Chemotherapy with benznidazole and itraconazole for mice infected with different Trypanosoma cruzi clonal genotypes

被引:122
作者
Toledo, MJD
Bahia, MT
Carneiro, CM
Martins-Filho, OA
Tibayrenc, M
Barnabé, C
Tafuri, WL
de Lana, M
机构
[1] Univ Estadual Maringa, Dept Anal Clin, Ctr Ciencias Saude, BR-87020900 Maringa, Parana, Brazil
[2] Univ Fed Minas Gerais, Dept Parasitol, Inst Ciencias Biol, Belo Horizonte, MG, Brazil
[3] Fundacao Oswaldo Cruz, Ctr Pesquisas Rene Rachou, Belo Horizonte, MG, Brazil
[4] Escola Farm, Dept Ciencias Biol, Inst Ciencias Exatas & Biol, Ouro Preto, MG, Brazil
[5] Escola Farm, Dept Anal Clin, Ouro Preto, MG, Brazil
[6] Univ Fed Ouro Preto, Ouro Preto, MG, Brazil
[7] Ctr Natl Rech Sci, Inst Rech Dev, Unite Mixte Rech 9926, F-34032 Montpellier 1, France
关键词
D O I
10.1128/AAC.47.1.223-230.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The benznidazole (BZ) and itraconazole (ITC) susceptibilities of a standard set of Trypanosoma cruzi natural stocks were evaluated during the acute phase and the chronic phase of experimental chagasic infection in BALB/c mice. Twenty laboratory-cloned stocks representative of the total phylogenetic diversity of T. cruzi, including genotypes 20 and 19 (T. cruzi I) and genotypes 39 and 32 (T. cruzi 11), were analyzed. Our results demonstrate important differences among stocks that could be pointed out as markers of biological behavior. Members of the T. cruzi I group were highly resistant to both BZ and ITC, whereas members of the T. cruzi 11 group were partially resistant to both drugs, despite their susceptibilities to ITC during the chronic phase of infection. The resistance to BZ observed for T. cruzi I was mainly triggered by genotype 20 isolates, whereas resistance to ITC was due to both genotype 20 and 19 isolates. Two polar patterns of response to BZ observed for genotype 39 isolates had a major impact on the partial resistance pattern observed for members of the T. cruzi 11 group. Genotype 32 isolates showed a typical profile of susceptibility. The correlation between the response to treatment and phylogenetic classification of T. cruzi stocks was clearer for ITC than for BZ. In conclusion, the data presented show a correlation between phylogenetic divergence among T. cruzi stocks and their susceptibilities to chemotherapeutic agents in vivo. Our results warn of the necessity to take into account the lesser genetic subdivisions of T. cruzi stocks since the upper subdivisions (T. cruzi I and 11) show a great deal of heterogeneity for in vivo drug susceptibility.
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收藏
页码:223 / 230
页数:8
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