Evidence map›Paper›PMID 26847396›Full record

ArticleJournal of the American Chemical Society2016

Antibacterial Flavonoids from Medicinal Plants Covalently Inactivate Type III Protein Secretion Substrates.

Lun K Tsou, María Lara-Tejero, Jordan RoseFigura, Zhenrun J Zhang, Yen-Chih Wang, Jacob S Yount, Matthew Lefebre, Paul D Dossa, Junya Kato, Fulan Guan and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
11.9field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 135 citations in OpenAlex.

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  18. Quercitrin Is a Novel Inhibitor ofMolecules (Basel, Switzerland) · 2023
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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

14 authors at 2 institutions in 1 country.

Lun K TsouLaboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University , New York, New York 10065, United States.
María Lara-TejeroDepartment of Microbial Pathogenesis, Yale University School of Medicine , New Haven, Connecticut 06536, United States.
Jordan RoseFiguraLaboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University , New York, New York 10065, United States.
Zhenrun J ZhangLaboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University , New York, New York 10065, United States.
Yen-Chih WangLaboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University , New York, New York 10065, United States.
Jacob S YountLaboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University , New York, New York 10065, United States.
Matthew LefebreDepartment of Microbial Pathogenesis, Yale University School of Medicine , New Haven, Connecticut 06536, United States.
Paul D DossaLaboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University , New York, New York 10065, United States.
Junya KatoDepartment of Microbial Pathogenesis, Yale University School of Medicine , New Haven, Connecticut 06536, United States.
Fulan GuanDepartment of Pharmacology, Yale University School of Medicine , New Haven, Connecticut 06520, United States.
Wing LamDepartment of Pharmacology, Yale University School of Medicine , New Haven, Connecticut 06520, United States.
Yung-Chi ChengDepartment of Pharmacology, Yale University School of Medicine , New Haven, Connecticut 06520, United States.
Jorge E GalánDepartment of Microbial Pathogenesis, Yale University School of Medicine , New Haven, Connecticut 06536, United States.
Howard C HangLaboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University , New York, New York 10065, United States.
Rockefeller University · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
MOLECULAR GENETIC ANALYSIS OF SALMONELLA CELL INVASIONR37AI030492 · NIAID · YALE UNIVERSITY · PI GALAN, JORGE E · 2000 to 2024
$10.1M
Clinical Study of PHY906, a Novel Chinese Herbal Medicine, as a Modulator of IrinP01CA154295 · NCI · YALE UNIVERSITY · PI CHENG, YUNG-CHI · 2011 to 2016
$6.4M
MOLECULAR GENETIC ANALYSIS OF SALMONELLA CELL INVASIONR01AI030492 · NIAID · YALE UNIVERSITY · PI Jorge E Galan · 1995 to 2026
$3.1M
Mechanistic analysis of flavonoids on bacterial virulenceR01AT007671 · NCCIH · ROCKEFELLER UNIVERSITY · PI GALAN, JORGE E, HANG, HOWARD C · 2012 to 2016
$2.4M
Molecular Control of IFITM3 in Restricting Influenza Virus InfectionR56AI114826 · NIAID · OHIO STATE UNIVERSITY · PI YOUNT, JACOB · 2015 to 2015
$366k
Chemical Probes for Type III Protein Secretion in Bacterial PathogensF32AI096890 · NIAID · ROCKEFELLER UNIVERSITY · PI ROSEFIGURA, JORDAN · 2012 to 2014
$150k
MOLECULAR GENETIC ANALYSIS OF SALMONELLA CELL INVASIONR29AI030492 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI GALAN, JORGE E · 1991 to 1995
–
NCATS NIH HHS UL1 TR001863NCCIH NIH HHS R01 AT007671NCCIH NIH HHS R01AT007671NCI NIH HHS P01 CA154295NCI NIH HHS P01CA154295NCI NIH HHS P30 CA016359NIAID NIH HHS AI096890NIAID NIH HHS AI30492NIAID NIH HHS F32 AI096890NIAID NIH HHS R01 AI030492NIAID NIH HHS R37 AI030492NIAID NIH HHS R56 AI114826
6 · The paper itself

Abstract

Traditional Chinese Medicines (TCMs) have been historically used to treat bacterial infections. However, the molecules responsible for these anti-infective properties and their potential mechanisms of action have remained elusive. Using a high-throughput assay for type III protein secretion in Salmonella enterica serovar Typhimurium, we discovered that several TCMs can attenuate this key virulence pathway without affecting bacterial growth. Among the active TCMs, we discovered that baicalein, a specific flavonoid from Scutellaria baicalensis, targets S. Typhimurium pathogenicity island-1 (SPI-1) type III secretion system (T3SS) effectors and translocases to inhibit bacterial invasion of epithelial cells. Structurally related flavonoids present in other TCMs, such as quercetin, also inactivated the SPI-1 T3SS and attenuated S. Typhimurium invasion. Our results demonstrate that specific plant metabolites from TCMs can directly interfere with key bacterial virulence pathways and reveal a previously unappreciated mechanism of action for anti-infective medicinal plants.

Indexed as

Anti-Bacterial AgentsDose-Response Relationship, DrugDrugs, Chinese HerbalFlavonoidsHigh-Throughput Screening AssaysMicrobial Sensitivity TestsMolecular StructurePlants, MedicinalSalmonella typhimuriumStructure-Activity RelationshipSubstrate SpecificityType III Secretion SystemsAnti-Bacterial AgentsDrugs, Chinese HerbalFlavonoidsType III Secretion Systems

Identifiers

PMID26847396
PMCPMC4831573
OpenAlexW2266508197

What OpenQuestion holds

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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.