Literature DB >> 23403434

Bis-(3'-5')-cyclic dimeric GMP regulates antimicrobial peptide resistance in Pseudomonas aeruginosa.

Song Lin Chua1, Sean Yang-Yi Tan, Morten Theil Rybtke, Yicai Chen, Scott A Rice, Staffan Kjelleberg, Tim Tolker-Nielsen, Liang Yang, Michael Givskov.   

Abstract

Bis-(3'-5')-cyclic dimeric GMP (c-di-GMP) is an intracellular second messenger that controls the lifestyles of many bacteria. A high intracellular level of c-di-GMP induces a biofilm lifestyle, whereas a low intracellular level of c-di-GMP stimulates dispersal of biofilms and promotes a planktonic lifestyle. Here, we used the expression of different reporters to show that planktonic cells, biofilm cells, and cells dispersed from biofilms (DCells) had distinct intracellular c-di-GMP levels. Proteomics analysis showed that the low intracellular c-di-GMP level of DCells induced the expression of proteins required for the virulence and development of antimicrobial peptide resistance in Pseudomonas aeruginosa. In accordance with this, P. aeruginosa cells with low c-di-GMP levels were found to be more resistant to colistin than P. aeruginosa cells with high c-di-GMP levels. This finding contradicts the current dogma stating that dispersed cells are inevitably more susceptible to antibiotics than their sessile counterparts.

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Year:  2013        PMID: 23403434      PMCID: PMC3632963          DOI: 10.1128/AAC.02499-12

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  43 in total

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Journal:  Mol Microbiol       Date:  2005-06       Impact factor: 3.501

5.  Broad-host-range expression vectors that carry the L-arabinose-inducible Escherichia coli araBAD promoter and the araC regulator.

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6.  Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development.

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7.  Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes.

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Journal:  Gene       Date:  1995-12-01       Impact factor: 3.688

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Authors:  S E West; H P Schweizer; C Dall; A K Sample; L J Runyen-Janecky
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9.  Analysis of Pseudomonas aeruginosa diguanylate cyclases and phosphodiesterases reveals a role for bis-(3'-5')-cyclic-GMP in virulence.

Authors:  Hemantha Kulasakara; Vincent Lee; Anja Brencic; Nicole Liberati; Jonathan Urbach; Sachiko Miyata; Daniel G Lee; Alice N Neely; Mamoru Hyodo; Yoshihiro Hayakawa; Frederick M Ausubel; Stephen Lory
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10.  The EAL domain protein VieA is a cyclic diguanylate phosphodiesterase.

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2.  Comparative systems biology analysis to study the mode of action of the isothiocyanate compound Iberin on Pseudomonas aeruginosa.

Authors:  Sean Yang-Yi Tan; Yang Liu; Song Lin Chua; Rebecca Munk Vejborg; Tim Holm Jakobsen; Su Chuen Chew; Yingying Li; Thomas E Nielsen; Tim Tolker-Nielsen; Liang Yang; Michael Givskov
Journal:  Antimicrob Agents Chemother       Date:  2014-08-25       Impact factor: 5.191

3.  Elevated levels of the second messenger c-di-GMP contribute to antimicrobial resistance of Pseudomonas aeruginosa.

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4.  In vitro and in vivo generation and characterization of Pseudomonas aeruginosa biofilm-dispersed cells via c-di-GMP manipulation.

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Review 5.  Proteomics dedicated to biofilmology: What have we learned from a decade of research?

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Journal:  Med Microbiol Immunol       Date:  2015-06-12       Impact factor: 3.402

6.  BrlR from Pseudomonas aeruginosa is a c-di-GMP-responsive transcription factor.

Authors:  Jacob R Chambers; Julie Liao; Michael J Schurr; Karin Sauer
Journal:  Mol Microbiol       Date:  2014-03-06       Impact factor: 3.501

Review 7.  Options and Limitations in Clinical Investigation of Bacterial Biofilms.

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8.  Pseudomonas aeruginosa Requires the DNA-Specific Endonuclease EndA To Degrade Extracellular Genomic DNA To Disperse from the Biofilm.

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9.  Insulin treatment enhances pseudomonas aeruginosa biofilm formation by increasing intracellular cyclic di-GMP levels, leading to chronic wound infection and delayed wound healing.

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10.  In Vitro Evaluation of Biofilm Dispersal as a Therapeutic Strategy To Restore Antimicrobial Efficacy.

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