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  1. Article ; Online: Relationship between hemagglutinin stability and influenza virus persistence after exposure to low pH or supraphysiological heating.

    Yang, Guohua / Ojha, Chet R / Russell, Charles J

    PLoS pathogens

    2021  Volume 17, Issue 9, Page(s) e1009910

    Abstract: The hemagglutinin (HA) surface glycoprotein is triggered by endosomal low pH to cause membrane fusion during influenza A virus (IAV) entry yet must remain sufficiently stable to avoid premature activation during virion transit between cells and hosts. HA ...

    Abstract The hemagglutinin (HA) surface glycoprotein is triggered by endosomal low pH to cause membrane fusion during influenza A virus (IAV) entry yet must remain sufficiently stable to avoid premature activation during virion transit between cells and hosts. HA activation pH and/or virion inactivation pH values less than pH 5.6 are thought to be required for IAV airborne transmissibility and human pandemic potential. To enable higher-throughput screening of emerging IAV strains for "humanized" stability, we developed a luciferase reporter assay that measures the threshold pH at which IAVs are inactivated. The reporter assay yielded results similar to TCID50 assay yet required one-fourth the time and one-tenth the virus. For four A/TN/09 (H1N1) HA mutants and 73 IAVs of varying subtype, virion inactivation pH was compared to HA activation pH and the rate of inactivation during 55°C heating. HA stability values correlated highly with virion acid and thermal stability values for isogenic viruses containing HA point mutations. HA stability also correlated with virion acid stability for human isolates but did not correlate with thermal stability at 55°C, raising doubt in the use of supraphysiological heating assays. Some animal isolates had virion inactivation pH values lower than HA activation pH, suggesting factors beyond HA stability can modulate virion stability. The coupling of HA activation pH and virion inactivation pH, and at a value below 5.6, was associated with human adaptation. This suggests that both virologic properties should be considered in risk assessment algorithms for pandemic potential.
    MeSH term(s) Animals ; Dogs ; Hemagglutinin Glycoproteins, Influenza Virus/chemistry ; High-Throughput Screening Assays ; Humans ; Hydrogen-Ion Concentration ; Influenza A Virus, H1N1 Subtype ; Influenza, Human/virology ; Madin Darby Canine Kidney Cells ; Orthomyxoviridae Infections/virology ; Protein Stability ; Virion/physiology
    Chemical Substances H1N1 virus hemagglutinin ; Hemagglutinin Glycoproteins, Influenza Virus
    Language English
    Publishing date 2021-09-03
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2205412-1
    ISSN 1553-7374 ; 1553-7366
    ISSN (online) 1553-7374
    ISSN 1553-7366
    DOI 10.1371/journal.ppat.1009910
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Potent dual block to HIV-1 infection using lentiviral vectors expressing fusion inhibitor peptide mC46- and Vif-resistant APOBEC3G.

    Delviks-Frankenberry, Krista A / Ojha, Chet R / Hermann, Kip J / Hu, Wei-Shau / Torbett, Bruce E / Pathak, Vinay K

    Molecular therapy. Nucleic acids

    2023  Volume 33, Page(s) 794–809

    Abstract: Gene therapy strategies that effectively inhibit HIV-1 replication are needed to reduce the requirement for lifelong antiviral therapy and potentially achieve a functional cure. We previously designed self-activating lentiviral vectors that efficiently ... ...

    Abstract Gene therapy strategies that effectively inhibit HIV-1 replication are needed to reduce the requirement for lifelong antiviral therapy and potentially achieve a functional cure. We previously designed self-activating lentiviral vectors that efficiently delivered and expressed a Vif-resistant mutant of APOBEC3G (A3G-D128K) to T cells, which potently inhibited HIV-1 replication and spread with no detectable virus. Here, we developed vectors that express A3G-D128K, membrane-associated fusion inhibitor peptide mC46, and O
    Language English
    Publishing date 2023-08-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2662631-7
    ISSN 2162-2531
    ISSN 2162-2531
    DOI 10.1016/j.omtn.2023.08.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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