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Updated: Aug 21, 2026

Quantitative 3D Imaging of Trypanosoma cruzi-Infected Cells, Dormant Amastigotes, and T Cells in Intact Clarified Organs
Published on: June 23, 2022
Trypanosoma cruzi Cardiomyopathy Diagnosed via Explant Tissue 28S Ribosomal Gene Sequencing Following Orthotopic
Aneurin C Fernandez1, Gerald J Berry2, Ragini Ahanonu3
1Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, USA.
Insights
Diagnosing Chagas cardiomyopathy is difficult, but ribosomal gene sequencing of heart tissue successfully identified Trypanosoma cruzi in a challenging case. This advanced molecular technique aids in definitive diagnosis and post-transplant monitoring.
Area of Science:
- Cardiology
- Infectious Diseases
- Molecular Diagnostics
Background:
- Chagas disease, caused by Trypanosoma cruzi, is a significant cause of infectious cardiomyopathy.
- Diagnosing chronic Chagas cardiomyopathy is challenging due to low parasite load in cardiac tissue.
Abstract:
Trypanosoma cruzi, the protozoal agent responsible for Chagas disease, is a well-established cause of infectious cardiomyopathy. Diagnosing chronic Chagas cardiomyopathy can be exceptionally challenging due to the sparse presence of amastigotes in explanted cardiac tissue. We present a case of a 53-year-old male originally from Veracruz, Mexico, residing in the United States, who presented with rapidly progressive biventricular heart failure refractory to goal-directed medical therapy. The patient developed cardiogenic shock necessitating mechanical circulatory support and subsequent orthotopic heart transplantation. Histopathological evaluation of the explanted heart revealed end-stage dilated cardiomyopathy with mixed inflammatory infiltrates and poorly formed granulomas, but no visible amastigotes. Given the granulomatous pathology, a lab-developed 28S ribosomal gene sequencing assay was performed on the myocardial tissue, successfully identifying Trypanosoma cruzi. Subsequent recipient serological testing confirmed the diagnosis. Post-transplant molecular surveillance remained negative for parasitic reactivation under immunosuppression. This case highlights the critical utility of advanced molecular diagnostic techniques, such as tissue-based ribosomal gene sequencing, alongside traditional dual-methodology serology, to establish a definitive diagnosis of Chagas disease in atypical presentations and ensure appropriate post-transplant monitoring.

