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PLoS Pathogens. Estimating the Fitness Advantage Conferred by Permissive Neuraminidase Mutations in Recent Oseltamivir-Resistant A(H1N1)pdm09 Influenza Viruses

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  • PLoS Pathogens. Estimating the Fitness Advantage Conferred by Permissive Neuraminidase Mutations in Recent Oseltamivir-Resistant A(H1N1)pdm09 Influenza Viruses

    [Source: PLoS Pathogens, full page: (LINK). Abstract, edited.]


    Open Access / Peer-Reviewed / Research Article

    Estimating the Fitness Advantage Conferred by Permissive Neuraminidase Mutations in Recent Oseltamivir-Resistant A(H1N1)pdm09 Influenza Viruses

    Jeff Butler, Kathryn A. Hooper, Stephen Petrie, Raphael Lee, Sebastian Maurer-Stroh, Lucia Reh, Teagan Guarnaccia, Chantal Baas, Lumin Xue, Sophie Vitesnik, Sook-Kwan Leang, Jodie McVernon, Anne Kelso, [ ... ], Ian G. Barr, James M. McCaw, Jesse D. Bloom, Aeron C. Hurt

    Published: April 03, 2014 / DOI: 10.1371/journal.ppat.1004065


    Abstract

    Oseltamivir is relied upon worldwide as the drug of choice for the treatment of human influenza infection. Surveillance for oseltamivir resistance is routinely performed to ensure the ongoing efficacy of oseltamivir against circulating viruses. Since the emergence of the pandemic 2009 A(H1N1) influenza virus (A(H1N1)pdm09), the proportion of A(H1N1)pdm09 viruses that are oseltamivir resistant (OR) has generally been low. However, a cluster of OR A(H1N1)pdm09 viruses, encoding the neuraminidase (NA) H275Y oseltamivir resistance mutation, was detected in Australia in 2011 amongst community patients that had not been treated with oseltamivir. Here we combine a competitive mixtures ferret model of influenza infection with a mathematical model to assess the fitness, both within and between hosts, of recent OR A(H1N1)pdm09 viruses. In conjunction with data from in vitro analyses of NA expression and activity we demonstrate that contemporary A(H1N1)pdm09 viruses are now more capable of acquiring H275Y without compromising their fitness, than earlier A(H1N1)pdm09 viruses circulating in 2009. Furthermore, using reverse engineered viruses we demonstrate that a pair of permissive secondary NA mutations, V241I and N369K, confers robust fitness on recent H275Y A(H1N1)pdm09 viruses, which correlated with enhanced surface expression and enzymatic activity of the A(H1N1)pdm09 NA protein. These permissive mutations first emerged in 2010 and are now present in almost all circulating A(H1N1)pdm09 viruses. Our findings suggest that recent A(H1N1)pdm09 viruses are now more permissive to the acquisition of H275Y than earlier A(H1N1)pdm09 viruses, increasing the risk that OR A(H1N1)pdm09 will emerge and spread worldwide.


    Author Summary

    Antimicrobial resistance is an increasing problem for the treatment of infectious diseases. In 2007–2008 human seasonal A(H1N1) influenza viruses rapidly acquired resistance to the most commonly used anti-influenza drug oseltamivir, via a H275Y amino acid mutation within the neuraminidase (NA) protein. In 2009 the oseltamivir sensitive A(H1N1)pdm09 virus (encoding NA 275H) emerged in the human population, rapidly replacing the oseltamivir resistant seasonal A(H1N1) virus. However, there is increasing concern that currently circulating A(H1N1)pdm09 viruses may similarly acquire oseltamivir resistance (via the NA H275Y mutation) and become widespread. Here we demonstrate that two novel amino acid changes present in virtually all recent A(H1N1)pdm09 viruses (NA V241I and N369K) enable the acquisition of the NA H275Y oseltamivir resistance mutation without compromising viral fitness. As such recent A(H1N1)pdm09 viruses are now one step closer to acquiring widespread oseltamivir resistance.
    _____

    Citation: Butler J, Hooper KA, Petrie S, Lee R, Maurer-Stroh S, et al. (2014) Estimating the Fitness Advantage Conferred by Permissive Neuraminidase Mutations in Recent Oseltamivir-Resistant A(H1N1)pdm09 Influenza Viruses. PLoS Pathog 10(4): e1004065. doi:10.1371/journal.ppat.1004065

