Evidence map›Paper›PMID 23658662›Full record

ArticlePloS one2013

Evaluation of genetically inactivated alpha toxin for protection in multiple mouse models of Staphylococcus aureus infection.

Rebecca A Brady, Christopher P Mocca, Ranjani Prabhakara, Roger D Plaut, Mark E Shirtliff, Tod J Merkel, Drusilla L Burns

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Host-Bacterium Interaction Mechanisms inInternational journal of molecular sciences · 2023
    Pooled it
  2. Infection and immunity · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The open microbiology journal · 2018
    Article
  13. Article
  14. Article
  15. Rapid Identification of Vancomycin ResistantJournal of clinical and diagnostic research : JCDR · 2017
    Article
  16. Article
  17. Article
  18. Multi-disciplinary antimicrobial strategies for improving orthopaedic implants to prevent prosthetic joint infections in hip and knee.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2016
    Review
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Rebecca A BradyCenter for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland, USA.
Christopher P Mocca
Ranjani Prabhakara
Roger D Plaut
Mark E Shirtliff
Tod J Merkel
Drusilla L Burns
Center for Biologics Evaluation and Research · USUniversity of Maryland, Baltimore · US

Funding

IMMUNITY AND INFECTIONT32AI007540 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 1998 to 2018
$2.2M
Staphylococcus aureus biofilms: in vitro and in vivo studiesR01AI069568 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SHIRTLIFF, MARK E · 2007 to 2011
$2.1M
NETWORK ON ANTIMICROBIAL RESISTANCE IN STAPHTLOCOCCUS AN01AI095359 · NIAID · FOCUS/MRL, INC.-MRL PHARMACEUTICAL SRVS · PI SAHM, DANIEL F · 1999 to 2000
$495k
NIAID NIH HHS AI69568NIAID NIH HHS AI-95359NIAID NIH HHS N01 AI095359NIAID NIH HHS R01 AI069568NIAID NIH HHS R01AI69568NIAID NIH HHS T32 AI007540
6 · The paper itself

Abstract

Staphylococcus aureus is a major human pathogen and a leading cause of nosocomial and community-acquired infections. Development of a vaccine against this pathogen is an important goal. While S. aureus protective antigens have been identified in the literature, the majority have only been tested in a single animal model of disease. We wished to evaluate the ability of one S. aureus vaccine antigen to protect in multiple mouse models, thus assessing whether protection in one model translates to protection in other models encompassing the full breadth of infections the pathogen can cause. We chose to focus on genetically inactivated alpha toxin mutant HlaH35L. We evaluated the protection afforded by this antigen in three models of infection using the same vaccine dose, regimen, route of immunization, adjuvant, and challenge strain. When mice were immunized with HlaH35L and challenged via a skin and soft tissue infection model, HlaH35L immunization led to a less severe infection and decreased S. aureus levels at the challenge site when compared to controls. Challenge of HlaH35L-immunized mice using a systemic infection model resulted in a limited, but statistically significant decrease in bacterial colonization as compared to that observed with control mice. In contrast, in a prosthetic implant model of chronic biofilm infection, there was no significant difference in bacterial levels when compared to controls. These results demonstrate that vaccines may confer protection against one form of S. aureus disease without conferring protection against other disease presentations and thus underscore a significant challenge in S. aureus vaccine development.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, BacterialAntigens, BacterialBacterial ToxinsBiofilmsColony Count, MicrobialDisease Models, AnimalFemaleImmunizationImmunoglobulin GMiceSoft Tissue InfectionsStaphylococcal InfectionsStaphylococcal Skin InfectionsStaphylococcal VaccinesAdjuvants, ImmunologicAntibodies, BacterialAntigens, BacterialBacterial ToxinsImmunoglobulin GStaphylococcal VaccinesVaccines, Attenuated

Identifiers

PMID23658662
PMCPMC3639205
OpenAlexW2102194988

What OpenQuestion holds

Textmetadata
LicenceCC0
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.