New small-molecule drug design strategies for fighting resistant influenza A
Identifieur interne : 000D01 ( Pmc/Corpus ); précédent : 000D00; suivant : 000D02New small-molecule drug design strategies for fighting resistant influenza A
Auteurs : Zuyuan Shen ; Kaiyan Lou ; Wei WangSource :
- Acta Pharmaceutica Sinica. B [ 2211-3835 ] ; 2015.
Abstract
Influenza A virus is the major cause of seasonal or pandemic flu worldwide. Two main treatment strategies–vaccination and small molecule anti-influenza drugs are currently available. As an effective vaccine usually takes at least 6 months to develop, anti-influenza small molecule drugs are more effective for the first line of protection against the virus during an epidemic outbreak, especially in the early stage. Two major classes of anti-influenza drugs currently available are admantane-based M2 protein blockers (amantadine and rimantadine) and neuraminidase (NA) inhibitors (oseltamivir, zanamivir, and peramivir). However, the continuous evolvement of influenza A virus and the rapid emergence of resistance to current drugs, particularly to amantadine, rimantadine, and oseltamivir, have raised an urgent need for developing new anti-influenza drugs against resistant forms of influenza A virus. In this review, we first give a brief introduction of the molecular mechanisms behind resistance, and then discuss new strategies in small-molecule drug development to overcome influenza A virus resistance targeting mutant M2 proteins and neuraminidases, and other viral proteins not associated with current drugs.
Url:
DOI: 10.1016/j.apsb.2015.07.006
PubMed: 26579472
PubMed Central: 4629447
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PMC:4629447Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">New small-molecule drug design strategies for fighting resistant influenza A</title><author><name sortKey="Shen, Zuyuan" sort="Shen, Zuyuan" uniqKey="Shen Z" first="Zuyuan" last="Shen">Zuyuan Shen</name><affiliation><nlm:aff id="aff0005">Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, and State Key Laboratory of Bioengineering Reactor, East China University of Science and Technology, Shanghai 200237, China</nlm:aff></affiliation></author><author><name sortKey="Lou, Kaiyan" sort="Lou, Kaiyan" uniqKey="Lou K" first="Kaiyan" last="Lou">Kaiyan Lou</name><affiliation><nlm:aff id="aff0005">Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, and State Key Laboratory of Bioengineering Reactor, East China University of Science and Technology, Shanghai 200237, China</nlm:aff></affiliation></author><author><name sortKey="Wang, Wei" sort="Wang, Wei" uniqKey="Wang W" first="Wei" last="Wang">Wei Wang</name><affiliation><nlm:aff id="aff0005">Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, and State Key Laboratory of Bioengineering Reactor, East China University of Science and Technology, Shanghai 200237, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff0010">Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, NM 87131-0001, USA</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">26579472</idno><idno type="pmc">4629447</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629447</idno><idno type="RBID">PMC:4629447</idno><idno type="doi">10.1016/j.apsb.2015.07.006</idno><date when="2015">2015</date><idno type="wicri:Area/Pmc/Corpus">000D01</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000D01</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">New small-molecule drug design strategies for fighting resistant influenza A</title><author><name sortKey="Shen, Zuyuan" sort="Shen, Zuyuan" uniqKey="Shen Z" first="Zuyuan" last="Shen">Zuyuan Shen</name><affiliation><nlm:aff id="aff0005">Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, and State Key Laboratory of Bioengineering Reactor, East China University of Science and Technology, Shanghai 200237, China</nlm:aff></affiliation></author><author><name sortKey="Lou, Kaiyan" sort="Lou, Kaiyan" uniqKey="Lou K" first="Kaiyan" last="Lou">Kaiyan Lou</name><affiliation><nlm:aff id="aff0005">Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, and State Key Laboratory of Bioengineering Reactor, East China University of Science and Technology, Shanghai 200237, China</nlm:aff></affiliation></author><author><name sortKey="Wang, Wei" sort="Wang, Wei" uniqKey="Wang W" first="Wei" last="Wang">Wei Wang</name><affiliation><nlm:aff id="aff0005">Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, and State Key Laboratory of Bioengineering Reactor, East China University of Science and Technology, Shanghai 200237, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff0010">Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, NM 87131-0001, USA</nlm:aff></affiliation></author></analytic><series><title level="j">Acta Pharmaceutica Sinica. B</title><idno type="ISSN">2211-3835</idno><idno type="eISSN">2211-3843</idno><imprint><date when="2015">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Influenza A virus is the major cause of seasonal or pandemic flu worldwide. Two main treatment strategies–vaccination and small molecule anti-influenza drugs are currently available. As an effective vaccine usually takes at least 6 months to develop, anti-influenza small molecule drugs are more effective for the first line of protection against the virus during an epidemic outbreak, especially in the early stage. Two major classes of anti-influenza drugs currently available are admantane-based M2 protein blockers (amantadine and rimantadine) and neuraminidase (NA) inhibitors (oseltamivir, zanamivir, and peramivir). However, the continuous evolvement of influenza A virus and the rapid emergence of resistance to current drugs, particularly to amantadine, rimantadine, and oseltamivir, have raised an urgent need for developing new anti-influenza drugs against resistant forms of influenza A virus. In this review, we first give a brief introduction of the molecular mechanisms behind resistance, and then discuss new strategies in small-molecule drug development to overcome influenza A virus resistance targeting mutant M2 proteins and neuraminidases, and other viral proteins not associated with current drugs.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Deyde, Vm" uniqKey="Deyde V">VM Deyde</name></author><author><name sortKey="Xu, Xy" uniqKey="Xu X">XY Xu</name></author><author><name sortKey="Bright, Ra" uniqKey="Bright R">RA Bright</name></author><author><name sortKey="Shaw, M" uniqKey="Shaw M">M Shaw</name></author><author><name sortKey="Smith, Cb" uniqKey="Smith C">CB Smith</name></author><author><name sortKey="Zhang, Y" uniqKey="Zhang Y">Y Zhang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Moscona, A" uniqKey="Moscona A">A. