Standing Genetic Variation and the Evolution of Drug Resistance in HIV

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Standing Genetic Variation and the Evolution of Drug Resistance in HIV

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Title: Standing Genetic Variation and the Evolution of Drug Resistance in HIV
Author: Pennings, Pleuni
Citation: Pennings, Pleuni S. 2012. Standing genetic variation and the evolution of drug resistance in HIV. PLoS Computational Biology 8(6): e1002527.
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Abstract: Drug due to mutations that were present before treatment starts or due to mutations that occur during treatment. The relative importance of these two sources is unknown. Resistance can also be transmitted between patients, but this process is not considered in the current study. We study three different situations in which HIV drug resistance may evolve: starting triple- drug therapy, treatment with a single dose of nevirapine and interruption of treatment. For each of these three cases good data are available from literature, which allows us to estimate the probability that resistance evolves from standing genetic variation. Depending on the treatment we find probabilities of the evolution of drug resistance due to standing genetic variation between 0 and 39%. For patients who start triple-drug combination therapy, we find that drug resistance evolves from standing genetic variation in approximately 6% of the patients. We use a population-dynamic and population-genetic model to understand the observations and to estimate important evolutionary parameters under the assumption that resistance remains a major problem for the treatment of HIV. Resistance can occur treatment failure is caused by the fixation of a single drug resistance mutation. We find that both, the effective population size of the virus before treatment, and the fitness of the resistant mutant during treatment, are key-parameters which determine the probability that resistance evolves from standing genetic variation. Importantly, clinical data indicate that both of these parameters can be manipulated by the kind of treatment that is used.
Published Version: doi:10.1371/journal.pcbi.1002527
Terms of Use: This article is made available under the terms and conditions applicable to Open Access Policy Articles, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#OAP
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:8553711

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  • FAS Scholarly Articles [7078]
    Peer reviewed scholarly articles from the Faculty of Arts and Sciences of Harvard University
 
 

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