Variability of the human immunodeficiency virus type 1 polymerase gene from treatment naive patients in Accra, Ghana
Identifieur interne : 000D34 ( Main/Exploration ); précédent : 000D33; suivant : 000D35Variability of the human immunodeficiency virus type 1 polymerase gene from treatment naive patients in Accra, Ghana
Auteurs : Kwamena William Coleman Sagoe [Ghana] ; Magdar Dwidar [États-Unis] ; Margaret Lartey [Ghana] ; Isaac Boamah [Ghana] ; AFRAKOMA ADJOA AGYEI [Ghana] ; ANNA ABA HAYFORD [Ghana] ; JULIUS ABRAHAM ADDO MINGLE [Ghana] ; Max Q. Arens [États-Unis]Source :
- Journal of clinical virology [ 1386-6532 ] ; 2007.
Descripteurs français
- Pascal (Inist)
- Wicri :
English descriptors
- KwdEn :
- AIDS, Gene, Ghana, HIV-1 virus, Human, Microbiology, Mutation, Resistance, Subtype, Treatment, Virology.
Abstract
Background: Little is known about the HIV-1 drug resistance mutations in Ghana. Objectives: To determine the background protease (PR) and reverse transcriptase (RT) mutations of HIV-1 from treatment naive patients in Ghana. Study design: Twenty-five plasma samples randomly selected were analyzed for drug resistance mutations. The molecular phylogeny and recombinant patterns of the polymerase gene of HIV-1 were also analysed. Results: No major drug-resistance mutations were seen in protease or reverse transcriptase genes. The L10I, L10V, V11I and E35G minor mutations were seen in four patients, while the V179E was observed in a patient with subtype G. An insertion of lysine was found at codon 36 of the protease gene of one patient. The predominant subtype was the CRF02_AG strain (n = 22), but 3 (13.6%) of these were recombinants with HIV- 1 subtype K and/or A 1. Two patients harboured unclassified/complex strains with D/CRF01 -AE and G/CRFAG_02 subtypes for the PR and RT, respectively, using the Stanford Database. Viral loads (VL) ranged from 2290 to >1,500,000 c/ml (mean = 339,065 c/ml). Conclusions: Treatment naive patients in Ghana before scale-up may have minor but not major PR mutations and high viral loads. The clinical effects of minor mutations/polymorphisms in the PR and RT genes and recombinants need to be investigated.
Affiliations:
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Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>AIDS</term>
<term>Gene</term>
<term>Ghana</term>
<term>HIV-1 virus</term>
<term>Human</term>
<term>Microbiology</term>
<term>Mutation</term>
<term>Resistance</term>
<term>Subtype</term>
<term>Treatment</term>
<term>Virology</term>
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<term>Homme</term>
<term>Gène</term>
<term>Traitement</term>
<term>Ghana</term>
<term>Soustype</term>
<term>Résistance</term>
<term>Mutation</term>
<term>Microbiologie</term>
<term>Virologie</term>
<term>SIDA</term>
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<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Ghana</term>
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<front><div type="abstract" xml:lang="en">Background: Little is known about the HIV-1 drug resistance mutations in Ghana. Objectives: To determine the background protease (PR) and reverse transcriptase (RT) mutations of HIV-1 from treatment naive patients in Ghana. Study design: Twenty-five plasma samples randomly selected were analyzed for drug resistance mutations. The molecular phylogeny and recombinant patterns of the polymerase gene of HIV-1 were also analysed. Results: No major drug-resistance mutations were seen in protease or reverse transcriptase genes. The L10I, L10V, V11I and E35G minor mutations were seen in four patients, while the V179E was observed in a patient with subtype G. An insertion of lysine was found at codon 36 of the protease gene of one patient. The predominant subtype was the CRF02_AG strain (n = 22), but 3 (13.6%) of these were recombinants with HIV- 1 subtype K and/or A 1. Two patients harboured unclassified/complex strains with D/CRF01 -AE and G/CRFAG_02 subtypes for the PR and RT, respectively, using the Stanford Database. Viral loads (VL) ranged from 2290 to >1,500,000 c/ml (mean = 339,065 c/ml). Conclusions: Treatment naive patients in Ghana before scale-up may have minor but not major PR mutations and high viral loads. The clinical effects of minor mutations/polymorphisms in the PR and RT genes and recombinants need to be investigated.</div>
</front>
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<name sortKey="Afrakoma Adjoa Agyei" sort="Afrakoma Adjoa Agyei" uniqKey="Afrakoma Adjoa Agyei" last="Afrakoma Adjoa Agyei">AFRAKOMA ADJOA AGYEI</name>
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