Evidence map›Paper›PMID 42681496›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

In Vivo Imaging of Bioluminescent Leptospires.

Frédérique Vernel-Pauillac, Catherine Werts

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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Frédérique Vernel-PauillacInstitut Pasteur, Biology and Genetic of the Bacterial Cell Wall Unit, Innate Immunity & Leptospira Group, Paris, France.
Catherine WertsInstitut Pasteur, Biology and Genetic of the Bacterial Cell Wall Unit, Innate Immunity & Leptospira Group, Paris, France. catherine.werts@pasteur.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study of pathological processes is often limited to in vitro or ex vivo assays, while understanding pathogenesis of an infectious disease requires in vivo analysis. The use of pathogens, genetically modified to express with luminescent enzymes, combined to charge coupled device (CCD) cameras constitutes a major technological advance for assessing the course of infection in an intact, living host in real time and in a non-invasive way. This technology, also called bioluminescence imaging, detects the photons emitted from biological sources of light through animal tissues. Here, we describe the method we developed to monitor leptospirosis in a mouse model, by following in a spatiotemporal scale, the dissemination and spread of leptospires. These bacteria have been genetically modified to express the firefly luciferase, which produces light in the presence of the substrate D-luciferin. This useful and accessible technology facilitates the study of the kinetics of blood and tissue dissemination of live leptospires, and the pharmacological impact of treatments and host-directed therapeutics.

Indexed as

LeptospiraLeptospirosisLuminescent MeasurementsAnimalsBenzothiazolesDisease Models, AnimalLuciferases, FireflyMiceBenzothiazolesD-luciferinLuciferases, FireflyBacterial disseminationBioluminescenceIn vivo live imagingIn vivo therapeutic monitoringLeptospiresLuciferaseSpaciotemporal kinetics

Identifiers

What OpenQuestion holds

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Registered trials

None linked

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.