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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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Cyclic diguanylate monophosphate directly binds to human siderocalin and inhibits its antibacterial activity

TL;DR: It is shown that c-di-GMP can directly target the human LCN2 protein to inhibit its antibacterial activity and can significantly reduceLCN2-mediated inhibition on the in vitro growth of Escherichia coli.
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Spermine Inhibits Vibrio cholerae Biofilm Formation Through The NspS-MbaA Polyamine Signaling System

TL;DR: It is reported that spermine acts as an exogenous cue that inhibits V. cholerae biofilm formation through the NspS–MbaA signaling system, and a model is proposed illustrating how this system may communicate exogenous polyamine content to the cell to controlBiofilm formation in the aquatic environment and within the human intestine.
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Ligand-dependent ribozymes

TL;DR: The occurrence of ligand‐dependent ribozymes in nature and the many examples realized by researchers that engineered ligand-dependent catalytic RNA motifs are summarized.
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Microbiological Examination of Erwinia amylovora Exopolysaccharide Ooze

TL;DR: Ooze is identified as a source of large, concentrated populations of E. amylovora that emerged from the host by rupturing host tissue and is already primed for infection should they be dispersed from ooze to new infection courts.
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