Evidence map›Paper›PMID 41633490›Full record

ArticleThe Journal of allergy and clinical immunology2026

Nasal microbiome and phageome profiles are associated with prospective respiratory viral infection risk in school-age children.

Michael S Kelly, Ching-Ying Huang, Minsik Kim, Dastan Haghnazari, Aribah Baig, Ye Sun, Bryan R Lenneman, Michael J Tisza, Amparito Cunningham, Diane Gold and 2 more

Abstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

12 authors.

Michael S KellyDivision of Pulmonary and Critical Care, Massachusetts General Hospital, Boston, Mass; Harvard Medical School, Boston, Mass.
Ching-Ying HuangDivision of Pulmonary and Critical Care, Massachusetts General Hospital, Boston, Mass.
Minsik KimDivision of Pulmonary and Critical Care, Massachusetts General Hospital, Boston, Mass; Harvard Medical School, Boston, Mass; Department of Biological Engineering, Inha University, Incheon, Korea.
Dastan HaghnazariDivision of Pulmonary and Critical Care, Massachusetts General Hospital, Boston, Mass.
Aribah BaigDivision of Pulmonary and Critical Care, Massachusetts General Hospital, Boston, Mass.
Ye SunDivision of Pulmonary Medicine, Boston Children's Hospital, Boston, Mass.
Bryan R LennemanHarvard Medical School, Boston, Mass; Mucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, Mass.
Michael J TiszaDepartment of Molecular Virology and Microbiology, Center for Metagenomics and Microbiome Research, Baylor College of Medicine, Houston, Tex.
Amparito CunninghamAllergy and Immunology, Boston Children's Hospital, Boston, Mass.
Diane GoldHarvard Medical School, Boston, Mass; Department of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Mass; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Mass.
Wanda PhipatanakulHarvard Medical School, Boston, Mass; Allergy and Immunology, Boston Children's Hospital, Boston, Mass.
Peggy S LaiDivision of Pulmonary and Critical Care, Massachusetts General Hospital, Boston, Mass; Harvard Medical School, Boston, Mass; Department of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Mass. Electronic address: PLAI@mgh.harvard.edu.

Funding

SICAS- Diversity SupplementU01AI110397 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI PHIPATANAKUL, WANDA · 2015 to 2020
$8.8M
The school microbiome and asthma morbidity in inner-city childrenR01AI144119 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LAI, PEGGY SUE · 2019 to 2023
$3.7M
High efficiency particulate air cleaner intervention to reduce respiratory virus exposure in elementary schoolsR21AI178155 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LAI, PEGGY SUE · 2023 to 2024
$490k
Molecular epidemiology of respiratory virus exposure in elementary schoolsR21AI175965 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LAI, PEGGY SUE · 2023 to 2024
$481k
Metagenomic Profiling of Dust Samples for School-based Viral SurveillanceF32AI194859 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI Ye Sun · 2025 to 2026
$188k
NIAID NIH HHS F32 AI194859NIAID NIH HHS R01 AI144119NIAID NIH HHS R21 AI175965NIAID NIH HHS R21 AI178155NIAID NIH HHS U01 AI110397
6 · The paper itself

Abstract

backgroundRespiratory viral infections are common and can trigger asthma exacerbations in children. The roles of the nasal microbiome and phageome (viruses that infect microbes) are not well understood.

objectiveWe sought to characterize the epidemiology of respiratory viral infections and the interplay between the nasal microbiome, phageome, and viral infections in school-age children with asthma.

methodsWe performed metagenomic sequencing and quantitative RT-PCR detection of respiratory viruses on 375 nasal samples from 227 school-age children with asthma collected routinely 3 times over a year. Surveys on parent-reported cold and asthma symptoms were administered routinely every 2 months. We evaluated multikingdom changes to the nasal microbiome during infection. A sparse partial least-squares discriminant analysis model identified microbial signatures associated with prospective viral infection risk.

resultsRespiratory viruses were identified in 124 (33%) samples, with rhinovirus being the most prevalent. Cold and asthma symptoms within the previous 14 days had a sensitivity of 79% and 59%, respectively, for quantitative RT-PCR-confirmed infection. Respiratory viral infection increased asthma symptoms and was accompanied by loss of nasal bacterial diversity and a reproducible bloom of pathobionts with no change in the mycobiome or phageome. A baseline bacteriome-dominated profile was protective (adjusted odds ratio, 0.41 [95% CI, 0.25-0.67]; P < .001), whereas phageome profiles increased risk (adjusted odds ratio, 3.74 [95% CI, 1.85-7.55]; P < .001) of viral infection. Specific phages inversely correlated with Staphylococcus epidermidis abundance, the most protective commensal against infection risk.

conclusionsThe nasal microbiome and phageome exert opposing influences on respiratory viral infection risk, highlighting their potential roles in modulating susceptibility to viral infections.

Indexed as

AsthmaMicrobiotaNoseRespiratory Tract InfectionsViromeVirus DiseasesChildFemaleHumansMaleProspective StudiesRhinovirusasthmametagenomic sequencingNasal microbiomephageomerespiratory viral infectionsRT-qPCRschool-age children

Identifiers

PMID41633490
PMCPMC12900554

What OpenQuestion holds

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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.