The impact of probiotic administration on experimental in vitro and in vivo infection by Trypanosoma cruzi.
- 2025
- Memorias do Instituto Oswaldo Cruz 120
- PubMed: 41124405
- DOI: 10.1590/0074-02760240272
Study Design
- Population
- mouse acute experimental models; peritoneal mouse macrophages (PMM) obtained from mice treated with 10^9 probiotics
- Methods
- The multi strain - PB8 and the Lactobacillus rhamnosus (LR) were orally administered [10^6-10^9 colony-forming units (CFU)] for seven days prior to mice infection followed for 14 daily administrations. Peritoneal mouse macrophages (PMM) were obtained from mice treated with 10^9 probiotics one day before collection and infected in vitro with or not benznidazole (BZ).
- Animal Study
Background
Chagas disease (CD) caused by Trypanosoma cruzi has limited therapy. Probiotics sustain healthy microbiota, playing roles in biological events.Objectives
Our aim was to determine the impact of probiotics on T. cruzi infection in vitro and in mouse acute experimental models.Methods
The multi strain - PB8 and the Lactobacillus rhamnosus (LR) were orally administered [106-109 colony-forming units (CFU)] for seven days prior to mice infection followed for 14 daily administrations. Peritoneal mouse macrophages (PMM) were obtained from mice treated with 109 probiotics one day before collection and infected in vitro with or not benznidazole (BZ).Findings
LR and PB8 reduced by 44-87% and 23-16% the parasitaemia peak in male and female mice, respectively, but did not protect against mortality. Histopathology showed mild reduction in cardiac nests due to probiotics' administration. PB8 and LR suppressed the parasite infection of PMM by 24 and 26%, reaching 65 and 42% of declines, respectively when 3% thioglycolate was performed. PB8 increased BZ activity at 1 µM, reaching 40% of parasitism' declines compared to BZ alone (25%). No gender difference was noticed during probiotic in vivo administration.Main conclusions
The results point to the potential of a combined therapeutic approach for CD, using probiotics and BZ.Research Insights
| Supplement | Dose | Health Outcome | Effect Type | Effect Size | Source |
|---|---|---|---|---|---|
| Bifidobacterium bifidum BB-06 | — | Improved Benznidazole Antiparasitic Activity | Beneficial | Small | View source"PB8 increased BZ activity at 1 µM, reaching 40% of parasitism' declines compared to BZ alone (25%)." |
| Bifidobacterium bifidum BB-06 | — | Reduced Parasite Infection in Peritoneal Mouse Macrophages | Beneficial | Small | View source"PB8 and LR suppressed the parasite infection of PMM by 24 and 26%" |
| Bifidobacterium bifidum BB-06 | — | Reduced Trypanosoma cruzi Parasitaemia | Beneficial | Moderate | View source"LR and PB8 reduced by 44-87% and 23-16% the parasitaemia peak in male and female mice, respectively" |
| Lactobacillus rhamnosus Lr-32 | — | Improved Benznidazole Antiparasitic Activity | Beneficial | Small | View source"PB8 increased BZ activity at 1 µM, reaching 40% of parasitism' declines compared to BZ alone (25%)." |
| Lactobacillus rhamnosus Lr-32 | — | Reduced Cardiac Parasite Burden | Beneficial | Small | View sourceHistopathology showed mild reduction in cardiac nests due to probiotics' administration. |
| Lactobacillus rhamnosus Lr-32 | — | Reduced Parasite Infection in Peritoneal Mouse Macrophages | Beneficial | Small | View source"PB8 and LR suppressed the parasite infection of PMM by 24 and 26%" |
| Lactobacillus rhamnosus Lr-32 | — | Reduced Trypanosoma cruzi Parasitaemia | Beneficial | Moderate | View source"LR and PB8 reduced by 44-87% and 23-16% the parasitaemia peak in male and female mice, respectively" |