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    Imposed mutational meltdown as an antiviral strategy

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    Authors
    Jensen, Jeffrey D.
    Stikeleather, Ryan A.
    Kowalik, Timothy F.
    Lynch, Michael
    UMass Chan Affiliations
    Department of Microbiology and Physiological Systems
    Document Type
    Journal Article
    Publication Date
    2020-10-13
    Keywords
    Antivirals
    SARS-CoV-2
    lethal mutagenesis
    mutational meltdown
    population genetics
    Evolution
    Genetics and Genomics
    Immunology and Infectious Disease
    Infectious Disease
    Microbiology
    Population Biology
    Therapeutics
    Virus Diseases
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    Link to Full Text
    https://doi.org/10.1111/evo.14107
    Abstract
    Following widespread infections of the most recent coronavirus known to infect humans, SARS-CoV-2, attention has turned to potential therapeutic options. With no drug or vaccine yet approved, one focal point of research is to evaluate the potential value of repurposing existing antiviral treatments, with the logical strategy being to identify at least a short-term intervention to prevent within-patient progression, whilst long-term vaccine strategies unfold. Here, we offer an evolutionary / population-genetic perspective on one approach that may overwhelm the capacity for pathogen defense (i.e., adaptation) - induced mutational meltdown - providing an overview of key concepts, review of previous theoretical and experimental work of relevance, and guidance for future research. Applied with appropriate care, including target specificity, induced mutational meltdown may provide a general, rapidly implemented approach for the within-patient eradication of a wide range of pathogens or other undesirable microorganisms.
    Source

    Jensen JD, Stikeleather RA, Kowalik TF, Lynch M. Imposed mutational meltdown as an antiviral strategy. Evolution. 2020 Oct 13. doi: 10.1111/evo.14107. Epub ahead of print. PMID: 33047822. Link to article on publisher's site

    DOI
    10.1111/evo.14107
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/27345
    PubMed ID
    33047822
    Related Resources

    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1111/evo.14107
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