Literature DB >> 27899451

Real Time, Spatial, and Temporal Mapping of the Distribution of c-di-GMP during Biofilm Development.

Harikrishnan A S Nair1,2, Saravanan Periasamy1, Liang Yang1,3, Staffan Kjelleberg1,3, Scott A Rice4,3.   

Abstract

Bis-(3'-5')-cyclic dimeric guanosine monophosphate (c-di-GMP) is a dynamic intracellular signaling molecule that plays a central role in the biofilm life cycle. Current methodologies for the quantification of c-di-GMP are typically based on chemical extraction, representing end point measurements. Chemical methodologies also fail to take into consideration the physiological heterogeneity of the biofilm and thus represent an average c-di-GMP concentration across the entire biofilm. To address these problems, a ratiometric, image-based quantification method has been developed based on expression of the green fluorescence protein (GFP) under the control of the c-di-GMP-responsive cdrA promoter (Rybtke, M. T., Borlee, B. R., Murakami, K., Irie, Y., Hentzer, M., Nielsen, T. E., Givskov, M., Parsek, M. R., and Tolker-Nielsen, T. (2012) Appl. Environ. Microbiol. 78, 5060-5069). The methodology uses the cyan fluorescent protein (CFP) as a biomass indicator and the GFP as a c-di-GMP reporter. Thus, the CFP/GFP ratio gives the effective c-di-GMP per biomass. A binary mask was applied to alleviate background fluorescence, and fluorescence was calibrated against known c-di-GMP concentrations. Using flow cells for biofilm formation, c-di-GMP showed a non-uniform distribution across the biofilm, with concentrated hot spots of c-di-GMP. Additionally, c-di-GMP was found to be localized at the outer boundary of mature colonies in contrast to a uniform distribution in early stage, small colonies. These data demonstrate the application of a method for the in situ, real time quantification of c-di-GMP and show that the amount of this biofilm-regulating second messenger was dynamic with time and colony size, reflecting the extent of biofilm heterogeneity in real time.
© 2017 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  Pseudomonas aeruginosa (P. aeruginosa); bacteria; biofilm development; bioreporter; cyclic di-GMP (c-di-GMP); development; image based quantification; nitric oxide

Mesh:

Substances:

Year:  2016        PMID: 27899451      PMCID: PMC5241725          DOI: 10.1074/jbc.M116.746743

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  38 in total

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2.  Hypothesis for the role of nutrient starvation in biofilm detachment.

Authors:  Stephen M Hunt; Erin M Werner; Baochuan Huang; Martin A Hamilton; Philip S Stewart
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3.  New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria.

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Review 4.  Mechanisms of cyclic-di-GMP signaling in bacteria.

Authors:  Urs Jenal; Jacob Malone
Journal:  Annu Rev Genet       Date:  2006       Impact factor: 16.830

5.  The Cyclic AMP-Vfr Signaling Pathway in Pseudomonas aeruginosa Is Inhibited by Cyclic Di-GMP.

Authors:  Henrik Almblad; Joe J Harrison; Morten Rybtke; Julie Groizeleau; Michael Givskov; Matthew R Parsek; Tim Tolker-Nielsen
Journal:  J Bacteriol       Date:  2015-04-20       Impact factor: 3.490

Review 6.  Cyclic di-GMP: the first 25 years of a universal bacterial second messenger.

Authors:  Ute Römling; Michael Y Galperin; Mark Gomelsky
Journal:  Microbiol Mol Biol Rev       Date:  2013-03       Impact factor: 11.056

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8.  Cyclic diguanosine monophosphate represses bacterial flagella synthesis by interacting with the Walker A motif of the enhancer-binding protein FleQ.

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9.  Fluorescence-based reporter for gauging cyclic di-GMP levels in Pseudomonas aeruginosa.

Authors:  Morten T Rybtke; Bradley R Borlee; Keiji Murakami; Yasuhiko Irie; Morten Hentzer; Thomas E Nielsen; Michael Givskov; Matthew R Parsek; Tim Tolker-Nielsen
Journal:  Appl Environ Microbiol       Date:  2012-05-11       Impact factor: 4.792

10.  Role of mutation in Pseudomonas aeruginosa biofilm development.

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1.  Regulation of flagellar motor switching by c-di-GMP phosphodiesterases in Pseudomonas aeruginosa.

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Authors:  Lisa-Marie Nisbett; Lucas Binnenkade; Bezalel Bacon; Sajjad Hossain; Nicholas J Kotloski; Evan D Brutinel; Raimo Hartmann; Knut Drescher; Dhruv P Arora; Sandhya Muralidharan; Kai M Thormann; Jeffrey A Gralnick; Elizabeth M Boon
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Review 3.  The biofilm life cycle: expanding the conceptual model of biofilm formation.

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Review 4.  Controlling Biofilm Development Through Cyclic di-GMP Signaling.

Authors:  Soyoung Park; Karin Sauer
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 3.650

Review 5.  Tracking the homeostasis of second messenger cyclic-di-GMP in bacteria.

Authors:  Anushya Petchiappan; Sujay Y Naik; Dipankar Chatterji
Journal:  Biophys Rev       Date:  2020-02-15

Review 6.  Biofilm dispersion.

Authors:  Kendra P Rumbaugh; Karin Sauer
Journal:  Nat Rev Microbiol       Date:  2020-06-12       Impact factor: 60.633

7.  Accumulation of dead cells from contact killing facilitates coexistence in bacterial biofilms.

Authors:  Gabi Steinbach; Cristian Crisan; Siu Lung Ng; Brian K Hammer; Peter J Yunker
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8.  The inducible chemical-genetic fluorescent marker FAST outperforms classical fluorescent proteins in the quantitative reporting of bacterial biofilm dynamics.

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9.  Pseudomonas aeruginosa type IV minor pilins and PilY1 regulate virulence by modulating FimS-AlgR activity.

Authors:  Victoria A Marko; Sara L N Kilmury; Lesley T MacNeil; Lori L Burrows
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10.  Cyclic Diguanylate Regulates Virulence Factor Genes via Multiple Riboswitches in Clostridium difficile.

Authors:  Robert W McKee; Carissa K Harvest; Rita Tamayo
Journal:  mSphere       Date:  2018-10-24       Impact factor: 4.389

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