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Acta Pharm Sin B</journal-id><journal-id journal-id-type="iso-abbrev">Acta Pharm Sin B</journal-id><journal-title-group><journal-title>Acta Pharmaceutica Sinica. B</journal-title></journal-title-group><issn pub-type="ppub">2211-3835</issn><issn pub-type="epub">2211-3843</issn><publisher><publisher-name>Elsevier</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">26579472</article-id><article-id pub-id-type="pmc">4629447</article-id><article-id pub-id-type="publisher-id">S2211-3835(15)00114-8</article-id><article-id pub-id-type="doi">10.1016/j.apsb.2015.07.006</article-id><article-categories><subj-group subj-group-type="heading"><subject>Review</subject></subj-group></article-categories><title-group><article-title>New small-molecule drug design strategies for fighting resistant influenza A</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Shen</surname><given-names>Zuyuan</given-names></name><xref rid="aff0005" ref-type="aff">a</xref></contrib><contrib contrib-type="author"><name><surname>Lou</surname><given-names>Kaiyan</given-names></name><email>kylou@ecust.edu.cn</email><xref rid="aff0005" ref-type="aff">a</xref><xref rid="cor1" ref-type="corresp">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Wei</given-names></name><email>wwang@unm.edu</email><xref rid="aff0005" ref-type="aff">a</xref><xref rid="aff0010" ref-type="aff">b</xref><xref rid="cor2" ref-type="corresp">⁎⁎</xref></contrib></contrib-group><aff id="aff0005"><label>a</label>Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, and State Key Laboratory of Bioengineering Reactor, East China University of Science and Technology, Shanghai 200237, China</aff><aff id="aff0010"><label>b</label>Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, NM 87131-0001, USA</aff><author-notes><corresp id="cor1"><label>⁎</label>Corresponding author. Tel./fax: +86 21 64253299. <email>kylou@ecust.edu.cn</email></corresp><corresp id="cor2"><label>⁎⁎</label>Corresponding author at: Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, NM 87131-0001, USA. Tel.: +1 505 2770756; fax: +1 505 2772609. <email>wwang@unm.edu</email></corresp></author-notes><pub-date pub-type="pmc-release"><day>06</day><month>9</month><year>2015</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>9</month><year>2015</year></pub-date><pub-date pub-type="epub"><day>06</day><month>9</month><year>2015</year></pub-date><volume>5</volume><issue>5</issue><fpage>419</fpage><lpage>430</lpage><history><date date-type="received"><day>19</day><month>6</month><year>2015</year></date><date date-type="accepted"><day>5</day><month>7</month><year>2015</year></date></history><permissions><copyright-statement>© 2015 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.</copyright-statement><copyright-year>2015</copyright-year><copyright-holder>Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences</copyright-holder><license license-type="CC BY-NC-ND" xlink:href="http://creativecommons.org/licenses/by-nc-nd/4.0/"><license-p>This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).</license-p></license></permissions><abstract><p>Influenza A virus is the major cause of seasonal or pandemic flu worldwide. Two main treatment strategies–vaccination and small molecule anti-influenza drugs are currently available. As an effective vaccine usually takes at least 6 months to develop, anti-influenza small molecule drugs are more effective for the first line of protection against the virus during an epidemic outbreak, especially in the early stage. Two major classes of anti-influenza drugs currently available are admantane-based M2 protein blockers (amantadine and rimantadine) and neuraminidase (NA) inhibitors (oseltamivir, zanamivir, and peramivir). However, the continuous evolvement of influenza A virus and the rapid emergence of resistance to current drugs, particularly to amantadine, rimantadine, and oseltamivir, have raised an urgent need for developing new anti-influenza drugs against resistant forms of influenza A virus. In this review, we first give a brief introduction of the molecular mechanisms behind resistance, and then discuss new strategies in small-molecule drug development to overcome influenza A virus resistance targeting mutant M2 proteins and neuraminidases, and other viral proteins not associated with current drugs.</p></abstract><abstract abstract-type="graphical"><title>Graphical abstract</title><p>Influenza A virus is the major cause of seasonal or pandemic flu worldwide. The continuous evolvement of influenza A virus and the rapid emergence of resistance to current drugs, particularly to amantadine, rimantadine, and oseltamivir, have raised an urgent need for developing new anti-influenza drugs against resistant forms of influenza A virus. In this review, we first give a brief introduction of the molecular mechanisms behind resistance, and then discuss new strategies in small-molecule drug development to overcome influenza A virus resistance targeting mutant M2 proteins and neuraminidases, and other viral proteins not associated with current drugs.<fig id="f0030" position="anchor"><graphic xlink:href="fx1"></graphic></fig></p></abstract><kwd-group><title>KEY WORDS</title><kwd>Influenza A virus</kwd><kwd>Drug discovery</kwd><kwd>Resistance</kwd><kwd>M2 ion channel</kwd><kwd>Neuraminidase</kwd></kwd-group></article-meta></front><body><sec id="s0005"><label>1</label><title>Introduction</title><p>Influenza A virus belongs to a family of RNA viruses termed the orthomyxoviridae. It is the main cause of seasonal or pandemic flu, an infectious disease characterized by high morbidity and significant mortality. Since influenza A virus is under continuous evolvement due to antigenic mutation, adaptation, and reassortment, highly virulent strains may appear unexpectedly, resulting in epidemics locally or pandemics worldwide such as the 1918 H1N1 (Spanish flu), 1957 H2N2 (Asian flu), 1968 H3N2 (Hong Kong flu), 2005 H5N1 (bird flu), 2009 H1N1 (swine flu), and more recently H7N9 (bird flu) of 2013. Influenza A virus pandemic may cause significant social health crisis and loss of life. For example, the pandemic of “Spanish flu” (H1N1) in 1918–1919 alone caused at least 20 million deaths. Besides, seasonal flu affects about 20% world population and causes 250,000 to 500,000 deaths per year based on a recent study<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref>.</p><p>The potential of devasting pandemic influenza outbreaks has attracted a great amount of resources and efforts in the search for possible prevention and effective treatment methods of influenza A infections. Currently, two main strategies against the virus are available, which are vaccination and small molecule anti-influenza drugs. Anti-influenza small molecule drugs present the first line of protection against the virus during an epidemic outbreak, especially in the early stages, as an effective vaccine usually takes at least 6 months to develop for the circulating strains. Furthermore, vaccination has limited effectiveness in treatment of immunocompromised patients. Moreover, anti-influenza drugs have demonstrated benefit in clinical practices in terms of shortening the disease duration and reducing the risk of influenza-caused serious complications and death if patients are treated in a timely fashion. For all of these reasons, anti-influenza drugs are necessary for the control of influenza A virus pandemics. Currently, two major classes of drugs are approved by FDA for anti-influenza A virus treatment: admantane-based M2 ion channel protein blockers (amantadine and rimantadine) and neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir). However, the continuous evolvement of influenza A virus and the rapid emergence of resistance to current drugs, particularly to admantanes<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> and oseltamivir<xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib4" ref-type="bibr">4</xref>, has raised great concern for a possible pandemic flu, highlighting an urgent need for developing new anti-influenza drugs against resistant influenza A virus. In this review, we discuss recent progress made in small-molecule drug development to overcome influenza A virus resistance with a focus on novel drug design strategies targeting the mutant M2 ion channel proteins and neuraminidases, as well as other viral proteins not associated with current drugs.