2001
DOI: 10.1006/expr.2001.4607
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Identification of Trypanosoma cruzi Genotypes Circulating in Chilean Chagasic Patients

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Cited by 51 publications
(54 citation statements)
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References 24 publications
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“…The current sampling extends epidemiological findings obtained by several groups of Latin America, 8,22,[30][31][32] and particularly of Argentina, 21,[33][34][35][36] showing the predominance of TcIId infection in human and mammalian hosts.…”
Section: Introductionsupporting
confidence: 84%
“…The current sampling extends epidemiological findings obtained by several groups of Latin America, 8,22,[30][31][32] and particularly of Argentina, 21,[33][34][35][36] showing the predominance of TcIId infection in human and mammalian hosts.…”
Section: Introductionsupporting
confidence: 84%
“…Our group verified that in mixed infections, interactions between populations of T. cruzi may occur, resulting in important changes in the biological characteristics of the parasite and the evolution of the infection (12,25,32). Moreover, the importance of mixed infections in the epidemiology of Chagas' disease (8,35) and the evidence that they may result in significant alterations in the host-parasite relationship motivated the studies on the efficacy of chemotherapy in dual infections. Therefore, the goal of the present investigation was to evaluate in BALB/c mice the impact of dual T. cruzi infections on chemotherapy effectiveness, compared with the respective single infections with stocks from distinct major T. cruzi genotypes.…”
Section: Discussionsupporting
confidence: 58%
“…The existence of mixed infections in vertebrate and invertebrate hosts has been verified (8,35) and raises questions about their relevance to the epidemiology of Chagas' disease. At least in experimental mixed infections, important interactions between subpopulations of the mixtures resulted in changes in parasite biological properties (12,13,25,32).…”
mentioning
confidence: 99%
“…The membranes were prehybridized for at least 2 hours at 55°C and hybridized with total T. cruzi kinetoplast P 32 -labeled DNA (1 × 10 6 cpm/ membrane). 29 After hybridization, each membrane was washed three times for 30 minutes with 2× SSC (0.3 M NaCl, 0.03 M sodium citrate), 0.1% sodium dodecyl sulfate at 55°C, and analyzed with the Molecular Imager FX (Bio-Rad Laboratories, Hercules, CA). For genotyping, different T. cruzi clones were used as probes to determine the parasite lineage infecting each animal (TCI, clonet 20 sp.104 cl1; TCIIb, clonet 33 CBB cl3; TCIId, clonet 39, NR cl3; and TCIIe, clonet 43 v195 cl1).…”
Section: Methodsmentioning
confidence: 99%
“…This method has been validated by hybridization with probes constructed by PCR amplification of T. cruzi DNA of other specific genotypes. [29][30][31] Hybridizations with genotype-specific T. cruzi probes were repeated twice, and genotyping was conducted with samples that showed a DNA fragment.…”
Section: Methodsmentioning
confidence: 99%