# Protein undernutrition alters the colonic bacteriome, disrupts intestinal immune homeostasis, and impairs control of Leishmania infantum infection in a murine model of visceral leishmaniasis

**Authors:** Renata Azevedo, Monica Losada-Barragán, Erika M. Costa, Heidi Pauer, Cristiane Cassiolato Pires Hardoim, Filipe Lima, Nathalia Pinho, Jonathan Durães, Felipe Gaitán-Albarracín, Sergio Cuervo-Escobar, Sebastián Arcila-Barrera, Adriana Umaña-Pérez, Luis Caetano M. Antunes, Patricia Cuervo

PMC · DOI: 10.3389/fnut.2025.1733703 · Frontiers in Nutrition · 2026-01-30

## TL;DR

This study shows that protein undernutrition worsens visceral leishmaniasis by disrupting gut bacteria and immune responses in mice.

## Contribution

The study reveals how protein undernutrition alters gut microbiota and immune responses to increase Leishmania infantum infection severity.

## Key findings

- Protein undernutrition reduces Bacteroidota and increases Desulfobacterota and Firmicutes in the colon.
- Undernutrition increases parasite load in the spleen due to immune and microbial disruptions.
- Elevated secretory IgA suggests a compensatory response to gut dysbiosis in undernourished mice.

## Abstract

Undernutrition is a significant global health issue that exacerbates susceptibility to infectious diseases, including visceral leishmaniasis (VL), caused by Leishmania infantum. Here, we investigated the interplay between undernutrition, immune responses, and the colonic microbiota composition in a murine model of VL.

We used BALB/c mice subjected to a low-protein diet and infected with L. infantum to analyze the effects on systemic and local immune responses, microbiota composition, and parasite load.

Undernutrition significantly downregulated the mRNA expression of cytokines such as IFN-γ, IL-10, IL-12, and IL-17A in the colon while increasing the colonic luminal levels of proinflammatory cytokines, including TNF-α, CCL5, and IL-17A. The protein-deficient diet also induced dysbiosis, characterized by reduced Bacteroidota and increased Desulfobacterota and Firmicutes. Additionally, secretory IgA levels were markedly elevated in undernourished animals, suggesting a compensatory response to dysbiosis. The parasite load was significantly increased in the spleens of undernourished, infected mice, potentially due to disrupted immune-endocrine communication involving intestinal inflammation and microbial imbalance.

These findings highlight the complex interplay between nutritional status, the microbiota, and host immunity in the progression of VL. Undernutrition exacerbates disease severity through local and systemic immune dysregulation and microbial shifts. Our results support new treatments targeting diet and microbiota to control VL.

## Linked entities

- **Diseases:** visceral leishmaniasis (MONDO:0005445)

## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Ccl5 (C-C motif chemokine ligand 5) [NCBI Gene 20304] {aka MuRantes, RANTES, SISd, Scya5, TCP228}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Igha (immunoglobulin heavy constant alpha) [NCBI Gene 238447] {aka IgA, Igh-2}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}
- **Diseases:** intestinal inflammation (MESH:D007249), Undernutrition (MESH:D044342), Leishmania infantum infection (MESH:D007896), dysbiosis (MESH:D064806), VL (MESH:D007898), immune dysregulation (OMIM:614878), infectious diseases (MESH:D003141)
- **Species:** Leishmania infantum (species) [taxon 5671], Mus musculus (house mouse, species) [taxon 10090], Bacillota (clostridial firmicutes, phylum) [taxon 1239]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12900761/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12900761/full.md

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Source: https://tomesphere.com/paper/PMC12900761