</p></sec><sec id="s0010"><label>2</label><title>Life cycle of influenza A virus: a brief introduction</title><p>Influenza A virus life cycle is divided into several sequential steps (see <xref rid="f0005" ref-type="fig">Fig. 1</xref>). The virus first attaches to host cell surface sialic acid (SA) receptor <italic>via</italic> the viral surface glycoprotein hemagglutinin. The influenza virus then enters into the cell <italic>via</italic> receptor-mediated endocytosis, followed by low-pH-induced membrane fusion of the viral envelope with the endosomal membrane of the cell. In this step, the viral M2 protein transports protons from the late endosome into interior of the virus. The resulting acidification induces the conformation change of viral hemagglutinin, which leads to hemagglutinin-mediated membrane fusion followed by the dissociation of viral M1 matrix protein from the viral ribonucleoprotein complexes (vRNPs), resulting in the release of vRNPs into cytoplasm. The vRNPs containing viral genome are then transported into the nucleus to start transcription; mRNAs formed in the transcription process are transported to cytoplasm and are translated into proteins necessary for viral particle replication. Newly synthesized viral genome segments and proteins are assembled to form new vRNPs in the nucleus, which are then transported from nucleus back into the cytoplasm for final packaging. The exportation of vRNPs from the nucleus requires viral nucleoprotein (NP). New virions are then assembled in the cell membrane in a process called budding. During the process, part of the cell membrane is wrapped around virions to form lipid viral envelopes. Finally, neuraminidase (NA) on the surface of new budding viruses cleaves terminal sialic acid (SA) residues from hemagglutinin (HA) and new viruses are released to start a new cycle of infection and replication. All of these steps in the life cycle of influenza A virus are essential for its virulence, replication, and transmission. Development of small molecule based inhibitors that block any of these steps can generate potential efficient strategies to treat or prevent influenza A infections. In the following sections, we will go through new strategies currently being used or proposed for overcoming the resistance of influenza A virus to current M2 ion channel blocker drugs (amantadine and rimantadine) and NA inhibitor drugs (<italic>e.g</italic>. oseltamivir).</p></sec><sec id="s0015"><label>3</label><title>Drug development targeting mutant M2 ion channel protein</title><p>M2 ion channel protein is a tetrameric transmembrane protein forming proton ion channels across the viral membrane<xref rid="bib6" ref-type="bibr"><sup>6</sup></xref>. It functions as a proton transporter which delivers protons from the late endosome into virus interior. The resulting acidification induces the hemagglutinin conformation change, leading to hemagglutinin-mediated membrane fusion and subsequent release virus RNA into cytoplasm of the host cell to initiate subsequent virus replication steps. M2 ion channel blockers bind to the interior of the ion channel, block the influx of protons, and prevent hemagglutinin-mediated membrane fusion. The proton blocking effects may result from an electrostatic repulsion potential from the charged amino group<xref rid="bib7" ref-type="bibr"><sup>7</sup></xref>. Currently, two M2 ion channel blockers approved by the FDA are amantadine (Symmetrel<sup>TM</sup>, Endo Pharmaceuticals) and rimantadine (Flumadine<sup>TM</sup>, Forest Pharmaceuticals). But the emergence of drug-resistant mutations of the M2 protein renders these two drugs ineffective against most circulating strains<xref rid="bib7" ref-type="bibr"><sup>7</sup></xref>. Three major mutations identified in transmissible strains are L26F, V27A, and S31N<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib8" ref-type="bibr">8</xref>, all of which are located on the transmembrane domain (residues 24–46) of the M2 protein. Among them, S31N mutation is the prevailing alteration presented in more than 95% of resistant viruses<xref rid="bib9" ref-type="bibr">9</xref>, <xref rid="bib10" ref-type="bibr">10</xref>.</p><p>Many efforts have been undertaken to make derivatives of amantadine in order to find new M2 inhibitors against these mutant M2 proteins <xref rid="f0010" ref-type="fig">Fig. 2</xref>). Replacement of the amine group with pyrrolidine, azetidine, and aziridine rings did not lead to compounds with better antiviral activities<xref rid="bib11" ref-type="bibr">11</xref>, <xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib13" ref-type="bibr">13</xref>. In 2010, Zarubaev, et al.<xref rid="bib14" ref-type="bibr"><sup>14</sup></xref>, reported a tetrazole derivative of adamantane (<bold>1</bold>) which exhibits a highly potent antiviral activity against a rimantadine-resistant influenza strain containing a S31N mutation. More recently, DeGrado and coworkers<xref rid="bib15" ref-type="bibr"><sup>15</sup></xref> rationally designed a spirane-adamantane derivative (<bold>2</bold>) with potent efficacy against both the V27A and L26P mutant strains of influenza virus with an activity comparable to amantadine to the wide-type strain. They also further developed the arylmethyl substituted amantadine derivative M2WJ332 (<bold>3</bold>) and the benzyl-substituted derivative (<bold>4</bold>). These two compounds showed both inhibitory activity against S31N and wild type M2 proteins. Notably, M2WJ332 has shown an even higher potency against the resistant S31N M2 protein than that of amantadine against wild type M2 protein. Evidences from NMR and molecular dynamic studies supported the drug bound inside the channel between the side chains of Asn31. Very recently, a new dual M2 inhibitor (<bold>5</bold>) was discovered by the same group to have novel flip-flop dual binding modes<xref rid="bib16" ref-type="bibr"><sup>16</sup></xref>. The drug binds to M2 proteins in different orientations depending upon whether it is a wide type S31 or mutant S31N M2 ion channel protein. Dual-binding inhibitors based upon the similar design strategy may provide new M2 blockers against amantadine or rimantadine resistant influenza virus A strains. Other scaffolds such as pinanamine derivatives<xref rid="bib17" ref-type="bibr">17</xref>, <xref rid="bib18" ref-type="bibr">18</xref>, <xref rid="bib19" ref-type="bibr">19</xref>, <xref rid="bib20" ref-type="bibr">20</xref> and spiranamine derivatives<xref rid="bib15" ref-type="bibr">15</xref>, <xref rid="bib21" ref-type="bibr">21</xref>, <xref rid="bib22" ref-type="bibr">22</xref> have also been explored as new M2 ion blockers. As exemplified by compound <bold>6</bold><xref rid="bib20" ref-type="bibr"><sup>20</sup></xref>, pinanamine derivatives have shown low inhibiting effects towards resistan S31 mutant virus, while several spiranamine analogs, such as the spiranamine and a silico analog <bold>7</bold>, have shown activity against V27A and L26P mutant virus.