Susceptibility to antiretroviral drugs of CRF01_AE, CRF02_AG, and subtype C viruses from untreated patients of Africa and asia : Comparative genotypic and phenotypic data
Non-B HIV-1 viruses are predominant in developing countries where access to antiretroviral drugs (ARVs) is progressively being intensified. It is important to obtain more data on the susceptibility of these viruses to available ARVs. CRF01_AE, CRF02_AG, and subtype C strains of HIV-1 obtained from u...
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creator | FLEURY, Herve J TONI, Thomas LEBEL-BINAY, Sophie CHERET, Arnaud MASQUELIER, Bernard LAN, N. T. H HUNG, P. V DESHPANDE, Alaka RECORDON-PINSON, Patricia BOUCHER, Sebastien LAZARO, Estibaliz JAUVIN, Valerie LAVIGNOLLE-AURILLAC, Valerie |
description | Non-B HIV-1 viruses are predominant in developing countries where access to antiretroviral drugs (ARVs) is progressively being intensified. It is important to obtain more data on the susceptibility of these viruses to available ARVs. CRF01_AE, CRF02_AG, and subtype C strains of HIV-1 obtained from untreated patients from Vietnam, Cote d'Ivoire, and India were analyzed for their in vitro susceptibility to NRTIs, NNRTIs, PIs, and an entry inhibitor (T-20) using a recombinant viral assay (PHENOSCRIPT). The corresponding viruses, which had been previously sequenced in reverse transcriptase (RT), protease (prot), plus envelope (env) C2/V3 genes and had therefore been fully characterized, were further sequenced in env HR1 + HR2 regions. CRF01_AE isolates are sensitive to NRTIs and NNRTIs with the exception of one isolate that exhibits a decreased susceptibility to NNRTIs associated with a I135T substitution in RT. CRF02_AG and subtype C viruses are sensitive to NRTIs and NNRTIs but some CRF02_AG isolates tend to be resistant to abacavir, potentially related to associated substitutions of RT at positions 123 (D123N) plus 135 (I135V). Whereas all but one CRF01_AE isolates are fully susceptible to PIs, some CRF02_AG and, more frequently, some subtype C isolates are resistant to atazanavir. The role of substitutions in prot at positions of secondary resistance mutations 20, 36, 63, and 82 is raised with a potentially crucial role of the V82I substitution. Finally, all viruses tested, regardless of the CRF or subtype, are fully susceptible to T-20. |
doi_str_mv | 10.1089/aid.2006.22.357 |
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T. H ; HUNG, P. V ; DESHPANDE, Alaka ; RECORDON-PINSON, Patricia ; BOUCHER, Sebastien ; LAZARO, Estibaliz ; JAUVIN, Valerie ; LAVIGNOLLE-AURILLAC, Valerie</creator><creatorcontrib>FLEURY, Herve J ; TONI, Thomas ; LEBEL-BINAY, Sophie ; CHERET, Arnaud ; MASQUELIER, Bernard ; LAN, N. T. H ; HUNG, P. V ; DESHPANDE, Alaka ; RECORDON-PINSON, Patricia ; BOUCHER, Sebastien ; LAZARO, Estibaliz ; JAUVIN, Valerie ; LAVIGNOLLE-AURILLAC, Valerie</creatorcontrib><description>Non-B HIV-1 viruses are predominant in developing countries where access to antiretroviral drugs (ARVs) is progressively being intensified. It is important to obtain more data on the susceptibility of these viruses to available ARVs. CRF01_AE, CRF02_AG, and subtype C strains of HIV-1 obtained from untreated patients from Vietnam, Cote d'Ivoire, and India were analyzed for their in vitro susceptibility to NRTIs, NNRTIs, PIs, and an entry inhibitor (T-20) using a recombinant viral assay (PHENOSCRIPT). The corresponding viruses, which had been previously sequenced in reverse transcriptase (RT), protease (prot), plus envelope (env) C2/V3 genes and had therefore been fully characterized, were further sequenced in env HR1 + HR2 regions. CRF01_AE isolates are sensitive to NRTIs and NNRTIs with the exception of one isolate that exhibits a decreased susceptibility to NNRTIs associated with a I135T substitution in RT. CRF02_AG and subtype C viruses are sensitive to NRTIs and NNRTIs but some CRF02_AG isolates tend to be resistant to abacavir, potentially related to associated substitutions of RT at positions 123 (D123N) plus 135 (I135V). Whereas all but one CRF01_AE isolates are fully susceptible to PIs, some CRF02_AG and, more frequently, some subtype C isolates are resistant to atazanavir. The role of substitutions in prot at positions of secondary resistance mutations 20, 36, 63, and 82 is raised with a potentially crucial role of the V82I substitution. Finally, all viruses tested, regardless of the CRF or subtype, are fully susceptible to T-20.