. Polymorphism rates equal or above 0.5% were found for 34% of the central core domain positions, 42% of the C-terminal domain positions, and 50% of the N-terminal domain positions. Among 727 ARV-naïve individuals in whom the complete pol gene was sequenced, integrase displayed significantly decreased inter- and intra-subtype diversity and a lower Shannon's entropy than protease or RT. All primary INI-resistance mutations with the exception of E157Q--which was present in 1.1% of sequences--were nonpolymorphic. Several accessory INI-resistance mutations including L74M, T97A, V151I, G163R, and S230N were also polymorphic with polymorphism rates ranging between 0.5% to 2.0%.

PMID:
18687142
PMCID:
PMC2546438
DOI:
10.1186/1742-4690-5-74
[Indexed for MEDLINE]
Free PMC Article

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