Evidence map›Paper›PMID 29643357›Full record

ArticleNature communications2018

Release of Staphylococcus aureus extracellular vesicles and their application as a vaccine platform.

Xiaogang Wang, Christopher D Thompson, Christopher Weidenmaier, Jean C Lee

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 209 papers.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed
18.4field-weighted citation impact, top 1% 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

209 citing papers in PubMed, 317 citations in OpenAlex.

  1. Review
  2. Article
  3. Towards a Scalable Production ofInternational journal of molecular sciences · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Identification of immunostimulatory antigens in Group AProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Review
  9. Membrane Vesicles ImproveMicroorganisms · 2026
    Article
  10. Review
  11. Review
  12. Frontiers in bacterial outer membrane vesicles: From basic characteristics to cancer therapy.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2026
    Article
  13. Article
  14. Biofilms: from the cradle of life to life support.NPJ biofilms and microbiomes · 2026
    Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Cytoplasmic membrane vesicles fromFrontiers in microbiology · 2026
    Article

149 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Xiaogang WangDivision of Infectious Diseases, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 181 Longwood Avenue, Boston, MA, 02115, USA.
Christopher D ThompsonDivision of Infectious Diseases, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 181 Longwood Avenue, Boston, MA, 02115, USA.
Christopher WeidenmaierInterfaculty Institute for Microbiology and Infection Medicine, University of Tuebingen, Elfriede Aulhorn Strasse 6, 72076, Tuebingen, Germany.ORCID http://orcid.org/0000-0003-4107-739X
Jean C LeeDivision of Infectious Diseases, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 181 Longwood Avenue, Boston, MA, 02115, USA. jclee@bwh.harvard.edu.
Brigham and Women's Hospital · USGerman Center for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Secretion of extracellular vesicles (EVs), a process common to eukaryotes, archae, and bacteria, represents a secretory pathway that allows cell-free intercellular communication. Microbial EVs package diverse proteins and influence the host-pathogen interaction, but the mechanisms underlying EV production in Gram-positive bacteria are poorly understood. Here we show that EVs purified from community-associated methicillin-resistant Staphylococcus aureus package cytosolic, surface, and secreted proteins, including cytolysins. Staphylococcal alpha-type phenol-soluble modulins promote EV biogenesis by disrupting the cytoplasmic membrane; whereas, peptidoglycan cross-linking and autolysin activity modulate EV production by altering the permeability of the cell wall. We demonstrate that EVs purified from a S. aureus mutant that is genetically engineered to express detoxified cytolysins are immunogenic in mice, elicit cytolysin-neutralizing antibodies, and protect the animals in a lethal sepsis model. Our study reveals mechanisms underlying S. aureus EV production and highlights the usefulness of EVs as a S. aureus vaccine platform.

Indexed as

AnimalsAntibodies, NeutralizingCell WallCytotoxinsExtracellular VesiclesFemaleGenetic EngineeringMethicillin-Resistant Staphylococcus aureusMicePeptidoglycanSepsisStaphylococcal InfectionsStaphylococcal VaccinesSurvival AnalysisVaccinationAntibodies, NeutralizingCytotoxinsPeptidoglycanStaphylococcal Vaccines

Identifiers

PMID29643357
PMCPMC5895597
OpenAlexW2797977351

What OpenQuestion holds

Textmetadata
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.