Evidence map›Paper›PMID 26086671›Full record

ArticlePloS one2015

Genomic Heterogeneity of Methicillin Resistant Staphylococcus aureus Associated with Variation in Severity of Illness among Children with Acute Hematogenous Osteomyelitis.

Claudia Gaviria-Agudelo, Chukwuemika Aroh, Naureen Tareen, Edward K Wakeland, MinSoo Kim, Lawson A Copley

Abstract readCase Reports
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. International journal of molecular sciences · 2023
    Pooled it
  2. Review
  3. Anti-Heliyon · 2024
    Article
  4. Article
  5. Article
  6. Virulence Determinants inFrontiers in microbiology · 2022
    Article
  7. Surveillance of osteoarticular infections caused byFrontiers in cellular and infection microbiology · 2022
    Article
  8. The impact ofHeliyon · 2018
    Article
  9. Procalcitonin and Pancreatic Stone Protein Function as Biomarkers in Early Diagnosis of Pediatric Acute Osteomyelitis.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  10. Article
  11. Article
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.

Claudia Gaviria-AgudeloDepartment of Pediatric Infectious Disease, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
Chukwuemika ArohDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
Naureen TareenChildren's Medical Center, Dallas, Texas, United States of America.
Edward K WakelandDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
MinSoo KimDepartment of Biomedical Informatics, University of Texas Southwestern Medical Center, Dallas, TX, United States of America.
Lawson A CopleyChildren's Medical Center, Dallas, Texas, United States of America; Texas Scottish Rite Hospital for Children, Dallas, Texas, United States of America; Department of Orthopaedic Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.

Funding

UT Southwestern Center for Translational Medicine (UL1/KL2/TL1)UL1TR001105 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$24.5M
UT-Southwestern Clinical and Translational Alliance for Research (UT-STAR) (TL1)UL1TR000451 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2012 to 2012
$6.3M
NCATS NIH HHS UL1 TR000451NCATS NIH HHS UL1TR000451NCATS NIH HHS UL1 TR001105
6 · The paper itself

Abstract

introductionThe association between severity of illness of children with osteomyelitis caused by Methicillin-resistant Staphylococcus aureus (MRSA) and genomic variation of the causative organism has not been previously investigated. The purpose of this study is to assess genomic heterogeneity among MRSA isolates from children with osteomyelitis who have diverse severity of illness. MATERIALS AND

methodsChildren with osteomyelitis were prospectively studied between 2010 and 2011. Severity of illness of the affected children was determined from clinical and laboratory parameters. MRSA isolates were analyzed with next generation sequencing (NGS) and optical mapping. Sequence data was used for multi-locus sequence typing (MLST), phylogenetic analysis by maximum likelihood (PAML), and identification of virulence genes and single nucleotide polymorphisms (SNP) relative to reference strains.

resultsThe twelve children studied demonstrated severity of illness scores ranging from 0 (mild) to 9 (severe). All isolates were USA300, ST 8, SCC mec IVa MRSA by MLST. The isolates differed from reference strains by 2 insertions (40 Kb each) and 2 deletions (10 and 25 Kb) but had no rearrangements or copy number variations. There was a higher occurrence of virulence genes among study isolates when compared to the reference strains (p = 0.0124). There were an average of 11 nonsynonymous SNPs per strain. PAML demonstrated heterogeneity of study isolates from each other and from the reference strains. DISCUSSION: Genomic heterogeneity exists among MRSA isolates causing osteomyelitis among children in a single community. These variations may play a role in the pathogenesis of variation in clinical severity among these children.

Indexed as

Severity of Illness IndexAcute DiseaseAdolescentChildChild, PreschoolDemographyGenetic HeterogeneityHigh-Throughput Nucleotide SequencingHumansInfantMethicillin-Resistant Staphylococcus aureusMultilocus Sequence TypingOsteomyelitisPhylogenyPolymorphism, Single NucleotideProspective Studies

Identifiers

PMID26086671
PMCPMC4473274

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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.