Evidence map›Paper›PMID 33733746›Full record

ArticleAccounts of chemical research2021

Leveraging Marine Natural Products as a Platform to Tackle Bacterial Resistance and Persistence.

M Alejandro Valdes-Pena, Nicholas P Massaro, You-Chen Lin, Joshua G Pierce

Open access · greenAbstract read
In one paragraph

Article in Accounts of chemical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.2field-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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Pyrrolidine-2,3-diones: heterocyclic scaffolds that inhibit and eradicateChemical communications (Cambridge, England) · 2024
    Article
  5. A Rhein-Based Derivative TargetsAntibiotics (Basel, Switzerland) · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. β-Lactams from the Ocean.Marine drugs · 2023
    Review
  10. Review
  11. 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.

M Alejandro Valdes-PenaDepartment of Chemistry and Comparative Medicine Institute, NC State University, Raleigh, North Carolina 27695, United States.
Nicholas P MassaroDepartment of Chemistry and Comparative Medicine Institute, NC State University, Raleigh, North Carolina 27695, United States.ORCID 0000-0002-6008-7676
You-Chen LinDepartment of Chemistry and Comparative Medicine Institute, NC State University, Raleigh, North Carolina 27695, United States.
Joshua G PierceDepartment of Chemistry and Comparative Medicine Institute, NC State University, Raleigh, North Carolina 27695, United States.ORCID 0000-0001-9194-3765
North Carolina State University · US

Funding

Synthesis and Chemical Biology of Bioactive Natural ProductsR35GM139583 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI PIERCE, JOSHUA G. · 2021 to 2025
$2.5M
Synthesis and Chemical Biology of Oxazolidinone and Pyrrolidine Natural ProductsR01GM110154 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI PIERCE, JOSHUA G. · 2015 to 2019
$1.3M
Synthesis and Chemical Biology of Bioactive Guanidine AlkaloidsR01GM117570 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI PIERCE, JOSHUA G. · 2016 to 2019
$1.2M
NIGMS NIH HHS R01 GM110154NIGMS NIH HHS R01 GM117570NIGMS NIH HHS R35 GM139583
6 · The paper itself

Abstract

Antimicrobial resistance to existing antibiotics represents one of the greatest threats to human health and is growing at an alarming rate. To further complicate treatment of bacterial infections, many chronic infections are the result of bacterial biofilms that are tolerant to treatment with antibiotics because of the presence of metabolically dormant persister cell populations. Together these threats are creating an increasing burden on the healthcare system, and a "preantibiotic" age is on the horizon if significant action is not taken by the scientific and medical communities. While the golden era of antibiotic discovery (1940s-1960s) produced most of the antibiotic classes in clinical use today, followed by several decades of limited development, there has been a resurgence in antibiotic drug discovery in recent years fueled by the academic and biotech sectors. Historically, great success has been achieved by developing next-generation variants of existing classes of antibiotics, but there remains a dire need for the identification of novel scaffolds and/or antimicrobial targets to drive future efforts to overcome resistance and tolerance. In this regard, there has been no more valuable source for the identification of antibiotics than natural products, with 69-77% of approved antibiotics either being such compounds or being derived from them.Our group has developed a program centered on the chemical synthesis and chemical microbiology of marine natural products with unusual structures and promising levels of activity against multidrug-resistant (MDR) bacterial pathogens. As we are motivated by preparing and studying the biological effects of these molecules, we are not initially pursuing a biological question but instead are allowing the observed phenotypes and activities to guide the ultimate project direction. In this Account, our recent efforts on the synoxazolidinone, lipoxazolidinone, and batzelladine natural products will be discussed and placed in the context of the field's greatest challenges and opportunities. Specifically, the synoxazolidinone family of 4-oxazolidinone-containing natural products has led to the development of several chemical methods to prepare antimicrobial scaffolds and has revealed compounds with potent activity as adjuvants to treat bacterial biofilms. Bearing the same 4-oxazolidinone core, the lipoxazolidinones have proven to be potent single-agent antibiotics. Finally, our synthetic efforts toward the batzelladines revealed analogues with activity against a number of MDR pathogens, highlighted by non-natural stereochemical isomers with superior activity and simplified synthetic access. Taken together, these studies provide several distinct platforms for the development of novel therapeutics that can add to our arsenal of scaffolds for preclinical development and can provide insight into the biochemical processes and pathways that can be targeted by small molecules in the fight against antimicrobial-resistant and -tolerant infections. We hope that this work will serve as inspiration for increased efforts by the scientific community to leverage synthetic chemistry and chemical microbiology toward novel antibiotics that can combat the growing crisis of MDR and tolerant bacterial infections.

Indexed as

AlkaloidsAnti-Bacterial AgentsBiofilmsBiological ProductsDrug Resistance, Multiple, BacterialGuanidineGuanidinesMicrobial Sensitivity TestsOxazolidinonesStaphylococcus aureusStereoisomerismStructure-Activity RelationshipAlkaloidsAnti-Bacterial Agentsbatzelladine ABiological ProductsGuanidineGuanidineslipoxazolidinone AOxazolidinonessynoxazolidinone A

Identifiers

PMID33733746
PMCPMC8428769
OpenAlexW3137932045

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.