Evidence map›Paper›PMID 37808661›Full record

ArticlebioRxiv : the preprint server for biology2023

Analysis of nasopharyngeal microbiome patterns in Zambian infants with fatal acute febrile illness.

Aubrey R Odom, Jessica McClintock, Christopher J Gill, Rachel Pieciak, Arshad Ismail, William B MacLeod, W Evan Johnson, Rotem Lapidot

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 0 citations in OpenAlex.

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

8 authors at 3 institutions in 2 countries.

Aubrey R OdomBioinformatics Program, Boston University, Boston, MA, 02118, USA.
Jessica McClintockDivision of Infectious Disease, Center for Data Science, Rutgers New Jersey Medical School, Newark, NJ, 07103, USA.
Christopher J GillDepartment of Global Health, Boston University School of Public Health, Boston, MA, 02118, USA.
Rachel PieciakDepartment of Global Health, Boston University School of Public Health, Boston, MA, 02118, USA.
Arshad IsmailSequencing Core Facility, National Institute for Communicable Diseases of the National Health Laboratory Service, 2131 Johannesburg, South Africa.
William B MacLeodDepartment of Global Health, Boston University School of Public Health, Boston, MA, 02118, USA.
W Evan JohnsonDivision of Infectious Disease, Center for Data Science, Rutgers New Jersey Medical School, Newark, NJ, 07103, USA.
Rotem LapidotPediatric Infectious Diseases, Boston Medical Center, Boston, MA, 02118, USA.
Boston University · USRutgers, The State University of New Jersey · USNational Health Laboratory Service · ZA

Funding

Biomarker Signatures of TB Infection in Young Children With and Without HIVR01AI175315 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Jerrold J. Ellner, William Evan Johnson · 2023 to 2026
$4.2M
Removing batch effects in high-throughput biomedical studiesR01GM127430 · NIGMS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI William Evan Johnson · 2018 to 2026
$2.4M
SAMIPS-NPC: Southern Africa Mother Infant Pertussis Study, Nasopharyngeal CarriageR01AI133080 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GILL, CHRISTOPHER J, MWANANYANDA, LAWRENCE · 2017 to 2019
$2.3M
Signature of profiling and staging the progression of TB from infection to disease.R21AI154387 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JOHNSON, WILLIAM EVAN · 2020 to 2021
$468k
NIAID NIH HHS R01 AI133080NIAID NIH HHS R01 AI175315NIAID NIH HHS R21 AI154387NIGMS NIH HHS R01 GM127430
6 · The paper itself

Abstract

Introduction: Associative connections have previously been identified between nasopharyngeal infections and infant mortality. The nasopharyngeal microbiome may potentially influence the severity of these infections. Methods: We conducted an analysis of a longitudinal prospective cohort study of 1,981 infants who underwent nasopharyngeal sampling from 1 week through 14 weeks of age at 2-3-week intervals. In all, 27 microbiome samples from 9 of the infants in the cohort who developed fatal acute febrile illness (fAFI) were analyzed in pooled comparisons with 69 samples from 10 healthy comparator infants. We completed 16S rRNA amplicon gene sequencing all infant NP samples and characterized the maturation of the infant NP microbiome among the fAFI(+) and fAFI(-) infant cohorts. Results: Beta diversity measures of fAFI(-) infants were markedly higher than those of fAFI(+) infants. The fAFI(+) infant NP microbiome was marked by higher abundances of Conclusions: Our results suggest that nasopharyngeal microbiome dysbiosis precedes fAFI in young infants. Early dysbiosis, involving microbes such as

Indexed as

16S rRNA sequencingbacteriadysbiosislongitudinal studymicrobiomenasopharyngeal

Identifiers

PMID37808661
PMCPMC10557644
OpenAlexW4387184126

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.