Evidence map›Paper›PMID 42751294›Full record

ArticleOpen forum infectious diseases2026

Genomic Surveillance Uncovers a Shift in Respiratory Syncytial Virus Subtype Dominance and the Local Expansion of Subclade B.D.E.1.7.

Emily LaVerriere, Sasha Behar, Yan Mei Liang, Marisa Nielsen, Manish Sagar, John H Connor

Abstract read
In one paragraph

Article in Open forum infectious diseases, 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

6 authors.

Emily LaVerriereDepartment of Virology, Immunology and Microbiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-4750-4199
Sasha BeharDepartment of Virology, Immunology and Microbiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID https://orcid.org/0009-0005-8883-7327
Yan Mei LiangDepartment of Virology, Immunology and Microbiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Marisa NielsenDepartment of Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-7434-9721
Manish SagarDepartment of Virology, Immunology and Microbiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-9803-6594
John H ConnorDepartment of Virology, Immunology and Microbiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-8867-7256

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Respiratory syncytial virus (RSV) is a leading cause of hospitalization among children under 5 and adults over 60 due to its ability to cause acute respiratory illness. Recent approvals of vaccines and monoclonal antibodies against RSV have raised concerns about the potential of prophylactic-evading viral mutations. Method: We analyzed 126 RSV-positive nasopharyngeal swabs from Boston Medical Center during the 2024-2025 respiratory season via amplicon-based whole-genome sequencing. We identified nucleotide variants, assigned clades, and built maximum-likelihood phylogenetic trees to examine genetic changes and evolution. Results: Out of the 126 genomes analyzed, 94 (74.6%) were RSV-A subtype, indicating a return to RSV-A dominance in the region. Within the RSV-B genomes, a large minority belong to the recently defined B.D.E.1.7 subclade (n = 12, 37.5% of RSV-B samples), which has only appeared sporadically in other US states. Mutations associated with monoclonal antibody or vaccine resistance were not observed. Conclusions: These findings show that in the Boston metropolitan area, RSV subtype dominance continues to flip between seasons. Investigation of the clades within both subtypes did not reveal evidence of any virus seeding from the preceding season. Though no mutations associated with prophylactic resistance were identified, surveillance of RSV remains critical to study evolution and transmission dynamics, particularly at the local level.

Indexed as

BostongenomicsMassachusettsmolecular epidemiologyphylogenetic analysisrespiratory syncytial virusrespiratory syncytial virusesrespiratory syncytial virus infectionsviruses

Identifiers

PMID42751294
PMCPMC13579484

What Socratic 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 Socratic graph.