Targeted gene expression profiling in Leishmania braziliensis and Leishmania guyanensis parasites isolated from Brazilian patients with different antimonial treatment outcomes

被引:35
作者
Torres, Davi Coe [2 ]
Adaui, Vanessa [3 ,4 ]
Ribeiro-Alves, Marcelo [5 ]
Romero, Gustavo A. S. [6 ]
Arevalo, Jorge [3 ]
Cupolillo, Elisa [1 ]
Dujardin, Jean-Claude [4 ]
机构
[1] Fiocruz MS, Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, Lab Pesquisas Leishmanioses, BR-21045900 Rio De Janeiro, Brazil
[2] Fiocruz MS, Inst Oswaldo Cruz, Lab Biol Computac & Sistemas, BR-21045900 Rio De Janeiro, Brazil
[3] Univ Peruana Cayetano Heredia, Inst Trop Med Alexander von Humboldt, Lima, Peru
[4] Inst Trop Med Antwerp, Unit Mol Parasitol, Dept Parasitol, Antwerp, Belgium
[5] Fiocruz MS, Inst Oswaldo Cruz, Ctr Desenvolvimento Tecnol Saude, BR-21045900 Rio De Janeiro, Brazil
[6] Univ Brasilia, Nucleo Med Trop, Lab Leishmanioses, Brasilia, DF, Brazil
关键词
Cutaneous leishmaniasis; Treatment failure; Targeted gene expression profiling; Leishmania braziliensis; Leishmania guyanensis; AMERICAN TEGUMENTARY LEISHMANIASIS; GAMMA-GLUTAMYLCYSTEINE SYNTHETASE; AQUAGLYCEROPORIN AQP1 GENE; DRUG-RESISTANT LEISHMANIA; ABC-TRANSPORTER MRPA; CUTANEOUS LEISHMANIASIS; MEGLUMINE ANTIMONIATE; SODIUM STIBOGLUCONATE; VIANNIA BRAZILIENSIS; DNA MICROARRAYS;
D O I
10.1016/j.meegid.2010.05.006
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
In Brazil, cutaneous leishmaniasis represents a serious public health problem, and chemotherapy is an important element of the clinical management of this disease. However, treatment efficacy is variable, a phenomenon that might be due to host and parasite (e.g., drug resistance) factors. To better understand the possible contribution of parasite factors to this phenomenon, we characterised 12 Leishmania braziliensis (LB) and 25 Leishmania guyanensis (LG) isolates collected from patients experiencing different antimonial treatment outcomes. For each isolate, promastigote cultures were grown in duplicate and were harvested at the late-log and stationary phases of growth. The RNA expression profiles of six genes encoding proteins with roles in antimony metabolism (AQP1, MRPA, GSH1, GSH2, TRYR and TDR1) were assessed by means of real-time quantitative PCR. Molecular data were compared to the clinical phenotypes. Within LB, we did not find statistically significant differences in the expression levels of the examined genes among isolates from patients with different treatment outcomes. In LG, GSH1 (encoding gamma-glutamylcysteine synthetase, gamma-GCS) was overexpressed in therapeutic failure isolates regardless of the growth curve phase. This finding reveals the predictive potential of promastigote expression curves for the prognosis of cutaneous leishmaniasis caused by LG in Brazil. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:727 / 733
页数:7
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