Evidence map›Paper›PMID 42902299›Full record

ArticleVirology journal2026

Merkel cell polyomavirus DNA in CSF of paediatric patients with suspected meningitis or encephalitis.

Negar Hemmati, Fatemeh Hoda Fallah, Bahman Abedi Kiasari

Abstract read
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Article in Virology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Negar HemmatiDepartment of Microbiology and Immunology, University of Tehran, Tehran, Iran.
Fatemeh Hoda FallahValiasr Hospital, Imam Khomeini Hospital, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Bahman Abedi KiasariDepartment of Microbiology and Immunology, University of Tehran, Tehran, Iran. abedikiasari.b@ut.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe clinical significance of Merkel cell polyomavirus (MCPyV) in pediatric central nervous system (CNS) infections remains uncertain, particularly in immunocompromised children.

objectiveTo determine the frequency of MCPyV DNA in cerebrospinal fluid (CSF) from children with suspected viral meningitis or encephalitis and evaluate its association with HIV infection, CSF findings, and clinical outcomes.

methodsCSF samples from 46 pediatric patients with suspected viral CNS infection were analyzed using TaqMan probe-based quantitative PCR targeting the large T-antigen gene. Positive specimens were confirmed by amplification of an independent VP1 target and bidirectional Sanger sequencing following conventional PCR re-amplification. Clinical, laboratory, and outcome data were compared using appropriate statistical tests.

resultsMCPyV DNA was detected in 6/46 patients (13.0%), all of whom were HIV-positive (p = 0.001; sensitivity analysis excluding patients with unknown HIV status, p = 0.002). Four isolates belonged to genotype I and two to genotype IIc. Compared with MCPyV-negative patients, MCPyV-positive patients had higher CSF lymphocyte percentages (89% vs. 84%; p = 0.048), higher protein concentrations (79 vs. 68 mg/dL; p = 0.022), lower glucose concentrations (51 vs. 55 mg/dL; p = 0.038), and more frequent altered consciousness (83.3% vs. 37.5%; p = 0.039). EBV DNA co-detection was identified in one MCPyV-positive patient.

conclusionsMCPyV DNA was detected exclusively in HIV-positive children and was associated with inflammatory CSF abnormalities. These findings suggest a possible association between MCPyV detection, immunosuppression, and CNS inflammation but do not establish causality. Larger multicenter studies are required.

Indexed as

Cerebrospinal FluidDNA, ViralEncephalitis, ViralMeningitis, ViralMerkel cell polyomavirusPolyomavirus InfectionsAdolescentChildChild, PreschoolFemaleGenotypeHIV InfectionsHumansInfantMaleDNA, ViralCSFEncephalitisHuman polyomavirusMeningitisMerkel cell polyomavirus (MCPyV)PCR

Identifiers

PMID42902299
PMCPMC13685387

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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.