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PMID: 15470704 Published · ppublish English Journal Article

Differential gene expression shows natural brominated furanones interfere with the autoinducer-2 bacterial signaling system of Escherichia coli.

Biotechnology and bioengineering ·Vol. 88 ·No. 5 ·2004-12-05 ·Pages 630-42

Ren D, Bedzyk LA, Ye RW, Thomas SM, Wood TK

Abstract

The quorum sensing disrupter (5Z)-4-bromo-5-(bromomethylene)-3-butyl-2(5H)-furanone (furanone) of the alga Delisea pulchra was previously found by us (Environ Microbiol 3:731-736, 2001) to inhibit quorum sensing in Escherichia coli via autoinducer-2 (AI-2, produced by LuxS). In this study, DNA microarrays were used to study the genetic basis of this natural furanone inhibition of AI-2 signaling (significant values with p < 0.05 are reported). Using DNA microarrays, the AI-2 mutant Escherichia coli DH5alpha was compared with the AI-2 wild-type strain, E. coli K12, to determine how AI-2 influenced gene expression. Escherichia coli K12 was also grown with 0 and 60 microg/mL furanone to study the inhibition of quorum sensing gene expression. It was found that 166 genes were differentially expressed by AI-2 (67 were induced and 99 were repressed) and 90 genes were differentially expressed by furanone (34 were induced and 56 were repressed). Importantly, 79% (44 out of 56) of the genes repressed by furanone were induced by AI-2, which indicated that furanone inhibited AI-2 signaling and influenced the same suite of genes as a regulon. Most of these genes have functions of chemotaxis, motility, and flagellar synthesis. Interestingly, the aerotaxis genes aer and tsr were discovered to be induced by AI-2 and repressed by furanone. Representative microarray results were confirmed by RNA dot blotting. Furthermore, the E. coli air-liquid interface biofilm formation was repressed by furanone, supporting the results that taxis and flagellar genes were repressed by furanone. The autoinducer bioassay indicated that 100 microg/mL furanone decreased the extracellular concentration of AI-2 2-fold, yet luxS and pfs transcription were not significantly altered. Hence, furanone appeared to alter AI-2 signaling post-transcriptionally.

MeSH Terms
Chemotaxis/drug effects,physiology Dose-Response Relationship, Drug Escherichia coli/drug effects,genetics,metabolism Escherichia coli Proteins/metabolism Furans/pharmacokinetics Gene Expression Profiling/methods Gene Expression Regulation, Bacterial/drug effects,physiology Homoserine/analogs & derivatives,genetics,metabolism Lactones/metabolism Signal Transduction/drug effects
Chemicals
Escherichia coli Proteins Furans Lactones N-octanoylhomoserine lactone Homoserine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ren Dacheng
Department of Chemical Engineering and Molecular & Cell Biology, University of Connecticut, 191 Auditorium Road, U-3222, Storrs, Connecticut 06269-3222, USA.
Bedzyk Laura A
Ye Rick W
Thomas Stuart M
Wood Thomas K
Article Info
Journal
Biotechnology and bioengineering
Abbr.
Biotechnol Bioeng
ISSN
0006-3592
Published
2004-12-05
Pages
630-42
Language
English
Region
United States
NLM ID
7502021
Subset
IM
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