Trypanosoma cruzi:: mixture of two populations can modify virulence and tissue tropism in rat

被引:38
作者
Franco, DJ
Vago, AR
Chiari, E
Meira, FCA
Galvao, LMC
Machado, CRS [1 ]
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Morfol, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Parasitol, BR-31270901 Belo Horizonte, MG, Brazil
关键词
Chagas' disease; Trypanosoma cruzi variability; myocarditis; myositis; kDNA;
D O I
10.1016/S0014-4894(03)00119-X
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
In rats, CL-Brener clone caused high mortality, severe acute myocarditis, and myositis that subsided completely in surviving animals. Accordingly, no parasite kDNA could be amplified in several organs after 4 months. The monoclonal JG strain caused null mortality, acute predominantly focal myocarditis, discrete and focal myositis, and a chronic phase with sparse inflammatory foci. Double infection with both Trypanosoma cruzi populations turned mortality very low or null. At the end of the acute phase, the heart exhibited only JG strain kDNA (LSSP-PCR), while skeletal muscles and rectum exhibited only CL-Brener kDNA. Molecular and histopathological findings were accordant. In double infection chronic phase, JG strain remains in heart and appeared in organs previously parasitized by CL-Brener clone. Understanding the virulence and histotropism shifts now described could be important to clarify the variable clinical course and epidemiological peculiarities of Chagas' disease. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:54 / 61
页数:8
相关论文
共 31 条
[1]   The mucin-like glycoprotein super-family of Trypanosoma cruzi:: structure and biological roles [J].
Acosta-Serrano, A ;
Almeida, IC ;
Freitas, LH ;
Yoshida, N ;
Schenkman, S .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 114 (02) :143-150
[2]   Trypanosoma cruzi infection modulates in vivo expression of major histocompatibility complex class II molecules on antigen-presenting cells and T-cell stimulatory activity of dendritic cells strain-dependent manner [J].
Soto, CDA ;
Mirkin, GA ;
Solana, ME ;
Cappa, SMG .
INFECTION AND IMMUNITY, 2003, 71 (03) :1194-1199
[3]   β-chemokines enhance parasite uptake and promote nitric oxide-dependent microbiostatic activity in murine inflammatory macrophages infected with Trypanosoma cruzi [J].
Aliberti, JCS ;
Machado, FS ;
Souto, JT ;
Campanelli, AP ;
Teixeira, MM ;
Gazzinelli, RT ;
Silva, JS .
INFECTION AND IMMUNITY, 1999, 67 (09) :4819-4826
[4]   Differential tissue distribution of diverse clones of Trypanosoma cruzi in infected mice [J].
Andrade, LO ;
Machado, CRS ;
Chiari, E ;
Pena, SDJ ;
Macedo, AM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1999, 100 (02) :163-172
[5]   Trypanosoma cruzi: role of host genetic background in the differential tissue distribution of parasite clonal populations [J].
Andrade, LO ;
Machado, CRS ;
Chiari, E ;
Pena, SDJ ;
Macedo, AM .
EXPERIMENTAL PARASITOLOGY, 2002, 100 (04) :269-275
[6]   INFLUENCE OF TRYPANOSOMA-CRUZI STRAIN ON THE PATHOGENESIS OF CHRONIC MYOCARDIOPATHY IN MICE [J].
ANDRADE, SG .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1990, 85 (01) :17-27
[7]   Infection with different Trypanosoma cruzi populations in rats:: Myocarditis, cardiac sympathetic denervation, and involvement of digestive organs [J].
Camargos, ERS ;
Franco, DJ ;
Garcia, CMMG ;
Dutra, AP ;
Teixeira, AL ;
Chiari, E ;
Machado, CRS .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2000, 62 (05) :604-612
[8]  
DIAS JCP, 1992, CHAGAS DIS AM TRYPAN, P49
[9]   Trypanosoma cruzi:: Optimization of polymerase chain reaction for detection in human blood [J].
Gomes, ML ;
Macedo, AM ;
Vago, AR ;
Pena, SDJ ;
Galvao, LMC ;
Chiari, E .
EXPERIMENTAL PARASITOLOGY, 1998, 88 (01) :28-33
[10]   Cyclophosphamide-induced immunosuppression protects cardiac noradrenergic nerve terminals from damage by Trypanosoma cruzi infection in adult rats [J].
Guerra, LB ;
Andrade, LO ;
Galvao, LMC ;
Macedo, AM ;
Machado, CRS .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2001, 95 (05) :505-509