Evidence map›Paper›PMID 26776731›Full record

ArticleCurrent biology : CB2016

Auto Poisoning of the Respiratory Chain by a Quorum-Sensing-Regulated Molecule Favors Biofilm Formation and Antibiotic Tolerance.

Ronen Hazan, Yok Ai Que, Damien Maura, Benjamin Strobel, Paul Anthony Majcherczyk, Laura Rose Hopper, David J Wilbur, Teri N Hreha, Blanca Barquera, Laurence G Rahme

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

108 citing papers in PubMed, 222 citations in OpenAlex.

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  8. TheJournal of bacteriology · 2026
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  11. BioMed research international · 2026
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  15. MvfR ShapesCells · 2025
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  16. In Vitro Analysis of Interactions BetweenAntibiotics (Basel, Switzerland) · 2025
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  18. Disruption ofMicrobiology (Reading, England) · 2025
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  20. Review

48 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Ronen HazanDepartment of Surgery and Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA; Department of Surgery, Center for Surgery, Innovation and Bioengineering, Massachusetts General Hospital, Boston, MA 02114, USA; Shriners Hospitals for Children Boston, Boston, MA 02114, USA.
Yok Ai QueDepartment of Surgery and Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA; Department of Surgery, Center for Surgery, Innovation and Bioengineering, Massachusetts General Hospital, Boston, MA 02114, USA; Shriners Hospitals for Children Boston, Boston, MA 02114, USA.
Damien MauraDepartment of Surgery and Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA; Department of Surgery, Center for Surgery, Innovation and Bioengineering, Massachusetts General Hospital, Boston, MA 02114, USA; Shriners Hospitals for Children Boston, Boston, MA 02114, USA.
Benjamin StrobelDepartment of Surgery and Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA; Department of Surgery, Center for Surgery, Innovation and Bioengineering, Massachusetts General Hospital, Boston, MA 02114, USA.
Paul Anthony MajcherczykDepartment of Fundamental Microbiology, University of Lausanne, Lausanne 1015, Switzerland.
Laura Rose HopperDepartment of Surgery and Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA; Department of Surgery, Center for Surgery, Innovation and Bioengineering, Massachusetts General Hospital, Boston, MA 02114, USA.
David J WilburDepartment of Chemistry, Tufts University, Medford, MA 02155, USA.
Teri N HrehaDepartment of Biological Sciences, CBIS, Rensselaer Polytechnic Institute, 110 8(th) Street, Troy, NY 12180, USA.
Blanca BarqueraDepartment of Biological Sciences, CBIS, Rensselaer Polytechnic Institute, 110 8(th) Street, Troy, NY 12180, USA.
Laurence G RahmeDepartment of Surgery and Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA; Department of Surgery, Center for Surgery, Innovation and Bioengineering, Massachusetts General Hospital, Boston, MA 02114, USA; Shriners Hospitals for Children Boston, Boston, MA 02114, USA. Electronic address: rahme@molbio.mgh.harvard.edu.
Massachusetts General Hospital · USRensselaer Polytechnic Institute · USHarvard University · USShriners Hospitals for Children - Boston · USTufts University · USUniversity of Lausanne · CH

Funding

Function of MVFR in Pseudomonas aeruginosa virulenceR01AI063433 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAHME, LAURENCE G · 2006 to 2010
$1.9M
Interruption of Signaling-Mediated Bacterial Persistent InfectionsR33AI105902 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAHME, LAURENCE G · 2015 to 2017
$1.8M
Interruption of Signaling-Mediated Bacterial Persistent InfectionsR21AI105902 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAHME, LAURENCE G · 2013 to 2014
$478k
Function of MVFR in Pseudomonas Aeruginosa VirulenceR56AI063433 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAHME, LAURENCE G · 2012 to 2012
$475k
NIAID NIH HHS R01 AI063433NIAID NIH HHS R21 AI105902NIAID NIH HHS R33 AI105902NIAID NIH HHS R33AI105902NIAID NIH HHS R56AI063433
6 · The paper itself

Abstract

Bacterial programmed cell death and quorum sensing are direct examples of prokaryote group behaviors, wherein cells coordinate their actions to function cooperatively like one organism for the benefit of the whole culture. We demonstrate here that 2-n-heptyl-4-hydroxyquinoline-N-oxide (HQNO), a Pseudomonas aeruginosa quorum-sensing-regulated low-molecular-weight excreted molecule, triggers autolysis by self-perturbing the electron transfer reactions of the cytochrome bc1 complex. HQNO induces specific self-poisoning by disrupting the flow of electrons through the respiratory chain at the cytochrome bc1 complex, causing a leak of reducing equivalents to O2 whereby electrons that would normally be passed to cytochrome c are donated directly to O2. The subsequent mass production of reactive oxygen species (ROS) reduces membrane potential and disrupts membrane integrity, causing bacterial cell autolysis and DNA release. DNA subsequently promotes biofilm formation and increases antibiotic tolerance to beta-lactams, suggesting that HQNO-dependent cell autolysis is advantageous to the bacterial populations. These data identify both a new programmed cell death system and a novel role for HQNO as a critical inducer of biofilm formation and antibiotic tolerance. This newly identified pathway suggests intriguing mechanistic similarities with the initial mitochondrial-mediated steps of eukaryotic apoptosis.

Indexed as

BiofilmsAnti-Bacterial AgentsBacterial ProteinsElectron TransportGene Expression Regulation, BacterialHydroxyquinolinesMitochondrial MembranesPseudomonas aeruginosaQuorum Sensing2-(n-heptyl)-4-hydroxyquinoline N-oxideAnti-Bacterial AgentsBacterial ProteinsHydroxyquinolines

Identifiers

PMID26776731
PMCPMC4729643
OpenAlexW2265995051

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.