Abstract

Trypanosoma cruzi has a complex life cycle comprising pools of cell populations which circulate among humans, vectors, sylvatic reservoirs and domestic animals. Recent experimental evidence has demonstrated the importance of clonal variations for parasite population dynamics, survival and evolution. By limiting dilution assays, we have isolated seven isogenic clonal cell lines derived from the Pan4 strain of T. cruzi. Applying different molecular techniques, we have been able to provide a comprehensive characterization of the expression heterogeneity in the mucin-associated surface protein (MASP) gene family, where all the clonal isogenic populations were transcriptionally different. Hierarchical cluster analysis and sequence comparison among different MASP cDNA libraries showed that, despite the great variability in MASP expression, some members of the transcriptome (including MASP pseudogenes) are conserved, not only in the life-cycle stages but also among different strains of T. cruzi. Finally, other important aspects for the parasite, such as growth, spontaneous metacyclogenesis or excretion of different catabolites, were also compared among the clones, demonstrating that T. cruzi populations of cells are also phenotypically heterogeneous. Although the evolutionary strategy that sustains the MASP expression polymorphism remains unknown, we suggest that MASP clonal variability and phenotypic heterogeneities found in this study might provide an advantage, allowing a rapid response to environmental pressure or changes during the life cycle of T. cruzi.

Highlights

  • Trypanosoma cruzi is a flagellate protozoan parasite belonging to the order Kinetoplastidae and is the aetiological agent of Chagas’ disease, a major public health problem in Central and South America

  • We amplified, cloned and analysed the sequences obtained of 15 MASPgenes belonging to the three mentioned strains

  • We obtained a total of 50 unique sequences with 49 mucin-associated surface protein (MASP) sequences, 37 genes (75.5%) and 12 pseudogenes (24.5%), plus a gene sequence codifying for a hypothetical protein

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Summary

Introduction

Trypanosoma cruzi is a flagellate protozoan parasite belonging to the order Kinetoplastidae and is the aetiological agent of Chagas’ disease, a major public health problem in Central and South America. Currently there are more than 8 million people infected with approximately 25 million people at risk of acquiring the disease, making it a significant problem for global public health worldwide with an estimated annual burden of $627.46 million in healthcare costs and 806 170 DALYs (disability-adjusted life years) [8,9,10] This flagellate needs a mammalian host and an insect vector to complete its life cycle. After approximately 8–15 days, the epimastigote forms develop into metacyclic trypomastigotes in the rectum of the triatomine These metacyclic forms, which are not replicative, are transmitted during the insect blood meal with the faeces and urine infecting mammalian host cells through the bite wound or the surrounding mucosal membranes.

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