A Dual-Mechanism Antibiotic Kills Gram-Negative Bacteria and Avoids Drug Resistance.


Journal

Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066

Informations de publication

Date de publication:
25 06 2020
Historique:
received: 06 06 2019
revised: 24 02 2020
accepted: 01 05 2020
pubmed: 5 6 2020
medline: 22 1 2021
entrez: 5 6 2020
Statut: ppublish

Résumé

The rise of antibiotic resistance and declining discovery of new antibiotics has created a global health crisis. Of particular concern, no new antibiotic classes have been approved for treating Gram-negative pathogens in decades. Here, we characterize a compound, SCH-79797, that kills both Gram-negative and Gram-positive bacteria through a unique dual-targeting mechanism of action (MoA) with undetectably low resistance frequencies. To characterize its MoA, we combined quantitative imaging, proteomic, genetic, metabolomic, and cell-based assays. This pipeline demonstrates that SCH-79797 has two independent cellular targets, folate metabolism and bacterial membrane integrity, and outperforms combination treatments in killing methicillin-resistant Staphylococcus aureus (MRSA) persisters. Building on the molecular core of SCH-79797, we developed a derivative, Irresistin-16, with increased potency and showed its efficacy against Neisseria gonorrhoeae in a mouse vaginal infection model. This promising antibiotic lead suggests that combining multiple MoAs onto a single chemical scaffold may be an underappreciated approach to targeting challenging bacterial pathogens.

Identifiants

pubmed: 32497502
pii: S0092-8674(20)30567-5
doi: 10.1016/j.cell.2020.05.005
pmc: PMC7780349
mid: NIHMS1597301
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
N3-cyclopropyl-7-((4-(1-methylethyl)phenyl)methyl)-7H-pyrrolo(3, 2-f)quinazoline-1,3-diamine 0
Pyrroles 0
Quinazolines 0
Folic Acid 935E97BOY8

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1518-1532.e14

Subventions

Organisme : NIAID NIH HHS
ID : DP1 AI124669
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA072720
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007388
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests A patent application describing the use of SCH-79797 as an antibiotic, as well as the pharmaceutical composition and use as antibiotic of derivatives is currently pending.

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Auteurs

James K Martin (JK)

Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.

Joseph P Sheehan (JP)

Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.

Benjamin P Bratton (BP)

Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.

Gabriel M Moore (GM)

Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.

André Mateus (A)

European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.

Sophia Hsin-Jung Li (SH)

Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.

Hahn Kim (H)

Department of Chemistry, Princeton University, Princeton, NJ 08544, USA; Princeton University Small Molecule Screening Center, Princeton University, Princeton, NJ 08544, USA.

Joshua D Rabinowitz (JD)

Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.

Athanasios Typas (A)

European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.

Mikhail M Savitski (MM)

European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.

Maxwell Z Wilson (MZ)

Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA; Department of Molecular, Cellular, and Developmental Biology, Center for BioEngineering, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.

Zemer Gitai (Z)

Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. Electronic address: zgitai@princeton.edu.

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Classifications MeSH