4.5 Article

Intraspecies Variation in Trypanosoma cruzi GPI-Mucins: Biological Activities and Differential Expression of α-Galactosyl Residues

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AMER SOC TROP MED & HYGIENE
DOI: 10.4269/ajtmh.2012.12-0015

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资金

  1. National Council for the Development of Research of Brazil (CNPq) [305042/2010-6]
  2. Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG)
  3. CNPq [552072/2009-5, PAPES-IV-400138/2006-9, PDJ-150880/2005-7]
  4. FAPEMIG
  5. National Institutes of Health [1R01AI070655-04, 3R01AI070655-04S1, 2G12RR008124-16A1, 2G12RR008124-16A1S1]
  6. Biomolecule Analysis Core Facility at the Border Biomedical Research Center/Biology/UTEP University of Texas at El Paso (National Institutes of Health) [2G12RR008124-16A1, 2G12RR008124-16A1S1, G12MD007592]

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The glycosylphosphatidylinositol (GPI)-anchored mucins of Trypanosoma cruzi trypomastigotes play an important immunomodulatory role during the course of Chagas disease. Here, some biological activities of tGPI-mucins from four T cruzi isolates, including benznidazole-susceptible (BZS-Y), benznidazole-resistant (BZR-Y), CL, and Colombiana, were evaluated. GPI-mucins were able to differentially trigger the production of interleukin-12 and nitric oxide in BALB/c macrophages and modulate LLC-MK2 cell invasion. The significance of these variations was assessed after analysis of the terminal alpha-galactosyl residues. Enzymatic treatment with alpha-galactosidase indicated a differential expression of O-linked alpha-galactosyl residues among the strains, with higher expression of this sugar in BZS-Y and BZR-Y T cruzi populations followed by Colombiana and CL. Unweighted pair group method analysis of the carbohydrate anchor profile and biological parameters allowed the clustering of two groups. One group includes Y and CL strains (T cruzi II and VI), and the other group is represented by Colombiana strain (T. cruzi I).

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