</description><identifier>ISSN: 0889-2229</identifier><identifier>EISSN: 1931-8405</identifier><identifier>DOI: 10.1089/aid.2006.22.357</identifier><identifier>PMID: 16623640</identifier><identifier>CODEN: ARHRE7</identifier><language>eng</language><publisher>Larchmont, NY: Liebert</publisher><subject>AIDS/HIV ; Anti-HIV Agents - therapeutic use ; Biological and medical sciences ; Cote d'Ivoire ; Drug Resistance, Multiple, Viral - genetics ; Fundamental and applied biological sciences. Psychology ; Genes, env ; Genetic Predisposition to Disease ; Genotype ; HIV Infections - drug therapy ; HIV Infections - virology ; HIV Protease - genetics ; HIV Reverse Transcriptase - genetics ; HIV-1 - classification ; HIV-1 - drug effects ; HIV-1 - enzymology ; HIV-1 - genetics ; HIV-1 - isolation & purification ; Human immunodeficiency virus 1 ; Human viral diseases ; Humans ; India ; Infectious diseases ; Medical sciences ; Microbiology ; Miscellaneous ; Phenotype ; Vietnam ; Viral diseases ; Virology</subject><ispartof>AIDS research and human retroviruses, 2006-04, Vol.22 (4), p.357-366</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-b2c3c757565298dba1ebbc05b264bf0a1f9d77f27bb1da94fb6c83e01e9c10443</citedby><cites>FETCH-LOGICAL-c356t-b2c3c757565298dba1ebbc05b264bf0a1f9d77f27bb1da94fb6c83e01e9c10443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3042,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17727689$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16623640$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FLEURY, Herve J</creatorcontrib><creatorcontrib>TONI, Thomas</creatorcontrib><creatorcontrib>LEBEL-BINAY, Sophie</creatorcontrib><creatorcontrib>CHERET, Arnaud</creatorcontrib><creatorcontrib>MASQUELIER, Bernard</creatorcontrib><creatorcontrib>LAN, N. T. H</creatorcontrib><creatorcontrib>HUNG, P. V</creatorcontrib><creatorcontrib>DESHPANDE, Alaka</creatorcontrib><creatorcontrib>RECORDON-PINSON, Patricia</creatorcontrib><creatorcontrib>BOUCHER, Sebastien</creatorcontrib><creatorcontrib>LAZARO, Estibaliz</creatorcontrib><creatorcontrib>JAUVIN, Valerie</creatorcontrib><creatorcontrib>LAVIGNOLLE-AURILLAC, Valerie</creatorcontrib><title>Susceptibility to antiretroviral drugs of CRF01_AE, CRF02_AG, and subtype C viruses from untreated patients of Africa and asia : Comparative genotypic and phenotypic data</title><title>AIDS research and human retroviruses</title><addtitle>AIDS Res Hum Retroviruses</addtitle><description>Non-B HIV-1 viruses are predominant in developing countries where access to antiretroviral drugs (ARVs) is progressively being intensified. It is important to obtain more data on the susceptibility of these viruses to available ARVs. CRF01_AE, CRF02_AG, and subtype C strains of HIV-1 obtained from untreated patients from Vietnam, Cote d'Ivoire, and India were analyzed for their in vitro susceptibility to NRTIs, NNRTIs, PIs, and an entry inhibitor (T-20) using a recombinant viral assay (PHENOSCRIPT). The corresponding viruses, which had been previously sequenced in reverse transcriptase (RT), protease (prot), plus envelope (env) C2/V3 genes and had therefore been fully characterized, were further sequenced in env HR1 + HR2 regions. CRF01_AE isolates are sensitive to NRTIs and NNRTIs with the exception of one isolate that exhibits a decreased susceptibility to NNRTIs associated with a I135T substitution in RT. CRF02_AG and subtype C viruses are sensitive to NRTIs and NNRTIs but some CRF02_AG isolates tend to be resistant to abacavir, potentially related to associated substitutions of RT at positions 123 (D123N) plus 135 (I135V). 