</p><p>At present, no M2 blocker is active against both wild type and all circulating M2-mutant strains, likely due to difficulties in tuning the structure of small molecule-based inhibitors to fit each of the individual mutant M2 ion channel proteins. Recently, the allosteric binding site outside of the ion channel of M2 protein was proposed to be a possible target for developing inhibitors against resistant M2 proteins<xref rid="bib23" ref-type="bibr"><sup>23</sup></xref>, though no small molecule has been identified as of yet.</p></sec><sec id="s0020"><label>4</label><title>Drugs development targeting neuraminidase (NA)</title><sec id="s0025"><label>4.1</label><title>NA and current NA inhibitor drugs</title><p>NA is one of the two major glycoproteins on the surface of viral lipid envelope. It functions as a sialidase to cleave off the terminal sialic acid (SA) on the budding virus, disrupting interactions between SA receptor and virus hemagglutinin<xref rid="bib24" ref-type="bibr">24</xref>, <xref rid="bib25" ref-type="bibr">25</xref>. The SA binding site of NA is highly conserved among different influenza A strains<xref rid="bib26" ref-type="bibr"><sup>26</sup></xref>. Therefore, NA inhibitors which mimic SA structure in its transition state during NA catalyzed hydrolysis, represent a class of anti-influenza drugs with broad activities against different influenza virus strains.</p><p>At present, three NA inhibitors have been approved by the FDA, which are zanamivir (Relenza<sup>TM</sup>, GlaxoSmithKline), oseltamivir (Tamiflu<sup>TM</sup>, Roche), and peramivir (Rapivab<sup>TM</sup>, BioCryst). Zanamivir, a 4-deoxy-4-guanidino derivative of SA<xref rid="bib27" ref-type="bibr"><sup>27</sup></xref>, was the first approved NA inhibitor. It is administered through inhalation due to its poor oral bioavailability. This route of administration is often not possible for young children or some patients with respiratory disease. Thus, it is not as widely used as oseltamivir, the only orally administered drug among the above three approved agents. Oseltamivir is a prodrug, which quickly converts to the active form, oseltamivir carboxylate (GS4071), by an esterase-catalyzed hydrolysis reaction inside the body<xref rid="bib28" ref-type="bibr"><sup>28</sup></xref>. The replacement of the glycerol moiety with a hydrophobic 3-pentyloxy as well as the replacement of 4-guanidino group with an amine group make oseltamivir more lipophilic than zanamivir, and thus achieve a higher oral bioavailability than zanamivir (80% <italic>vs</italic>. 20%). The third drug paramivir, administered intravenously<xref rid="bib29" ref-type="bibr"><sup>29</sup></xref>, was recently approved by the FDA in December 2014 to treat adult influenza A infections. Structurally, paramivir is distinct from zanamivir and oseltamivir since it contains a unique five-membered ring. On the other hand, it contains structural features of both zanamivir and oseltamivir, the hydrophilic pharmacorphore of 4-guanidino group of zanamivir and the hydrophobic 3-pentanyloxy moiety of oseltamivir. Laninamivir<xref rid="bib30" ref-type="bibr"><sup>30</sup></xref>, another drug which is structurally similar to zanamivir, has been approved in Japan as an octanoyl prodrug (Inavir<sup>TM</sup>, Daiichi Sankyo. Biota). It is currently involved in clinical trials in the United States.</p></sec><sec id="s0030"><label>4.2</label><title>An overview of resistance to NA inhibitors</title><p>Although the SA binding site of the viral NA is highly conserved, a number of mutations arise as a result of drug-induced selective pressure<xref rid="bib31" ref-type="bibr"><sup>31</sup></xref>, leading to the decreased sensitivity to NA inhibitors. The frequency of resistant mutations induced by NA inhibitors is relatively low compared with amantadine and rimantadine<xref rid="bib32" ref-type="bibr"><sup>32</sup></xref>, as the mutation often significantly reduces viral fitness in infection and replication. However, emergence of compensatory mutations may restore viral infectivity and ability to replicate in the host cell<xref rid="bib33" ref-type="bibr"><sup>33</sup></xref>. Understanding the mutation type and molecular mechanism behind the observed resistance helps to design new NA inhibitors against resistant strains.</p><p>Residues surrounding the active site provide direct interactions with SA and SA-mimicing drugs (<xref rid="f0015" ref-type="fig">Fig. 3</xref>). To understand the cause of resistance, the details of the drug binding mode must also be understood. In the case of oseltamivir, the predominating resistant mutation is H274Y. Notably, it does not cause zanamivir resistance. The hydrophobic 3-pentyloxy group in oseltamivir induces a reposition of the Glu276 side chain to achieve optimal hydrophobic interactions. The H274Y mutation blocks these side chain conformational changes and thus reduces the drug binding efficiency of oseltamivir<xref rid="bib35" ref-type="bibr"><sup>35</sup></xref>. While the hydrophilic glycerol moiety in zanamivir interacts with Glu276 through hydrogen bonding in the same way as the natural substrate SA, no conformational rearrangement is required. Therefore, H274 mutation does not cause zanamivir resistance. As paramivir shares the similar hydrophobic interaction with Glu276 as does oseltamivir, H274 mutation may also reduce paramivir sensitivity<xref rid="bib31" ref-type="bibr"><sup>31</sup></xref>. Compared to oseltamivir, drug resistance to zanamivir and laninamivir are rare in clinic to date<xref rid="bib31" ref-type="bibr"><sup>31</sup></xref>, likely due to two reasons. First, their structures are more similar to the natural substrate SA. Secondly, these two drugs are less frequently administered. Therefore, the drug-induced selectivity pressure is low. However, resistance to these drugs is still possible, as a recombinant H3N2 virus containing the E276D mutation has shown resistance to both zanamivir and oseltamivir in one study<xref rid="bib26" ref-type="bibr"><sup>26</sup></xref>. In addition, compensatory mutation residues outside the binding pocket may also contribute to resistance fitness. For example, the compensatory mutations R222Q and V234M associated with H274Y significantly enhance the influenza virus infectivity and its ability to replicate in the host cells, likely due to the restoration of the flexibility of the Glu276 residue previously restricted by the mutation H274Y<xref rid="bib33" ref-type="bibr"><sup>33</sup></xref>.