# TLR4 competence and mouse models of sublethal leptospirosis

**Authors:** Olifan Zewdie Abil, Suman Kundu, Leonardo Moura Midon, Maria Gomes-Solecki, Joseph Vinetz, Joseph Vinetz, Joseph Vinetz

PMC · DOI: 10.1371/journal.pntd.0013163 · PLOS Neglected Tropical Diseases · 2025-05-30

## TL;DR

This study compares mouse models of leptospirosis and finds that TLR4 function does not determine susceptibility to the disease.

## Contribution

The study demonstrates that TLR4 competence is not sufficient to cause susceptibility to sublethal leptospirosis in mice.

## Key findings

- TLR4 competent strains showed similar clinical and molecular signs of leptospirosis as hyporesponsive strains.
- Serologic immune factors showed increased IgM and IgG3 with no significant inflammatory markers.
- C3H/HeN and C57BL/6 are suitable models for sublethal leptospirosis.

## Abstract

Mice are slowly being accepted as alternative models for investigation of leptospiral infection. The strain often used to analyze sublethal disease (C3H/HeJ) expresses a hyporesponsive tlr4 gene in its cells and thus the model is deemed immunocompromised. To help resolve this scientific concern we compared infection of mice expressing competent tlr4 (C3H/HeN, C57BL6) versus tlr4 hyporesponsive mice (C3H/HeJ) with Leptospira interrogans serovar Copenhageni strain Fiocruz L1-130 over a period of two weeks. We found that the two mouse strains with a functional tlr4 gene (C3H/HeN and C57BL/6) developed clinical and molecular signs of leptospirosis less pronounced but not significantly different than tlr4 hyporesponsive C3H/HeJ, as quantified by weight loss, survival curves, presence of Leptospira 16S rRNA in blood and urine and burden of viable spirochetes in kidney as compared to the respective uninfected controls. Analysis of serologic immune factors in the three strains revealed increased IgM and IgG3, and a general absence of inflammatory markers at two weeks post infection. Our data suggests that TLR4 function is not sufficient to cause susceptibility to leptospirosis. We conclude that C3H/HeN and C57BL/6 are appropriate mouse models of sublethal leptospirosis.

We did a comparative study using mouse strains immunocompetent and hyporesponsive to tlr4. The data shows that tlr4 competent strains (C3H/HeN and C57BL/6) developed clinical and molecular signs of sublethal leptospirosis not much different than tlr4 hyporesponsive C3H/HeJ. Thus, competent recognition of L. interrogans serovar Copenhageni FioCruz factors by murine TLR4 does not determine susceptibility to leptospirosis.

## Linked entities

- **Genes:** TLR4 (toll like receptor 4) [NCBI Gene 7099]
- **Diseases:** leptospirosis (MONDO:0005825)
- **Species:** Mus musculus (taxon 10090), Leptospira interrogans (taxon 173)

## Full-text entities

- **Genes:** Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}
- **Diseases:** infection (MESH:D007239), inflammatory (MESH:D007249), leptospirosis (MESH:D007922), weight loss (MESH:D015431)
- **Species:** Leptospira interrogans serovar Copenhageni (no rank) [taxon 44275], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12151470/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12151470/full.md

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Source: https://tomesphere.com/paper/PMC12151470