Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Understanding and Sensitizing Density-Dependent Persistence to Quinolone Antibiotics

Understanding and Sensitizing Density-Dependent Persistence to Quinolone Antibiotics

Thumbnail Image
Download
Name

1-s2.0-S1097276517308717-main.pdf

Size

1.87 MB

Format

Adobe PDF

Checksum (MD5)

6a15f744e66272bf9d38530cf52017e8

Download all files submitted through automated deposit
sword-2018-08-27.original.zip (1.17 MB)
Author(s)
Hamblin, Meagan
•
Gutierrez, Arnaud
•
Jain, Saloni R.
•
Saluja, Prerna Bhargava
•
Lobritz, Michael Andrew
•
Collins, James J.
Date Issued
December 2017
Journal
Molecular Cell
Publisher
Elsevier BV
Citation
Gutierrez, Arnaud et al. “Understanding and Sensitizing Density-Dependent Persistence to Quinolone Antibiotics.” Molecular Cell 68, 6 (December 2017): 1147–1154 © 2017 The Authors
Version
Final published version
Abstract
Physiologic and environmental factors can modulate antibiotic activity and thus pose a significant challenge to antibiotic treatment. The quinolone class of antibiotics, which targets bacterial topoisomerases, fails to kill bacteria that have grown to high density; however, the mechanistic basis for this persistence is unclear. Here, we show that exhaustion of the metabolic inputs that couple carbon catabolism to oxidative phosphorylation is a primary cause of growth phase-dependent persistence to quinolone antibiotics. Supplementation of stationary-phase cultures with glucose and a suitable terminal electron acceptor to stimulate respiratory metabolism is sufficient to sensitize cells to quinolone killing. Using this approach, we successfully sensitize high-density populations of Escherichia coli, Staphylococcus aureus, and Mycobacterium smegmatis to quinolone antibiotics. Our findings link growth-dependent quinolone persistence to discrete impairments in respiratory metabolism and identify a strategy to kill non-dividing bacteria. Gutierrez et al. show that activation of cellular respiration is sufficient to sensitize antibiotic refractory bacteria at high densities to drugs targeting DNA topoisomerases. This suggests that the nutrient environment and metabolic state are key components of bacterial persistence phenotypes. Keywords: quinolones; drug persistence; antibiotic; oxidative phosphorylation
MIT Department
Institute for Medical Engineering and Science
Massachusetts Institute of Technology. Department of Biological Engineering
Terms of Use
Creative Commons Attribution-NonCommercial-NoDerivs License
http://creativecommons.org/licenses/by-nc-nd/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/117581
DOI of Published Version
https://doi.org/10.1016/J.MOLCEL.2017.11.012
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.