</p></sec><sec id="s0035"><label>4.3</label><title>Drug development targeting mutant NA</title><p>Currently, NA-based drug development against resistant influenza A virus aims to search for novel compounds effective to treat predominant H274 mutant strains. Although zanamivir and laninamivir are still effective against H274 mutation, they are also associated with unfavorable pharmacokinetics and must be administered through inhalation or intravenously. New generations of NA inhibitors should have both excellent activity against resistant strains and improved oral bioavailability. Several strategies are employed to achieve this goal.</p><sec id="s0040"><label>4.3.1</label><title>Structure-based rational drug design</title><p>Structure-based drug design is centered upon an understanding of the dynamic process of NA binding with a substrate and provides new opportunities to design new NA inhibitors. Crystal structures of N1 and N8 NA when each immerged with oseltamivir for a short period time revealed the presence of a transient “150-cavity” near the substrate binding pocket<xref rid="bib36" ref-type="bibr"><sup>36</sup></xref>. The initial binding of SA or NA inhibitors requires the adaptive opening of a 150-loop, and thus generates the 150-cavity. Several C-3 or C-4 modified Neu5Ac2en derivatives (<italic>e.g</italic>. <bold>8</bold>, <xref rid="f0020" ref-type="fig">Fig. 4</xref>)<xref rid="bib37" ref-type="bibr">37</xref>, <xref rid="bib38" ref-type="bibr">38</xref>, zanamivir derivatives (<italic>e.g.</italic><bold>9</bold>)<xref rid="bib39" ref-type="bibr"><sup>39</sup></xref>, and oseltamivir derivatives (<italic>e.g</italic>. <bold>10</bold>)<xref rid="bib40" ref-type="bibr"><sup>40</sup></xref> were designed and synthesized. The extended side chain at the 3 or 4 positions was believed to bind with the 150-cavity. These compounds demonstrated antiviral activity against both wide-type and oseltamivir-resistant influenza A virus, suggesting the use of the 150-cavity as a novel drug target in NA inhibitor design against resistant strains. However, there is a limitation for 150-cavity targeting NA inhibitors since the 150 cavity is likely be seen only in group 1 influenza A virus (N1, N4, N5, N8), but not in group 2 (N2, N9). Recently, the flexible “430-loop” generated cavity near the active SA binding site was proposed to be a new potential target to design NA inhibitors against both group-1 and group-2 NAs<xref rid="bib41" ref-type="bibr">41</xref>, <xref rid="bib42" ref-type="bibr">42</xref>. This cavity is much larger than SA binding site and thus could possibly accommodate a larger molecular scaffold than current NA inhibiting drugs. An and coworkers reported that the small molecule NA inhibitor NSC89853 (<bold>11</bold>), which is structurally different from other SA mimics, could possibly bind to the pocket formed by the 430-loop based on molecular modeling<xref rid="bib43" ref-type="bibr"><sup>43</sup></xref>. Feng, et al.<xref rid="bib44" ref-type="bibr"><sup>44</sup></xref> , recently designed and synthesized a series of zanamivir analogs with an extended side chain at 1-position (<italic>e.g</italic>., <bold>12</bold>) projected towards the 430-loop. The most potent compound <bold>12</bold> shows an IC<sub>50</sub> in low nmol/L range against both group-1 and group-2 NAs, demonstrating the potential of “430-cavity” as a powerful strategy in the design of new NA inhibitors.</p></sec><sec id="s0045"><label>4.3.2</label><title>Bioisosteric design</title><p>Bioisosteric replacement of substituents in current NA inhibitors remains a powerful strategy in the design of new NA inhibitors. Fang and coworkers<xref rid="bib45" ref-type="bibr"><sup>45</sup></xref> replaced the 2-carboxylic acid group with a phosphonic acid and the obtained phosphonate congeners exhibiting strong antiviral activities against both wide and H274 mutants. Continuous efforts in structural modification of oseltamivir, particularly the replacement of the 5-amino group with other bioisosteric groups such as guanidine (<bold>13</bold>)<xref rid="bib46" ref-type="bibr"><sup>46</sup></xref>, <italic>N</italic>-methylguanidine (<bold>14</bold>)<xref rid="bib47" ref-type="bibr"><sup>47</sup></xref>, amidine (<bold>15</bold>)<xref rid="bib48" ref-type="bibr"><sup>48</sup></xref>, amidoxime (<bold>16</bold>)<xref rid="bib48" ref-type="bibr"><sup>48</sup></xref>, <italic>etc.</italic>, led to a number of potent NA inhibitors. Many of them were effective against the H274 mutation, but most of them were not able to retain the superior oral bioavailability of oseltamivir. Very recently, Schade and coworkers<xref rid="bib48" ref-type="bibr"><sup>48</sup></xref> reported a 5-amidoxime substituted oseltamivir analog <bold>16</bold> which not only has a superior antiviral activity, but also has an oral bioavailability comparable to oseltamivir.</p></sec><sec id="s0050"><label>4.3.3</label><title>Screening of natural products</title><p>Natural products including extracts from traditional medicinal plants continue to serve as a source of new anti-influenza drug leads. Grienke and coworkers<xref rid="bib49" ref-type="bibr"><sup>49</sup></xref> screened the seed extracts of <italic>Alpinia katsumadain</italic>, and identified the extract compound katsumadain A with a NA-inhibiting activity at low mM ranges against several strains of H1N1 swine influenza virus including one oseltamivir-resistant strain. Due to the large molecular volume, the binding site of katsumadain A is likely extended into the cavities formed by 430-loop or 245-loop based on docking analysis. Katsumadian A could serve as a leading compound for rational design of new NA inhibitors with novel binding modes. Other studies on tropical medicinal plants<xref rid="bib50" ref-type="bibr"><sup>50</sup></xref>, flavonoids<xref rid="bib51" ref-type="bibr">51</xref>, <xref rid="bib52" ref-type="bibr">52</xref>, and chalcones<xref rid="bib53" ref-type="bibr"><sup>53</sup></xref> have also been reported. These natural products may help in the development of safer and less toxic NA inhibitors for resistant influenza virus A strains.</p></sec></sec></sec><sec id="s0055"><label>5</label><title>Drug development targeting other viral proteins</title><p>Influenza A virus has eight segmented RNA genes and encodes twelve known peptides: PA, PB1, PB2, PB1-F2, N40, HA, NA, NP, M2 ion channel, M1 matrix proteins, NS1, and NS2. Besides the M2 ion channel protein and NA discussed previously, other viral proteins may also have potentials as drug targets. Many of them have already been under investigation for drug development against resistant influenza A virus.</p><sec id="s0060"><label>5.1</label><title>Hemagglutinin based anti-influenza drug development</title><p>Hemagglutinin (HA) is a membrane-binding glycoprotein on the surface of an influenza virus. It is responsible for virus attachment to sialic acid receptors on the cell membrane in the initial stage of virus infection. It also facilitates the fusion of viral and cell membranes after the virus enters the cell <italic>via</italic> receptor-mediated endocytosis for subsequent release of viral nucleocapsids into cell cytoplasm<xref rid="bib54" ref-type="bibr"><sup>54</sup></xref>. Accordingly, two strategies have been adopted in anti-virus drug development.