Molecular diagnosis and typing of Trypanosoma cruzi populations and lineages in cerebral Chagas disease in a patient with AIDS

被引:63
作者
Burgos, JM
Begher, SB
Freitas, JM
Bisio, M
Duffy, T
Altcheh, J
Teijeiro, R
Alcoba, HL
Deccarlini, F
Freilij, H
Levin, MJ
Levalle, J
Macedo, AM
Schijman, AG [1 ]
机构
[1] Consejo Nacl Invest Cient & Tecn, INGEBI, Lab Biol Mol Enfermedad Chagas, Buenos Aires, DF, Argentina
[2] Hosp Ignacio Pirovano, Unidad Clin Med & Infectol 2, Gobierno Ciudad Buenos Aires, Buenos Aires, DF, Argentina
[3] Hosp Ninos Dr Ricardo Gutierrez, Lab Parasitol & Enfermedad Chagas, Buenos Aires, DF, Argentina
[4] Univ Fed Minas Gerais, ICB, Dept Bioquim & Imunol, Belo Horizonte, MG, Brazil
[5] UBA, FCEyN, Dept Fisiol & Biol Mol & Celular, Buenos Aires, DF, Argentina
关键词
D O I
10.4269/ajtmh.2005.73.1016
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Trypanosoma cruzi DNA was amplified from an intracranial biopsy and peripheral blood of an HIV patient with encephalitis; this episode was indicative of AIDS and congenital Chagas disease. The analysis of a microsatellite locus revealed a multiclonal parasite population at the brain lesion with a more complex minicircle signature than that profiled in blood using restriction fragment length polymorphism (RFLP)-PCR and low stringency single primer (LSSP) PCR. Interestingly, different sublineages of T cruzi II were detected in blood and brain by means of spliced-leader and 24 alpha ribosomal-DNA amplifications. Quantitative-competitive PCR monitored the decrease of parasitic load during treatment and secondary prophylaxis with benznidazole. The synergy between parasiticidal plus anti-retroviral treatments probably allowed the patient a longer survival than usually achieved in similar episodes. This is the first case report demonstrating a differential distribution of natural parasite populations and sublineages in Chagas disease reactivation, showing the proliferation of cerebral variants not detectable in peripheral blood.
引用
收藏
页码:1016 / 1018
页数:3
相关论文
共 17 条
[1]   Identification of six Trypanosoma cruzi phylogenetic lineages by random amplified polymorphic DNA and multilocus enzyme electrophoresis [J].
Brisse, S ;
Barnabé, C ;
Tibayrenc, M .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2000, 30 (01) :35-44
[2]  
CAHN P, 2001, MANAGEMENT HIV INFEC, V31, P513
[3]   AIDS and Chagas' disease [J].
Corti, M .
AIDS PATIENT CARE AND STDS, 2000, 14 (11) :581-588
[4]   CONGENITAL CHAGAS-DISEASE - DIAGNOSTIC AND CLINICAL ASPECTS [J].
FREILIJ, H ;
ALTCHEH, J .
CLINICAL INFECTIOUS DISEASES, 1995, 21 (03) :551-555
[5]  
Gürtler RE, 2003, EMERG INFECT DIS, V9, P29
[6]   USE OF THE POLYMERASE CHAIN-REACTION TO DETECT TOXOPLASMA-GONDII IN HUMAN BLOOD-SAMPLES [J].
HOYEN, DO ;
JOSS, AWL ;
BALFOUR, AH ;
SMYTH, ETM ;
BAIRD, D ;
CHATTERTON, JMW .
JOURNAL OF CLINICAL PATHOLOGY, 1992, 45 (10) :910-913
[7]   Trypanosoma cruzi:: Genetic structure of populations and relevance of genetic variability to the pathogenesis of Chagas disease [J].
Macedo, AM ;
Machado, CR ;
Oliveira, RP ;
Pena, SDJ .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2004, 99 (01) :1-12
[8]   Genetic variability of Trypanosoma cruzi:: Implications for the pathogenesis of Chagas disease [J].
Macedo, AM ;
Pena, SDJ .
PARASITOLOGY TODAY, 1998, 14 (03) :119-124
[9]   Usefulness of microsatellite typing in population genetic studies of Trypanosoma cruzi [J].
Macedo, AM ;
Pimenta, JR ;
de Aguiar, RS ;
Melo, AIR ;
Chiari, E ;
Zingales, B ;
Pena, SDJ ;
Oliveira, RP .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2001, 96 (03) :407-413
[10]  
Perez-Ramirez L, 1999, AM J TROP MED HYG, V61, P198