Molecular characterization of the kinetoplastid membrane protein-11 genes from the parasite Trypanosoma rangeli

Trypanosomatids are early divergent parasites which include several species of medical interest. Trypanosoma rangeli is not pathogenic for humans but shows a high immunological cross-reactivity with Trypanosoma cruzi, the causative agent of Chagas' disease that affects more than 17 million peop...

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Published inParasitology Vol. 130; no. 6; pp. 643 - 651
Main Authors DIEZ, H., THOMAS, M. C., URUEÑA, C. P., SANTANDER, S. P., CUERVO, C. L., LÓPEZ, M. C., PUERTA, C. J.
Format Journal Article
LanguageEnglish
Published Cambridge, UK Cambridge University Press 01.06.2005
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Summary:Trypanosomatids are early divergent parasites which include several species of medical interest. Trypanosoma rangeli is not pathogenic for humans but shows a high immunological cross-reactivity with Trypanosoma cruzi, the causative agent of Chagas' disease that affects more than 17 million people throughout the world. Recent studies have suggested that T. cruzi KMP-11 antigen could be a good candidate for the induction of immunoprotective cytotoxic responses against T. cruzi natural infection. In the present paper the genes coding for the T. rangeli kinetoplastid membrane protein-11 have been characterized. The results show that the locus encoding this protein is formed by 4 gene units measuring 550 nucleotides in length, organized in tandem, and located in different chromosomes in KP1(+) and KP1(−) strains. The gene units are transcribed as a single mRNA of 530 nucleotides in length. Alignment of the T. rangeli KMP-11 deduced amino acid sequence with the homologous KMP-11 protein from T. cruzi revealed an identity of 97%. Interestingly, the T and B cell epitopes of the T. cruzi KMP-11 protein are conserved in the T. rangeli KMP-11 amino acid sequence.
Bibliography:istex:B46A181F1311CAE66ADA574A2DF64BDC05F649E4
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PII:S0031182004006936
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content type line 23
ISSN:0031-1820
1469-8161
DOI:10.1017/S0031182004006936