Evidence map›Paper›PMID 32459815›Full record

ArticlePLoS pathogens2020

Inhibition of the NAD salvage pathway in schistosomes impairs metabolism, reproduction, and parasite survival.

Michael D Schultz, Tulin Dadali, Sylvain A Jacques, Hélène Muller-Steffner, Jeremy B Foote, Leonardo Sorci, Esther Kellenberger, Davide Botta, Frances E Lund

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 26% of its field
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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Schistosoma mansoni and the purinergic halo.Trends in parasitology · 2022
    Review
  5. NADSignal transduction and targeted therapy · 2020
    Review
  6. Review
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

9 authors at 3 institutions in 3 countries.

Michael D SchultzDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Tulin DadaliDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Sylvain A JacquesLaboratoire d'Innovation Thérapeutique, LIT UMR 7200 CNRS-Université de Strasbourg, MEDALIS Drug Discovery Center, Faculté de Pharmacie, Illkirch, France.
Hélène Muller-SteffnerLaboratoire des Systèmes Chimiques Fonctionnels, CAMB UMR 7199 CNRS-Université de Strasbourg, MEDALIS Drug Discovery Center, Faculté de Pharmacie, Illkirch, France.
Jeremy B FooteDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Leonardo SorciDepartment of Materials, Environmental Sciences and Urban Planning, Division of Bioinformatics and Biochemistry, Polytechnic University of Marche, Ancona, Italy.ORCID 0000-0002-4356-8873
Esther KellenbergerLaboratoire d'Innovation Thérapeutique, LIT UMR 7200 CNRS-Université de Strasbourg, MEDALIS Drug Discovery Center, Faculté de Pharmacie, Illkirch, France.ORCID 0000-0002-9320-4840
Davide BottaDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID 0000-0003-3926-0662
Frances E LundDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID 0000-0003-3083-1246
University of Alabama at Birmingham · USCentre National de la Recherche Scientifique · FRMarche Polytechnic University · IT

Funding

IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
NIAID NIH HHS HHSN272201700014CNIAID NIH HHS T32 AI007051
6 · The paper itself

Abstract

NAD, a key co-enzyme required for cell metabolism, is synthesized via two pathways in most organisms. Since schistosomes apparently lack enzymes required for de novo NAD biosynthesis, we evaluated whether these parasites, which infect >200 million people worldwide, maintain NAD homeostasis via the NAD salvage biosynthetic pathway. We found that intracellular NAD levels decline in schistosomes treated with drugs that block production of nicotinamide or nicotinamide mononucleotide-known NAD precursors in the non-deamidating salvage pathway. Moreover, in vitro inhibition of the NAD salvage pathway in schistosomes impaired egg production, disrupted the outer membranes of both immature and mature parasites and caused loss of mobility and death. Inhibiting the NAD salvage pathway in schistosome-infected mice significantly decreased NAD levels in adult parasites, which correlated with reduced egg production, fewer liver granulomas and parasite death. Thus, schistosomes, unlike their mammalian hosts, appear limited to one metabolic pathway to maintain NAD-dependent metabolic processes.

Indexed as

AnimalsFemaleHost-Parasite InteractionsMiceNADReproductionSchistosoma mansoniSchistosomiasis mansoniNAD

Identifiers

PMID32459815
PMCPMC7252647
OpenAlexW3028723143

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.