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Psychology</topic><topic>Genes, env</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - virology</topic><topic>HIV Protease - genetics</topic><topic>HIV Reverse Transcriptase - genetics</topic><topic>HIV-1 - classification</topic><topic>HIV-1 - drug effects</topic><topic>HIV-1 - enzymology</topic><topic>HIV-1 - genetics</topic><topic>HIV-1 - isolation & purification</topic><topic>Human immunodeficiency virus 1</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>India</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Phenotype</topic><topic>Vietnam</topic><topic>Viral diseases</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FLEURY, Herve J</creatorcontrib><creatorcontrib>TONI, Thomas</creatorcontrib><creatorcontrib>LEBEL-BINAY, Sophie</creatorcontrib><creatorcontrib>CHERET, Arnaud</creatorcontrib><creatorcontrib>MASQUELIER, Bernard</creatorcontrib><creatorcontrib>LAN, N. T. H</creatorcontrib><creatorcontrib>HUNG, P. 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T. H</au><au>HUNG, P. V</au><au>DESHPANDE, Alaka</au><au>RECORDON-PINSON, Patricia</au><au>BOUCHER, Sebastien</au><au>LAZARO, Estibaliz</au><au>JAUVIN, Valerie</au><au>LAVIGNOLLE-AURILLAC, Valerie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Susceptibility to antiretroviral drugs of CRF01_AE, CRF02_AG, and subtype C viruses from untreated patients of Africa and asia : Comparative genotypic and phenotypic data</atitle><jtitle>AIDS research and human retroviruses</jtitle><addtitle>AIDS Res Hum Retroviruses</addtitle><date>2006-04-01</date><risdate>2006</risdate><volume>22</volume><issue>4</issue><spage>357</spage><epage>366</epage><pages>357-366</pages><issn>0889-2229</issn><eissn>1931-8405</eissn><coden>ARHRE7</coden><abstract>Non-B HIV-1 viruses are predominant in developing countries where access to antiretroviral drugs (ARVs) is progressively being intensified. It is important to obtain more data on the susceptibility of these viruses to available ARVs. CRF01_AE, CRF02_AG, and subtype C strains of HIV-1 obtained from untreated patients from Vietnam, Cote d'Ivoire, and India were analyzed for their in vitro susceptibility to NRTIs, NNRTIs, PIs, and an entry inhibitor (T-20) using a recombinant viral assay (PHENOSCRIPT). The corresponding viruses, which had been previously sequenced in reverse transcriptase (RT), protease (prot), plus envelope (env) C2/V3 genes and had therefore been fully characterized, were further sequenced in env HR1 + HR2 regions. CRF01_AE isolates are sensitive to NRTIs and NNRTIs with the exception of one isolate that exhibits a decreased susceptibility to NNRTIs associated with a I135T substitution in RT. CRF02_AG and subtype C viruses are sensitive to NRTIs and NNRTIs but some CRF02_AG isolates tend to be resistant to abacavir, potentially related to associated substitutions of RT at positions 123 (D123N) plus 135 (I135V). Whereas all but one CRF01_AE isolates are fully susceptible to PIs, some CRF02_AG and, more frequently, some subtype C isolates are resistant to atazanavir. The role of substitutions in prot at positions of secondary resistance mutations 20, 36, 63, and 82 is raised with a potentially crucial role of the V82I substitution. Finally, all viruses tested, regardless of the CRF or subtype, are fully susceptible to T-20.</abstract><cop>Larchmont, NY</cop><pub>Liebert</pub><pmid>16623640</pmid><doi>10.1089/aid.2006.22.357</doi><tpages>10</tpages></addata></record> |
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subjects | AIDS/HIV Anti-HIV Agents - therapeutic use Biological and medical sciences Cote d'Ivoire Drug Resistance, Multiple, Viral - genetics Fundamental and applied biological sciences. Psychology Genes, env Genetic Predisposition to Disease Genotype HIV Infections - drug therapy HIV Infections - virology HIV Protease - genetics HIV Reverse Transcriptase - genetics HIV-1 - classification HIV-1 - drug effects HIV-1 - enzymology HIV-1 - genetics HIV-1 - isolation & purification Human immunodeficiency virus 1 Human viral diseases Humans India Infectious diseases Medical sciences Microbiology Miscellaneous Phenotype Vietnam Viral diseases Virology |
title | Susceptibility to antiretroviral drugs of CRF01_AE, CRF02_AG, and subtype C viruses from untreated patients of Africa and asia : Comparative genotypic and phenotypic data |
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