Evidence map›Paper›PMID 38682956›Full record

ArticlemBio2024

Exploring the pediatric nasopharyngeal bacterial microbiota with culture-based MALDI-TOF mass spectrometry and targeted metagenomic sequencing.

Sreymom Pol, Teemu Kallonen, Tommi Mäklin, Poda Sar, Jill Hopkins, Sona Soeng, Thyl Miliya, Clare L Ling, Stephen D Bentley, Jukka Corander and 1 more

Abstract read
In one paragraph

Article in mBio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Nasal microbiome inhabitants with anti-Microbiology spectrum · 2025
    Article
  3. 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

11 authors.

Sreymom Pol *Cambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0001-8393-659X
Teemu Kallonen *Department of Biostatistics, University of Oslo, Oslo, Norway.ORCID 0000-0003-1741-6486
Tommi MäklinDepartment of Mathematics and Statistics, University of Helsinki, Helsinki, Finland.ORCID 0000-0003-0970-3514
Poda SarCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Jill HopkinsCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0003-1989-8618
Sona SoengCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Thyl MiliyaCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Clare L LingCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0002-5188-0349
Stephen D BentleyWellcome Sanger Institute, Hinxton, United Kingdom.ORCID 0000-0001-8094-3751
Jukka Corander *Department of Biostatistics, University of Oslo, Oslo, Norway.ORCID 0000-0002-7752-1942
Paul Turner *Cambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0002-1013-7815

Funding

EC | European Research Council (ERC) 742154Norwegian Research Council 299941Wellcome TrustWellcome Trust 206194Wellcome Trust 220211
6 · The paper itself

Abstract

The nasopharynx is an important reservoir of disease-associated and antimicrobial-resistant bacterial species. This proof-of-concept study assessed the utility of a combined culture, matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS), and targeted metagenomic sequencing workflow for the study of the pediatric nasopharyngeal bacterial microbiota. Nasopharyngeal swabs and clinical metadata were collected from Cambodian children during a hospital outpatient visit and then biweekly for 12 weeks. Swabs were cultured on chocolate and blood-gentamicin agar, and all colony morphotypes were identified by MALDI-TOF MS. Metagenomic sequencing was done on a scrape of all colonies from a chocolate agar culture and processed using the mSWEEP pipeline. One hundred one children were enrolled, yielding 620 swabs. MALDI-TOF MS identified 106 bacterial species/40 genera: 20 species accounted for 88.5% (2,190/2,474) of isolates. Colonization by IMPORTANCE: The human upper respiratory tract is an important source of disease-causing and antibiotic-resistant bacteria. However, understanding the interactions and stability of these bacterial populations is technically challenging. We used a combination of approaches to determine colonization patterns over a 3-month period in 101 Cambodian children. The combined approach was feasible to implement, and each component gave complementary data to enable a better understanding of the complex patterns of bacterial colonization.

Indexed as

BacteriaMetagenomicsMicrobiotaNasopharynxSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationCambodiaChildChild, PreschoolFemaleHaemophilus influenzaeHumansInfantMaleCambodiacolonizationHaemophilus influenzaeMALDI-TOFmetagenomic sequencingpediatricsStaphylococcus aureusStreptococcus pneumoniae

Identifiers

PMID38682956
PMCPMC11237702

What OpenQuestion holds

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LicenceCC BY
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.