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    <titleInfo>
      <title>Antibacterial and leishmanicidal activities of temporin-SHd, a 17-residue long membrane-damaging peptide</title>
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    <abstract>Temporins are a family of short antimicrobial peptides (8-17 residues) that mostly show potent activity against Gram-positive bacteria. Herein, we demonstrate that temporin-SHd, a 17-residue peptide with a net charge of +2 (FLPAALAGIGGILGKLF(amide)) expressed a broad spectrum of antimicrobial activity. This peptide displayed potent antibacterial activities against Gram-negative and Gram-positive bacteria, including multi-drug resistant Staphylococcus aureus strains, as well as antiparasitic activity against promastigote and the intracellular stage (amastigote) of Leishmania infantum, at concentration not toxic for the macrophages. Temporin-SHd that is structured in a non-amphipathic alpha-helix in anionic membrane-mimetic environments, strongly and selectively perturbs anionic bilayer membranes by interacting with the polar head groups and acyl region of the phospholipids, with formation of regions of two coexisting phases: one phase rich in peptide and the other lipid-rich. The disruption of lipid packing within the bilayer may lead to the formation of transient pores and membrane permeation/disruption once a threshold peptide accumulation is reached. To our knowledge, Temporin-SHd represents the first known 17-residue long temporin expressing such broad spectrum of antimicrobial activity including members of the trypanosomatidae family. Additionally, since only a few shorter members (13 residues) of the temporin family are known to display antileishmanial activity (temporins-TA, -TB and -SHa), SHd is an interesting tool to analyze the antiparasitic mechanism of action of temporins.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>Antimicrobial peptide</topic>
      <topic>Amphibian</topic>
      <topic>Temporin-SH</topic>
      <topic>Circular dichroism</topic>
      <topic>Membrane interaction/permeabilization</topic>
      <topic>Antiparasitic activity</topic>
    </subject>
    <classification authority="local">020</classification>
    <classification authority="local">052</classification>
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      <titleInfo>
        <title>Biochimie</title>
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      <part>
        <detail type="volume">
          <number>95</number>
        </detail>
        <detail type="volume">
          <number>2</number>
        </detail>
        <extent unit="pages">
          <list> 388-399</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2013</dateIssued>
      </originInfo>
      <identifier type="issn">0300-9084</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010060735</identifier>
    <identifier type="doi">10.1016/j.biochi.2012.10.015</identifier>
    <identifier type="issn">0300-9084</identifier>
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      <recordCreationDate encoding="w3cdtf">2013-05-02</recordCreationDate>
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      <recordIdentifier>fdi:010060735</recordIdentifier>
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