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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBELLECAVE, Pantxika
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorMALATO, Laurent
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorCALMELS, Christina
dc.contributor.authorREIGADAS, Sandrine
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPARISSI, Vincent
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorANDREOLA, Marie-Line
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorFLEURY, Hervé
dc.date.accessioned2024-11-05T13:22:07Z
dc.date.available2024-11-05T13:22:07Z
dc.date.issued2014-08-01
dc.identifier.issn1872-7913en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203129
dc.description.abstractEnThe antiviral efficacy of raltegravir (RAL) has been proven against human immunodeficiency virus type 1 (HIV-1) subtypes B and C but remained to be determined against other subtypes. Therefore, the enzymatic activities as well as RAL resistance of HIV-1 subtype A and CRF01_AE integrases (INs) were investigated. Previously published subtype A and CRF01_AE IN sequences from RAL-naïve patients were aligned to generate consensus sequences for both IN subtypes. Subtype A and CRF01_AE INs encoded by these consensus sequences as well as the corresponding enzymes harbouring the N155H resistance mutation were expressed and purified. Enzymatic activities of subtype A and CRF01_AE INs were analysed with regard to typical 3'-end processing (3'-P) and strand transfer (ST) activities both in the presence and absence of RAL and were compared with subtype B IN as well as with the corresponding INs harbouring the N155H resistance mutation. Subtypes B, A and CRF01_AE INs showed similar 3'-P and ST activities. In the presence of RAL, the three wild-type INs exhibited ST activity IC50 values (50% inhibitory concentrations) of 86.3 ± 32.5, 158.3 ± 99.0 and 100.0 ± 65.7 nM, respectively. Analysis of 3'-P activity in the presence of RAL revealed IC(50) > 10 μM for all three enzymes. The three INs harbouring the N155H mutation presented in vitro low but similar resistance levels to RAL. In conclusion, INs from HIV-1 subtypes B, A and CRF01_AE showed similar responses to RAL in vitro, suggesting the potency of this antiretroviral drug to treat HIV-1 subtype A- and CRF01_AE-infected patients.
dc.language.isoENen_US
dc.subject.enAnti-HIV Agents
dc.subject.enCloning
dc.subject.enMolecular
dc.subject.enGene Expression
dc.subject.enGenotype
dc.subject.enHIV Integrase
dc.subject.enHIV-1
dc.subject.enHumans
dc.subject.enInhibitory Concentration 50
dc.subject.enMicrobial Sensitivity Tests
dc.subject.enMutant Proteins
dc.subject.enPyrrolidinones
dc.subject.enRaltegravir Potassium
dc.title.enIn vitro analysis of the susceptibility of HIV-1 subtype A and CRF01_AE integrases to raltegravir.
dc.title.alternativeInt J Antimicrob Agentsen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.ijantimicag.2014.04.013en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed24935032en_US
bordeaux.journalInternational Journal of Antimicrobial Agentsen_US
bordeaux.page168-72en_US
bordeaux.volume44en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue2en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=International%20Journal%20of%20Antimicrobial%20Agents&rft.date=2014-08-01&rft.volume=44&rft.issue=2&rft.spage=168-72&rft.epage=168-72&rft.eissn=1872-7913&rft.issn=1872-7913&rft.au=BELLECAVE,%20Pantxika&MALATO,%20Laurent&CALMELS,%20Christina&REIGADAS,%20Sandrine&PARISSI,%20Vincent&rft.genre=article


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