    Editor: Daniel R. Perez, Virginia-Maryland Regional College of Veterinary Medicine, United States of America

    Received: December 18, 2013; Accepted: February 27, 2014; Published: April 3, 2014

    Copyright: © 2014 Butler et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

    Funding: The Melbourne WHO Collaborating Centre for Reference and Research on Influenza is supported by the Australian Government Department of Health. JMM is supported by an Australian Research Council Future Fellowship (FT110100250) and the Defence Science Institute. JM is supported by a National Health and Medical Research Council Career Development Fellowship. Funding for this research was also kindly provided by the University of Melbourne Research Grants Support Scheme. JDB and KAH were supported by a grant from the NIAID of the National Institutes of Health under award K22AI093789. The authors acknowledge use of computing resources for the quantification of within-host fitness provided by the NeCTAR research cloud (an Australian Government project conducted as part of the Super Science initiative and financed by the Education Investment Fund) and by the Victorian Life Sciences Computation Initiative (VLSCI), grant number VR0274, on its Peak Computing Facility at the University of Melbourne (an initiative of the Victorian Government, Australia.). This work was partially supported by the Australian NHMRC and A*STAR Singapore through the joint grant 12/1/06/24/5793 to ACH and SMS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

    Competing interests: I have read the journal's policy and have the following conflicts: Oseltamivir phosphate and carboxylate was provided to the WHO Collaborating Centre for Reference and Research on Influenza free of charge by Hoffmann-La Roche Ltd., Basel, Switzerland. AK, IGB and ACH hold a small number of shares in CSL Limited, a company that manufactures influenza vaccine. This does not alter our adherence to all PLOS policies on sharing data and materials.


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  • #2
    Re: PLoS Pathogens. Estimating the Fitness Advantage Conferred by Permissive Neuraminidase Mutations in Recent Oseltamivir-Resistant A(H1N1)pdm09 Influenza Viruses

    Red color and underlining mine.

    PLoS Pathogens: Fitness Advantage From Permissive NA Mutations In Oseltamivir Resistant pH1N1





    # 8429

    Hopefully today’s blog won’t be as tedious as the title might first suggest.

    Oseltamivir (aka Tamiflu &#174 – an NAI (Neuraminidase Inhibiting) antiviral drug – is our primary pharmaceutical weapon against influenza. While it doesn’t `cure’ the flu - when started early enough (preferentially within 48 hrs of onset of symptoms) - it can reduce both the severity and duration of infection (see Effectiveness Of NAI Antivirals In Reducing Mortality In Hospitalized H1N1pdm09 Cases).

    Up until the middle of the last decade, we had another class of antiviral drugs - M2 ion channel blockers (e.g. Amantadine, Rimantadine) – which were first developed in the late 1950s. But excessive use over the years (including in agricultural settings) eventually led to widespread resistance.
    The replacement antivirals introduced during the last decade include Oseltamivir (Tamiflu), Zanamivir (Relenza), and Peramivir. Of these, Oseltamivir is by far the most widely used, and has been stockpiled by many governments for use in the event of a pandemic.

    While occasional instances of Oseltamivir resistance was recorded prior to 2007, in nearly every case, it developed after a person was placed on the drug (`spontaneous mutations’). While of concern to the patient being treated, it occurred in only about 1% of treated cases, and studies suggested that these resistant strains were `less biologically fit’, and were therefore believed to be unlikely to spread.
    Which of course, is exactly what they did do. Between 2007 and 2008, the incidence of resistant seasonal H1N1 viruses literally exploded around the globe.
    So much so, that by the end of 2008, nearly all of the H1N1 samples tested in the United States were resistant to oseltamivir and the CDC was forced to issue major new guidance for the use of antivirals (see CIDRAP articleWith H1N1 resistance, CDC changes advice on flu drugs).
    This resistance was primarily due to an H275Y mutation - where a single amino acid substitution (histidine (H) to tyrosine (Y)) occurs at the neuraminidase position 275 (Note: some scientists use 'N2 numbering' (H274Y)).

    While this mutation had been seen before, obviously something had changed between 2006 and 2008 to allow the resistant form of the virus to spread so quickly.

