Evidence map›Paper›PMID 42370689›Full record

ArticleJournal of clinical microbiology2026

Diagnostic value of HHV-6A/B genotyping in immunocompromised adults.

Virginia Rodríguez-Lorente, Paola Charry, Ares Guardia, Francesc Fernández-Avilés, Montserrat Rovira, María Queralt Salas, Carmen Martínez, Laura Rosiñol, Marta Bodro, Ana Belén Pérez and 6 more

Abstract read
In one paragraph

Article in Journal of clinical microbiology, 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

16 authors.

Virginia Rodríguez-LorenteMicrobiology Department, Hospital Clínic de Barcelona, Universitat de Barcelona, Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi Sunyer (FRCB-IDIBAPS), Barcelona, Spain.ORCID 0009-0008-7497-1041
Paola CharryHematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0000-0002-4777-9643
Ares GuardiaHematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.
Francesc Fernández-AvilésHematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0000-0002-3733-590X
Montserrat RoviraHematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.
María Queralt SalasHematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0000-0003-4567-3682
Carmen MartínezHematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0000-0002-8401-7306
Laura RosiñolHematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0000-0002-2534-9239
Marta BodroInfectious Diseases Department, Hospital Clínic de Barcelona, Universitat de Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0000-0002-0520-8279
Ana Belén PérezCentro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), CIBER-ISCIII, Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0001-9655-817X
Isabel MachucaCentro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), CIBER-ISCIII, Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0003-3343-0085
Ana CervillaMicrobiology Department, Hospital Clinic of Barcelona, Barcelona, Spain.
María Del Mar MosqueraMicrobiology Department, Hospital Clínic de Barcelona, Universitat de Barcelona, Instituto de Salud Global de Barcelona (ISGlobal), Barcelona, Spain.ORCID 0000-0001-5863-7424
Miguel J MartínezCentro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), CIBER-ISCIII, Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0002-0682-1075
María Suárez-Lledó *Hematology Department, Hospital Clínic de Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0009-0004-4573-0581
María Ángeles Marcos *Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), CIBER-ISCIII, Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0001-8250-3311

Funding

HHV-6 Foundation 501[c][3] EIN #20-1043981
6 · The paper itself

Abstract

Human herpesvirus 6 (HHV-6) comprises two genetically and biologically distinct species, HHV-6A and HHV-6B, yet species-level differentiation is rarely performed in clinical practice. We conducted a retrospective study of 119 immunocompromised adults with detectable HHV-6 DNA between 2020 and 2025 to characterize species distribution, compare epidemiological, clinical, and virological features, and evaluate the diagnostic relevance of genotyping. Viral species were detected by real-time polymerase chain reaction (PCR) across multiple sample types, and suspected chromosomal integration was confirmed through detection of endogenous HHV-6 (eHHV-6) DNA in hair follicles by quantitative real-time PCR. HHV-6B accounted for ~96% of infections and was significantly associated with organ involvement, predominantly gastrointestinal disease, irrespective of plasma viral load. In contrast, HHV-6A was less frequently detected in tissues and was consistently associated with viremia and chromosomal integration, independent of viral load. Genotypic concordance across plasma, biopsy, cerebrospinal fluid, bronchoalveolar lavage, and hair follicle samples from the same patient was complete. Incorporating species-level genotyping and targeted testing for chromosomal integration (eHHV-6) into diagnostic workflows may improve interpretation of viral detection and help prevent unnecessary antiviral therapy.IMPORTANCESpecies-specific identification of human herpesvirus 6 (HHV-6A/B) has critical diagnostic implications in immunocompromised patients, although it is rarely performed in diagnostic laboratories. Our study showed that HHV-6A detection is associated with chromosomal integration, whereas HHV-6B is the main species linked to clinically relevant disease and invasive tissue infection. This study emphasizes that implementing species-specific PCR and testing for eHHV-6 in clinical microbiology laboratories may help interpret viral DNA detection, prevent misclassification of integrated virus as active infection, and avoid unnecessary antiviral therapy.

Indexed as

GenotypeGenotyping TechniquesHerpesvirus 6, HumanImmunocompromised HostRoseolovirus InfectionsAdultAgedAged, 80 and overDNA, ViralFemaleHumansMaleMiddle AgedReal-Time Polymerase Chain ReactionRetrospective StudiesViral LoadDNA, ViralDNA genotypingendogenous human herpesvirus 6human herpesvirus 6Ahuman herpesvirus 6Breal-time PCR

Identifiers

PMID42370689
PMCPMC13463904

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.