Evidence map›Paper›PMID 32786281›Full record

ReviewACS infectious diseases2020

Periplasmic Targets for the Development of Effective Antimicrobials against Gram-Negative Bacteria.

Ankit Pandeya, Isoiza Ojo, Olaniyi Alegun, Yinan Wei

Open access · greenAbstract readReview
In one paragraph

Review in ACS infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Antibiotic Resistance inAntibiotics (Basel, Switzerland) · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Targeting Iron - Respiratory Reciprocity Promotes Bacterial Death.bioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Exploring the inhibitory potential ofFrontiers in molecular biosciences · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. 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

4 authors at 1 institution in 1 country.

Ankit PandeyaDepartment of Chemistry, University of Kentucky, Lexington, Kentucky 40506, United States.
Isoiza OjoDepartment of Chemistry, University of Kentucky, Lexington, Kentucky 40506, United States.
Olaniyi AlegunDepartment of Chemistry, University of Kentucky, Lexington, Kentucky 40506, United States.ORCID 0000-0002-5774-6431
Yinan WeiDepartment of Chemistry, University of Kentucky, Lexington, Kentucky 40506, United States.ORCID 0000-0002-9936-7149
University of Kentucky · US

Funding

A novel mechanism of immunosuppression in sepsis: Depletion of monocytes and macrophagesR01GM132443 · NIGMS · UNIVERSITY OF KENTUCKY · PI LI, ZHENYU, WEI, YINAN · 2019 to 2022
$1.7M
Rules for penetrating the Gram-negative bacterial envelopeR56AI137020 · NIAID · UNIVERSITY OF KENTUCKY · PI WEI, YINAN · 2018 to 2018
$565k
Inhibition of GSDMD as a new treatment for infectionR21AI142063 · NIAID · UNIVERSITY OF KENTUCKY · PI WEI, YINAN · 2019 to 2020
$405k
NIAID NIH HHS R21 AI142063NIAID NIH HHS R56 AI137020NIGMS NIH HHS R01 GM132443
6 · The paper itself

Abstract

Antibiotic resistance has emerged as a serious threat to global public health in recent years. Lack of novel antimicrobials, especially new classes of compounds, further aggravates the situation. For Gram-negative bacteria, their double layered cell envelope and an array of efflux pumps act as formidable barriers for antimicrobials to penetrate. While cytoplasmic targets are hard to reach, proteins in the periplasm are clearly more accessible, as the drug only needs to breach the outer membrane. In this review, we summarized recent efforts on the validation and testing of periplasmic proteins as potential antimicrobial targets and the development of related inhibitors that either inhibit the growth of a bacterial pathogen or reduce its virulence during interaction with host cells. We conclude that the periplasm contains a promising pool of novel antimicrobial targets that should be scrutinized more closely for the development of effective treatment against multidrug-resistant Gram-negative bacteria.

Indexed as

Gram-Negative BacteriaPeriplasmAnti-Bacterial AgentsBacteriaDrug Resistance, Multiple, BacterialAnti-Bacterial Agentsantimicrobial resistanceantimicrobial targetchaperoneefflux pumpGram-negative bacteriuminhibitorperiplasmvirulence

Identifiers

PMID32786281
PMCPMC8187054
OpenAlexW3047115808

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.