Evidence map›Paper›PMID 42160378›Full record

ArticlePLoS pathogens2026

p1/s1, a 3'-nucleotidase/nuclease, allows Leishmania major to circumvent host innate immune response mechanisms.

Stella M Schmelzle, Michaela Bergmann, Bianca Walber, Jamal Shamsara, Tanja Ziesmann, Ute Distler, Csaba Miskey, Liam Childs, Peter Kolb, Stefan Tenzer and 2 more

Abstract read
In one paragraph

Article in PLoS pathogens, 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

12 authors.

Stella M SchmelzleDivision of Immunology, Paul-Ehrlich-Institut, Langen, Germany.
Michaela BergmannDivision of Immunology, Paul-Ehrlich-Institut, Langen, Germany.
Bianca WalberDivision of Immunology, Paul-Ehrlich-Institut, Langen, Germany.
Jamal ShamsaraInstitute for Pharmaceutical Chemistry, Philipps-Universität Marburg, Marburg, Germany.
Tanja ZiesmannInstitute for Immunology, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Ute DistlerInstitute for Immunology, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Csaba MiskeyDivision Haematology, Cell and Gene Therapy, Genomics Core Facility, Paul-Ehrlich-Institut, Langen, Germany.
Liam ChildsResearch Group Host-Pathogen Interactions, Paul-Ehrlich-Institut, Langen, Germany.
Peter KolbInstitute for Pharmaceutical Chemistry, Philipps-Universität Marburg, Marburg, Germany.
Stefan TenzerInstitute for Immunology, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Katrin BagolaDivision of Immunology, Paul-Ehrlich-Institut, Langen, Germany.
Ger van ZandbergenDivision of Immunology, Paul-Ehrlich-Institut, Langen, Germany.ORCID https://orcid.org/0000-0001-5218-4962

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

3'-nucleotidases/nucleases, distinct class I nucleases of protozoan parasites, play a pivotal role in extracellular purine salvage. As Leishmania are purine auxotrophs and lack de novo synthesis, ectoenzymes facilitating nucleotide and nucleic acid cleavage are indispensable for subsequent uptake. Employing quantitative proteomics, we characterized a class I nuclease p1/s1 cluster in L. major that comprises enzymes exhibiting dual 3'-nucleotidase and endonuclease activity. Expression of these enzymes is induced upon miltefosine or staurosporine treatment and was specifically detected in stationary-phase, but not in logarithmic-phase promastigotes. After confirming secretion of p1/s1, ecto-enzymatic activity was detected on parasites and in the culture supernatant. Viable null mutants deficient for the p1/s1 cluster were only obtained when a diCre-based inducible knockout system was applied, whereas direct deletion approaches were lethal. The viable knockout strains exhibited significantly reduced 3'-nucleotidase/nuclease activity. Notably, these parasites adapted by compensatory enrichment of various alternative purine salvage proteins at the proteomic level. Furthermore, both enzymatic functions implied mechanisms of host-pathogen interactions to facilitate infection establishment: Utilizing 3'-nucleotidase activity, Leishmania generate extracellular adenosine to suppress inflammatory cytokine secretion from macrophages and reduce lymphocyte proliferation in a human primary cell model. The presence of ecto-nucleases also allowed these parasites to degrade and survive neutrophil extracellular traps, a potent first-line innate immune mechanism in pathogen defense. In summary, our integrative approach combining proteomics, immunological and genome editing methods expands current knowledge about Leishmania major 3'-nucleotidases/nucleases. By offering new insights into the diverse involvements in host-pathogen interactions, we highlight p1/s1 as pivotal factor during infection and potential drug target.

Indexed as

Host-Parasite InteractionsImmune EvasionImmunity, InnateLeishmania majorLeishmaniasisNucleotidasesProtozoan ProteinsAnimalsHumans3'-nucleotidaseNucleotidasesProtozoan Proteins

Identifiers

PMID42160378
PMCPMC13232948

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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.