    In 2010 Bloom, Gong & Baltimore discussed these `enabling’ changes in the Journal Science in a report called Permissive Secondary Mutations Enable the Evolution of Influenza Oseltamivir Resistance.
    ABSTACT
    The His<sup>274</sup>→Tyr<sup>274</sup> (H274Y) mutation confers oseltamivir resistance on N1 influenza neuraminidase but had long been thought to compromise viral fitness. However, beginning in 2007–2008, viruses containing H274Y rapidly became predominant among human seasonal H1N1 isolates. We show that H274Y decreases the amount of neuraminidase that reaches the cell surface and that this defect can be counteracted by secondary mutations that also restore viral fitness.
    Two such mutations occurred in seasonal H1N1 shortly before the widespread appearance of H274Y. The evolution of oseltamivir resistance was therefore enabled by “permissive” mutations that allowed the virus to tolerate subsequent occurrences of H274Y. An understanding of this process may provide a basis for predicting the evolution of oseltamivir resistance in other influenza strains.
    In 2011 Abed, Pizzorno, Bouhy & Boivin identified several `permissive’ neuraminidase mutations that occurred just prior to the spread of resistant H1N1 - that when combined with H275Y - `enabled’ its efficient transmission (see PLoS Pathogens Role of Permissive Neuraminidase Mutations in Influenza A/Brisbane/59/2007-like (H1N1) Viruses).
    This pervasive spread of resistant H1N1 would have been a much bigger deal had it not been for the arrival of the 2009 H1N1 pandemic virus, which effectively supplanted the old (resistant) H1N1, and replaced it with a new – but fortunately, still susceptible to NAIs – H1N1 virus.
    Fast forward five years, and the (now seasonal, formerly pandemic) pH1N1 virus remains overwhelmingly susceptible to Oseltamivir and other NAI antiviral drugs, although we have seen a few signs of `creeping resistance’.
    Reassuringly, the latest FluViewreport (week 12) indicated that of 4524 viruses tested this flu season in the United States, only 54 (1.2%) showed signs of NA Inhibitor resistance.


    But we have seen a few worrisome clusters of NAI resistant flu (see Eurosurveillance: Community Cluster Of Antiviral Resistant pH1N1 in Japan & NEJM: Oseltamivir Resistant H1N1 in Australia), which has raised concerns that we could see a repeat of the 2007-2008 rise in antiviral resistance in our current H1N1 strain.

    All of which serves as prelude to a new study that appears in PloS Pathogens, that looks at the potential of pH1N1 following the same course as its predecessor. Their assessment is not particularly rosy.
    Estimating the Fitness Advantage Conferred by Permissive Neuraminidase Mutations in Recent Oseltamivir-Resistant A(H1N1)pdm09 Influenza Viruses
    Jeff Butler, Kathryn A. Hooper, Stephen Petrie, Raphael Lee, Sebastian Maurer-Stroh, Lucia Reh, Teagan Guarnaccia, Chantal Baas, Lumin Xue, Sophie Vitesnik, Sook-Kwan Leang, Jodie McVernon, Anne Kelso, Ian G. Barr, James M. McCaw, Jesse D. Bloom, Aeron C. Hurt mail
    Published: April 03, 2014 DOI: 10.1371/journal.ppat.1004065

    Abstract Oseltamivir is relied upon worldwide as the drug of choice for the treatment of human influenza infection. Surveillance for oseltamivir resistance is routinely performed to ensure the ongoing efficacy of oseltamivir against circulating viruses.
    Since the emergence of the pandemic 2009 A(H1N1) influenza virus (A(H1N1)pdm09), the proportion of A(H1N1)pdm09 viruses that are oseltamivir resistant (OR) has generally been low. However, a cluster of OR A(H1N1)pdm09 viruses, encoding the neuraminidase (NA) H275Y oseltamivir resistance mutation, was detected in Australia in 2011 amongst community patients that had not been treated with oseltamivir. Here we combine a competitive mixtures ferret model of influenza infection with a mathematical model to assess the fitness, both within and between hosts, of recent OR A(H1N1)pdm09 viruses.
    In conjunction with data from in vitro analyses of NA expression and activity we demonstrate that contemporary A(H1N1)pdm09 viruses are now more capable of acquiring H275Y without compromising their fitness, than earlier A(H1N1)pdm09 viruses circulating in 2009. Furthermore, using reverse engineered viruses we demonstrate that a pair of permissive secondary NA mutations, V241I and N369K, confers robust fitness on recent H275Y A(H1N1)pdm09 viruses, which correlated with enhanced surface expression and enzymatic activity of the A(H1N1)pdm09 NA protein.
    These permissive mutations first emerged in 2010 and are now present in almost all circulating A(H1N1)pdm09 viruses.

