Evidence map›Paper›PMID 41092742›Full record

ArticlePlacenta2025

Pan-viral metagenomic sequencing demonstrates that cryptic viral infection is rarely observed in villitis of unknown etiology.

Andrew P Norgan, Qandeel Sadiq, Bohdana Fedyshyn, Matthew J Wolf, Elizabeth Ann L Enninga

Abstract read
In one paragraph

Article in Placenta, 2025. 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

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Andrew P NorganDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA. Electronic address: norgan.andrew@mayo.edu.
Qandeel SadiqDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Bohdana FedyshynDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN, USA.
Matthew J WolfDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Elizabeth Ann L EnningaDepartment of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN, USA; Department of Immunology, Mayo Clinic, Rochester, MN, USA. Electronic address: enninga.elizabethann@mayo.edu.

Funding

Defining T cell-placenta immune mechanisms in chronic villitisR56AI177472 · NIAID · MAYO CLINIC ROCHESTER · PI ENNINGA, ELIZABETH ANN LIESER · 2024 to 2024
$326k
NIAID NIH HHS R56 AI177472
6 · The paper itself

Abstract

introductionAberrant maternal immune responses are implicated in villitis of unknown etiology (VUE), but the underlying cause of this loss of tolerance, including cryptic causative or precipitating infections, has been difficult to define. Herein, we performed pan-viral metagenomic sequencing of placentas with VUE to investigate the possibility of cryptic viral infection as a contributing factor in this inflammatory pathology.

methodsPlacentas evaluated at a single tertiary medical center between 2010 and 2024 were included in this study. Overall, the cohort included infectious villitis due to cytomegalovirus (CMV; n = 4), VUE (n = 25), and a reference group composed of pathologically unremarkable placentas (n = 17). Total nucleic acid was extracted from formalin-fixed paraffin embedded (FFPE) placental tissues and subjected to pan-viral metagenomic sequencing (PVMS) to identify viral-associated reads.

resultsPVMS detected reads mapping to CMV in 4 (of 4) of CMV cases. For VUE cases, 22 (of 25) had no identifiable viral reads, while 1 case demonstrated CMV reads and two had papillomavirus reads. The control samples demonstrated no identifiable reads in 13 (of 17) samples, while 3 cases had reads mapping to human papillomavirus 16 and one case had reads mapping to human Herpesvirus 6. DISCUSSION: Utilizing PVMS, we did not identify cryptic viral sequences in 88 % of morphologic VUE cases. In one clinical VUE case, CMV sequences were identified, suggesting a misclassification of infectious villitis. Both papillomavirus and herpesvirus sequences have previously been identified in the placenta, with unknown clinical significance. Overall, these findings exclude active viral infection as a potential etiology of VUE.

Indexed as

Chorionic VilliCytomegalovirus InfectionsPlacenta DiseasesPregnancy Complications, InfectiousVirus DiseasesAdultCytomegalovirusFemaleHumansMetagenomicsPlacentaPregnancyInfectionInflammationMetagenomicsPlacentaVillitisVirus

Identifiers

PMID41092742
PMCPMC12628840

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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.