Author/Authors :
Câmara، نويسنده , , A.C.J. and Varela-Freire، نويسنده , , A.A. and Valadares، نويسنده , , H.M.S. and Macedo، نويسنده , , A.M. and D’?vila، نويسنده , , D.A. and Machado، نويسنده , , C.R. and Lages-Silva، نويسنده , , E. and Chiari، نويسنده , , E. and Galv?o، نويسنده , , L.M.C.، نويسنده ,
Abstract :
Trypanosoma cruzi genetic diversity was investigated in 25 isolates (vectors and humans) from the semiarid zone of the State of Rio Grande do Norte, Brazil. Molecular markers (3′ region of the 24Sα rRNA; mitochondrial cytochrome oxidase subunit 2 (COII) gene; spliced leader intergenic region (SL-IR) gene; allelic size microsatellite polymorphism) identified 56% TcIII (100% Panstrongylus lutzi; 50% Triatoma brasiliensis); 40% TcII (91.7% humans; 50% T. brasiliensis) and 4% TcI (human). Microsatellite analysis revealed monoclonal and heterozygous patterns on one or more microsatellite loci in 64% of T. cruzi isolates (92.3% triatomines; 33.3% humans) and 36% putative polyclonal populations (66.7% humans; 7.7% triatomines) by loci SCLE10, SCLE11, TcTAT20, TcAAAT6, all belonging to TcII. Identical T. cruzi polyclonal profiles (88.9%) were detected, mostly from humans. The adaptative natural plasticity of TcII and TcIII and their potential for maintaining human infection in T. brasiliensis were confirmed. Intraspecific and phylogenetic T. cruzi diversity in the sylvatic and domestic transmission cycles in this specific region will provide exclusive control strategies.
Keywords :
Trypanosoma cruzi , Chagas disease infection , Genomic markers , Triatoma brasiliensis , Panstrongylus lutzi , T. cruzi III