Evidence map›Paper›PMID 42075749›Full record

ReviewPathogens (Basel, Switzerland)2026

Polyamines as Gatekeepers of Virus Replication and Central Nervous System Homeostasis.

Samantha P Stacey, Bryan C Mounce

Abstract readReview
In one paragraph

Review in Pathogens (Basel, Switzerland), 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.

Samantha P StaceyDepartment of Microbiology and Immunology, Loyola University Chicago, Maywood, IL 60153, USA.
Bryan C MounceDepartment of Microbiology and Immunology, Loyola University Chicago, Maywood, IL 60153, USA.ORCID 0000-0003-1710-5362

Funding

Uncovering and harnessing connected metabolic pathways essential to virus infection.R35GM138199 · NIGMS · LOYOLA UNIVERSITY CHICAGO · PI Bryan C Mounce · 2020 to 2026
$2.7M
NIGMS NIH HHS R35 GM138199NIGMS NIH HHS R35GM138199
6 · The paper itself

Abstract

Polyamines are small, positively charged molecules essential for fundamental cellular processes, including transcription, translation, and membrane fluidity. In the central nervous system (CNS), these molecules serve as homeostatic gatekeepers by modulating neuroreceptors like NMDA and supporting autophagic clearance. While basal polyamine levels are necessary for proper neuronal differentiation and memory formation, their dysregulation is a hallmark of neurodegenerative pathologies such as Alzheimer's and Parkinson's diseases. Neurotropic viruses, including poliovirus, Zika virus, and human cytomegalovirus are significant human pathogens that rely on cellular metabolites for their replication, including polyamines. These pathogens exploit polyamines at multiple stages of their life cycles, relying on them for virion stability, cellular attachment, and the stimulation of viral enzyme activity. Notably, diverse viral families share this dependence, making polyamine biosynthesis a prime target for broad-spectrum antiviral therapies. This review covers the current understanding of polyamine metabolism in virus infection and CNS health and disease, as well as considering antiviral therapies targeting host polyamines to limit neurotropic virus infection.

Indexed as

Central Nervous SystemHomeostasisPolyaminesVirus ReplicationAnimalsHumansPolyaminescentral nervous systemmetabolismneurotropic virusespolyamines

Identifiers

PMID42075749
PMCPMC13118667

What Socratic 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 Socratic graph.