</p><p>The first strategy is to interfere with hemagglutinin binding to sialic acid receptors. One approach is the addition of SA-containing receptor-mimics as competing inhibitors. Such inhibitors include sialic acid containing natural compounds<xref rid="bib55" ref-type="bibr">55</xref>, <xref rid="bib56" ref-type="bibr">56</xref> and synthetic multivalent SA-containing inhibitors<xref rid="bib57" ref-type="bibr"><sup>57</sup></xref>. Multivalent SA-containing inhibitors offer better results than monovalent ones in inhibiting virus attachment<xref rid="bib58" ref-type="bibr"><sup>58</sup></xref>. However, multivalent SA-containing compounds often suffer from poor solubility, immunoreactivity, and toxicity issues<xref rid="bib59" ref-type="bibr"><sup>59</sup></xref>. One solution is to use liposome-based drug delivery system to encapsulate inhibitors as exemplified by the sialylneolacto-<italic>N</italic>-tetraose c (LSTc)-bearing liposomes developed by Hendricks, et al.<xref rid="bib57" ref-type="bibr"><sup>57</sup></xref>.</p><p>The second strategy involves prevention the formation of a low-pH induced conformation of hemagglutinin, a key step leading to fusion of the host endosomal membrane and the viral lipid envelop. The antiviral activity of this group of compounds is derived from their capability of stabilizing the nonfusogenic conformation of the hemagglutinin. The first compound in this class is <italic>tert</italic>-butylhydroquinone, which was discovered in 1993<xref rid="bib60" ref-type="bibr"><sup>60</sup></xref>. Evidence from NMR study has shown that it binds to the stem loop region in H7 HA and stabilizes the neutral pH conformation<xref rid="bib61" ref-type="bibr"><sup>61</sup></xref>. Several anti-influenza A virus compounds with a similar mechanism were found later. Most of the compounds in this class were subtype-dependent with a low resistance barrier, and underwent no further investigation<xref rid="bib60" ref-type="bibr">60</xref>, <xref rid="bib62" ref-type="bibr">62</xref>, <xref rid="bib63" ref-type="bibr">63</xref>, <xref rid="bib64" ref-type="bibr">64</xref>, <xref rid="bib65" ref-type="bibr">65</xref>. One exception is arbidol (ARB), currently an approved drug in Russia and China to treat influenza virus infection (Fig. <xref rid="f0025" ref-type="fig">5</xref>)<xref rid="bib66" ref-type="bibr">66</xref>, <xref rid="bib67" ref-type="bibr">67</xref>. Aribidol was shown to stabilize the HA by a 0.2 pH unit reduction at the transition phase<xref rid="bib66" ref-type="bibr"><sup>66</sup></xref>. Recent studies pointed out that both the binding of the ARB to the polar head groups of phospholipids in the cell membrane and the presence of the aromatic residues of the viral surface proteins could contribute to its antivirus activity<xref rid="bib67" ref-type="bibr"><sup>67</sup></xref>. A better understanding the details of the drug binding mode and resulting effects on hemagglutinin and lipid interaction would help to design new ARB-like molecules.</p></sec><sec id="s0065"><label>5.2</label><title>RNA polymerase as the drug target</title><p>Influenza A׳s RNA polymerase is a heterotrimeric protein containing three subunits PB1, PB2, and PA. It is responsible for transcription and replication of the virus genome. All three subunits are important for its functions. PB1 has polymerase activity, and PB2 is involved in cap-binding of host cell pre-mRNAs, whereas PA possesses the endonuclease domain which cleaves capped host pre-mRNAs and initiates transcription. Influenza virus polymerase is highly conserved among different strains<xref rid="bib68" ref-type="bibr"><sup>68</sup></xref> and contains multiple sites for potential anti-virus drug development. Currently, three major classes of drugs are under development: RNA synthesis inhibitors, cap-snatching inhibitors, and inhibitors targeting protein–protein interactions between the three polymerase subunits (<italic>e.g</italic>. PA–PB1, PB1–PB2).</p><p>RNA synthesis inhibitors are mainly nucleoside mimics such as favipiravir (T-705)<xref rid="bib69" ref-type="bibr"><sup>69</sup></xref> and ribavirin (<xref rid="f0025" ref-type="fig">Fig. 5</xref>)<xref rid="bib70" ref-type="bibr"><sup>70</sup></xref>. Inside the cells, T-705 is metabolized to its active form T-705 ribofuransosyl 5-triphosphate and functions as a purine mimic to inhibit viral RNA-dependent RNA polymerase. Notably, favipiravir does not interfere with mammalian cell RNA or DNA synthesis, so it is nontoxic to the host cell. Moreover, the drug has been shown to be effective against a broad range of influenza strains including amantadine and oseltamivir resistant strains. It demonstrated anti-virus activity against the H5N1 avian flu, recently emerged 2009 H1N1 swine flu, and 2013 H7N9 bird flu<xref rid="bib71" ref-type="bibr"><sup>71</sup></xref>. Additionally, favipiravir was reported to have a low resistance rate<xref rid="bib69" ref-type="bibr"><sup>69</sup></xref>. Favipiravir was approved in Japan in 2014 as a stockpiling drug (Avigan<sup>TM</sup>) during periods of a possible influenza pandemic. Currently, favipiravir is under clinical trials in the United States. Ribavirin, another compound in this class, is converted to ribavirin monophosphate and functions as an inosine 5′-monophosphate (IMP) dehydrogenase in the guanosine 5′-triphosphate sodium salt hydrate (GTP) synthesis pathway, leading to the inhibition of viral RNA synthesis<xref rid="bib70" ref-type="bibr"><sup>70</sup></xref>.</p><p>Cap-snatching is a key process in virus RNA transcription. During the cap-snatching process, PB2 first binds to the 5′-methyl cap of host pre-mRNA which is then cleaved by PA׳s endonuclease site to produce a capped primer for transcription initiation<xref rid="bib72" ref-type="bibr"><sup>72</sup></xref>. Both the PB2 cap-binding site and PA′s endonuclease site appear to be potential drug targets. From their calcuations, Lv, et al.<xref rid="bib73" ref-type="bibr"><sup>73</sup></xref>, found two small molecules RO and PPT28, which have a higher affinity with the viral PB 2 cap-binding domain than a known cap analog, m7GTP. RO and PPT28 could serve as potential anti-influenza drugs targeting PB2 cap-binding domain. PA׳s endonuclease active site resides in the N-terminal region of PA and is highly conserved. X-ray crystal structures reveal a conserved cleft in the active site<xref rid="bib74" ref-type="bibr">74</xref>, <xref rid="bib75" ref-type="bibr">75</xref>. A number of cap-snatching inhibitors discovered targeting the endonuclease site have been reported including 4-substituted 2,4-dioxobutanoic acid derivatives<xref rid="bib76" ref-type="bibr"><sup>76</sup></xref>, flutimide (<xref rid="f0025" ref-type="fig">Fig. 5</xref>)<xref rid="bib77" ref-type="bibr"><sup>77</sup></xref>, and <italic>N</italic>-hydroxamic acid/<italic>N</italic>-hydroxyimide<xref rid="bib78" ref-type="bibr"><sup>78</sup></xref>. Most of these compounds did not undergo further development, partially due to their unknown binding mode to allow for further optimization of their structures. Recently, the X-ray crystal structures of the PA endonuclease domain bound with several inhibitors in this class were reported by two different groups<xref rid="bib79" ref-type="bibr">79</xref>, <xref rid="bib80" ref-type="bibr">80</xref>. These structures provide a better understanding of the binding of the inhibitors at the PA endonuclease active site and may help in designing new PA inhibitors with improved activities.