Evidence map›Paper›PMID 28917089›Full record

ArticleCarbohydrate research2017

The trehalose-specific transporter LpqY-SugABC is required for antimicrobial and anti-biofilm activity of trehalose analogues in Mycobacterium smegmatis.

Jeffrey M Wolber, Bailey L Urbanek, Lisa M Meints, Brent F Piligian, Irene C Lopez-Casillas, Kailey M Zochowski, Peter J Woodruff, Benjamin M Swarts

Open access · greenAbstract read
In one paragraph

Article in Carbohydrate research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-weighted citation impact, top 9% 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, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Mycobacterial Biofilm: Mechanisms, Clinical Problems, and Treatments.International journal of molecular sciences · 2024
    Review
  7. Review
  8. TargetingACS infectious diseases · 2024
    Article
  9. Article
  10. Molecular recognition of trehalose and trehalose analogues byProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Article
  12. Article
  13. TargetingViruses · 2023
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  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

8 authors at 2 institutions in 1 country.

Jeffrey M WolberDepartment of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, United States.
Bailey L UrbanekDepartment of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, United States.
Lisa M MeintsDepartment of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, United States.
Brent F PiligianDepartment of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, United States.
Irene C Lopez-CasillasDepartment of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, United States.
Kailey M ZochowskiDepartment of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, United States.
Peter J WoodruffDepartment of Chemistry, University of Southern Maine, Portland, ME 04104, United States.
Benjamin M SwartsDepartment of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, United States. Electronic address: ben.swarts@cmich.edu.
Central Michigan University · USUniversity of Southern Maine · US

Funding

Chemoenzymatic synthesis of trehalose analogues as tools for investigating mycobacteriaR15AI117670 · NIAID · CENTRAL MICHIGAN UNIVERSITY · PI SWARTS, BENJAMIN MICHAEL, WOODRUFF, PETER J · 2015 to 2024
$1.3M
NIAID NIH HHS R15 AI117670
6 · The paper itself

Abstract

Mycobacteria, including the bacterial pathogen that causes human tuberculosis, possess distinctive pathways for synthesizing and utilizing the non-mammalian disaccharide trehalose. Trehalose metabolism is essential for mycobacterial viability and has been linked to in vitro biofilm formation, which may bear relevance to in vivo drug tolerance. Previous research has shown that some trehalose analogues bearing modifications at the 6-position inhibit growth of various mycobacterial species. In this work, 2-, 5-, and 6-position-modified trehalose analogues were synthesized using our previously reported one-step chemoenzymatic method and shown to inhibit growth and biofilm formation in the two-to three-digit micromolar range in Mycobacterium smegmatis. The trehalose-specific ABC transporter LpqY-SugABC was essential for antimicrobial and anti-biofilm activity, suggesting that inhibition by monosubstituted trehalose analogues requires cellular uptake and does not proceed via direct action on extracellular targets such as antigen 85 acyltransferases or trehalose dimycolate hydrolase. Although the potency of the described compounds in in vitro growth and biofilm assays is moderate, this study reports the first trehalose-based mycobacterial biofilm inhibitors and reinforces the concept of exploiting unique sugar uptake pathways to deliver inhibitors and other chemical cargo to mycobacteria.

Indexed as

Anti-Bacterial AgentsATP-Binding Cassette TransportersBacterial ProteinsBiofilmsDose-Response Relationship, DrugMycobacterium smegmatisProtein TransportTrehaloseAnti-Bacterial AgentsATP-Binding Cassette TransportersBacterial ProteinsTrehalose

Identifiers

PMID28917089
PMCPMC5693249
OpenAlexW2745267660

What OpenQuestion holds

Textmetadata
LicenceTDM
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.