Evidence map›Paper›PMID 24664176›Full record

ArticlePloS one2014

Chitinases are negative regulators of Francisella novicida biofilms.

Myung-Chul Chung, Scott Dean, Ekaterina S Marakasova, Albert O Nwabueze, Monique L van Hoek

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. An overview of viral chitinases: General properties and biotechnological potential.Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  9. Review
  10. Review
  11. Article
  12. Frontiers in microbiology · 2023
    Article
  13. Review
  14. Contribution of NmSystems · 2021
    Article
  15. Review
  16. Article
  17. Genetic Determinants of Antibiotic Resistance inFrontiers in microbiology · 2021
    Review
  18. Article
  19. Review
  20. Biofilm architecture: An emerging synthetic biology target.Synthetic and systems biotechnology · 2020
    Review
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

5 authors at 1 institution in 1 country.

Myung-Chul ChungSchool of Systems Biology and the National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, Virginia, United States of America.
Scott DeanSchool of Systems Biology and the National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, Virginia, United States of America.
Ekaterina S MarakasovaSchool of Systems Biology and the National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, Virginia, United States of America.
Albert O NwabuezeSchool of Systems Biology and the National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, Virginia, United States of America.
Monique L van HoekSchool of Systems Biology and the National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, Virginia, United States of America.
George Mason University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biofilms, multicellular communities of bacteria, may be an environmental survival and transmission mechanism of Francisella tularensis. Chitinases of F. tularensis ssp. novicida (Fn) have been suggested to regulate biofilm formation on chitin surfaces. However, the underlying mechanisms of how chitinases may regulate biofilm formation are not fully determined. We hypothesized that Fn chitinase modulates bacterial surface properties resulting in the alteration of biofilm formation. We analyzed biofilm formation under diverse conditions using chitinase mutants and their counterpart parental strain. Substratum surface charges affected biofilm formation and initial attachments. Biophysical analysis of bacterial surfaces confirmed that the chi mutants had a net negative-charge. Lectin binding assays suggest that chitinase cleavage of its substrates could have exposed the concanavalin A-binding epitope. Fn biofilm was sensitive to chitinase, proteinase and DNase, suggesting that Fn biofilm contains exopolysaccharides, proteins and extracellular DNA. Exogenous chitinase increased the drug susceptibility of Fn biofilms to gentamicin while decreasing the amount of biofilm. In addition, chitinase modulated bacterial adhesion and invasion of A549 and J774A.1 cells as well as intracellular bacterial replication. Our results support a key role of the chitinase(s) in biofilm formation through modulation of the bacterial surface properties. Our findings position chitinase as a potential anti-biofilm enzyme in Francisella species.

Indexed as

MutationAnti-Bacterial AgentsBacterial AdhesionBacterial ProteinsBiofilmsCell LineChitinasesFrancisellaGentamicinsHumansAnti-Bacterial AgentsBacterial ProteinsChitinasesGentamicins

Identifiers

PMID24664176
PMCPMC3963990
OpenAlexW2015446041

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.