Evidence map›Paper›PMID 37347167›Full record

ArticleInfection and immunity2023

Crucial Role for Lipoteichoic Acid Assembly in the Metabolic Versatility and Antibiotic Resistance of Staphylococcus aureus.

Troy A Burtchett, John C Shook, Laura E Hesse, Philip C Delekta, Robert S Brzozowski, Alhakam Nouri, Alexa J Calas, Catherine M Spanoudis, Prahathees J Eswara, Neal D Hammer

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. A novel polysaccharide in the envelope ofJournal of bacteriology · 2025
    Article
  5. Article
  6. Article
  7. 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

10 authors at 2 institutions in 1 country.

Troy A BurtchettDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.
John C ShookDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.
Laura E HesseDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.
Philip C DelektaDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.
Robert S BrzozowskiDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida, USA.
Alhakam NouriDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.
Alexa J CalasDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.
Catherine M SpanoudisDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida, USA.
Prahathees J EswaraDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida, USA.ORCID 0000-0003-4430-261X
Neal D HammerDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.ORCID 0000-0001-6148-7850
Michigan State University · USUniversity of South Florida · US

Funding

Division site determination in Gram-positive bacteriaR35GM133617 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI ESWARA, PRAHATHEES JAI · 2019 to 2023
$2.3M
Isoprenoid synthesis and allocation in Staphylococcus aureusR21AI144504 · NIAID · MICHIGAN STATE UNIVERSITY · PI HAMMER, NEAL D. · 2019 to 2020
$426k
NIAID NIH HHS R21 AI144504NIGMS NIH HHS R35 GM133617
6 · The paper itself

Abstract

Staphylococcus aureus is a public health threat due to the prevalence of antibiotic resistance and the capacity of this organism to infect numerous organs in vertebrates. To generate energy needed to proliferate within tissues, S. aureus transitions between aerobic respiration and fermentation. Fermentation results in a distinct colony morphology called the small-colony variant (SCV) due to decreased membrane potential and ATP production. These traits promote increased resistance to aminoglycoside antibiotics. Consequently, SCVs are associated with persistent infections. We hypothesize that dedicated physiological pathways support fermentative growth of S. aureus that represent potential targets for treatment of resistant infections. Lipoteichoic acid (LTA) is an essential component of the Gram-positive cell envelope that functions to maintain ion homeostasis, resist osmotic stress, and regulate autolytic activity. Previous studies revealed that perturbation of LTA reduces viability of metabolically restricted S. aureus, but the mechanism by which LTA supports S. aureus metabolic versatility is unknown. Though LTA is essential, the enzyme that synthesizes the modified lipid anchor, YpfP, is dispensable. However,

Indexed as

Staphylococcal InfectionsStaphylococcus aureusAnimalsDrug Resistance, MicrobialLipopolysaccharidesMutationTeichoic AcidsLipopolysaccharideslipoteichoic acidTeichoic Acidscationglycolipid anchorion homeostasislipoteichoic acidmembrane potentialmetabolismsmall-colony variantStaphylococcus aureusypfP

Identifiers

PMID37347167
PMCPMC10353449
OpenAlexW4381597372

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.