Evidence map›Paper›PMID 24053623›Full record

ArticleBMC genomics2013

Comparative genomics reveals distinct host-interacting traits of three major human-associated propionibacteria.

Tim N Mak, Monika Schmid, Elzbieta Brzuszkiewicz, Guanghong Zeng, Rikke Meyer, Karen S Sfanos, Volker Brinkmann, Thomas F Meyer, Holger Brüggemann

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 48 citations in OpenAlex.

  1. Bacterial skin colonization with a specificMicrobiology spectrum · 2025
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  2. Prostate and urinary microbiomes in prostate cancer development: focus onFrontiers in cellular and infection microbiology · 2025
    Review
  3. Microorganisms · 2024
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  4. Comparative Genomic Analysis ofMicroorganisms · 2023
    Article
  5. Acne conglobata caused byPostepy dermatologii i alergologii · 2022
    Article
  6. Article
  7. Solution Structure of theFrontiers in cellular and infection microbiology · 2022
    Article
  8. Microorganisms · 2021
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Composition of the Biofilm Matrix ofFrontiers in microbiology · 2019
    Article
  14. Review
  15. Article
  16. Review
  17. Propionibacterium avidum: A Virulent Pathogen Causing Hip Periprosthetic Joint Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2018
    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

9 authors at 5 institutions in 3 countries.

Tim N MakDepartment of Biomedicine, Aarhus University, Aarhus, Denmark. brueggemann@microbiology.au.dk.
Monika Schmid
Elzbieta Brzuszkiewicz
Guanghong Zeng
Rikke Meyer
Karen S Sfanos
Volker Brinkmann
Thomas F Meyer
Holger Brüggemann
Aarhus University · DKMax Planck Institute for Infection Biology · DEJohns Hopkins Medicine · USMax Planck Society · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPropionibacteria are part of the human microbiota. Many studies have addressed the predominant colonizer of sebaceous follicles of the skin, Propionibacterium acnes, and investigated its association with the skin disorder acne vulgaris, and lately with prostate cancer. Much less is known about two other propionibacterial species frequently found on human tissue sites, Propionibacterium granulosum and Propionibacterium avidum. Here we analyzed two and three genomes of P. granulosum and P. avidum, respectively, and compared them to two genomes of P. acnes; we further highlight differences among the three cutaneous species with proteomic and microscopy approaches.

resultsElectron and atomic force microscopy revealed an exopolysaccharide (EPS)-like structure surrounding P. avidum cells, that is absent in P. acnes and P. granulosum. In contrast, P. granulosum possesses pili-like appendices, which was confirmed by surface proteome analysis. The corresponding genes were identified; they are clustered with genes encoding sortases. Both, P. granulosum and P. avidum lack surface or secreted proteins for predicted host-interacting factors of P. acnes, including several CAMP factors, sialidases, dermatan-sulphate adhesins, hyaluronidase and a SH3 domain-containing lipoprotein; accordingly, only P. acnes exhibits neuraminidase and hyaluronidase activities. These functions are encoded on previously unrecognized island-like regions in the genome of P. acnes.

conclusionsDespite their omnipresence on human skin little is known about the role of cutaneous propionibacteria. All three species are associated with a variety of diseases, including postoperative and device-related abscesses and infections. We showed that the three organisms have evolved distinct features to interact with their human host. Whereas P. avidum and P. granulosum produce an EPS-like surface structure and pili-like appendices, respectively, P. acnes possesses a number of unique surface-exposed proteins with host-interacting properties. The different surface properties of the three cutaneous propionibacteria are likely to determine their colonizing ability and pathogenic potential on the skin and at non-skin sites.

Indexed as

Comparative Genomic HybridizationGenome, BacterialDNA, BacterialHost-Pathogen InteractionsHumansMicroscopy, Atomic ForceMicroscopy, Electron, ScanningPropionibacteriumSequence Analysis, DNASkinDNA, Bacterial

Identifiers

PMID24053623
PMCPMC3848858
OpenAlexW1980136113

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.