Evidence map›Paper›PMID 42432696›Full record

ArticleGenome medicine2026

Metagenomic analysis of blood virome in ischemic stroke reveals an increase in herpesvirus transcripts and host immune activation.

Michael D Clarke, Sarina Falcione, Roobina Boghozian, Raluca Todoran, Yiran Zhang, Maria Guadalupe C Real, Alexis StPierre, Twinkle Joy, Glen C Jickling

Abstract read
In one paragraph

Article in Genome medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Michael D ClarkeFaculty of Medicine and Dentistry, Department of Medical Microbiology and Immunology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada. mdclarke@ualberta.ca.ORCID http://orcid.org/0000-0003-1901-8035
Sarina FalcioneFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.
Roobina BoghozianFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.
Raluca TodoranFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.
Yiran ZhangFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.
Maria Guadalupe C RealFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.
Alexis StPierreFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.
Twinkle JoyFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.
Glen C JicklingFaculty of Medicine and Dentistry, Department of Medicine, Division of Neurology, University of Alberta, 87 Ave 114 St., Edmonton, AB, T6G 2J7, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundViral infections may influence stroke pathophysiology. Several infections have been linked to increased risk of stroke, however our understanding of these viral interactions with immune and host tissue is limited. We performed a transcriptomic analysis of the blood virome following ischemic stroke to study these interactions.

methodsViruses were measured by RNA sequencing of blood from 37 patients with ischemic stroke and 32 matched controls. RNA reads are aligned against a human reference genome, as well as a comprehensive database of human virus genomes. Host gene expression following stroke is examined in relation to the presence of viral transcripts.

resultsViral RNAs were detected in the blood samples of both ischemic stroke and control groups. Viral reads with a prevalence > 3% and raw counts > 2 were from a total of 6 viral families. This included several human herpesviruses (HHVs), adenoviruses, and papillomaviruses, as well as human pegivirus, respiratory syncytial virus, and human endogenous retrovirus K (HERV-K). Combined, counts from HHVs were higher in stroke compared to control by a fold change of 2.13. Coinfection with multiple HHVs was more common in stroke, with a 1.23 fold increase in the number of detected herpesviruses. Reads from two viral genes were increased in stroke, UL95 from cytomegalovirus (CMV), and EBNA2 from Epstein-Barr virus (EBV). Genes associated with stroke, including APOE, C3, PDGF, and CXCL2 were differentially expressed in stroke samples which contained high counts of one or both of UL95 and EBNA2.

conclusionViral RNAs from multiple families can be detected within the human blood virome. HHV transcripts were the most abundant of viral RNAs detected. Among stroke patients, HHV transcripts were more prevalent, with higher counts, and indicated a higher rate of coinfection with multiple HHV species. Expression of the EBV gene EBNA2 and the CMV gene UL95 may relate to changes in immune gene expression following stroke. Further evaluation is needed to determine the effects that the human virome have on stroke risk, immune response to stroke, and long-term outcome.

Indexed as

HerpesviridaeIschemic StrokeMetagenomicsStrokeViromeAgedFemaleHost-Pathogen InteractionsHumansMaleMiddle AgedRNA, ViralRNA, ViralCytomegalovirusEpstein-Barr VirusIschemic StrokeNeuroinflammationVirome

Identifiers

PMID42432696
PMCPMC13644114

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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.