</p><p>The interactions between the polymerase′s subunits have recently been proposed to be attractive targets<xref rid="bib81" ref-type="bibr"><sup>81</sup></xref>, as their proper assembly is crucial for the normal activities of the polymerase. Evidence from crystallography data show that the protein–protein interactions between subunits PA and PB1 involve relatively few residues<xref rid="bib82" ref-type="bibr">82</xref>, <xref rid="bib83" ref-type="bibr">83</xref>, suggesting great promise in designing small-molecule based inhibitors. Muratore, et al.<xref rid="bib84" ref-type="bibr"><sup>84</sup></xref>, screened a library of 3 million compounds <italic>in silico</italic> based on one of the reported crystal structures<xref rid="bib82" ref-type="bibr"><sup>82</sup></xref>, and identified several compounds (<bold>17</bold>–<bold>19</bold>) as effective inhibitors against PA–PB1 binding in an ELISA-based assay and in cells (<xref rid="f0025" ref-type="fig">Fig. 5</xref>). Particularly, compound <bold>17</bold> was demonstrated to be active against an oseltamivir-resistant strain<xref rid="bib84" ref-type="bibr"><sup>84</sup></xref>. These compounds were identified as lead compounds for further antivirus drug development<xref rid="bib85" ref-type="bibr"><sup>85</sup></xref>. Studies with compound <bold>19</bold> and its analogs have shown that cycloheptathiophene-3-carboxamide scaffold is promising for new anti-influenza virus drug development<xref rid="bib85" ref-type="bibr"><sup>85</sup></xref>. Very recently, continuous efforts along this line led to the discovery of new RNA-dependent RNA polymerase (RdRP) inhibitors (<bold>20</bold>, <bold>21</bold>) through dissection of the thiophene-3-carboxamide molecule via a molecular interaction field (MIF)-based scaffold-hopping method<xref rid="bib86" ref-type="bibr"><sup>86</sup></xref>. Serendipitously, the same group also discovered that the compound AL18 (<bold>22</bold>), previously reported as a potent inhibitor of human cytomegalovirus DNA polymerase<xref rid="bib87" ref-type="bibr"><sup>87</sup></xref>, blocks the PA/PB1 interaction and inhibits influenza A virus replication<xref rid="bib88" ref-type="bibr"><sup>88</sup></xref>. In another study, Fukuoka and coworkers<xref rid="bib89" ref-type="bibr"><sup>89</sup></xref> performed a docking simulation-based screening of ~4000 drugs. Benzbromarone, diclazuril, and trenbolone acetate, were identified as three successful hit compounds with strong anti-influenza activities (<xref rid="f0025" ref-type="fig">Fig. 5</xref>). Two compounds, benzbromarone and diclazuril, were confirmed to be bound to PA and decreased the activity of the viral RNA polymerase<xref rid="bib89" ref-type="bibr"><sup>89</sup></xref>. More recently, Kessler, et al., discovered benzofurazan-based novel inhibitors targeting PA–PB1 binding interfaces using an ELISA-based high-throughput screening method. However, this serie of compounds has unfavorable toxicity profiles for <italic>in vivo</italic> use. Overall, the PA–PB1 binding interface has emerged to be a potential fruitful target for a new generation of anti-influenza A drug development.</p><p>Similar anti-viral opportunities are also seen in PB1–PB2 interactions, since the crystal structure of the binding interface of PB1–PB2 shows that only a small section of PB1 (residues 678–757) and of PB2 (residues 1–37) are involved in the interface<xref rid="bib90" ref-type="bibr"><sup>90</sup></xref>. To date, several synthetic-peptide-based inhibitors have been reported to be able to interfere with PB1–PB2 interactions and disrupt normal function of the polymerase<xref rid="bib91" ref-type="bibr">91</xref>, <xref rid="bib92" ref-type="bibr">92</xref>. However, nonpeptide small-molecule based inhibitors remain to be discovered. One particular challenge is to design small-molecules fitting in the flat PB1–PB2 interface.</p></sec><sec id="s0070"><label>5.3</label><title>Nucleoprotein (NP) as the drug target</title><p>The influenza virus nucleoprotein (NP) is one of the most abundant viral proteins produced in the virus replication process inside the host cell. During the viral life cycle, NP binds with influenza viral RNA and polymerase subunits (PB1, PB2, and PA) to form the viral ribonucleoprotein complexes (vRNPs). It also involved in vRNPs nuclear import, replication, and export<xref rid="bib93" ref-type="bibr">93</xref>, <xref rid="bib94" ref-type="bibr">94</xref>. NP has emerged as a novel target for anti-virus drug development because of its important structural and regulatory roles in virus replication. Recent large-scale sequence analysis of influenza A virus NP has identified several already known functional region as well as new highly conserved sites as potential drug-targets<xref rid="bib95" ref-type="bibr"><sup>95</sup></xref>.</p><p>Currently, NP-based antiviral drug development has formed two major classes of inhibitors that target on NP interaction with virus RNA<xref rid="bib96" ref-type="bibr"><sup>96</sup></xref> and block formation of vRNPs by the mechanism of NP oligomerization<xref rid="bib97" ref-type="bibr">97</xref>, <xref rid="bib98" ref-type="bibr">98</xref>, <xref rid="bib99" ref-type="bibr">99</xref>. Naproxen, an approved nonsteroidal anti-inflammatory drug that inhibits inducible cyclooxygenase-2 (COX-2), was the first inhibitor discovered through <italic>in silico</italic> virtual screening to inhibit the NP-RNA interactions (<xref rid="f0025" ref-type="fig">Fig. 5</xref>)<xref rid="bib96" ref-type="bibr"><sup>96</sup></xref>. It is effective against H1N1 and H3N2 strains both <italic>in vitro</italic> and <italic>in vivo</italic>. Single-point mutation experiments indicated that naproxen targets the RNA binding groove of NP and prevents its interaction with virus RNA. Naproxen serves as a lead compound for further development, particularly as a dual-functional drug with both antiviral and anti-inflammatory benefits. Nucleozin (<xref rid="f0025" ref-type="fig">Fig. 5</xref>) and its derivatives represent the other class of small molecules targeting NP oligomerization<xref rid="bib97" ref-type="bibr">97</xref>, <xref rid="bib98" ref-type="bibr">98</xref>, <xref rid="bib99" ref-type="bibr">99</xref>. Nucleozin was first identified in 2010 by two independent groups<xref rid="bib97" ref-type="bibr">97</xref>, <xref rid="bib100" ref-type="bibr">100</xref>. It appears to exert inhibitory effects at both early and late stages in the influenza virus life cycle<xref rid="bib101" ref-type="bibr"><sup>101</sup></xref>. Nucleozin not only inhibits viral RNA and protein synthesis, but also stabilizes NP self-oligomerization and promotes nonfunctional aggregates of NP. Moreover, it blocks the exportation of the vRNPs from the nucleus and facilitates the formation of large perinuclear aggregates of vRNPs along with the cellular protein Rab11<xref rid="bib101" ref-type="bibr"><sup>101</sup></xref>.