Literature DB >> 6407346

Studies of Trypanosoma cruzi clones in inbred mice. I. A comparison of the course of infection of C3H/HEN- mice with two clones isolated from a common source.

M Postan, J A Dvorak, J P McDaniel.   

Abstract

Two single-cell-isolate cloned stocks of the Sylvio-X10 strain, recovered from an acute human Trypanosoma cruzi infection, were used to infect C3H/HEN mice. The Sylvio-X10/4 clone produced a chronic infection in mice; clone Sylvio-X10/7 produced an acute lethal infection under identical experimental conditions. The course of infection of mice with the Sylvio-X10/7 clone was characterized by higher peripheral blood parasitemia and greater tissue involvement, an earlier appearance of specific anti-T. cruzi plasma IgG and shorter survival times than in mice infected with the Sylvio-X10/4 clone. The course of infection in mice with the Sylvio-X10 strain was intermediate between that of the two clones. This is the first demonstration of the pluripotential pathogenetic nature of a T. cruzi strain due to genetic heterogeneity of the population of parasites that constitute the strain. This experimental system is highly stable and reproducible. Consequently, the use of inbred mice and T. cruzi clones appears to provide an excellent model to study factors which influence the course of Chagas' disease.

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Year:  1983        PMID: 6407346     DOI: 10.4269/ajtmh.1983.32.497

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  32 in total

1.  Trypanosoma cruzi: properties of a clone isolated from CL strain.

Authors:  M T Lima; A M Jansen; E Rondinelli; C R Gattass
Journal:  Parasitol Res       Date:  1991       Impact factor: 2.289

2.  The chemokines CXCL9 and CXCL10 promote a protective immune response but do not contribute to cardiac inflammation following infection with Trypanosoma cruzi.

Authors:  Jenny L Hardison; Ruth A Wrightsman; Philip M Carpenter; Thomas E Lane; Jerry E Manning
Journal:  Infect Immun       Date:  2006-01       Impact factor: 3.441

3.  The CC chemokine receptor 5 is important in control of parasite replication and acute cardiac inflammation following infection with Trypanosoma cruzi.

Authors:  Jenny L Hardison; Ruth A Wrightsman; Philip M Carpenter; William A Kuziel; Thomas E Lane; Jerry E Manning
Journal:  Infect Immun       Date:  2006-01       Impact factor: 3.441

4.  Differential expression of Trypanosoma cruzi neuraminidase in intra- and extracellular trypomastigotes.

Authors:  I A Rosenberg; R P Prioli; J S Mejia; M E Pereira
Journal:  Infect Immun       Date:  1991-01       Impact factor: 3.441

5.  Changes in the total content of iron, copper, and zinc in serum, heart, liver, spleen, and skeletal muscle tissues of rats infected with Trypanosoma cruzi.

Authors:  A J Matousek de Abel de la Cruz; J L Burguera; M Burguera; N Añez
Journal:  Biol Trace Elem Res       Date:  1993-04       Impact factor: 3.738

6.  Elaboration by mammalian mesenchymal cells infected with Trypanosoma cruzi of a fibroblast-stimulating factor that may contribute to chagasic cardiomyopathy.

Authors:  D J Wyler; P Libby; S Prakash; R P Prioli; M E Pereira
Journal:  Infect Immun       Date:  1987-12       Impact factor: 3.441

7.  Trypanosoma cruzi promotes neuronal and glial cell survival through the neurotrophic receptor TrkC.

Authors:  Craig Weinkauf; Mercio Pereiraperrin
Journal:  Infect Immun       Date:  2009-01-29       Impact factor: 3.441

8.  Intracellular growth of Trypanosoma cruzi in cardiac myocytes is inhibited by cytokine-induced nitric oxide release.

Authors:  Laura Edith Fichera; Maria Cecilia Albareda; Susana Adriana Laucella; Miriam Postan
Journal:  Infect Immun       Date:  2004-01       Impact factor: 3.441

9.  Macrophages Promote Oxidative Metabolism To Drive Nitric Oxide Generation in Response to Trypanosoma cruzi.

Authors:  Sue-Jie Koo; Imran H Chowdhury; Bartosz Szczesny; Xianxiu Wan; Nisha J Garg
Journal:  Infect Immun       Date:  2016-11-18       Impact factor: 3.441

10.  Challenge of chronically infected mice with homologous trypanosoma cruzi parasites enhances the immune response but does not modify cardiopathy: implications for the design of a therapeutic vaccine.

Authors:  Christian Emerson Rosas-Jorquera; Luiz Roberto Sardinha; Fernando Delgado Pretel; André Luis Bombeiro; Maria Regina D'Império Lima; José Maria Alvarez
Journal:  Clin Vaccine Immunol       Date:  2012-12-19
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