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In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir.

In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir. Research Abstract Details 

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  • In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir. Abstract Text:

    sherie masseSherie Masse,xiaozhi luXiaozhi Lu,tatyana dekhtyarTatyana Dekhtyar,liangjun luLiangjun Lu,gennadiy koevGennadiy Koev,feng gaoFeng Gao,hongmei moHongmei Mo,dale kempfDale Kempf,barry bernsteinBarry Bernstein,george j hannaGeorge J Hanna,akhteruzzaman mollaAkhteruzzaman Molla,sherie masseSherie Masse,xiaozhi luXiaozhi Lu,tatyana dekhtyarTatyana Dekhtyar,liangjun luLiangjun Lu,gennadiy koevGennadiy Koev,feng gaoFeng Gao,hongmei moHongmei Mo,dale kempfDale Kempf,barry bernsteinBarry Bernstein,george j hannaGeorge J Hanna,akhteruzzaman mollaAkhteruzzaman Molla,

    Lopinavir (LPV)-ritonavir has demonstrated durable antiviral activity in human immunodeficiency virus type 1 (HIV-1)-infected antiretroviral-naïve and protease inhibitor (PI)-experienced patients. However, information on LPV activity against HIV-2 and the patterns of mutations in HIV-2 in response to selection by LPV is limited. The activity of LPV against three strains of HIV-2 was assessed and compared to activity against a reference HIV-1 strain. LPV demonstrated activity similar to that observed against HIV-1 in two HIV-2 strains (HIV-2(MS) and HIV-2(CBL-23)) tested. On the other hand, approximately 10-fold-reduced susceptibility was observed with the third HIV-2 strain, HIV-2(CDC310319). Passage of HIV-2(MS) with increasing concentrations of LPV selected mutations V47A and D17N in the HIV-2 protease gene. The introduction of both 17N and 47A either individually or together into HIV-2(ROD) molecular infectious clones showed that the single V47A substitution in HIV-2 resulted in a substantial reduction in susceptibility to LPV. In contrast, this mutant retained wild-type susceptibility to other PIs and appeared to be hypersusceptible to atazanavir and saquinavir.

    In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir. Publishing Authors By Initials

    s masseS Masse,x luX Lu,t dekhtyarT Dekhtyar,l luL Lu,g koevG Koev,f gaoF Gao,h moH Mo,d kempfD Kempf,b bernsteinB Bernstein,gj hannaGJ Hanna,a mollaA Molla,s masseS Masse,x luX Lu,t dekhtyarT Dekhtyar,l luL Lu,g koevG Koev,f gaoF Gao,h moH Mo,d kempfD Kempf,b bernsteinB Bernstein,gj hannaGJ Hanna,a mollaA Molla,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Antimicrobial agents and chemotherapy

    VOLUME: 51

    Page Numbers: 3075-80

    Journal Abbreviation: Antimicrob. Agents Chemother.

    ISSN: 0066-4804

    DAY: 18

    MONTH: 06

    YEAR: 2007

    In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 315061

    In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir. Information

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    Grant and Affiliation Information for In vitro selection and characterization of human immunodeficiency virus type 2 with decreased susceptibility to lopinavir.

    AFFILIATION: Antiviral Research, Global Pharmaceutical Research and Development, AP52N-1 Rm. 1133, 200 Abbott Park Road, Abbott Park, IL 60064, USA. Sherie.masse@abbott.com

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: GM 065057

    ACRONYM: GM

    MEDLINETA: Antimicrob Agents Chemother

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