Inhibition of Protein Secretion in


Journal

Antimicrobial agents and chemotherapy
ISSN: 1098-6596
Titre abrégé: Antimicrob Agents Chemother
Pays: United States
ID NLM: 0315061

Informations de publication

Date de publication:
02 2019
Historique:
received: 18 06 2018
accepted: 04 11 2018
pubmed: 14 11 2018
medline: 28 1 2020
entrez: 14 11 2018
Statut: epublish

Résumé

At sufficient concentrations, antibiotics effectively eradicate many bacterial infections. However, during therapy, bacteria are unavoidably exposed to lower antibiotic concentrations, and sub-MIC exposure can result in a wide variety of other effects, including the induction of virulence, which can complicate therapy, or horizontal gene transfer (HGT), which can accelerate the spread of resistance genes. Bacterial type I signal peptidase (SPase) is an essential protein that acts at the final step of the general secretory pathway. This pathway is required for the secretion of many proteins, including many required for virulence, and the arylomycins are a class of natural product antibiotics that target SPase. Here, we investigated the consequences of exposing

Identifiants

pubmed: 30420476
pii: AAC.01253-18
doi: 10.1128/AAC.01253-18
pmc: PMC6355593
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bacterial Proteins 0
Membrane Proteins 0
Serine Endopeptidases EC 3.4.21.-
type I signal peptidase EC 3.4.21.89

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

Subventions

Organisme : NIAID NIH HHS
ID : R21 AI081126
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA231991
Pays : United States
Organisme : NCI NIH HHS
ID : R50 CA211526
Pays : United States

Informations de copyright

Copyright © 2019 American Society for Microbiology.

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Auteurs

Shawn I Walsh (SI)

Department of Chemistry, The Scripps Research Institute, La Jolla, California, USA.

David S Peters (DS)

Department of Chemistry, The Scripps Research Institute, La Jolla, California, USA.

Peter A Smith (PA)

Department of Chemistry, The Scripps Research Institute, La Jolla, California, USA.

Arryn Craney (A)

Department of Chemistry, The Scripps Research Institute, La Jolla, California, USA.

Melissa M Dix (MM)

The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, California, USA.
Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California, USA.

Benjamin F Cravatt (BF)

The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, California, USA.
Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California, USA.

Floyd E Romesberg (FE)

Department of Chemistry, The Scripps Research Institute, La Jolla, California, USA floyd@scripps.edu.

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Classifications MeSH