Evidence map›Paper›PMID 36877063›Full record

ArticleInfection and immunity2023

Hyperglycemia Increases Severity of Staphylococcus aureus Osteomyelitis and Influences Bacterial Genes Required for Survival in Bone.

Casey E Butrico, Nathan Klopfenstein, Erin R Green, Joshua R Johnson, Sun H Peck, Carolyn B Ibberson, C Henrique Serezani, James E Cassat

Open access · hybridAbstract read
In one paragraph

Article in Infection and immunity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.4field-weighted citation impact, top 4% of its field
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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. D-alanine aminotransferase (Dat) promotesbioRxiv : the preprint server for biology · 2026
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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 1 country.

Casey E ButricoDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Nathan KlopfensteinDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Erin R GreenDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Joshua R JohnsonVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Sun H PeckVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Carolyn B IbbersonDepartment of Microbiology and Plant Biology, The University of Oklahoma, Norman, Oklahoma, USA.
C Henrique SerezaniDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
James E CassatDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0002-1199-1167
Vanderbilt University Medical Center · USVanderbilt University · USUniversity of Oklahoma · US

Funding

Interdisciplinary Training Program in Lung ResearchT32HL094296 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ray Stokes Peebles · 2008 to 2026
$6.3M
Phosphatase and tensin homolog PTEN actions in polymicrobial sepsisR01HL124159 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SEREZANI, C. HENRIQUE · 2014 to 2022
$4.2M
Chemical Biology of Infectious Diseases (CBID) Training ProgramT32AI112541 · NIAID · VANDERBILT UNIVERSITY · PI Eric P Skaar · 2015 to 2026
$4.0M
Defining the impact of host factors on the molecular architecture and bacterial physiology of Staphylococcus aureus abscessesR01AI145992 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CASSAT, JAMES E, SKAAR, ERIC P · 2020 to 2024
$3.8M
Differential Inflammasome Regulation in the pathogenesis of S. aureus osteomyelitisR01AI161022 · NIAID · WASHINGTON UNIVERSITY · PI CASSAT, JAMES E, MBALAVIELE, GABRIEL · 2021 to 2025
$3.4M
Hyperglycemia and increased severity to Staphylococcus aureus infections.R01AI180777 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI C. Henrique Serezani · 2024 to 2026
$2.1M
The impact of hypoxia on Staphylococcus aureus metabolism and virulence during osteomyelitisR01AI132560 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CASSAT, JAMES E · 2017 to 2021
$1.9M
Prostaglandin E2 Actions and Enhanced Susceptibility to Skin Infection in Diabetic MiceR01DK122147 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SEREZANI, C. HENRIQUE · 2020 to 2022
$1.7M
Immunological Mechanisms of Disease Training ProgramT32AI138932 · NIAID · VANDERBILT UNIVERSITY · PI MAJOR, AMY S, RATHMELL, JEFFREY C. · 2019 to 2023
$1.4M
Mechanisms underlying poor skin host defense in diabetic conditionsR21AI149207 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SEREZANI, C. HENRIQUE · 2020 to 2021
$467k
Novel ultrahigh resolution microCT imaging systemS10RR027631 · NCRR · VANDERBILT UNIVERSITY · PI PERRIEN, DANIEL S · 2010 to 2010
$460k
Defining mechanisms of microbe-microbe interactions in chronic wound infectionK22AI155927 · NIAID · UNIVERSITY OF OKLAHOMA · PI IBBERSON, CAROLYN BROOK · 2022 to 2023
$267k
BLRD VA IK2 BX005401NCRR NIH HHS S10 RR027631NHLBI NIH HHS R01 HL124159NHLBI NIH HHS R01HL124159-01NHLBI NIH HHS T32 HL094296NHLBI NIH HHS T32HL094296NIAID NIH HHS AI149207ANIAID NIH HHS K22 AI155927NIAID NIH HHS K22AI155927NIAID NIH HHS R01 AI132560NIAID NIH HHS R01AI132560NIAID NIH HHS R01 AI145992NIAID NIH HHS R01AI145992NIAID NIH HHS R01 AI161022NIAID NIH HHS R01AI161022NIAID NIH HHS R01 AI180777NIAID NIH HHS R21 AI149207NIAID NIH HHS T32 AI112541NIAID NIH HHS T32AI112541NIAID NIH HHS T32 AI138932NIAID NIH HHS T32AI138932NIDDK NIH HHS DK122147-01A1NIDDK NIH HHS R01 DK122147VA 1IK2BX005401
6 · The paper itself

Abstract

Hyperglycemia, or elevated blood glucose, renders individuals more prone to developing severe Staphylococcus aureus infections. S. aureus is the most common etiological agent of musculoskeletal infection, which is a common manifestation of disease in hyperglycemic patients. However, the mechanisms by which S. aureus causes severe musculoskeletal infection during hyperglycemia are incompletely characterized. To examine the influence of hyperglycemia on S. aureus virulence during invasive infection, we used a murine model of osteomyelitis and induced hyperglycemia with streptozotocin. We discovered that hyperglycemic mice exhibited increased bacterial burdens in bone and enhanced dissemination compared to control mice. Furthermore, infected hyperglycemic mice sustained increased bone destruction relative to euglycemic controls, suggesting that hyperglycemia exacerbates infection-associated bone loss. To identify genes contributing to S. aureus pathogenesis during osteomyelitis in hyperglycemic animals relative to euglycemic controls, we used transposon sequencing (TnSeq). We identified 71 genes uniquely essential for S. aureus survival in osteomyelitis in hyperglycemic mice and another 61 mutants with compromised fitness. Among the genes essential for S. aureus survival in hyperglycemic mice was the gene encoding superoxide dismutase A (

Indexed as

HyperglycemiaOsteomyelitisStaphylococcal InfectionsAnimalsGenes, BacterialGlucoseMiceMice, ObeseStaphylococcus aureusGlucosehyperglycemiaosteomyelitisStaphylococcus aureussuperoxide dismutasetransposon sequencing

Identifiers

PMID36877063
PMCPMC10112148
OpenAlexW4323294064

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.