Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-24T11:22:29.800Z Has data issue: false hasContentIssue false
  • English
  • Français

Variation of transient gene expression within single lineages of Trypanosoma cruzi

Published online by Cambridge University Press:  16 October 2009

J.-P. LAURENT  and
J. SWINDLE
J.-P. LAURENT
Affiliation:
Seattle Biomedical Research Institute, 4 Nickerson Street no. 200, Seattle, WA 98109-1631, USA
J. SWINDLE
Affiliation:
Seattle Biomedical Research Institute, 4 Nickerson Street no. 200, Seattle, WA 98109-1631, USA
Get access Rights & Permissions [Opens in a new window]

Abstract

The biodiversity of Trypanosoma cruzi is one of the main factors complicating the understanding of its molecular epidemiology. As an alternative to classical genetic methods, investigators have used DNA-mediated transformation techniques to study this diversity. Recently, transient expression data were shown to correlate with the genetic data. This led investigators to speculate on a potential speciation within clonal populations of Trypanosoma cruzi. To further test the phylogenetic significance of transient expression analysis in Trypanosoma cruzi, multiple plasmids were used to drive the expression of a reporter gene in different parasite populations. In our study, population specific expression of the reporter gene was observed but the variability revealed by these transient expression assays was very large and did not follow the grouping of Trypanosoma cruzi populations in 2 lineages. In this report, we discuss some of the limitations of transient assays on such a diverse parasite.

Keywords

Trypanosoma cruziphylogenytransfectionchloramphenicol acetyl transferase genecalmodulin–ubiquitin associated gene (CUB)Chagas' disease
Type
Research Article
Information
Parasitology , Volume 119 , Issue 6 , December 1999 , pp. 583 - 589
Copyright
© 1999 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)