Evidence map›Paper›PMID 42223211›Full record

ArticleVirulence2026

Do BKPyV genomic features underlie clinical divergence between kidney and hematopoietic transplant recipients?

Aurélien Aubry, Baptiste Demey, Virginie Morel, Véronique Descamps, Ophélie Fourdinier, Maud Salmona, Louison Collet, François Helle, Etienne Brochot

Abstract read
In one paragraph

Article in Virulence, 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.

Aurélien AubryVirology Department, Centre Hospitalier Universitaire Amiens-Picardie, Amiens, France.ORCID 0009-0007-0842-5723
Baptiste DemeyVirology Department, Centre Hospitalier Universitaire Amiens-Picardie, Amiens, France.ORCID 0000-0002-5456-6654
Virginie MorelVirology Department, Centre Hospitalier Universitaire Amiens-Picardie, Amiens, France.ORCID 0000-0003-2406-5223
Véronique DescampsVirology Department, Centre Hospitalier Universitaire Amiens-Picardie, Amiens, France.ORCID 0009-0001-0310-4150
Ophélie FourdinierInfectious Agents, Resistance and Chemotherapy Research Unit, AGIR UR4294 Université de Picardie Jules Verne, Amiens, France.ORCID 0009-0008-5085-2785
Maud SalmonaVirology Department, Hopital Saint-Louis, Paris, France.ORCID 0000-0001-7985-6132
Louison ColletInfectious Agents, Resistance and Chemotherapy Research Unit, AGIR UR4294 Université de Picardie Jules Verne, Amiens, France.
François HelleInfectious Agents, Resistance and Chemotherapy Research Unit, AGIR UR4294 Université de Picardie Jules Verne, Amiens, France.ORCID 0000-0001-6884-2456
Etienne BrochotVirology Department, Centre Hospitalier Universitaire Amiens-Picardie, Amiens, France.ORCID 0000-0002-8677-6349

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BK polyomavirus (BKPyV) persists in the renourinary tract of most adults and can replicate under immunosuppression. In kidney transplant recipients (KTR), it may cause BKPyV-associated nephropathy (BKPyVAN), while in hematopoietic stem cell transplant recipients (HSCT), it is more often linked to hemorrhagic cystitis (HC). These clinical differences are generally attributed to the type of graft and immunosuppressive regimen. However, viral factors such as genotype or mutations might also influence tissue tropism and pathogenesis. This study aimed to compare the virological features of BKPyV between KTR and HSCT recipients and to explore possible associations with clinical manifestations. This retrospective study included 101 transplanted patients (66 KTR, 35 HSCT) at Amiens-Picardie University Hospital (France) between 2019 and 2023, with at least one episode of BKPyV DNAuria during post-allograft follow-up. Viral genotyping was performed by Sanger sequencing, while NGS (Next-generation Sequencing) provided complete coding genome sequences for 51 patients. Genotype distribution was similar in both groups, with Ib2 as the most frequent subtype. No genotype or mutation was associated with a specific graft type or complication, except for the small t antigen gene, which appeared to be more frequently mutated in KTRs. Viral replication occurred earlier and at higher levels in HSCT patients (mean peak DNAuria: 9.3 log

Indexed as

BK VirusGenome, ViralHematopoietic Stem Cell TransplantationKidney TransplantationPolyomavirus InfectionsTransplant RecipientsTumor Virus InfectionsAdultAgedCystitis, HemorrhagicFemaleFranceGenotypeHumansKidney DiseasesMaleBK polyomavirushematopoietic stem cell transplantationhemorrhagic cystitiskidney transplantationnephropathywhole genome sequencing

Identifiers

PMID42223211
PMCPMC13228933

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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.