Evidence map›Paper›PMID 42832601›Full record

ArticlePloS one2026

Characterization of the dual functions of Leishmania CK1.2 in both the parasite and the macrophage.

Daniel Martel, Olivier Leclercq, Florent Dingli, Victor Laigle, Nawal Hajj Sleiman, Damarys Loew, Gerald F Späth, Najma Rachidi

Abstract read
In one paragraph

Article in PloS one, 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

8 authors.

Daniel MartelInstitut Pasteur, Université Paris Cité and INSERM U1347, Groupe de signalisation et interactions hôte-parasite, Paris, France.
Olivier LeclercqInstitut Pasteur, Université Paris Cité and INSERM U1347, Groupe de signalisation et interactions hôte-parasite, Paris, France.
Florent DingliLaboratoire de Spectrométrie de Masse Protéomique (LSMP), Centre de Recherche, Institut Curie, PSL Research University, Paris, France.ORCID https://orcid.org/0000-0002-7715-2446
Victor LaigleLaboratoire de Spectrométrie de Masse Protéomique (LSMP), Centre de Recherche, Institut Curie, PSL Research University, Paris, France.ORCID https://orcid.org/0000-0001-5739-5742
Nawal Hajj SleimanInstitut Pasteur, Université Paris Cité and INSERM U1347, Groupe de signalisation et interactions hôte-parasite, Paris, France.ORCID https://orcid.org/0000-0002-0385-543X
Damarys LoewLaboratoire de Spectrométrie de Masse Protéomique (LSMP), Centre de Recherche, Institut Curie, PSL Research University, Paris, France.ORCID https://orcid.org/0000-0002-9111-8842
Gerald F SpäthInstitut Pasteur, Université Paris Cité and INSERM U1347, Unité de Parasitologie moléculaire et Signalisation, Paris, France.ORCID https://orcid.org/0000-0002-0256-2029
Najma RachidiInstitut Pasteur, Université Paris Cité and INSERM U1347, Groupe de signalisation et interactions hôte-parasite, Paris, France.ORCID https://orcid.org/0000-0002-1247-7768

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leishmania CK1.2 (L-CK1.2) is a serine/threonine protein kinase essential for the survival of the protozoan parasite Leishmania, the causative agent of leishmaniasis. This study investigates the dynamic localization pattern of L-CK1.2 and the broad spectrum of its interacting partners within the parasite. Using proteomic analysis and confocal microscopy, we identified 230 L-CK1.2-associated proteins across the major parasite life stages. This analysis revealed the ubiquitous presence of L-CK1.2 in various cellular structures, including the cytoskeleton, basal body, and flagellum. Using an in vitro system, sixty-four host proteins, involved in critical host biological processes such as immune response, apoptosis, and purine biosynthesis, were identified as potential interacting partners of L-CK1.2. These processes are known to be regulated by Leishmania during infection. The study highlights the potential dual function of L-CK1.2, in the parasite (cis) and within the host cell (trans), positioning this kinase as a key player in host-pathogen interactions. This work provides a comprehensive map of L-CK1.2 interactions and suggests its potential importance in regulating intracellular Leishmania survival, providing potential targets for leishmaniasis therapy. Furthermore, given the evolutionary conservation of CK1.2 across other parasitic organisms, our findings may have broader implications for understanding and managing parasitic infections.

Indexed as

LeishmaniaMacrophagesProtozoan ProteinsAnimalsHost-Parasite InteractionsHumansMiceProteomicsProtozoan Proteins

Identifiers

PMID42832601
PMCPMC13638044

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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.