Evidence map›Paper›PMID 25575312›Full record

ArticleThe ISME journal2015

Culture and molecular-based profiles show shifts in bacterial communities of the upper respiratory tract that occur with age.

Jennifer C Stearns, Carla J Davidson, Suzanne McKeon, Fiona J Whelan, Michelle E Fontes, Anthony B Schryvers, Dawn M E Bowdish, James D Kellner, Michael G Surette

Erratum issuedAbstract read
In one paragraph

Article in The ISME journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 110 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed, 2 pooled it
–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

110 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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  15. Article
  16. Upper Respiratory Microbiome in Vasculitis.Rheumatic diseases clinics of North America · 2025
    Review
  17. The neonate respiratory microbiome.Acta physiologica (Oxford, England) · 2025
    Review
  18. Article
  19. Frontiers in cellular and infection microbiology · 2025
    Review
  20. Article

50 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jennifer C StearnsDepartment of Medicine, McMaster University, Hamilton, Ontario, Canada.ORCID 0000000286036607
Carla J DavidsonDepartment of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada.
Suzanne McKeonDepartment of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada.
Fiona J WhelanDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Michelle E FontesDepartment of Medicine, McMaster University, Hamilton, Ontario, Canada.
Anthony B SchryversDepartment of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada.
Dawn M E BowdishDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
James D Kellner1] Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada [2] Department of Paediatrics, University of Calgary, Calgary, Alberta, Canada.
Michael G Surette1] Department of Medicine, McMaster University, Hamilton, Ontario, Canada [2] Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada [3] Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

The upper respiratory tract (URT) is a crucial site for host defense, as it is home to bacterial communities that both modulate host immune defense and serve as a reservoir of potential pathogens. Young children are at high risk of respiratory illness, yet the composition of their URT microbiota is not well understood. Microbial profiling of the respiratory tract has traditionally focused on culturing common respiratory pathogens, whereas recent culture-independent microbiome profiling can only report the relative abundance of bacterial populations. In the current study, we used both molecular profiling of the bacterial 16S rRNA gene and laboratory culture to examine the bacterial diversity from the oropharynx and nasopharynx of 51 healthy children with a median age of 1.1 years (range 1-4.5 years) along with 19 accompanying parents. The resulting profiles suggest that in young children the nasopharyngeal microbiota, much like the gastrointestinal tract microbiome, changes from an immature state, where it is colonized by a few dominant taxa, to a more diverse state as it matures to resemble the adult microbiota. Importantly, this difference in bacterial diversity between adults and children accompanies a change in bacterial load of three orders of magnitude. This indicates that the bacterial communities in the nasopharynx of young children have a fundamentally different structure from those in adults and suggests that maturation of this community occurs sometime during the first few years of life, a period that includes ages at which children are at the highest risk for respiratory disease.

Indexed as

AdultAge FactorsBacterial InfectionsBacterial LoadChildChild, PreschoolDNA, BacterialGastrointestinal TractHealthy VolunteersHumansInfantMicrobiotaNasopharynxOropharynxPhylogenyRNA, Ribosomal, 16SDNA, BacterialRNA, Ribosomal, 16S

Identifiers

PMID25575312
PMCPMC4409167

What OpenQuestion holds

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Registered trials

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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.