Bioluminescent imaging of Trypanosoma cruzi infection

被引:49
作者
Hyland, Kenneth V.
Asfaw, Sofya H.
Olson, Cheryl L.
Daniels, Melvin D.
Engman, David M. [1 ]
机构
[1] Northwestern Univ, Dept Microbiol Immunol, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
Trypanosoma cruzi; Luciferase; Bioluminescent imaging; Chagas disease;
D O I
10.1016/j.ijpara.2008.04.002
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
Chagas disease, caused by infection with the protozoan parasite Trypanosoma cruzi, is a major public health problem in Central and South America. The pathogenesis of Chagas disease is complex and the natural course of infection is not completely understood. The recent development of bioluminescence imaging technology has facilitated studies of a number of infectious and non-infectious diseases. We developed luminescent T. cruzi to facilitate similar studies of Chagas disease pathogenesis. Luminescent T cruzi trypomastigotes and amastigotes were imaged in infections of rat myoblast cultures, which demonstrated a clear correlation of photon emission signal strength to the number of parasites used. This was also observed in mice infected with different numbers of luminescent parasites, where a stringent correlation of photon emission to parasite number was observed early at the site of inoculation, followed by dissemination of parasites to different sites over the course of a 25-day infection. Whole animal imaging from ventral, dorsal and lateral perspectives provided clear evidence of parasite dissemination. The tissue distribution of T cruzi was further determined by imaging heart, spleen, skeletal muscle, lungs, kidneys, liver and intestines ex vivo. These results illustrate the natural dissemination of T cruzi during infection and unveil a new tool for studying a number of aspects of Chagas disease, including rapid in vitro screening of potential therapeutical agents, roles of parasite and host factors in the outcome of infection, and analysis of differential tissue tropism in various parasite-host strain combinations. (C) 2008 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1391 / 1400
页数:10
相关论文
共 54 条
[1]   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
[2]   Myocardial parasite persistence in chronic Chagasic patients [J].
Añez, N ;
Carrasco, H ;
Parada, H ;
Crisante, G ;
Rojas, A ;
Fuenmayor, C ;
Gonzalez, N ;
Percoco, G ;
Borges, R ;
Guevara, P ;
Ramirez, JL .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1999, 60 (05) :726-732
[3]   Use of Leishmania donovani field isolates expressing the luciferase reporter gene in in vitro drug screening [J].
Ashutosh ;
Gupta, S ;
Ramesh ;
Sundar, S ;
Goyal, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (09) :3776-3783
[4]   In vivo detection of Trypanosoma cruzi antigens in hearts of patients with chronic Chagas' heart disease [J].
Bellotti, G ;
Bocchi, EA ;
deMoraes, AV ;
Higuchi, MD ;
BarberoMarcial, M ;
Sosa, E ;
EstevesFilho, A ;
Kalil, R ;
Weiss, R ;
Jatene, A ;
Pileggi, F .
AMERICAN HEART JOURNAL, 1996, 131 (02) :301-307
[5]  
BEN YCA, 1988, T R SOC TROP MED HYG, V82, P77
[6]   Toxoplasma gondii:: Inconsistent dissemination patterns following oral infection in mice [J].
Boyle, Jon P. ;
Saeij, Jeroen P. J. ;
Boothroyd, John C. .
EXPERIMENTAL PARASITOLOGY, 2007, 116 (03) :302-305
[7]   Glycoinositolphospholipids from Trypanosoma cruzi interfere with macrophages and dendritic cell responses [J].
Brodskyn, C ;
Patricio, J ;
Oliveira, R ;
Lobo, L ;
Arnholdt, A ;
Mendonça-Previato, L ;
Barral, A ;
Barral-Netto, M .
INFECTION AND IMMUNITY, 2002, 70 (07) :3736-3743
[8]   TRYPANOSOMA-CRUZI INFECTION IN IMMUNOSUPPRESSED MICE [J].
CALABRESE, KS ;
BAUER, PG ;
LAGRANGE, PH ;
DACOSTA, SCG .
IMMUNOLOGY LETTERS, 1992, 31 (01) :91-96
[9]   Immunosuppressive drugs as a tool to explore immunopathology in experimental Chagas disease [J].
Calabrese, KS .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1999, 94 :273-276
[10]   IMMUNOFLUORESCENCE AS AN ADJUNCT TO THE HISTOPATHOLOGIC DIAGNOSIS OF CHAGAS-DISEASE [J].
CHANDLER, FW ;
WATTS, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (03) :567-569