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Open AccessJournal ArticleDOI

Cyclic di-GMP: the First 25 Years of a Universal Bacterial Second Messenger

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TLDR
A historic perspective on the development of the field is provided, common trends are emphasized, and new directions in c-di-GMP research are highlighted that will give a deeper understanding of this truly universal bacterial second messenger.
Abstract
SUMMARY Twenty-five years have passed since the discovery of cyclic dimeric (3′→5′) GMP (cyclic di-GMP or c-di-GMP). From the relative obscurity of an allosteric activator of a bacterial cellulose synthase, c-di-GMP has emerged as one of the most common and important bacterial second messengers. Cyclic di-GMP has been shown to regulate biofilm formation, motility, virulence, the cell cycle, differentiation, and other processes. Most c-di-GMP-dependent signaling pathways control the ability of bacteria to interact with abiotic surfaces or with other bacterial and eukaryotic cells. Cyclic di-GMP plays key roles in lifestyle changes of many bacteria, including transition from the motile to the sessile state, which aids in the establishment of multicellular biofilm communities, and from the virulent state in acute infections to the less virulent but more resilient state characteristic of chronic infectious diseases. From a practical standpoint, modulating c-di-GMP signaling pathways in bacteria could represent a new way of controlling formation and dispersal of biofilms in medical and industrial settings. Cyclic di-GMP participates in interkingdom signaling. It is recognized by mammalian immune systems as a uniquely bacterial molecule and therefore is considered a promising vaccine adjuvant. The purpose of this review is not to overview the whole body of data in the burgeoning field of c-di-GMP-dependent signaling. Instead, we provide a historic perspective on the development of the field, emphasize common trends, and illustrate them with the best available examples. We also identify unresolved questions and highlight new directions in c-di-GMP research that will give us a deeper understanding of this truly universal bacterial second messenger.

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Citations
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Journal ArticleDOI

The ever-expanding world of bacterial cyclic oligonucleotide second messengers.

TL;DR: In the past 15 years, three more cyclic dinucleotide (cdN) second messengers have been discovered: 3′−5′, 3′-5′ and 3′ −5′ cyclic di-GMP (c-di-AMP) as discussed by the authors.
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A Diguanylate Cyclase Acts as a Cell Division Inhibitor in a Two-Step Response to Reductive and Envelope Stresses

TL;DR: An unexpected second role is found for YfiN, a conserved diguanylate cyclase in Gram-negative bacteria, known to contribute to persistence in the host, that acts as a cell division inhibitor in response to envelope stress.
Journal ArticleDOI

Prospects for Anti-Biofilm Pharmaceuticals.

TL;DR: This commentary highlights several avenues currently being pursued in research labs to the development of new anti-biofilm pharmaceuticals, including discovering new antimicrobial agents that kill microorganisms in biofilms more effectively than do existing antibiotics.
Journal ArticleDOI

Thermoregulation of Biofilm Formation in Burkholderia pseudomallei Is Disrupted by Mutation of a Putative Diguanylate Cyclase.

TL;DR: Evaluating predicted cyclic di-GMP binding and metabolic proteins from Burkholderia pseudomallei 1026b concludes that a predicted hydrolase and a phosphodiesterase that modulate swimming motility were identified, in addition to a diguanylate cyclase thatmodulates biofilm formation and motility in response to temperature.
Book ChapterDOI

The Challenging World of Biofilm Physiology.

TL;DR: The highly complex nature and the rapid adaptability of the biofilm population impede understanding of the process of biofilm formation, but an important role for oxygen-binding proteins herein is clear.
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