# Infectivity of Aflagellar Epimastigotes of Trypanosoma caninum in the DH82 Cell Line and Mouse Peritoneal Macrophages

**Authors:** Kátia Cristina Silva Nascimento, Sandra Maria de Oliveira Souza, Aline Fagundes, Roger Magno Macedo Silva, Francisco Odencio Rodrigues de Oliveira Junior, Samanta Cristina das Chagas Xavier, Gilbert Q. Santos, Suzana Corte-Real, Juliana Helena da Silva Barros

PMC · DOI: 10.1155/japr/7057514 · 2025-03-07

## TL;DR

This study shows that aflagellar epimastigotes of Trypanosoma caninum can infect mouse macrophages and transform into amastigotes, offering new insights into the parasite's life cycle.

## Contribution

The study demonstrates for the first time that aflagellar epimastigotes of T. caninum can infect macrophages and transform into amastigotes.

## Key findings

- Aflagellar epimastigotes of T. caninum infect macrophages and transform into amastigotes.
- Amastigotes proliferate within parasitophorous vacuoles in macrophages within 15 minutes.
- Some parasites revert to the flagellar epimastigote form after 48 hours.

## Abstract

Background:
Trypanosoma caninum presents aflagellar and flagellar epimastigote, trypomastigote, and spheromastigote forms in axenic cultures. Attempts to utilize trypomastigote forms of T. caninum to develop in vitro and in vivo infection models have failed. To investigate the infection potential of aflagellar epimastigotes, T. caninum interaction studies were performed using DH82 cells and BALB/c mouse peritoneal macrophages in Dulbecco's modified Eagle medium (DMEM)/F-12 medium supplemented with fetal bovine serum and bovine serum albumin. Light-field microscopy, scanning electron microscopy, and transmission electron microscopy were used to analyze these interactions. Regarding T. caninum–macrophage interactions, the following previously unseen results were obtained: (1) the aflagellar epimastigote form of T. caninum infects macrophages, and (2) T. caninum epimastigotes transformed into amastigotes inside macrophages. Aflagellar epimastigotes were seen adhering to and entering macrophages and differentiating to the amastigote form; amastigotes proliferated within the parasitophorous vacuole in macrophages after 15 min. At the final time point (48 h), there were few macrophages arranged on the coverslips, but interacting with free amastigotes of T. caninum, while some of the parasites changed to the flagellar epimastigote form. Considering the lack of information on T. caninum and its importance in public health, this study provides new insights into the biological cycle of T. caninum and parasite–host relationships.

## Linked entities

- **Species:** Trypanosoma caninum (taxon 629700)

## Full-text entities

- **Diseases:** Aflagellar Epimastigotes of Trypanosoma caninum (MESH:D014355), infection (MESH:D007239)
- **Chemicals:** F-12 (MESH:C007782), DMEM (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Trypanosoma caninum (species) [taxon 629700]
- **Cell lines:** DH82 — Canis lupus familiaris (Dog), Canine histiocytic sarcoma, Cancer cell line (CVCL_2018), BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11991806/full.md

---
Source: https://tomesphere.com/paper/PMC11991806