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      <title>Exploring the FL-160-CRP gene family through sequence variability of the complement regulatory protein (CRP) expressed by the trypomastigote stage of #Trypanosoma cruzi$</title>
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      <namePart type="family">Mathieu-Daudé</namePart>
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    <abstract>The complement regulatory protein (CRP) of Trypanosoma cruzi is a surface glycoprotein which confers to the infectious trypomastigote forms a protection against the lytic activity of the host complement. CRP belongs to the large family of the trans-sialidase-like proteins and its sequence is highly similar to those of the flagellar FL-160 and chronic exoantigen proteins, encoded by a multigene family. To further define the gene family encoding the CRP, we investigated the protein diversity among several strains of T cruzi through the sequencing of trypomastigote transcripts, and used a phylogenetic analysis based on the multiple alignment of these proteins with the top scoring sequences detected by a database sequence homology search. Intrastrain variations in CRP sequences revealed the existence of several copies per strain. The interstrain variability of CRP was consistent with the genetic subdivisions of T cruzi into lineages and discrete typing units. The phylogenetic analysis based on a 227 amino acid alignment of CRP sequences with the 200 putative proteins retrieved from the protein databases (including the sequences from the T cruzi genome project) revealed that the CRP sequences clustered with the FL-160 proteins into a monophyletic group characterized by the presence of the 12 amino acid mimicry epitope that mimics nervous tissues. The phylogeny did not differentiate between the CRP and the FL-160 proteins. The identification of this group of CRP-like proteins and the high sequence similarity observed within it open up new prospects for the exploration of the localization, structure and function of these proteins and a better understanding of their involvement in key aspects of host-parasite interactions, such as the resistance to the complement. This work provides also information for the T cruzi genome annotation of the trans-sialidase-like putative proteins.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>Trypanosoma cruzi</topic>
      <topic>complement regulatory protein</topic>
      <topic>FL 160</topic>
      <topic>trans sialidase like proteins</topic>
    </subject>
    <classification authority="local">052</classification>
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      <titleInfo>
        <title>Infection Genetics and Evolution</title>
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      <part>
        <detail type="volume">
          <number>8</number>
        </detail>
        <detail type="volume">
          <number>3</number>
        </detail>
        <extent unit="pages">
          <list> 258-266</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2008</dateIssued>
      </originInfo>
      <identifier type="issn">1567-1348</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010042624</identifier>
    <identifier type="doi">10.1016/j.meegid.2007.12.010</identifier>
    <identifier type="issn">1567-1348</identifier>
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