    Our findings suggest that recent A(H1N1)pdm09 viruses are now more permissive to the acquisition of H275Y than earlier A(H1N1)pdm09 viruses, increasing the risk that OR A(H1N1)pdm09 will emerge and spread worldwide.


    Fair warning: the methods and materials section is lengthy, complex, and pretty tough sledding for those without a solid background in virology. Those interested in the details (or with a masochistic bent) will want to read this report in its entirety.

    The bottom line, however, is that since the 2009 H1N1 virus emerged five years ago, it has managed to pick up a series of `permissive’ mutations that are believed to increase its ability to replicate when it carries the H275Y resistance mutation.
    Which in theory, should promote its spread.
    Given that these mutations are already entrenched, it is a bit surprising we haven’t already seen an expansion in resistant pH1N1, beyond a couple of documented clusters in Australia and Japan. The authors write:
    One explanation is that a high level of circulating A(H1N1)pdm09 viruses may be required for a A(H1N1)pdm09 OR virus to become established and spread. The Australian HNE2011 virus cluster emerged [25], [26] during a season when A(H1N1)pdm09 viruses accounted for almost 40% of all influenza A and B viruses detected globally but, in 2012 and 2013, the proportion of A(H1N1)pdm09 viruses circulating has been considerably lower (9% and 25% respectively) [52].
    In the most recent 2013/14 Northern Hemisphere influenza season, a cluster of A(H1N1)pdm09 H275Y OR viruses that contained both the V241I and N369K PPMs plus an additional N386K NA mutation, was detected in Sapporo, Japan [53], during a period of the season where A(H1N1)pdm09 viruses contributed approximately 50% of the circulating influenza strains [54].
    We’ve just come through an H1N1 dominated flu season in North America, and the incidence of H274Y has remained low, so other factors may be involved. The authors suggest:
    Apart from NA PPMs, it may be that other properties, such as antigenic novelty, are also necessary for an OR virus to spread widely. In 2007–2008, the H275Y NA mutation became fixed in a new seasonal A(H1N1) antigenic variant (A/Brisbane/59/2007-like), suggesting that the antigenic novelty of the OR virus assisted its prolific spread.
    In this vein, the authors warn:
    A(H1N1)pdm09 viruses have now been circulating in humans for over four years, but are yet to undergo a significant antigenic change (as evidenced by the continued inclusion of A/California/7/2009 in the human seasonal influenza vaccine since 2009).
    As the H1 component of the vaccine has been updated, on average, every 2.8 years (range 1 to 8 years), and the H3 component every 1.8 years (range 1 to 4 years) since 1980, it is reasonable to anticipate that A(H1N1)pdm09 viruses will undergo antigenic change in the near future.
    The significance being that an antigenic change in the virus might be the spark needed to spread the resistant mutation, and at the same time would reduce the effectiveness of the current vaccine (and evade herd immunity), and therefore increase our need for effective antiviral medications.
    Viruses and bacteria evolve and adapt very quickly. The sobering truth is pharmacological victories over them tend to be fleeting. New classes of drugs are going to be needed, along with prudent stewardship of the drugs currently in our arsenal.
    The authors of this study wrap up by saying:
    Here we demonstrate that contemporary A(H1N1)pdm09 viruses have acquired NA mutations which permit the acquisition of NA H275Y without compromising viral fitness. These mutations, which are now present in virtually all circulating A(H1N1)pdm09 viruses, enhance the surface expression and enzymatic activity of the A(H1N1)pdm09 H275Y NA protein in vitro and result in enhanced viral fitness in vivo.
    Hence, the risk that H275Y A(H1N1)pdm09 viruses will spread globally, in a similar manner to OR seasonal A(H1N1) viruses in 2007–2008, now appears greater than at any time since the A(H1N1)pdm09 lineage emerged in 2009.
    Posted by Michael Coston at <a class="timestamp-link" href="http://afludiary.blogspot.com/2014/04/plos-pathogens-fitness-advantage-from.html" rel="bookmark" title="permanent link"><abbr class="published" itemprop="datePublished" title="2014-04-04T07:13:00-04:00">7:13 AM</abbr>
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