Evidence map›Paper›PMID 22205797›Full record

ArticleJournal of clinical microbiology2012

Presence of genes encoding panton-valentine leukocidin is not the primary determinant of outcome in patients with hospital-acquired pneumonia due to Staphylococcus aureus.

Batu K Sharma-Kuinkel, Sun H Ahn, Thomas H Rude, Yurong Zhang, Steven Y C Tong, Felicia Ruffin, Fredric C Genter, Kevin R Braughton, Frank R Deleo, Steven L Barriere and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
2.7field-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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Microbes and the fate of neutrophils.Immunological reviews · 2023
    Review
  6. Observational
  7. Article
  8. Impact ofMicrobiology spectrum · 2021
    Article
  9. Article
  10. Frontiers in microbiology · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Life After USA300: The Rise and Fall of a Superbug.The Journal of infectious diseases · 2017
    Review
  16. Article
  17. Article
  18. Article
  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

11 authors at 5 institutions in 2 countries.

Batu K Sharma-KuinkelDepartment of Medicine, Duke University Medical Center, Durham, North Carolina, USA.
Sun H Ahn
Thomas H Rude
Yurong Zhang
Steven Y C Tong
Felicia Ruffin
Fredric C Genter
Kevin R Braughton
Frank R Deleo
Steven L Barriere
Vance G Fowler
Duke Medical Center · USTheravance Biopharma (United States) · USMenzies School of Health Research · AUNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

Mechanisms of Staphylococcus aureus virulenceZIAAI001079 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DELEO, FRANK · 2009 to 2025
$11.8M
Mentoring Patient Oriented Research in Antibiotic-Resistant BacteriaK24AI093969 · NIAID · DUKE UNIVERSITY · PI FOWLER, VANCE G. · 2011 to 2020
$1.6M
NIAID NIH HHS K24 AI093969
6 · The paper itself

Abstract

The impact of Panton-Valentine leukocidin (PVL) on the outcome in Staphylococcus aureus pneumonia is controversial. We genotyped S. aureus isolates from patients with hospital-acquired pneumonia (HAP) enrolled in two registrational multinational clinical trials for the genetic elements carrying pvl and 30 other virulence genes. A total of 287 isolates (173 methicillin-resistant S. aureus [MRSA] and 114 methicillin-susceptible S. aureus [MSSA] isolates) from patients from 127 centers in 34 countries for whom clinical outcomes of cure or failure were available underwent genotyping. Of these, pvl was detected by PCR and its product confirmed in 23 isolates (8.0%) (MRSA, 18/173 isolates [10.4%]; MSSA, 5/114 isolates [4.4%]). The presence of pvl was not associated with a higher risk for clinical failure (4/23 [17.4%] versus 48/264 [18.2%]; P = 1.00) or mortality. These findings persisted after adjustment for multiple potential confounding variables. No significant associations between clinical outcome and (i) presence of any of the 30 other virulence genes tested, (ii) presence of specific bacterial clone, (iii) levels of alpha-hemolysin, or (iv) delta-hemolysin production were identified. This study suggests that neither pvl presence nor in vitro level of alpha-hemolysin production is the primary determinant of outcome among patients with HAP caused by S. aureus.

Indexed as

AdultAgedAged, 80 and overBacterial ToxinsCross InfectionExotoxinsFemaleGenotypeHumansLeukocidinsMaleMiddle AgedMolecular TypingPneumonia, StaphylococcalRisk AssessmentStaphylococcus aureusBacterial ToxinsExotoxinsLeukocidinsPanton-Valentine leukocidinVirulence Factors

Identifiers

PMID22205797
PMCPMC3295120
OpenAlexW1983938091

What OpenQuestion holds

Textmetadata
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.