</p></sec><sec id="s0075"><label>5.4</label><title>Nonstructrual protein I (NS1) as the drug target</title><p>The NS1 protein of influenza A virus has multiple functions<xref rid="bib102" ref-type="bibr"><sup>102</sup></xref>. It suppresses the host responses to the virus infection, in particular the interferon(IFN)-mediated response<xref rid="bib103" ref-type="bibr"><sup>103</sup></xref>, through binding with viral dsRNA<xref rid="bib104" ref-type="bibr"><sup>104</sup></xref>, CPSF30<xref rid="bib105" ref-type="bibr"><sup>105</sup></xref>, the ubiquitin-ligase TRIM25<xref rid="bib106" ref-type="bibr"><sup>106</sup></xref>, and phosphoinositide 3-kinase (PI3K)<xref rid="bib107" ref-type="bibr"><sup>107</sup></xref>. The distinct binding sites of NS1 with these biomolecules provide potential opportunities for drug discovery<xref rid="bib108" ref-type="bibr"><sup>108</sup></xref>. Currently, drug development targeting the NS1 protein is still in the early stages.</p><p>Serving as a proof of concept that NS1 could be a feasible target, a few lead compounds that inhibit NS1 functions were identified by either a yeast-based assay<xref rid="bib109" ref-type="bibr"><sup>109</sup></xref> or virtual screening<xref rid="bib110" ref-type="bibr"><sup>110</sup></xref>. Engel and coworkers<xref rid="bib109" ref-type="bibr"><sup>109</sup></xref> tested 2000 compounds in yeast model expressing NS1. Four compounds were found to reverse the growth inhibiting effect of NS1. These compounds potentially exhibited antivirus activity by blocking NS1-mediated IFN response. Further derivatization of these compounds leads to the compound JJ3297 (<bold>23</bold>) (<xref rid="f0025" ref-type="fig">Fig. 5</xref>)<xref rid="bib111" ref-type="bibr"><sup>111</sup></xref>, which facilitated the restoration of an IFN-like antiviral state and inhibited virus replication and spread in a RNase L dependent manner. Very recently, Ai et al.<xref rid="bib110" ref-type="bibr"><sup>110</sup></xref> screened a library of more than 30,000 compounds from traditional Chinese medicine using a structural-based docking method, and identified two compounds 32056 and 31674 that show antiviral activities by stably binding to the CPSF30-binding site of NS1. In addition, several compounds interfering with NS1/viral RNA binding were identified either through virtual<xref rid="bib112" ref-type="bibr"><sup>112</sup></xref> or high-throughput screening methods<xref rid="bib113" ref-type="bibr">113</xref>, <xref rid="bib114" ref-type="bibr">114</xref>.</p></sec></sec><sec id="s0080"><label>6</label><title>Combination therapy</title><p>Combination therapy uses several antivirus drugs with different mechanisms of action in one regime to achieve greater efficacy than one drug dose alone based on drug synergistic effect. It allows for lower doses of each component, resulting in reduced side effects. In addition, it may significantly increase the selection barrier for resistance. Thus, it presents a promising strategy for the treatment of influenza A virus, particularly for severe and immunocompromised patients<xref rid="bib115" ref-type="bibr"><sup>115</sup></xref>. A combination of amantadine+oseltamivir<xref rid="bib116" ref-type="bibr"><sup>116</sup></xref> as well as favirpiravir+oseltamivir<xref rid="bib117" ref-type="bibr"><sup>117</sup></xref> have demonstrated enhanced drug efficacy in H5N1 infected mice. Recently, combination therapy with three antiviral drugs (amantadine, ribavirin, and oseltamivir) in patients with severe A/H1N1 2009 (pH1N1) influenza in Korea has reduced the 14-day mortality<xref rid="bib118" ref-type="bibr"><sup>118</sup></xref>. In another study, triple-combination antiviral drug therapy showed similar pharmacokinetics to mono-drug therapy and demonstrated increased safety in immunocompromised patients<xref rid="bib118" ref-type="bibr">118</xref>, <xref rid="bib119" ref-type="bibr">119</xref>. Currently, several combination therapies based on approved and/or new drugs are under investigation.</p></sec><sec id="s0085"><label>7</label><title>Conclusions</title><p>The rapid emergence of influenza virus A resistance to current anti-virus drugs and the unpredictable nature of a potential influenza pandemic outbreak has impelled scientists and researchers to search for new antiviral strategies to overcome resistance and provide for better prophylactic and therapeutic outcomes than what current drugs can offer us. Recent progress in basic molecular biology, biophysics, and virology has provided important information regarding the molecular and structural basis behind the resistant influenza A virus and has helped to guide new drug development strategies for antiviral treatments. These new strategies target the mutant M2 proteins, neuraminidases, or other viral proteins. Ideally, the next generation of antivirus drug should have strong potency against a broad range of current resistant strains with a much higher resistance barrier. A number of small-molecule based drugs have been identified through structure-based drug design and <italic>in vitro</italic> or <italic>in vivo</italic> screening. A few have advanced into different phases of clinical trials. They may provide new options for drug treatment and prevention of influenza virus A infections in the near future, either alone or in combination with other drugs, to keep flu pandemics under check.</p></sec></body><back><ref-list><title>References</title><ref id="bib1"><label>1</label><mixed-citation publication-type="other" id="othref0005">World Health Organization. Influenza (seasonal ) fact sheet N˚211. 2014. 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We also would like to thank William Hanafin at the Univeristy of Illinois for his editing suggestions.</p></ack><fn-group><fn id="d32e59"><p>Peer review under responsibility of Institute of Materia Medica, Chinese Academy of Medical Sciences and Chinese Pharmaceutical Association.</p></fn></fn-group></back><floats-group><fig id="f0005"><label>Figure 1</label><caption><p>A schematic presentation of influenza A virus life cycle (adapted with permission from Ref. <xref rid="bib5" ref-type="bibr">5</xref> life cycle Copyright 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim).</p></caption><graphic xlink:href="gr1"></graphic></fig><fig id="f0010"><label>Figure 2</label><caption><p>Structures of M2 ion channel blockers.</p></caption><graphic xlink:href="gr2"></graphic></fig><fig id="f0015"><label>Figure 3</label><caption><p>Residues around the SA active site of NA (N1) with oseltamivir and the relative positions of 150 and 430 loop of N1 <italic>versus</italic> N9 (N1: light blue, PDB 2HU0, N9: yellow, PDB 2C4A) (adapted with permission from Ref. <xref rid="bib34" ref-type="bibr">34</xref>, Copyright 2012 Elsevier Ltd.).</p></caption><graphic xlink:href="gr3"></graphic></fig><fig id="f0020"><label>Figure 4</label><caption><p>Sialic acid and neuraminidase (NA) inhibitors.</p></caption><graphic xlink:href="gr4"></graphic></fig><fig id="f0025"><label>Figure 5</label><caption><p>Anti-influenza drugs targeting other viral proteins besides M2 ion channel and NA.</p></caption><graphic xlink:href="gr5"></graphic></fig></floats-group></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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