Literature DB >> 31811038

Antimicrobial Activity of, and Cellular Pathways Targeted by, p-Anisaldehyde and Epigallocatechin Gallate in the Opportunistic Human Pathogen Pseudomonas aeruginosa.

Yetunde Adewunmi1, Sanchirmaa Namjilsuren1, William D Walker2, Dahlia N Amato2, Douglas V Amato2, Olga V Mavrodi1,3, Derek L Patton4, Dmitri V Mavrodi5.   

Abstract

Plant-derived aldehydes are constituents of essential oils that possess broad-spectrum antimicrobial activity and kill microorganisms without promoting resistance. In our previous study, we incorporated p-anisaldehyde from star anise into a polymer network called proantimicrobial networks via degradable acetals (PANDAs) and used it as a novel drug delivery platform. PANDAs released p-anisaldehyde upon a change in pH and humidity and controlled the growth of the multidrug-resistant pathogen Pseudomonas aeruginosa PAO1. In this study, we identified the cellular pathways targeted by p-anisaldehyde by generating 10,000 transposon mutants of PAO1 and screened them for hypersensitivity to p-anisaldehyde. To improve the antimicrobial efficacy of p-anisaldehyde, we combined it with epigallocatechin gallate (EGCG), a polyphenol from green tea, and demonstrated that it acts synergistically with p-anisaldehyde in killing P. aeruginosa We then used transcriptome sequencing to profile the responses of P. aeruginosa to p-anisaldehyde, EGCG, and their combination. The exposure to p-anisaldehyde altered the expression of genes involved in modification of the cell envelope, membrane transport, drug efflux, energy metabolism, molybdenum cofactor biosynthesis, and the stress response. We also demonstrate that the addition of EGCG reversed many p-anisaldehyde-coping effects and induced oxidative stress. Our results provide insight into the antimicrobial activity of p-anisaldehyde and its interactions with EGCG and may aid in the rational identification of new synergistically acting combinations of plant metabolites. Our study also confirms the utility of the thiol-ene polymer platform for the sustained and effective delivery of hydrophobic and volatile antimicrobial compounds.IMPORTANCE Essential oils (EOs) are plant-derived products that have long been exploited for their antimicrobial activities in medicine, agriculture, and food preservation. EOs represent a promising alternative to conventional antibiotics due to their broad-range antimicrobial activity, low toxicity to human commensal bacteria, and capacity to kill microorganisms without promoting resistance. Despite the progress in the understanding of the biological activity of EOs, our understanding of many aspects of their mode of action remains inconclusive. The overarching aim of this work was to address these gaps by studying the molecular interactions between an antimicrobial plant aldehyde and the opportunistic human pathogen Pseudomonas aeruginosa The results of this study identify the microbial genes and associated pathways involved in the response to antimicrobial phytoaldehydes and provide insights into the molecular mechanisms governing the synergistic effects of individual constituents within essential oils.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  Pseudomonas aeruginosa; antimicrobial activity; cellular targets; epigallocatechin gallate; p-anisaldehyde

Year:  2020        PMID: 31811038      PMCID: PMC6997733          DOI: 10.1128/AEM.02482-19

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  56 in total

Review 1.  Bacterial molybdoenzymes: old enzymes for new purposes.

Authors:  Silke Leimkühler; Chantal Iobbi-Nivol
Journal:  FEMS Microbiol Rev       Date:  2015-10-13       Impact factor: 16.408

2.  Organization of heat shock dnaK and groE operons of the nosocomial pathogen Enterococcus faecium.

Authors:  Marinella S Laport; Leonardo Lima Dos Santos; José A C Lemos; Maria do Carmo F Bastos; Robert A Burne; Marcia Giambiagi-Demarval
Journal:  Res Microbiol       Date:  2005-08-08       Impact factor: 3.992

3.  Inactivation of efflux pumps abolishes bacterial biofilm formation.

Authors:  Malin Kvist; Viktoria Hancock; Per Klemm
Journal:  Appl Environ Microbiol       Date:  2008-10-03       Impact factor: 4.792

4.  Interplay of efflux system, ampC, and oprD expression in carbapenem resistance of Pseudomonas aeruginosa clinical isolates.

Authors:  John Quale; Simona Bratu; Jyoti Gupta; David Landman
Journal:  Antimicrob Agents Chemother       Date:  2006-05       Impact factor: 5.191

5.  Potential Use of Dimethyl Sulfoxide in Treatment of Infections Caused by Pseudomonas aeruginosa.

Authors:  Qiao Guo; Qiaolian Wu; Dangdang Bai; Yang Liu; Lin Chen; Sheng Jin; Yuting Wu; Kangmin Duan
Journal:  Antimicrob Agents Chemother       Date:  2016-11-21       Impact factor: 5.191

Review 6.  Homeostasis and catabolism of choline and glycine betaine: lessons from Pseudomonas aeruginosa.

Authors:  Matthew J Wargo
Journal:  Appl Environ Microbiol       Date:  2013-01-25       Impact factor: 4.792

7.  Transcriptional tradeoff between metabolic and stress-response programs in Pseudomonas putida KT2440 cells exposed to toluene.

Authors:  Patricia Domínguez-Cuevas; José-Eduardo González-Pastor; Silvia Marqués; Juan-Luis Ramos; Víctor de Lorenzo
Journal:  J Biol Chem       Date:  2006-02-22       Impact factor: 5.157

8.  Epigallocatechin-gallate enhances the activity of tetracycline in staphylococci by inhibiting its efflux from bacterial cells.

Authors:  Andrea Sudano Roccaro; Anna Rita Blanco; Francesco Giuliano; Dario Rusciano; Vincenzo Enea
Journal:  Antimicrob Agents Chemother       Date:  2004-06       Impact factor: 5.191

Review 9.  How to manage Pseudomonas aeruginosa infections.

Authors:  Matteo Bassetti; Antonio Vena; Antony Croxatto; Elda Righi; Benoit Guery
Journal:  Drugs Context       Date:  2018-05-29

10.  Effects of disruption of heat shock genes on susceptibility of Escherichia coli to fluoroquinolones.

Authors:  Yuko Yamaguchi; Toshifumi Tomoyasu; Akiko Takaya; Mizue Morioka; Tomoko Yamamoto
Journal:  BMC Microbiol       Date:  2003-08-12       Impact factor: 3.605

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  3 in total

1.  Membrane Depolarization Sensitizes Pseudomonas aeruginosa Against Tannic Acid.

Authors:  Md Aashique; Amrita Roy; Rekha Yamini Kosuru; Soumen Bera
Journal:  Curr Microbiol       Date:  2021-01-07       Impact factor: 2.188

2.  2E,4E-Decadienoic Acid, a Novel Anti-Oomycete Agent from Coculture of Bacillus subtilis and Trichoderma asperellum.

Authors:  Xi-Fen Zhang; Qing-Yu Li; Mei Wang; Si-Qi Ma; Yan-Fen Zheng; Yi-Qiang Li; Dong-Lin Zhao; Cheng-Sheng Zhang
Journal:  Microbiol Spectr       Date:  2022-08-09

3.  Impact of Phytochemicals on Viability and Cereulide Toxin Synthesis in Bacillus cereus Revealed by a Novel High-Throughput Method, Coupling an AlamarBlue-Based Assay with UPLC-MS/MS.

Authors:  Markus Kranzler; Elrike Frenzel; Veronika Walser; Thomas F Hofmann; Timo D Stark; Monika Ehling-Schulz
Journal:  Toxins (Basel)       Date:  2021-09-21       Impact factor: 4.546

  3 in total

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