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Differential gene expression of virulence factors modulates infectivity of TcI Trypanosoma cruzi strains

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Abstract

Trypanosoma cruzi is the etiological agent of Chagas disease, whose clinical outcome ranges from asymptomatic individuals to chronic fatal megasyndromes. Despite being central to pathogenesis, the regulation of parasite virulence factors’ expression remains largely unknown. In this work, the relative expression of several parasite virulence factors between two TcI strains (Ninoa, low virulence and Qro, high virulence) was assessed by qRT-PCR of total and of polysome-associated mRNA, as well as by western blots. Trypomastigotes were also incubated with specific anti-sense morpholino oligonucleotides to block the translation of a selected virulence factor, calreticulin, in both strains. Ninoa trypomastigotes showed significantly lower levels of trypomastigote-decay acceleration factor, complement regulatory protein, complement C2 receptor inhibitor trispanning, and glycoproteins 82 and 90 mRNAs compared with Qro. There was a significantly lower recruitment of complement regulatory protein and complement C2 receptor inhibitor trispanning mRNAs to polysomes and higher recruitment of MASP mRNA to monosomes in Ninoa strain. Calreticulin mRNA displayed both a higher total mRNA level and recruitment to translationally active polysomes in the Ninoa strain (low virulence) than in the Qro strain (high virulence). When calreticulin was downregulated by ≈ 50% by anti-sense morpholino oligonucleotides, a significant decrease of parasite invasion in mammalian cells was found in both strains. Calreticulin downregulation, however, only increased significantly the activation of the complement system by Ninoa trypomastigotes. These results suggest a role for the regulation of virulence factors’ gene expression in the differential virulence among T. cruzi strains. Furthermore, a possible function of calreticulin in parasite invasion not related to its binding to complement factors is shown.

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Acknowledgments

We thank Mayra Cruz-Rivera for her kind donation of TsCRT antibody. We also thank Dr. Alberto Pizaña for his generous guinea pig donations.

Funding

Funding was provided by grant PAPIIT IN208417 from DGAPA, Universidad Nacional Autónoma de México.

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Correspondence to Bertha Espinoza.

Ethics declarations

All animals utilized for this project were anesthetized and sacrificed in accordance with the norm issued by the National Autonomous University of Mexico in their Animal Care guidelines (http://www.biomedicas.unam.mx/wp-content/pdf/intranet/reglamentos/codigo-etico-iibo.pdf?x21431) and the official Mexican standard NOM-062-ZOO-1999. This project was approved by the Committee for the Care and Use of laboratory animals (Instituto de Investigaciones Biomedicas, Universidad Nacional Autonoma de Mexico).

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The authors declare that they have no conflict of interest.

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Section Editor: Panagiotis Karanis

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Arroyo-Olarte, R.D., Martínez, I., Lujan, E. et al. Differential gene expression of virulence factors modulates infectivity of TcI Trypanosoma cruzi strains. Parasitol Res 119, 3803–3815 (2020). https://doi.org/10.1007/s00436-020-06891-1

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  • DOI: https://doi.org/10.1007/s00436-020-06891-1

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