Evidence map›Paper›PMID 40445994›Full record

ArticlePLoS neglected tropical diseases2025

TLR4 competence and mouse models of sublethal leptospirosis.

Olifan Zewdie Abil, Suman Kundu, Leonardo Moura Midon, Maria Gomes-Solecki

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Olifan Zewdie AbilDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, United States of America.ORCID 0000-0001-8886-9760
Suman KunduDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, United States of America.
Leonardo Moura MidonDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, United States of America.
Maria Gomes-SoleckiDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, United States of America.ORCID 0000-0002-3715-4543

Funding

Intranasal Vaccine Against Lyme DiseaseR44AI167605 · NIAID · IMMUNO TECHNOLOGIES, INC. · PI GOMES-SOLECKI, MARIA · 2022 to 2024
$3.0M
ImmunoPET Probes for the Imaging of Lyme DiseaseR01AI175417 · NIAID · HUNTER COLLEGE · PI Maria Gomes-Solecki, WEIGANG QIU · 2023 to 2026
$2.2M
Role of TLR4 in persistent Leptospira infectionR21AI142129 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI GOMES-SOLECKI, MARIA · 2019 to 2020
$418k
NIAID NIH HHS R01 AI175417NIAID NIH HHS R21 AI142129NIAID NIH HHS R44 AI167605
6 · The paper itself

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.

Indexed as

Disease Models, AnimalLeptospira interrogansLeptospirosisToll-Like Receptor 4AnimalsAntibodies, BacterialFemaleImmunoglobulin MKidneyMaleMiceMice, Inbred C3HMice, Inbred C57BLRNA, Ribosomal, 16SAntibodies, BacterialImmunoglobulin MRNA, Ribosomal, 16STlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID40445994
PMCPMC12151470

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.