Publication
HIV-2 Integrase Polymorphisms and Longitudinal Genotypic Analysis of HIV-2 Infected Patients Failing a Raltegravir-Containing Regimen
dc.contributor.author | Cavaco-Silva, J | |
dc.contributor.author | Abecasis, A | |
dc.contributor.author | Miranda, AC | |
dc.contributor.author | Poças, J | |
dc.contributor.author | Narciso, J | |
dc.contributor.author | Águas, MJ | |
dc.contributor.author | Maltez, F | |
dc.contributor.author | Almeida, I | |
dc.contributor.author | Germano, I | |
dc.contributor.author | Diniz, A | |
dc.contributor.author | Gonçalves, MF | |
dc.contributor.author | Gomes, P | |
dc.contributor.author | Cunha, C | |
dc.contributor.author | Camacho, RJ | |
dc.date.accessioned | 2014-04-02T11:50:18Z | |
dc.date.available | 2014-04-02T11:50:18Z | |
dc.date.issued | 2014 | |
dc.description.abstract | To characterize the HIV-2 integrase gene polymorphisms and the pathways to resistance of HIV-2 patients failing a raltegravir-containing regimen, we studied 63 integrase strand transfer inhibitors (INSTI)-naïve patients, and 10 heavily pretreated patients exhibiting virological failure while receiving a salvage raltegravir-containing regimen. All patients were infected by HIV-2 group A. 61.4% of the integrase residues were conserved, including the catalytic motif residues. No INSTI-major resistance mutations were detected in the virus population from naïve patients, but two amino acids that are secondary resistance mutations to INSTIs in HIV-1 were observed. The 10 raltegravir-experienced patients exhibited resistance mutations via three main genetic pathways: N155H, Q148R, and eventually E92Q - T97A. The 155 pathway was preferentially used (7/10 patients). Other mutations associated to raltegravir resistance in HIV-1 were also observed in our HIV-2 population (V151I and D232N), along with several novel mutations previously unreported. Data retrieved from this study should help build a more robust HIV-2-specific algorithm for the genotypic interpretation of raltegravir resistance, and contribute to improve the clinical monitoring of HIV-2-infected patients. | por |
dc.identifier.citation | PLoS One. 2014 Mar 28;9(3):e92747 | por |
dc.identifier.uri | http://hdl.handle.net/10400.17/1771 | |
dc.language.iso | eng | por |
dc.peerreviewed | yes | por |
dc.publisher | PLOS One | por |
dc.subject | HCC INF | por |
dc.subject | Drug Resistance, Viral/genetics | por |
dc.subject | Genotype | por |
dc.subject | HIV Infections/drug therapy | |
dc.subject | HIV Integrase/genetics | |
dc.subject | HIV Integrase Inhibitors/therapeutic use | |
dc.subject | HIV-1/drug effects | |
dc.subject | HIV-2/drug effects | |
dc.subject | HIV-2/genetics | |
dc.subject | Polymorphism, Genetic/genetics | |
dc.subject | Pyrrolidinones/therapeutic use | |
dc.title | HIV-2 Integrase Polymorphisms and Longitudinal Genotypic Analysis of HIV-2 Infected Patients Failing a Raltegravir-Containing Regimen | por |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.title | Plos One | por |
rcaap.rights | openAccess | por |
rcaap.type | article | por |
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